KNUDSEN STEEN (DK)
DAHLEN ANNA ET AL: "Activation of the GLl oncogene through fusion with the beta-actin gene (ACTB) in a group of distinctive pericytic neoplasms - Pericytoma with t(7;12)", AMERICAN JOURNAL OF PATHOLOGY, vol. 164, no. 5, May 2004 (2004-05-01), pages 1645 - 1653, XP002494073, ISSN: 0002-9440
FOURNIER MARCIA V ET AL: "Gene expression signature in organized and growth-arrested mammary acini predicts good outcome in breast cancer", CANCER RESEARCH, vol. 66, no. 14, July 2006 (2006-07-01), pages 7095 - 7102, XP002494058, ISSN: 0008-5472
VEER VAN 'T L J ET AL: "Gene expression profiling predicts clinical outcome of breast cancer", NATURE, NATURE PUBLISHING GROUP, LONDON, UK, vol. 415, no. 6871, 31 January 2002 (2002-01-31), pages 530 - 536, XP002259781, ISSN: 0028-0836
What is claimed is:
CLAIMS
1. A method of determining sensitivity of a cancer patient to a treatment for cancer comprising measuring a level of expression of at least one gene in a cell of said patient, said gene selected from the group consisting of ACTB, ACTN4, ADA, ADAM9, ADAMTSl, ADDl, AFlQ, AIFl, AKAPl, AKAP13, AKRlCl, AKTl, ALDH2, ALDOC, ALG5, ALMSl, ALOXl 5B, AMIG02, AMPD2, AMPD3, ANAPC5, ANP32A, ANP32B, ANXAl, AP1G2, AP0BEC3B, APRT, ARHE, ARHGAP15, ARHGAP25, ARHGDIB, ARHGEF6, ARL7, ASAHl, ASPH, ATF3, ATIC, ATP2A2, ATP2A3, ATP5D, ATP5G2, ATP6V1B2, BC008967, BCATl, BCHE, BCLl IB, BDNF, BHLHB2, BIN2, BLMH, BMIl , BNIP3, BRDT, BRRNl, BTN3A3, Cl Iorf2, C14orfl39, C15orf25, C18orflO, Clorf24, Clorf29, Clorf38, ClQRl, C22orfl8, C6orf32, CACNAlG, CACNB3, CALMl , CALML4, CALU, CAP350, CASP2, CASP6, CASP7, CAST, CBLB, CCNA2, CCNBlIPl, CCND3, CCR7, CCR9, CDlA, CDlC, CDlD, CDlE, CD2, CD28, CD3D, CD3E, CD3G, CD3Z, CD44, CD47, CD59, CD6, CD63, CD8A, CD8B1, CD99, CDClO, CDC14B, CDHI l , CDH2, CDKL5, CDKN2A, CDW52, CECRl, CENPB, CENTBl , CENTG2, CEPl, CG018, CHRNA3, CHSl, CIAPINl, CKAP4, CKIP-I, CNP, COL4A1, COL5A2, COL6A1, COROl C, CRABPl, CRK, CRYl, CSDA, CTBPl, CTSC, CTSL, CUGBP2, CUTC, CXCLl, CXCR4, CXorf9, CYFIP2, CYLD, CYR61, DATFl, DAZAPl, DBNl, DBT, DCTNl, DDX18, DDX5, DGKA, DIAPHl, DKCl, DKFZP434J154, DKFZP564C186, DKFZP564G2022, DKFZp564J157, DKFZP564K0822, DNAJClO, DNAJC7, DNAPTP6, DOCKlO, D0CK2, DPAGTl , DPEP2, DPYSL3, DSIPI, DUSPl , DXS9879E, EEF1B2, EFNB2, EHD2, EIF5A, ELK3, ENO2, EPASl , EPB41L4B, ERCC2, ERG, ERP70, EVERl, EVI2A, EVL, EXTl, EZH2, F2R, FABP5, FAD 104, FAM46A, FAU, FCGR2A, FCGR2C, FER1L3, FHLl , FHODl , FKBPlA, FKBP9, FLJ10350, FLJ10539, FLJ10774, FLJ12270, FLJ13373, FLJ20859, FLJ21 159, FLJ22457, FLJ35036, FLJ46603, FLNC, FLOTl, FMNLl, FNBPl, FOLHl, FOXF2, FSCNl , FTL, FYB, FYN, G0S2, G6PD, GALIG, GALNT6, GATA2, GATA3, GFPTl, GIMAP5, GIT2, GJAl , GLRB, GLTSCR2, GLUL, GMDS, GNAQ, GNB2, GNB5, GOT2, GPR65, GPRASPl , GPSM3, GRP58, GSTM2, GTF3A, GTSEl, GZMA, GZMB, HlFO, Hl FX, H2AFX, H3F3A, HA-I , HEXB, HIC, HIST1H4C, HKl , HLA- A, HLA-B, HLA-DRA, HMGAl, HMGN2, HMMR, HNRPAl, HNRPD, HNRPM, HOXA9, HRMTlLl, HSA9761 , HSPA5, HSU79274, HTATSFl, ICAMl , ICAM2, IER3, IFI16, IFI44, IFITM2, IFITM3, IFRG28, IGFBP2, IGSF4, IL13RA2, IL21R, IL2RG, IL4R, IL6, IL6R, IL6ST, IL8, IMPDH2, INPP5D, INSIGl, IQGAPl, IQG AP2, IRS2, ITGA5, ITM2A, JARID2, JUNB, K-ALPHA-I, KHDRBSl, KIAA0355, KIAA0802, KIAA0877, KIAA0922, KIAA1078, KIAAl 128, KIAA1393, KIFCl , LAIRl, LAMBl, LAMB3, LAT, LBR, LCK, LCPl, LCP2, LEFl, LEPREl, LGALSl , LGALS9, LHFPL2, LNK, LOC54103, LOC55831, LOC81558, LOC94105, LONP, LOX, LOXL2, LPHN2, LPXN, LRMP, LRP12, LRRC5, LRRN3, LSTl, LTB, LUM, LY9, LY96, MAGEB2, MAL, MAPlB, MAP1LC3B, MAP4K1, MAPKl, MARCKS, MAZ, MCAM, MCLl, MCM5, MCM7, MDH2, MDNl, MEF2C, MFNG, MGCl 7330, MGC21654, MGC2744, MGC4083, MGC8721, MGC8902, MGLL, MLPH, MPHOSPH6, MPPl, MPZLl, MRP63, MRPS2, MTlE, MTlK, MUFl , MVP, MYB, MYL9, MYOlB, NAPlLl, NAPl L2, NARF, NASP, NCOR2, NDN, NDUFABl, NDUFS6, NFKBIA, NID2, NIPA2, NME4, NME7, NNMT, NOL5A, NOL8, NOMO2, NOTCHl, NPCl, NQOl, NR1D2, NUDC, NUP210, NUP88, NVL, NXFl , OBFCl, OCRL, OGT, OXAlL, P2RX5, P4HA1, PACAP, PAF53, PAFAH1B3, PALM2- AKAP2, PAX6, PCBP2, PCCB, PFDN5, PFNl, PFN2, PGAMl, PHEMX, PHLDAl, PIM2, PITPNCl, PLAC8, PLAGLl, PLAUR, PLCBl, PLEK2, PLEKHCl, PLOD2, PLSCRl, PNAS-4, PNMA2, POLR2F, PPAP2B, PRFl, PRGl , PRIMl, PRKCH, PRKCQ, PRKD2, PRNP, PRP19, PRPF8, PRSS23, PSCDBP, PSMB9, PSMC3, PSME2, PTGER4, PTGES2, PTOVl, PTP4A3, PTPN7, PTPNSl, PTRF, PURA, PWPl, PYGL, QKI, RAB3GAP, RAB7L1, RAB9P40, RAC2, RAFTLIN, RAG2, RAPlB, RASGRP2, RBPMS, RCNl, RFC3, RFC5, RGC32, RGS3, RHOH, RIMS3, RI0K3, RIPK2, RISl, RNASE6, RNF144, RPLlO, RPLlOA, RPL12, RPL13A, RPL17, RPL18, RPL36A, RPLPO, RPLP2, RPS15, RPS19, RPS2, RPS4X, RPS4Y1 , RRAS, RRAS2, RRBPl, RRM2, RUNXl, RUNX3, S100A4, SART3, SATBl , SCAPl , SCARBl, SCN3A, SEC31L2, SEC61G, SELL, SELPLG, SEMA4G, SEPTlO, SEPT6, SERPINAl , SERPINBl, SERPINB6, SFRS5, SFRS6, SFRS7, SH2D1A, SH3GL3, SH3TC1 , SHDl, SHMT2, SIATl , SKBl, SKP2, SLA, SLC1A4, SLC20A1, SLC25A15, SLC25A5, SLC39A14, SLC39A6, SLC43A3, SLC4A2, SLC7A1 1 , SLC7A6, SMAD3, SMOX, SNRPA, SNRPB, SOD2, SOX4, SP140, SPANXC, SPIl , SRF, SRM, SSA2, SSBP2, SSRPl, SSSCAl, STAG3, STATl , STAT4, STAT5A, STCl , STC2, STOML2, T3JAM, TACCl, TACC3, TAF5, TALI, TAPl, TARP, TBCA, TCF 12, TCF4, TFDP2, TFPI, TIMM 17 A, TIMPl, TJPl, TK2, TM4SF1, TM4SF2, TM4SF8, TM6SF1, TMEM2, TMEM22, TMSBlO, TMSNB, TNFAIP3, TNFAIP8, TNFRSFlOB, TNFRSFlA, TNFRSF7, TNIK, TNPOl, TOBl, TOMM20, TOX, TPKl, TPM2, TRA@, TRAl, TRAM2, TRB@, TRD@, TRIM, TRIM14, TRIM22, TRIM28, TRIPl 3, TRPV2, TUBGCP3, TUSC3, TXN, TXNDC5, UBASH3A, UBE2A, UBE2L6, UBE2S, UCHLl, UCK2, UCP2, UFDlL, UGDH, ULK2, UMPS, UNG, USP34, USP4, VASP, VAVl, VLDLR, VWF, WASPIP, WBSCR20A, WBSCR20C, WHSCl, WNT5A, ZAP70, ZFP36L1, ZNF32, ZNF335, ZNF593, ZNFNlAl, and ZYX, wherein said level of expression of said gene indicates said cell is sensitive to said treatment.
2. The method of claim 1, wherein said at least one gene is selected from the group consisting of RPS4X, S100A4, NDUFS6, C14orfl39, SLC25A5, RPLlO, RPL12, EIF5A, RPL36A, BLMH, CTBPl, TBCA, MDH2, and DXS9879E, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of UBB, B2M, MANlAl , and SUIl, or wherein the method further comprises measuring a level of at least one microRNA selected from the group consisting of Hcd892, Hcd678, hsa-mir-007-l-prec, MPR243, Hcd654, hsa-mir-487, Hcd794, Hcd739, and Hcd562, wherein said level of expression of said gene or said level of said microRNA indicates that said cell is sensitive to Vincristine.
3. The method of claim 1, wherein said at least one gene is selected from the group consisting of ClQRl, SLA, PTPN7, ZNFNlAl , CENTBl, IFI 16, ARHGEF6, SEC31 L2, CD3Z, GZMB, CD3D, MAP4K1, GPR65, PRFl, ARHGAPl 5, TM6SF1 , and TCF4, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of HCLSl, CD53, PTPRCAP, and PTPRC, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of HUMTRF, HPRl 87, hsa- mir-450-1 , hsa-mir-155-prec, hsa-mir-515-15p, hsa-mir-181b-prec, hsa-mir-124a-l- precl, hsa-mir-450-2, Hcd923, hsa-mir-342, hsa-mir-142-prec, hsa-mir-223-prec, Hcd754, and Hcd213_HPR182, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Cisplatin.
4. The method of claim 1, wherein said at least one gene is selected from the group consisting of SRM, SCARBl, SIATl, CUGBP2, ICAMl, WASPIP, ITM2A, PALM2- AKAP2, PTPNSl, MPPl, LNK, FCGR2A, RUNX3, EVI2A, BTN3A3, LCP2, BCHE, LY96, LCPl, IFI 16, MCAM, MEF2C, SLC1A4, FYN, ClorOδ, CHSl, FCGR2C, TNIK, AMPD2, SEPT6, RAFTLIN, SLC43A3, RAC2, LPXN, CKIP-I , FLJ10539, FLJ35036, DOCKlO, TRPV2, IFRG28, LEFl, and ADAMTSl, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of MSN, SPARC, VIM, GAS7, ANPEP, EMP3, BTN3A2, FNl , and CAPN3, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of MPRl 21, HUMTRS, hsa- mir-213-prec, hsa-mir-155-prec, hsa-mir-147-prec, hsa-mir-100, hsa-mir-138-l-prec, hsa-mir-140, hsa-mir-146-prec, hsa-mir-509, hsa-mir-146b, Hcd514, Hcd397, Hcd731, hsa-mir-034-prec, and hsa-mir-lOO-l/2-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Azaguanine.
5. The method of claim 1, wherein said at least one gene is selected from the group consisting of CD99, INSIGl , PRGl, MUFl , SLA, SSBP2, GNB5, MFNG, PSMB9, EVI2A, PTPN7, PTGER4, CXorf9, ZNFNl Al , CENTBl, NAPlLl, HLA-DRA, IFIl 6, ARHGEF6, PSCDBP, SELPLG, LAT, SEC31L2, CD3Z, SH2D1A, GZMB, SCN3A, RAFTLIN, D0CK2, CD3D, RAC2, ZAP70, GPR65, PRFl, ARHGAPl 5, NOTCHl , and UBASH3A, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of LAPTM5, HCLSl , CD53, GMFG, PTPRCAP, PTPRC, COROlA, and ITK, or wherein the method further comprises measuring a level of expression of at least one micro RNA selected from the group consisting of Hcd415, Hcd768, HUMTRF, Hcd866, Hcdl45, HUMTRAB, Hcd913, HPR163, Hcd697, Hcd755, Hcd716, MPR207, HSTRNL, HPR206, MPR243, Hcd654, MPRl 30, Hcd782, Hcd794, Hcd739, hsa-mir-142-prec, HSHELAOl , HUMTRVlA, and Hcd754, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Etoposide.
6. The method of claim 1, wherein said at least one gene is selected from the group consisting of CD99, ALDOC, SLA, SSBP2, IL2RG, CXorf9, RHOH, ZNFNlAl, CENTBl, CDlC, MAP4K1, CD3G, CCR9, CXCR4, ARHGEF6, SELPLG, LAT, SEC31L2, CD3Z, SH2D1A, CDlA, LAIRl, TRB@, CD3D, WBSCR20C, ZAP70, IFI44, GPR65, AIFl, ARHGAP15, NARF, and PACAP, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of LAPTM5, HCLSl, CD53, GMFG, PTPRCAP, TCF7, CDlB, PTPRC, COROlA, HEMl, and ITK, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of Hcd768, hsa-mir-483, Hcdl45, hsa-mir-197-prec, hsa-mir-212-prec, HPR163, Hcd654, hsa-mir- 342, Hcd794, hsa-mir-142-prec, and Hcd754, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Adriamycin.
7. The method of claim 1, wherein said at least one gene is selected from the group consisting of RPL12, RPLP2, MYB, ZNFNlAl, SCAPl, STAT4, SP140, AMPD3, TNFAIP8, DDXl 8, TAF5, RPS2, DOCK2, GPR65, H0XA9, FLJ12270, and HNRPD, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of RPL32, FBL, and PTPRC, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-096-prec-7, Hcd605, hsa-mir-007-2-prec, hsa-mir-019b-2-prec, MPR216, hsa-mir-019b-l-prec, hsa- mir-135-2-prec, HSTRNL, hsa-mir-025-prec, hsa-mir-007-l-prec, hsa-mir-019a-prec, hsa-mir-380-5p, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir-142-prec, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Aclarubicin.
8. The method of claim 1, wherein said at least one gene is selected from the group consisting of PGAMl, DPYSL3, INSIGl , GJAl, BNIP3, PRGl , G6PD, PLOD2, LOXL2, SSBP2, Clorf29, TOX, STCl, TNFRSFlA, NC0R2, NAPlLl, LOC94105, ARHGEF6, GATA3, TFPI, LAT, CD3Z, AFlQ, MAPlB, TRIM22, CD3D, BCATl , IFI44, CUTC, NAPl L2, NME7, FLJ21 159, and COL5A2, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of BASPl, COL6A2, PTPRC, PRKCA, CCL2, and RAB31, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of Hcd768, HUMTRF, hsa-mir-213-prec, hsa-mir-181b-prec, MPR244, hsa-mir-409-3p, HSTRNL, hsa-mir-382, hsa-mir-342, hsa-mir-142-prec, and Hcd200, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Mitoxantrone.
9. The method of claim 1, wherein said at least one gene is selected from the group consisting of STCl , GPR65, DOCKlO, COL5A2, FAM46A, and LOC54103, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of HUMTRF, Hcdl48_HPR2251eft, Hcd938, MPRl 74, and hsa-mir-4323p, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Mitomycin.
10. The method of claim 1, wherein said at least one gene is selected from the group consisting of RPLlO, RPS4X, NUDC, DKCl , DKFZP564C 186, PRP19, RAB9P40, HSA9761 , GMDS, CEPl, IL13RA2, MAGEB2, HMGN2, ALMSl, GPR65, FLJ 10774, NOL8, DAZAPl, SLC25A15, PAF53, DXS9879E, PITPNCl, SPANXC, and
KIAAl 393, or wherein the method further comprises measuring a level of expression of RALY, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-096-prec-7, hsa-mir-l Ol-prec-9, hsa-mir-20b, hsa-mir-019b-2-prec, hsa-mir- 032-prec, MPR156, hsa-mir-019b- 1-prec, hsa-mir-135-2-prec, hsa-mir-025-prec, hsa- mir-007-l-prec, hsa-mir-361, hsa-mir-093-prec-7.1=093-1 , hsa-mir- 106-prec-X, hsa- mir-098-prec-X, hsa-mir- 142-prec, HPRl 69, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Paclitaxel.
1 1. The method of claim 1 , wherein said at least one gene is selected from the group consisting of PFNl, PGAMl, K-ALPHA-I, CSDA, UCHLl , PWPl, PALM2-AKAP2, TNFRSFlA, ATP5G2, AFlQ, NME4, and FHODl , or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir- 123-prec, Hcd257, hsa-mir- 155-prec, ath-MIR180a, Hcd448, HSTRNL, MPRl 74, Hcd200, hsa-mir-4323p, and HPR244, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Gemcitabine.
12. The method of claim 1, wherein said at least one gene is selected from the group consisting of ANP32B, GTF3A, RRM2, TRIM 14, SKP2, TRIP13, RFC3, CASP7, TXN, MCM5, PTGES2, OBFCl , EPB41L4B, and CALML4, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-096-prec-7, hsa-mir-095-prec-4, HSTRNL, and hsa-mir-007-l-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Taxotere.
13. The method of claim 1 , wherein said at least one gene is selected from the group consisting of IFITM2, UBE2L6, USP4, ITM2A, IL2RG, GPRASPl, PTPN7, CXorf9, RHOH, GIT2, ZNFNlAl, CEPl , TNFRSF7, MAP4K1 , CCR7, CD3G, ATP2A3, UCP2, GATA3, CDKN2A, TARP, LAIRl, SH2D1A, SEPT6, HA-I , ERCC2, CD3D, LSTl, AIFl, ADA, DATFl, ARHGAP15, PLAC8, CECRl , LOC81558, and EHD2, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of LAPTM5, ITGB2, ANPEP, CD53, CD37, AD0RA2A, GNA15, PTPRC, COROlA, HEMl, FLII, and CREB3L1, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of MPR141 , hsa-mir-424, Hcd690, Hcd783, hsa-mir- 150-prec, Hcd266, hsa-mir-503, hsa-mir-128b-prec, Hcd397, and hsa-mir-484, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Dexamethasone.
14. The method of claim 1 , wherein said at least one gene is selected from the group consisting of ITM2A, RHOH, PRIMl, CENTBl, NAPlLl, ATP5G2, GATA3, PRKCQ, SH2D1A, SEPT6, NME4, CD3D, CDlE, ADA, and FHODl, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of GNAl 5, PTPRC, and RPL13, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of HUMTRF, hsa-mir-155-prec, hsa-mir-515-15p, Hcd938, Hcd642, Hcdl20, hsa-mir-380-5p, hsa-mir-342, hsa-mir-142-prec, hsa-mir-223-prec, and hsa-mir-4323p, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Ara-C.
15. The method of claim 1 , wherein said at least one gene is selected from the group consisting of CD99, ARHGDIB, VWF, ITM2A, LGALS9, INPP5D, SATBl, TFDP2, SLA, IL2RG, MFNG, SELL, CDW52, LRMP, ICAM2, RIMS3, PTPN7, ARHGAP25, LCK, CXorrø, RHOH, GIT2, ZNFNlAl , CENTBl , LCP2, SPIl, GZMA, CEPl, CD8A, SCAPl , CD2, CDlC, TNFRSF7, VAVl , MAP4K1, CCR7, C6orf32, ALOXl 5B, BRDT, CD3G, LTB, ATP2A3, NVL, RASGRP2, LCPl, CXCR4, PRKD2, GATA3, TRA@, KIAA0922, TARP, SEC31L2, PRKCQ, SH2D1A, CHRN A3, CDlA, LSTl, LAIRl, CACNAlG, TRB@, SEPT6, HA-I, D0CK2, CD3D, TRD@, T3JAM, FNBPl, CD6, AIFl , FOLHl , CDlE, LY9, ADA, CDKL5, TRIM, EVL, DATFl, RGC32, PRKCH, ARHGAP15, NOTCHl, BIN2, SEMA4G, DPEP2, CECRl,
BCLl IB, STAG3, GALNT6, UBASH3A, PHEMX, FLJ 13373, LEFl, IL21R, MGCl 7330, AKAP13, ZNF335, and GIMAP5, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of SRRMl , LAPTM 5, ITGB2, CD53, CD37, GMFG, PTPRCAP, GNAl 5, BLM, PTPRC, COROlA, PRKCBl, HEMl, and UGT2B17, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of Hcd544, hsa-mir-181c-prec, Hcd517, MPR151 , hsa-mir- 213-prec, hsa-mir-181b-prec, hsa-mir-150-prec, hsa-mir-153-l-precl , hsa-mir-128b- prec, Hcd812, hsa-mir-195-prec, hsa-mir-342, hsa-mir-370, hsa-mir-142-prec, hsa-mir- 223-prec, and hsa-mir-484, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Methylprednisolone.
16. The method of claim 1, wherein said at least one gene is selected from the group consisting of PRPF8, RPL18, GOT2, RPL13A, RPS15, RPLP2, CSDA, KHDRBSl , SNRPA, IMPDH2, RPS 19, NUP88, ATP5D, PCBP2, ZNF593, HSU79274, PRIMl, PFDN5, OXAlL, H3F3A, ATIC, CIAPINl, RPS2, PCCB, SHMT2, RPLPO, HNRPAl, STOML2, SKBl, GLTSCR2, CCNBlIPl, MRPS2, FLJ20859, and FLJ 12270, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of RNPSl, RPL32, EEFlG, PTMA, RPL13, FBL, RBMX, and RPS9, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir- 092-prec-X=092-2, hsa-mir-096-prec-7, hsa-mir-123-prec, Hcd250, hsa-mir-518e, HPR232, Hcd263, hsa-mir-516-33p, Hcd605, Hcd373, MPR254, MPR215, HUMTRF, hsa-mir-106a, hsa-mir-20b, Hcd361, Hcd412, Hcd781, hsa-mir-019b-2-prec, HPR214, Hcd807, Hcd817, Hcd788, Hcd970, Hcdl48_HPR2251eft, HcdlO2, Hcd246, HPR199, HPR233, Hcd383, MPR224, HPR172, MPR216, hsa-mir-321, Hcd586, Hcd587, Hcd249, Hcd279, HPR159, Hcd689, Hcd691, hsa-mir-019b-l-prec, Hcd413, Hcd581, Hcd536_HPR104, Hcd230, HPRl 54, Hcd270, Hcd649, Hcd889, Hcd938, HPR266, hsa-mir-025-prec, Hcd355_HPR190, MPRl 62, Hcd923, MPR237, MPRl 74, hsa-mir- 019a-prec, hsa_mir_490_Hcd20, hsa-mir-380-5p, hsa-mir-093-prec-7.1=093-l , hsa- mir-106-prec-X, Hcd627, hsa-mir-142-prec, HPRl 69, hsa-mir-OOlb-2-prec, hsa-mir- 018-prec, hsa-mir-020-prec, Hcd404, hsa-mir-384, and hsa-mir-4323p, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Methotrexate.
17. The method of claim 1, wherein said at least one gene is selected from the group consisting of PFNl, HKl , MCLl, ZYX, RAPlB, GNB2, EPASl, PGAMl, CKAP4, DUSPl , MYL9, K-ALPHA-I , LGALSl , CSDA, IFITM2, ITGA5, DPYSL3, JUNB, NFKBIA, LAMBl, FHLl , INSIGl , TIMPl, GJAl, PSME2, PRGl , EXTl, DKFZP434J154, MVP, VASP, ARL7, NNMT, TAPl , PLOD2, ATF3, PALM2- AKAP2, IL8, LOXL2, IL4R, DGKA, STC2, SEC61G, RGS3, F2R, TPM2, PSMB9, LOX, STCl, PTGER4, IL6, SMAD3, WNT5A, BDNF, TNFRSFlA, FLNC, DKFZP564K0822, FLOTl , PTRF, HLA-B, MGC4083, TNFRSFlOB, PLAGLl, PNM A2, TFPI, LAT, GZMB, CYR61, PLAUR, FSCNl, ERP70, AFlQ, HIC, COL6A1, IFITM3, MAPlB, FLJ46603, RAFTLIN, RRAS, FTL, KIAA0877, MTlE, CDClO, D0CK2, TRIM22, RISl, BCATl , PRFl, DBNl, MTl K, TMSBlO, FLJ10350, Clorf24, NME7, TMEM22, TPKl, COL5A2, ELK3, CYLD, ADAMTSl, EHD2, and ACTB, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of MSN, ACTR2, AKRlBl , VIM, ITGA3, OPTN, M6PRBP1, COLlAl, BASPl, ANPEP, TGFBl, NFIL3, NK4, CSPG2, PLAU, COL6A2, UBC, FGFRl, BAX, COL4A2, and RAB31 , or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-376a, hsa-mir-155-prec, hsa-mir-409-3p, hsa-mir- 495, Hcd498, hsa-mir-199a-2-prec, hsa-mir-382, HPR271, hsa-mir-145-prec, and hsa- mir-199a-l-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Bleomycin.
18. The method of claim 1 , wherein said at least one gene is selected from the group consisting of SSRPl , NUDC, CTSC, AP1G2, PSME2, LBR, EFNB2, SERPINAl, SSSCAl , EZH2, MYB, PRIMl, H2AFX, HMGAl, HMMR, TK2, WHSCl, DIAPHl, LAMB3, DPAGTl , UCK2, SERPINBl , MDNl , BRRNl , G0S2, RAC2, MGC21654, GTSEl, TACC3, PLEK2, PLAC8, HNRPD, and PNAS-4, or wherein the method further comprises measuring the level of expression of PTMA, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-lOl -prec-9, hsa-mir- 144-prec, hsa-mir-519a-l, hsa-mir-519b, hsa-mir-015b-prec, hsa-mir-106a, hsa-mir-16- 1 , hsa-mir-181d, hsa-mir-017-prec, hsa-mir-019b-2-prec, hsa-mir-192, hsa-mir-213- prec, hsa-mir-215-prec, hsa-mir-107, hsa-mir-200b, hsa-mir-103-prec-5= 103-1 , hsa- mir-519a-l/526c, MPR216, hsa-mir-019b-l-prec, hsa-mir-107-prec-lO, hsa-mir-135-2- prec, hsa-mir-103-2-prec, hsa-mir-519a-2, hsa-mir-025-prec, hsa-mir-16-2, MPR95, hsa-mir-016b-chr3, Hcd948, hsa-mir-195-prec, hsa-mir-093-prec-7.1=093-1 , hsa-mir- 106-prec-X, hsa-mir-142-prec, hsa-mir-519c/526c, hsa-mir-200a-prec, hsa-mir-016a- chrl3, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Methyl-GAG.
19. The method of claim 1, wherein said at least one gene is selected from the group consisting of ITGA5, TNFAIP3, WNT5A, FOXF2, LOC94105, IFI 16, LRRN3, DOCKlO, LEPREl, COL5A2, and ADAMTSl, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of MSN, VIM, CSPG2, and FGFRl, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of Hcd829, HUMTRF, HPR187, Hcd210_HPR205, hsa-mir-379, hsa- mir-213-prec, hsa-mir-4325p, hsa-mir-450-1, hsa-mir-155-prec, Hcd28_HPR39right, MPR244, hsa-mir-409-3p, hsa-mir-124a- 1 -prec 1 , hsa-mir-154-precl , hsa-mir-495, hsa- mir-515-23p, Hcd43 8right, Hcd770; hsa-mir-382, hsa-mir-223-prec, Hcd754, and Hcd213_HPR182, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Carboplatin.
20. The method of claim 1, wherein said at least one gene is selected from the group consisting of RPL 18, RPLlOA, ANAPC5, EEF 1B2, RPLl 3 A, RPSl 5, AKAPl, NDUFABl , APRT, ZNF593, MRP63, IL6R, SART3, UCK2, RPLl 7, RPS2, PCCB, TOMM20, SHMT2, RPLPO, GTF3A, STOML2, DKFZp564J157, MRPS2, ALG5, and CALML4, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of RNPSl, RPLl 3, RPS6, and RPL3, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-096-prec-7, hsa-mir- 429, Hcd693, HPR214, Hcd586, Hcd249, Hcd689, hsa-mir-194-2, Hcd581, Hcd270, hsa-mir-025-prec, Hcd340, hsa-mir-007-l-prec, hsa-mir-093-prec-7.1=093-1 , hsa-mir- 106-prec-X, Hcd794, hsa-mir-020-prec, and hsa-mir-4323p, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to 5-FU (5- Fluorouracil).
21. The method of claim 1 , wherein said at least one gene is selected from the group consisting of KIFCl , VLDLR, RUNXl , P AF AHl B3, HlFX, RNF 144, TMSNB, CRYl , MAZ, SLA, SRF, UMPS, CD3Z, PRKCQ, HNRPM, ZAP70, ADDl , RFC5, TM4SF2, PFN2, BMIl, TUBGCP3, ATP6V1B2, CDlD, ADA, CD99, CD2, CNP, ERG, CD3E, CDlA, PSMC3, RPS4Y1, AKTl , TALI, UBE2A, TCF12, UBE2S, CCND3, PAX6, RAG2, GSTM2, SATBl, NASP, IGFBP2, CDH2, CRABPl, DBNl, AKRlCl, CACNB3, CASP2, CASP2, LCP2, CASP6, MYB, SFRS6, GLRB, NDN, GNAQ, TUSC3, GNAQ, JARID2, OCRL, FHLl, EZH2, SMOX, SLC4A2, UFDlL, ZNF32, HTATSFl, SHDl, PTOVl, NXFl, FYB, TRIM28, BC008967, TRB@, HlFO 5 CD3D, CD3G, CENPB, ALDH2, ANXAl, H2AFX, CDlE, DDX5, CCNA2, ENO2, SNRPB, GATA3, RRM2, GLUL, SOX4, MAL, UNG, ARHGDIB, RUNXl , MPH0SPH6, DCTNl , SH3GL3, PLEKHCl, CD47, POLR2F, RHOH, and ADDl , or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of ITK, RALY, PSMC5, MYL6, CDlB, STMNl, GNAl 5, MDK, CAPG, ACTNl, CTNNAl, FARSLA, E2F4, CPSFl, SEPWl, TFRC, ABLl , TCF7, FGFRl, NUCB2, SMA3, FAT, VIM, and ATP2A3, wherein said level of expression of said gene indicates that said cell is sensitive to Rituximab.
22. The method of claim 1 , wherein said at least one gene is selected from the group consisting of TRAl , ACTN4, CALMl, CD63, FKBPlA, CALU, IQGAPl , MGC8721 , STATl , TACCl, TM4SF8, CD59, CKAP4, DUSPl, RCNl, MGC8902, LGALSl, BHLHB2, RRBPl, PRNP, IER3, MARCKS, LUM, FER1L3, SLC20A1 , HEXB, EXTl, TJPl, CTSL, SLC39A6, RI0K3, CRK, NNMT, TRAM2, ADAM9, DNAJC7, PLSCRl, PRSS23, PLOD2, NPCl, TOBl , GFPTl , IL8, PYGL, L0XL2, KIAA0355, UGDH, PURA, ULK2, CENTG2, NID2, CAP350, CXCLl , BTN3A3, IL6, WNT5A, F0XF2, LPHN2, CDHl 1, P4HA1, GRP58, DSIPI, MAP1LC3B, GALIG, IGSF4, IRS2, ATP2A2, OGT, TNFRSFlOB, KIAAl 128, TM4SF1, RBPMS, RIPK2, CBLB, NRl D2, SLC7A1 1, MPZLl, SSA2, NQOl, ASPH, ASAHl, MGLL, SERPINB6, HSPA5, ZFP36L1, COL4A1 , CD44, SLC39A14, NIPA2, FKBP9, IL6ST, DKFZP564G2022, PPAP2B, MAPlB, MAPKl , MYOlB, CAST, RRAS2, QKI, LHFPL2, 38970, ARHE, KIAA 1078, FTL, KIAA0877, PLCBl, KIAA0802, RAB3GAP, SERPINBl, TIMM 17A, SOD2, HLA-A, NOMO2, LOC55831 , PHLDAl, TMEM2, MLPH, FAD104, LRRC5, RAB7L1, FLJ35036, DOCKlO, LRP12, TXNDC5, CDC14B, HRMTlLl, COROlC, DNAJClO, TNPOl, LONP, AMIGO2, DNAPTP6, and ADAMTS 1 , or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of WARS, CD81, CTSB, PKM2, PPP2CB, CNN3, ANXA2, JAKl, EIF4G3, COLlAl, DYRK2, NFIL3, ACTNl, CAPN2, BTN3A2, IGFBP3, FNl, COL4A2, and KPNBl, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-136-prec, Hcd570, Hcd873, Hcd282PO, Hcd799, Hcd829, Hcd210_HPR205, hsa-mir-219-prec, hsa-mir-202, hsa-mir-429, Hcd693, hsa- mir-022-prec, MPR88, hsa-mir-198-prec, hsa-mir-199b-prec, Hcdl45, hsa-mir- 124a-2- prec, hsa-mir- 138-2-prec, Hcd960, Hcd869, Hcd384, hsa-mir-027b-prec, Hcd444, hsa- mir-194-2, hsa-mir- 197-prec, Hcd913, HPR163, hsa-mir- 138- 1-prec, hsa-mir-OlOa- prec, hsa-mir-023b-prec, hsa-mir- 193b, Hcd654, Hcd542, hsa-mir- 199a-2-prec, hsa- mir-214-prec, Hcd608, Hcd684, hsa-mir- 145-prec, hsa-mir-023a-prec, hsa-mir-024-2- prec, and hsa-mir- 199a- 1 -prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to radiation therapy.
23. The method of claim 1, wherein said at least one gene is selected from the group consisting of FAU, N0L5A, ANP32A, ARHGDIB, LBR, FABP5, ITM2A, SFRS5, IQGAP2, SLC7A6, SLA, IL2RG, MFNG, GPSM3, PIM2, EVERl, LRMP, ICAM2, RIMS3, FMNLl, MYB, PTPN7, LCK, CXorf9, RHOH, ZNFNlAl , CENTBl, LCP2, DBT, CEPl , IL6R, VAVl, MAP4K1, CD28, PTP4A3, CD3G, LTB, USP34, NVL, CD8B1 , SFRS6, LCPl , CXCR4, PSCDBP, SELPLG, CD3Z, PRKCQ, CDlA, GAT A2, P2RX5, LAIRl , Clorf38, SH2D1A, TRB@, SEPT6, HA-I, DOCK2, WBSCR20C, CD3D, RNASE6, SFRS7, WBSCR20A, NUP210, CD6, HNRPAl, AIFl, CYFIP2, GLTSCR2, Cl lorf2, ARHGAP15, BIN2, SH3TC1, STAG3, TM6SF1, C15orf25, FLJ22457, PACAP, and MGC2744, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-123-prec, hsa-mir-106a, hsa-mir-20b, hsa-mir-017-prec, hsa-mir-019b-2-prec, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1, hsa-mir-122a-prec, Hcd783, MPR216, hsa-mir-019b-l-prec, hsa-mir-135-2-prec, hsa- mir-128b-prec, hsa-mir-025-prec, Hcd511, hsa-mir-093-prec-7.1=093-1, hsa-mir-106- prec-X, hsa-mir-142-prec, HPRl 69, hsa-mir-223-prec, hsa-mir-018-prec, and hsa-mir- 020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to PXDlOl (belinostat).
24. The method of claim 1, wherein said at least one gene is selected from the group consisting of CD99, SNRPA, CUGBP2, STAT5A, SLA, IL2RG, GTSEl, MYB, PTPN7, CXorf9, RHOH, ZNFNlAl, CENTBl , LCP2, HIST1H4C, CCR7, APOBEC3B, MCM7, LCPl, SELPLG, CD3Z, PRKCQ, GZMB, SCN3A, LAIRl, SH2D1A, SEPT6, CGOl 8, CD3D, C18orflO, PRFl, AIFl, MCM5, LPXN, C22orfl8, ARHGAPl 5, and LEFl , or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir- 096-prec-7, Hcd605, hsa-mir-20b, hsa-miR-373*, HUMTRAB, hsa-mir-019b- 1-prec, HPR163, hsa-mir-371, hsa-mir-025-prec, hsa-mir-18b, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir-142-prec, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to 5-Aza-2'- deoxycytidine (Decitabine).
25. The method of claim 1 , wherein said at least one gene is selected from the group consisting of SLC9A3R1, RPS 19, ITM2A, SSBP2, CXorf9, RHOH, ZNFNlAl , FXYD2, CCR9, NAPlLl, CXCR4, SH2D1A, CDlA, TRB@, SEPT6, RPS2, DOCK2, CD3D, CD6, ZAP70, AIFl, CDlE, CYFIP2, ADA, TRIM, GLTSCR2, FLJ10858, BCLl IB, GIMAP6, STAG3, UBASH3A or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of MRPS24, TRIM22, TRIM41, LAT, CDlC, MRPS22, ADAMI l, RPL13, RPS27, RPL13, RPS25, RPL18A, COROlA, PTPRCAP, GMFG, ITK, CDlB, GMFG, PTPRCAP, COROlA, ITGB2, HCLSl , and ATP2A3, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of HUMTRF, hsa-mir-483, MPR74, hsa-mir- 122a-prec, ath-MIR180a, hsa-mir-128b-prec, Hcd923, hsa-mir- 106-prec-X, hsa-mir-342, hsa-mir- 142-prec, HPRl 69, hsa-mir-223-prec, Hcd754, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Idarubicin.
26. The method of claim 1, wherein said at least one gene is selected from the group consisting of CD99, HLA-DPBl, ARHGDIB, IFITMl, UBE2L6, ITM2A, SERPINAl, STAT5A, INPP5D, DGKA, SATBl, SEMA4D, TFDP2, SLA, IL2RG, CD48, MFNG, AL0X5AP, GPSM3, PSMB9, KIAA071 1, SELL, ADA, EDGl, RIMS3, FMNLl , MYB, PTPN7, LCK, CXorf9, RHOH, ZNFNlAl, CENTBl, LCP2, FXYD2, CDlD, BATF, STAT4, VAVl, MAP4K1, CCR7, PDE4C, CD3G, CCR9, SPl 10, LCPl, IFI16, CXCR4, ARHGEF6, GAT A3, SELPLG, SEC31L2, CD3Z, PRKCQ, SH2D1A, GZMB, CDlA, SCN3A, LAIRl, FYB, TRB@, SEPT6, HA-I, DOCK2, CGOl 8, CD3D, T3JAM, FNBPl, CD6, ZAP70, LSTl, GPR65, PRFl, AIFl, FLJ20331, RAG2, WDR45, CDlE, CYFIP2, TARP, TRIM, RPLlOL, GLTSCR2, GIMAP5, ARHGAP15, NOTCHl, BIN2, C13orfl8, CECRl, BCLl IB, GIMAP6, STAG3, TM6SF1, HSDl 7B7, UBASH3A, MGC5566, FLJ22457, TPKl, PHFl 1, and DKFZP434B0335, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of FLJ 10534, PTPRC, TRIM22, C18orfl , EVL, TRIM41, PSME2, LAT, CDlC, MYBBPlA, ICAM3, ADAMl 1, CD53, FARSLA, RPL13, RAC2, RPL13, GNA15, PGF, LAPTM5, RPL18A, CD53, COROlA, PTPRCAP, PTPRC, HEMl, GMFG, GNAl 5, ITK, CDlB, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl , GNA15, TCF7, ITGB2, PTPRC, HCLSl, ATP2A3, MYBLl , and FARSLA, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir- 124a-3-prec, hsa-mir-181a-prec, Hcd773, Hcd683, Hcd796, HUMTRF, HUMTRS, hsa- mir-181b-2, Hcd294, hsa-mir-20b, hsa-mir-181d, hsa-mir-213-prec, Hcdl48_HPR2251eft, hsa-mir-515-15p, hsa-mir-181b-prec, Hcd783, HUMTRAB, HUMTRN, hsa-mir-181b-l, hsa-mir-124a-l-precl, hsa-mir-367, hsa-mir-128b-prec, Hcd43 8right, hsa-mir-025-prec, hsa-mir-216-prec, Hcd731 , hsa-mir-093-prec-7.1=093- 1, hsa-mir-106-prec-X, hsa-mir-342, hsa-mir-142-prec, HSHELAOl, HUMTRVlA, hsa-mir-223-prec, Hcd754, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Melphalan.
27. The method of claim 1 , wherein said at least one gene is selected from the group consisting of MCLl, DDX23, JUNB, ZFP36, IFITMl, CKSlB, SERPINAl, IL4R, CLDN3, ARL4A, HMMR, FLJ 12671, ANKHDl, KIF2C, RPA3, MCCC2, CDH17, LSM5, PRFl, RODl, FLJ12666, SUV420H1, MUC13, C13orfl8, and CDCA8, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of ETS2, ARIDlA, IDl, DDC, NID2, CCT3, ID2, NFIL3, and AREG, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of Hcd829, hsa-mir-197-prec, HPRl 63, and hsa-mir-150-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to IL4-PE38 fusion protein.
28. The method of claim 1 , wherein said at least one gene is selected from the group consisting of MCLl , DDX23, JUNB, ZFP36, IFITMl, CKSlB, SERPINAl, IL13R, CLDN3, ARL4A, HMMR, FLJ 12671, ANKHDl, KIF2C, RP A3, MCCC2, CDH 17, LSM5, PRFl, RODl, FLJ12666, SUV420H1, MUC13, C13orfl8, and CDCA8, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of ETS2, ARIDlA, IDl, DDC, NID2, CCT3, ID2, NFIL3, and AREG, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of Hcd829, hsa-mir-197-prec, HPR163, and hsa-mir-150-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to IL13-PE38QQR fusion protein (cintredekin besudotox).
29. The method of claim 1 , wherein said at least one gene is selected from the group consisting of STOM, TNFAIP3, ASNS, GARS, CXCR4, EGLN3, LBH, and GDF 15, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of STOMLl and KIAA0746, or wherein the method further comprises measuring a level of expression of at least one micro RN A selected from the group consisting of hsa-mir-034prec, Hcd255, Hcd712, Hcd965, Hcd891, Hcd210_HPR205, hsa-mir-429, Hcd753, Hcd693, MPR203, Hcd704, Hcd863PO, hsa-mir-122a-prec, Hcd760, Hcd338, HPR213, Hcd852, Hcd366, MPR103, Hcd669, and hsa-mir-188-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Valproic acid (VPA).
30. The method of claim 1 , wherein said at least one gene is selected from the group consisting of PPIB, ZFP36L2, IFI30, USP7, SRM, SH3BP5, ALDOC, FADS2, GUSB, PSCDl, IQGAP2, STS, MFNG, FLIl, PIM2, INPP4A, LRMP, ICAM2, EVI2A, MAL, BTN3A3, PTPN7, ILlORA, SPIl, TRAFl, ITGB7, ARHGAP6, MAP4K1, CD28, PTP4A3, LTB, Clorf38, WBSCR22, CD8B1, LCPl, FLJ13052, MEF2C, PSCDBP, IL 16, SELPLG, MAGEA9, LAIRl, TNFRSF25, EVI2B, IGJ, PDCD4, RAS A4, HA-I, PLCL2, RNASE6, WBSCR20C, NUP210, RPLlOL, Cl Iorf2, CABCl , ARHGEF3, TAPBPL, CHST12, FKBPl 1 , FLJ35036, MYLIP, TXNDC5, PACAP, TOSO, PNAS-4, IL21R, and TCF4, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of CLTB, BTN3A2, BCL2, SETBPl, ICAM3, BCL2, BCL2, BCL2, CD53, CCND2, CLTB, CLTB, BCL2L1 1 , BTN3A2, CD37, MYCL2, CTSS, LAPTM5, CD53, COROlA, HEMl, CD53, COROlA, HEMl , HCLSl, BCL2L11, MYCLl, MYC, and MANlAl, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of Hcd257, hsa-mir-148-prec, Hcd512, HPR227, Hcd421, MPR203, hsa-mir-017-prec, hsa-mir-219-2, hsa-mir-328, Hcd783, Hcdl81, HPR213, hsa-mir-191-prec, hsa-mir-375, hsa-mir-212-prec, Hcd913, Hcd716, MPR207, HPR206, hsa-mir-016b-chr3, Hcd654, hsa-mir-195-prec, Hcd425, hsa-mir- 148a, hsa-mir-142-prec, and hsa-mir-016a-chrl3, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to All-trans retinoic acid (ATRA).
31. The method of claim 1 , wherein said at least one gene is selected from the group consisting of C6orf29, TRIM31, CD69, LRRN3, GPR35, and CDW52, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of Hcd99, hsa-mir-520c/526a, hsa-mir-191-prec, hsa-mir-205-prec, hsa-mir-375, hsa-mir-423, hsa-mir-449, and hsa-mir-196-2-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Cytoxan.
32. The method of claim 1, wherein said at least one gene is selected from the group consisting of K-ALPHA-I , CSDA, UCHLl, NAPlLl, ATP5G2, HDGFRP3, and IFI44, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of HUMTRF, MPR74, hsa-mir-213-prec, hsa-mir-155-prec, hsa-mir-181b-prec, hsa-mir-342, and hsa-mir-4323p, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Topotecan (Hycamtin).
33. The method of claim 1, wherein said at least one gene is selected from the group consisting of NOL5A, STOM, SIATl, CUGBP2, GUSB, ITM2A, JARID2, RUNX3, ICAM2, PTPN7, VAVl, PTP4A3, MCAM, MEF2C, IDH3B, RFP, SEPT6, SLC43A3, WBSCR20C, SHMT2, GLTSCR2, CABCl, FLJ20859, FLJ20010, MGC10993, and FKBPl 1, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of STOMLl, EIF4A1, PDE3B, BCLl IA, INPP4B, HLA-DMA, TRFP, EIF4A1, GAS7, MYCL2, HCLSl , MYCLl, and MYC, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-092-prec-X=092- 2, hsa-mir-123-prec, hsa-mir-514-1, hsa-mir-lOl-prec-9, hsa-mir-148-prec, hsa-mir- 106a, hsa-mir-20b, Hcd781 , hsa-mir-017-prec, hsa-mir-019b-2-prec, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1, hsa-mir-107, hsa-mir- 103-prec-5= 103-1 , MPR216, hsa- mir-29b-2=102prec7.1=7.2, hsa-mir-019b-l-prec, hsa-mir-107-prec-lO, hsa-mir- 135-2- prec, Hcd581, hsa-mir- 103-2-prec, Hcd230, hsa-mir-025-prec, hsa-mir-208-prec, hsa- mir- 18b, hsa-mir-093-prec-7.1=093-1 , hsa-mir- 106-prec-X, hsa-mir- 142-prec, HPRl 69, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Suberoylanilide hydroxamic acid (SAHA, vorinostat, Zolinza).
34. The method of claim 1, wherein said at least one gene is selected from the group consisting of ZFP36L2, TRIB2, LCP2, C6orf32, IL16, CACNAlG, SPDEF, HABl, TOSO, and ARHGAP25, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of SGCD and CAPN3, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of Hcd415, hsa-mir-147-prec, hsa-mir-033b-prec, Hcd778, hsa-mir-127-prec, hsa-mir-324, Hcd794, and Hcd634, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Depsipeptide (FR901228).
35. The method of claim 1, wherein said at least one gene is selected from the group consisting of PLEKHB2, ARPC 1 B, MX 1 , CUGBP2, IFI 16, TNFRSF 14, SPI lO, ELF 1 , LPXN, IFRG28, LEFl, and PYCARD, or wherein the method further comprises measuring a level of expression of HMXl, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of MPR121 , Hcdl 15, Hcd693, Hcd704, HPRlOO, Hcd760, hsa-mir-147-prec, hsa-mir-033b-prec, hsa-mir-146-prec, Hcdl 42, hsa-mir-501, Hcd716, MPR207, Hcd777, hsa-mir-204-prec, hsa-mir-146b, Hcd51 1, Hcd397, MPRl 30, Hcd782, hsa- mir-324, Hcd794, and Hcd739, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Bortezomib.
36. The method of claim 1, wherein said at least one gene is selected from the group consisting of SSRPl, ALDOC, ClQRl, TTFl , PRIMl, USP34, TK2, GOLGIN-67, NPD014, KIAA0220, SLC43A3, WBSCR20C, ICAM2, TEXlO, CHD7, SAMSNl, and TPRT, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of PTPRC, CD53, RNPSl , H3F3A, NUDC, SMARCA4, RPL32, PTMA, CD53, PTPRCAP, PTPRC, RPL32, PTPRCAP, PTPRC, CD53, PTPRC, HCLSl, and SLC 19Al , or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-096-prec-7, hsa-mir-123-prec, MPR249, HPR232, hsa-mir-lOl-prec-9, hsa-mir-106a, hsa-mir-20b, Hcd861, hsa-mir- 017-prec, hsa-mir-019b-2-prec, hsa-mir-033-prec, HcdlO2, MPR216, Hcd975, hsa-mir- 019b-l-prec, hsa-mir-135-2-prec, Hcd581, Hcd536_HPR104, hsa-mir-128b-prec, HSTRNL, hsa-mir-025-prec, hsa-mir-18b, HPR262, Hcd923, Hcd434, Hcd658, HPR129, hsa-mir-380-5p, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, Hcd627, hsa-mir-142-prec, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Leukeran.
37. The method of claim 1, wherein said at least one gene is selected from the group consisting of HLA-E, BAT3, ENO2, UBE2L6, CUGBP2, ITM2A, PALM2-AKAP2, JARID2, DGKA, SLC7A6, TFDP2, ADA, EDGl, ICAM2, PTPN7, CXorf9, RHOH, MX2, ZNFNlAl, COCH, LCP2, CLGN, BNCl , FLNC, HLA-DRB3, UCP2, HLA- DRBl, GAT A3, PRKCQ, SH2D1 A, NFATC3, TRB@, FNBPl, SEPT6, NME4, DKFZP434C171, ZC3HAV1, SLC43A3, CD3D, AIFl, SPTANl, CDlE, TRIM, DATFl, FHODl, ARHGAP15, STAG3, SAP130, and CYLD, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of PTPRC, MX2004PA1 1424, TRIM22, TRIM41, CDlC, CHD8, ADAMl 1 , ANPEP, RBMX2, RAC2, GNAl 5, LAPTM5, PTPRCAP, PTPRC, GNAl 5, CDlB, PTPRCAP, PTPRC, GNAl 5, PTPRC, and ATP2A3, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of Hcd773, Hcd248, hsa-mir-181d, MPR74, hsa-mir-213- prec, hsa-mir-155-prec, MPR197, hsa-mir-181b-prec, hsa-mir-29b-2=102prec7.1=7.2, hsa-mir-029c-prec, Hcd318, hsa-mir-128b-prec, hsa-mir-130a-prec, hsa-mir-140, hsa- mir-16-2, hsa-mir-526a-2, hsa-mir-016b-chr3, hsa-mir-195-prec, hsa-mir-216-prec, hsa- mir-342, hsa-mir-29b-l , Hcd627, hsa-mir-102-prec-l, hsa-mir-142-prec, hsa-mir-223- prec, hsa-let-7f-2-prec2, and hsa-mir-016a-chrl3, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Fludarabine.
38. The method of claim 1 , wherein said at least one gene is CD99, or wherein the method further comprises measuring a level of expression of at least one micro RN A selected from the group consisting of Hcd794 and Hcd754, wherein said level of expression of said gene or microRN A indicates that said cell is sensitive to Vinblastine.
39. The method of claim 1, wherein said at least one gene is selected from the group consisting of RPLP2, BTGl, CSDA, ARHGDIB, INSIGl , ALDOC, WASPIP, ClQRl, EDEMl, SLA, MFNG, GPSM3, ADA, LRMP, EVI2A, FMNLl, PTPN7, RHOH, ZNFNlAl, CENTBl, MAP4K1, CD28, SPl 10, NAPlLl, IFI16, ARHGEF6, SELPLG, CD3Z, SH2D1A, LAIRl, RAFTLIN, HA-I, D0CK2, CD3D, T3JAM, ZAP70, GPR65, CYFIP2, LPXN, RPLlOL, GLTSCR2, ARHGAP15, BCLl IB, TM6SF1, PACAP, and TCF4, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of PTPRC, BCL2, LAT, ICAM3, BCL2, BCL2, BCL2, ADAMI l, CD53, FARSLA, BCL2L1 1, RPL13, RAC2, RPL13, MYCL2, LAPTM5, RPLl 8A, CD53, COROlA, PTPRCAP, PTPRC, HEMl , GMFG, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl, PTPRC, HCLSl , BCL2L1 1, MYCLl, FARSLA, and MYC, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa- mir-096-prec-7, hsa-mir-124a-3-prec, hsa-mir-lOl-prec-9, Hcd712, Hcd693, hsa-mir- 219-2, Hcdl45, hsa-mir-155-prec, HPR213, hsa-mir-212-prec, Hcd913, Hcd716, MPR207, Hcd559, Hcd654, Hcd739, and hsa-mir-142-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Busulfan.
40. The method of claim 1 , wherein said at least one gene is selected from the group consisting of ARHGDIB, ITM2A, SSBP2, PIM2, SELL, ICAM2, EVI2A, MAL, PTPN7, ZNFNlAl, LCP2, ARHGAP6, CD28, CD8B1, LCPl , NPD014, CD69, NFATC3, TRB@, IGJ, SLC43A3, D0CK2, FHODl , and PACAP, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of ICAM3, CD53, SMARCA4, CD37, LAPTM5, CD53, COROlA, HEMl , GMFG, GMFG, CD53, COROlA, HEMl , and HCLSl , or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir- 123-prec, hsa-mir-lOl-prec-9, Hcd517, Hcd796, Hcd749, Hcd674, hsa-mir-019b-2- prec, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1 , hsa-mir-124a-2-prec, hsa-mir-143- prec, hsa-mir-516-43p, hsa-mir-216-prec, Hcd731 , hsa-mir-106-prec-X, hsa-mir-142- prec, hsa-mir-223-prec, Hcd754, and hsa-mir-018-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Dacarbazine.
41. The method of claim 1 , wherein said at least one gene is selected from the group consisting of RPL18, RPLlOA, RPS3A, EEF1B2, GOT2, RPL13A, RPS15, NOL5A, RPLP2, SLC9A3R1, EIF3S3, MTHFD2, IMPDH2, ALDOC, FABP5, ITM2A, PCK2, MFNG, GCHl, PIM2, ADA, ICAM2, TTFl , MYB, PTPN7, RHOH, ZNFNlAl, PRIMl, FHIT, ASS, SYK, OXAlL, LCPl, DDX 18, NOLA2, KIAA0922, PRKCQ, NFATC3, ANAPC5, TRB@, CXCR4, FNBP4, SEPT6, RPS2, MDNl, PCCB, RASA4, WBSCR20C, SFRS7, WBSCR20A, NUP210, SHMT2, RPLPO, MAP4K1 , HNRPAl, CYFIP2, RPLlOL, GLTSCR2, MRPL16, MRPS2, FLJ12270, CDK5RAP3, ARHGAPl 5, CUTC, FKBPl 1, ADPGK, FLJ22457, PUS3, PACAP, and CALML4, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of MRPS24, DUSP2, EIF4A1, BRD2, BCLl IA, RASSF2, MRPL37, MRPL30, RASSFl, MYBBPlA, LASS2, MRPS22, ADAMI l, CD53, RPS6KB1 , RNPSl, BRD2, EIF4A1 , FBL, BRD2, RPL36A, RPL13, RPL38, H3F3A, KIAA0182, RPS27, RPS6, EEFlG, RPL13, MYCL2, FBLNl, RPS25, RPL32, PTMA, RPL18A, RPL3, CD53, COROlA, HEMl, GMFG, RPL32, GMFG, CD53, COROlA, HEMl , HCLSl, ATP2A3, RASSF7, MYCLl, MYBLl, MYC, RPSl 5 A, RASSF2, and LASS6, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa- mir-092-prec-X=092-2, hsa-mir-148-prec, hsa-mir-20b, hsa-mir-007-2-prec, hsa-mir- 017-prec, hsa-mir-019b-2-prec, Hcd760, Hcd783, MPR216, hsa-mir-375, hsa-mir- 019b-l-prec, hsa-mir-135-2-prec, hsa-mir-150-prec, hsa-mir-128b-prec, hsa-mir-499, hsa-mir-025-prec, hsa-mir-007-l-prec, hsa-mir-019a-prec, hsa-mir-093-prec-7.1=093-1 , hsa-mir-106-prec-X, hsa-mir-142-prec, HPR169, hsa-mir-018-prec, hsa-mir-020-prec, and hsa-mir-484, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Oxaliplatin.
42. The method of claim 1 , wherein said at least one gene is selected from the group consisting of CSDA, INSIGl, UBE2L6, PRGl , ITM2A, DGKA, SLA, PCBP2, IL2RG, AL0X5AP, PSMB9, LRMP, ICAM2, PTPN7, CXorf9, RHOH, ZNFNlAl , CENTBl , LCP2, STAT4, CCR7, CD3G, SPl 10, TNFAIP8, IFI 16, CXCR4, ARHGEF6, SELPLG, CD3Z, PRKCQ, SH2D1 A, CDlA, NFATC3, LAIRl, TRB@, SEPT6, RAFTLIN, D0CK2, CD3D, CD6, AIFl, CDlE, CYFIP2, TARP, ADA, ARHGAPl 5, GIMAP6, STAG3, FLJ22457, PACAP, and TCF4, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of PTPRC, TRIM22, PSME2, LAT, CDlC, ICAM3, ADAMl 1, CD53, FARSLA, RPL13, RAC2, RPL13, NK4, LAPTM5, CD53, COROlA, PTPRCAP, PTPRC, HEMl , GMFG, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl, ITGB2, PTPRC, HCLSl, ATP2A3, and FARSLA, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of Hcd257, Hcd768, Hcd796, HUMTRF, HUMTRS, MPR74, hsa-mir-213-prec, hsa-mir- 155-prec, Hcd763, hsa-mir-181b-prec, ath-MIR180a, hsa-mir-216-prec, hsa-mir-342, hsa-mir-142-prec, HSHELAOl, HUMTRVlA, hsa-mir-223-prec, Hcd754, and hsa-mir- 020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Hydroxyurea.
43. The method of claim 1, wherein said at least one gene is selected from the group consisting of RPLl 1, RPL17, ANAPC5, RPL13A, STOM, TUFM, SCARBl, FABP5, KIAA071 1 , IL6R, WBSCR22, UCK2, GZMB, Clorf38, PCBP2, GPR65, GLTSCR2, and FKBPl 1 , or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of STOMLl, MRPL37, MRPL30, RPL36A, RPL38, HSPDl, MIF, RPL32, RPL3, and RPL32, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of Hcd257, Hcd946, Hcd503, hsa-mir-429, Hcd693, hsa-miR-373*, Hcd738, hsa-mir-328, Hcd783, Hcdl 81 , Hcd631, Hcd279, hsa-mir-194- 2, hsa-mir-197-prec, HPR163, hsa-mir-150-prec, Hcd323, hsa-mir-103-2-prec, Hcd243, Hcd938, hsa-mir-025-prec, hsa-mir-007-l-prec, MPR243, Hcd51 1 , Hcd654, hsa-mir- 199a-2-prec, hsa-mir-214-prec, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, Hcd794, Hcd530, HSHELAOl , Hcd754, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Tegafur.
44. The method of claim 1, wherein said at least one gene is selected from the group consisting of ALDOC, ITM2A, SLA, SSBP2, IL2RG, MFNG, SELL, STCl, LRMP, MYB, PTPN7, CXorf9, RHOH, ZNFNlAl, CENTBl, MAP4K1, CCR7, CD3G, CCR9, CBFA2T3, CXCR4, ARHGEF6, SELPLG, SEC31L2, CD3Z, SH2D1A, CDlA, SCN3A, LAIRl , TRB@, DOCK2, WBSCR20C, CD3D, T3JAM, CD6, ZAP70, GPR65, AIFl, WDR45, CDlE, CYFIP2, TARP, TRIM, ARHGAPl 5, NOTCHl, STAG3, UBASH3A, MGC5566, and PACAP, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of PTPRC, TRIM22, TRIM41, LAT, CDlC, MYBBPlA, CD53, FARSLA, PPP2CA, LAPTM5, CD53, COROlA, PTPRCAP, PTPRC, HEMl, GMFG, ITK, CDlB, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl, TCF7, PTPRC, HCLSl, ATP2A3, MYBLl, and FARSLA, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of Hcd768, HUMTRF, Hcdl45, Hcd923, hsa-mir-216-prec, hsa-mir-093-prec-7.1=093-1, hsa-mir- 342, Hcd794, hsa-mir-142-prec, HSHELAOl, hsa-mir-223-prec, and Hcd754, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Daunorubicin.
45. The method of claim 1 , wherein said at least one gene is selected from the group consisting of PFNl, CALU, ZYX, PSMD2, RAPlB, EPASl, PGAMl, STATl, CKAP4, DUSPl , RCNl , UCHLl , ITGA5, NFKBIA, LAMBl , TGFBI, FHLl , GJAl, PRGl, EXTl, MVP, NNMT, TAPl , CRIMl, PLOD2, RPS 19, AXL, PALM2-AKAP2, IL8, LOXL2, PAPSS2, CAVl, F2R, PSMB9, LOX, Clorf29, STCl, LIF, KCNJ8, SMAD3, HPCALl , WNT5A, BDNF, TNFRSFlA, NCOR2, FLNC, HMGA2, HLA-B, FLOTl, PTRF, IFI16, MGC4083, TNFRSFlOB, PNMA2, TFPI, CLECSF2, SPl 10, PLAUR, ASPH, FSCNl, HIC, HLA-C, COL6A1, IL6ST, IFITM3, MAPlB, FLJ46603, RAFTLIN, FTL, KIAA0877, MTlE, CDClO, ZNF258, BCATl , IFI44, SOD2, TMSBlO, FLJ10350, Clorf24, EFHD2, RPS27L, TNFRSF12A, FAD104, RAB7L1 , NME7, TMEM22, TPKl, ELK3, CYLD, AMIGO2, ADAMTSl, and ACTB, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of ACLY, MPZLl, STC2, BAX, RAB31, RAB31,, (UBC12, LOXLl , EMP3, FGFRlOP, IL6, TRIM22, OPTN, CYR61, METAPl , SHCl, FNl , EMP3, RAB31, LOXLl , BAX, BAX, RAB31, FNl , CD44, ANXAl, COL5A2, LGALSl, FGFRl, PLAU, TFPI2, TFPI2, VCAMl, SHCl, CSF2RA, EMP3, COLlAl, TGFBl, COL6A2, FGFRl, ITGA3, AKRlBl , MSN, EMP3, VIM, EMP3, COL6A2, MSN, PSMC5, UBC, FGFRl, BASPl, ANXAl 1, CSPG2, M6PRBP1, PRKCA, OPTN, OPTN, SPARC, CCL2, and ITGA3, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-125b-2-prec, hsa-mir-022- prec, hsa-mir-125b-l, hsa-mir-155-prec, hsa-mir-100, hsa-mir-409-3p, hsa-mir-495, hsa-mir-199a-2-prec, hsa-mir-382, and hsa-mir-lOO-l/2-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Bleomycin.
46. The method of claim 1 , wherein said at least one gene is selected from the group consisting of HSPCB, LDHA, and TM4SF7, or wherein the method further comprises measuring a level of expression of LY6E, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of Hcd338, hsa-mir-099b-prec-19, and hsa-mir-149-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Estramustine.
47. The method of claim 1, wherein said at least one gene is selected from the group consisting of CSDA, INSIGl, UBE2L6, PRGl, ITM2A, DGKA, TFDP2, SLA, IL2RG, AL0X5AP, GPSM3, PSMB9, SELL, ADA, EDGl, FMNLl, PTPN7, CXorf9, RHOH, ZNFNlAl, CENTBl, LCP2, CDlD, STAT4, VAVl , MAP4K1 , CCR7, PDE4C, CD3G, CCR9, SPl 10, TNFAIP8, LCPl , IFI 16, CXCR4, ARHGEF6, SELPLG, SEC31L2, CD3Z, PRKCQ, SH2D1A, GZMB, CDlA, LAIRl, AFlQ, TRB@, SEPT6, DOCK2, RPS19, CD3D, T3JAM, FNBPl , CD6, ZAP70, LSTl , BCATl, PRFl , AIFl , RAG2, CDl E, CYF1P2, TARP, TRIM, GLTSCR2, G1MAP5, ARHGAPl 5, NOTCHl , BCLl IB, GIMAP6, STAG3, TM6SF1 , UBASH3A, MGC5566, FLJ22457, and TPKl, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of PTPRC, TRIM22, EVL, TRIM41, PSME2, LAT, CDlC, ADAMl 1 , CD53, FARSLA, RPL13, RAC2, RPL13, GNA15, LAPTM5, RPL18A, CD53, COROlA, PTPRCAP, PTPRC, HEMl, GMFG, GNA15, ITK, CDlB, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl, GNAl 5, ITGB2, PTPRC, HCLSl, ATP2A3, and FARSLA, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa- mir-181a-prec, hsa-mir-181c-prec, HUMTRF, hsa-mir-181d, MPR74, Hcd817, hsa-mir- 213-prec, hsa-mir-155-prec, Hcdl48_HPR2251eft, hsa-mir-515-15p, hsa-mir-181b-prec, HUMTRN, hsa-mir-128b-prec, hsa-mir-450-2, hsa-mir-216-prec, hsa-mir-342, hsa-mir- 142-prec, hsa-mir-223-prec, Hcd754, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Chlorambucil.
48. The method of claim 1, wherein said at least one gene is selected from the group consisting of PRGl, SLC2A3, RPS 19, PSMBlO, ITM2A, DGKA, SEMA4D, SLA, IL2RG, MFNG, AL0X5AP, GPSM3, PSMB9, SELL, ADA, FMNLl, MYB, PTPN7, CXorf9, RHOH, ZNFNlAl, CENTBl, FXYD2, CDlD, STAT4, MAP4K1 , CCR7, PDE4C, CD3G, CCR9, SPl 10, TK2, TNFAIP8, NAPlLl, SELPLG, SEC31L2, CD3Z, PRKCQ, SH2D1A, GZMB, CDlA, LAIRl, TRB@, SEPT6, D0CK2, CGOl 8, WBSCR20C, CD3D, CD6, LSTl, GPR65, PRFl, ALMSl , AIFl, CDlE, CYFIP2, TARP, GLTSCR2, FLJ12270, ARHGAP15, NAP1L2, CECRl, GIMAP6, STAG3, TM6SF1, C15orf25, MGC5566, FLJ22457, ET, TPKl, and PHFl 1, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of ETS2, PTPRC, PETER, SETBPl, LAT, MYBBPlA, ETV5, METAPl, ETSl , ADAMl 1, CD53, FARSLA, RPL13, ARMET, TETRAN, BETl, RPL13, MET, LAPTM5, CD53, COROlA, PTPRCAP, PTPRC, HEMl, GMFG, CDlB, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl, ETV4, ITGB2, PTPRC, HCLSl , MYBLl, FARSLA, and METAP2, or wherein the method further comprises measuring a level of expression of at least one micro RN A selected from the group consisting of hsa-mir-124a-3-prec, Hcd946, Hcd683, HPR264, MPR185, HUMTRF, Hcd294, Hcd503, hsa-mir-20b, MPR74, MPR234, Hcd447, Hcd817, Hcdl48_HPR2251eft, hsa-mir-515-15p, Hcd383, hsa-mir-181b-prec, Hcd783, MPR224, HPR172, MPR216, HUMTRN, hsa-mir-321 , HPR159, MPR228, ath-MIR180a, hsa- mir-197-prec, hsa-mir-124a-l-precl, hsa-mir-128b-prec, Hcd28_HPR391eft, Hcd889,
Hcd350, hsa-mir-025-prec, hsa-mir-208-prec, hsa-mir-450-2, Hcd923, Hcd434, HPRl 29, HPR220, hsa-mir-380-5p, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir-342, hsa-mir-142-prec, HSHELAOl, hsa-mir-223-prec, Hcd754, hsa-mir-020- prec, and hsa-mir-4323p, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Mechlorethamine.
49. The method of claim 1, wherein said at least one gene is selected from the group consisting of PGKl, SCD, INSIGl, IGBPl, TNFAIP3, TNFSFlO, ABCAl , AGA, ABCA8, DBCl, PTGER2, UGT1A3, ClOorflO, TM4SF13, CGI-90, LXN, DNAJC12, HIPK2, and C9orf95, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of FGFRlOP, PLXNAl, PSCD2L, TUBB, FGFRl, TUBB2, PAGA, TUBB2, UBB, TUBB2, FGFRl, FGFRl , and TUBB-P ARALOG, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa- mir-483, Hcd631, hsa-mir-212-prec, Hcd938, MPR133, Hcd794, Hcd438, and Hcd886, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Streptozocin.
50. The method of claim 1 , wherein said at least one gene is selected from the group consisting of RPLP2, CD99, IFITMl, INSIGl , ALDOC, ITM2A, SERPINAl, ClQRl , STAT5A, INPP5D, SATBl , VPS 16, SLA, IL2RG, MFNG, SELL, LRMP, ICAM2, MYB, PTPN7, ARHGAP25, LCK, CXorf9, RHOH, ZNFNlAl , CENTBl, ADD2, LCP2, SPIl, DBT, GZMA, CD2, BATF, HISTl H4C, ARHGAP6, VAVl , MAP4K1 , CCR7, PDE4C, CD3G, CCR9, SP 140, TK2, LCPl 5 IFI 16, CXCR4, ARHGEF6, PSCDBP, SELPLG, SEC31L2, CD3Z, PRKCQ, SH2D1A, GZMB, CDlA, GATA2, LY9, LAIRl, TRB@, SEPT6, HA-I, SLC43A3, DOCK2, CG018, MLCl, CD3D, T3JAM, CD6, ZAP70, DOK2, LSTl , GPR65, PRFl , ALMSl, AIFl , PRDX2, FLJ12151 , FBXW12, CDlE, CYFIP2, TARP, TRIM, RPLlOL, GLTSCR2, CKIP-I, NRNl, ARHGAPl 5, NOTCHl, PSCD4, C13orfl8, BCLI lB, GIMAP6, STAG3, NARF, TM6SF1, C15orf25, FLJ 11795, SAMSNl, UBASH3A, PACAP, LEFl, IL21R, TCF4, and DKFZP434B0335, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of FLJ 10534, PTPRC, CD27BP, TRIM22, TRIM41 , PSCD2L, CDlC, MYBBPlA, ICAM3, CD53, FARSLA, GAS7, ABCD2, CD24, CD29, RAC2, CD37, GNAl 5, PGF, LAPTM5, RPL18A, CD53, COROlA, PTPRCAP, PTPRC, HEMl, GMFG, GNA15, ITK, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl , GNAl 5, TCF7, ITGB2, PTPRC, HCLSl, PRKCBl, ATP2A3, PRKCBl, MYBLl, and FARSLA, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-092-prec-X=092-2, Hcd517, Hcd796, HUMTRF, hsa-mir-20b, hsa-mir-019b-2-prec, hsa-mir-033-prec, hsa-mir-092- prec- 13=092-1, Hcdl48_HPR2251eft, HUMTRAB, Hcd975, hsa-mir-135-2-prec, hsa- mir-128b-prec, hsa-mir-143-prec, hsa-mir-025-prec, hsa-mir-216-prec, hsa-mir-093- prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir-142-prec, HSHELAOl , HUMTRVlA, hsa-mir-223-prec, Hcd754, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Carmustine.
51. The method of claim 1, wherein said at least one gene is selected from the group consisting of RPS15, INSIGl, ALDOC, ITM2A, ClQRl , STAT5A, INPP5D, VPS16, SLA, USP20, IL2RG, MFNG, LRMP, EVI2A, PTPN7, ARHG AP25, RHOH, ZNFNlAl, CENTBl, LCP2, SPIl, ARHGAP6, MAP4K1, CCR7, LY96, C6orf32, MAGEAl, SP 140, LCPl, IFI 16, ARHGEF6, PSCDBP, SELPLG, CD3Z, PRKCQ, GZMB, LAIRl, SH2D1A, TRB@, RFP, SEPT6, HA-I, SLC43A3, CD3D, T3JAM, GPR65, PRFl , AIFl , LPXN, RPLlOL, SITPEC, ARHGAP15, C13orfl8, NARF, TM6SF1 , PACAP, and TCF4, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of PTPRC, ICAM3, TRFP, CD53, FARSLA, RAC2, MAGEAl 1 , LAPTM5, CD53, COROlA, PTPRCAP, PTPRC, HEMl, GMFG, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl, PTPRC, HCLSl , SLC 19Al, FARSLA, and RPS 15 A, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-lOl-prec-9, Hcd796, hsa-mir-20b, HUMTRAB, hsa-mir-135-2-prec, hsa-mir-153-l-precl , hsa-mir-025-prec, hsa-mir-093-prec- 7.1=093-1, hsa-mir-106-prec-X, hsa-mir-142-prec, HUMTRVlA, Hcd754, hsa-mir- 018-prec, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Lomustine.
52. The method of claim 1, wherein said at least one gene is selected from the group consisting of SSRPl, ALDOC, ClQRl, TTFl, PRIMl, USP34, TK2, GOLGIN-67, NPD014, KIAA0220, SLC43A3, WBSCR20C, ICAM2, TEXlO, CHD7, SAMSNl, and TPRT, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of PTPRC, CD53, RNPSl, H3F3A, NUDC, SMARCA4, RPL32, PTMA, CD53, PTPRCAP, PTPRC, RPL32, PTPRCAP, PTPRC, CD53, PTPRC, HCLSl, and SLC 19Al , or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-096-prec-7, hsa-mir-123-prec, MPR249, HPR232, hsa-mir-101-prec-9, hsa-mir-106a, hsa-mir-20b, Hcd861, hsa-mir- 017-prec, hsa-mir-019b-2-prec, hsa-mir-033-prec, HcdlO2, MPR216, Hcd975, hsa-mir- 019b-l-prec, hsa-mir-135-2-prec, Hcd581, Hcd536_HPR104, hsa-mir-128b-prec, HSTRNL, hsa-mir-025-prec, hsa-mir-18b, HPR262, Hcd923, Hcd434, Hcd658, HPRl 29, hsa-mir-380-5p, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, Hcd627, hsa-mir-142-prec, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Mercaptopurine.
53. The method of claim 1, wherein said at least one gene is selected from the group consisting of CD99, INSIGl , PRGl, ALDOC, ITM2A, SLA, SSBP2, IL2RG, MFNG, ALOX5AP, Clorf29, SELL, STCl , LRMP, MYB, PTPN7, CXorf9, RHOH, ZNFNlAl, CENTBl , ADD2, CDlD, BATF, MAP4K1, CCR7, PDE4C, CD3G, CCR9, SPl 10, TNFAIP8, NAPl Ll, CXCR4, ARHGEF6, GATA3, SELPLG, SEC31L2, CD3Z, SH2D1A, GZMB, CDlA, SCN3A, LAIRl , AFlQ, TRB@, DOCK2, MLCl, CD3D, T3JAM, CD6, ZAP70, IFI44, GPR65, PRFl, AIFl, WDR45, CDlE, CYFIP2, TARP, TRIM, ARHGAP 15, NOTCHl, STAG3, NARF, TM6SF1, UBASH3A, and MGC5566, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of FLJ 10534, PTPRC, TRIM22, C18orfl, TRIM41, LAT, CDlC, MYBBPlA, CD53, FARSLA, PPP2CA, COL5A2, LAPTM5, CD53, COROlA, PTPRCAP, PTPRC, HEMl, GMFG, ITK, CDlB, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl, TCF7, PTPRC, HCLSl, ATP2A3, MYBLl, and FARSLA, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir- 124a-3-prec, Hcd768, HUMTRF, hsa-mir-213-prec, hsa-mir-181b-prec, Hcd783, hsa- mir-212-prec, hsa-mir-124a-l-precl, hsa-mir-342, hsa-mir-142-prec, HSHELAOl, hsa- mir-223-prec, and Hcd754, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Teniposide.
54. The method of claim 1, wherein said at least one gene is selected from the group consisting of ALDOC, ClQRl , SLA, WBSCR20A, MFNG, SELL, MYB, RHOH, ZNFNlAl, LCP2, MAP4K1, CBFA2T3, LCPl, SELPLG, CD3Z, LAIRl , WBSCR20C, CD3D, GPR65, ARHGAP15, FLJ10178, NARF, and PUS3, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of PTPRC, MYBBPlA, ICAM3, CD53, FARSLA, CD53, PTPRCAP, PTPRC, HEMl, GMFG, GMFG, PTPRCAP, PTPRC, CD53, HEMl , PTPRC, HCLSl, PRKCBl, PRKCBl, MYBLl, and FARSLA, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-025-prec, hsa-mir-007-l-prec, hsa-mir- 093-prec-7.1=093-1 , Hcd794, and hsa-mir-142-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Dactinomycin.
55. The method of claim 1 , wherein said at least one gene is selected from the group consisting of PPIB, ZFP36L2, IFI30, USP7, SRM, SH3BP5, ALDOC, FADS2, GUSB, PSCDl, IQGAP2, STS, MFNG, FLIl , PIM2, INPP4A, LRMP, ICAM2, EVI2A, MAL, BTN3A3, PTPN7, ILlORA, SPIl, TRAFl , ITGB7, ARHGAP6, MAP4K1 , CD28, PTP4A3, LTB, Clorf38, WBSCR22, CD8B1, LCPl , FLJ13052, MEF2C, PSCDBP, ILl 6, SELPLG, MAGEA9, LAIRl, TNFRSF25, EVI2B, IGJ, PDCD4, RASA4, HA-I, PLCL2, RNASE6, WBSCR20C, NUP210, RPLlOL, Cl Iorf2, CABCl, ARHGEF3, TAPBPL, CHSTl 2, FKBPl 1, FLJ35036, MYLIP, TXNDC5, PACAP, TOSO, PNAS-4, IL21R, and TCF4, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of CLTB, BTN3A2, BCL2, SETBPl, ICAM3, BCL2, BCL2, BCL2, CD53, CCND2, CLTB, CLTB, BCL2L1 1, BTN3A2, CD37, MYCL2, CTSS, LAPTM5, CD53, COROlA, HEMl, CD53, COROlA, HEMl, HCLSl , BCL2L11, MYCLl, MYC, and MANlAl, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of Hcd257, hsa-mir-148-prec, Hcd512, HPR227, Hcd421, MPR203, hsa-mir-017-prec, hsa-mir-219-2, hsa-mir-328, Hcd783, Hcdl81, HPR213, hsa-mir-191-prec, hsa-mir-375, hsa-mir-212-prec, Hcd913, Hcd716, MPR207, HPR206, hsa-mir-016b-chr3, Hcd654, hsa-mir-195-prec, Hcd425, hsa-mir- 148a, hsa-mir-142-prec, and hsa-mir-016a-chrl3, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Tretinoin.
56. The method of claim 1, wherein said at least one gene is selected from the group consisting of PDGFRB, KDR, KIT, and FLT3, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of FLTl , FLT4, PDGFRA, and CSFlR, wherein said level of expression of said gene indicates that said cell is sensitive to sunitinib.
57. The method of claim 1 , wherein said at least one gene is BCL2, wherein said level of expression of said gene indicates that said cell is sensitive to SPC2996.
58. The method of claim 1, wherein said at least one gene is selected from the group consisting of ARHGDIB, ZFP36L2, ITM2A, LGALS9, INPP5D, SATBl , TFDP2, IL2RG, CD48, SELL, ADA, LRMP, RIMS3, LCK, CXorf9, RHOH, ZNFNlAl, LCP2, CDlD, CD2, ZNF91 , MAP4K1, CCR7, IGLLl, CD3G, ZNF430, CCR9, CXCR4, KIAA0922, TARP, FYN, SH2D1A, CDlA, LSTl, LAIRl, TRB@, SEPT6, CD3D, CD6, AIFl , CDlE, TRIM, GLTSCR2, ARHGAP15, BIN2, SH3TC1 , CECRl, BCLl IB, GIMAP6, STAG3, GALNT6, MGC5566, PACAP, and LEFl, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of CD27BP, TRIM22, TRA@, C18orfl, EVL, PRKCH, TRIM41, PSCD2L, CDlC, ADAMI l, ABCD2, CD24, CD29, CD37, GNAl 5, LAPTM5, COROlA, HEMl, GMFG, GNA15, CDlB, ' GMFG, COROlA, HEMl, GNAl 5, ITGB2, PRKCBl, ATP2 A3, and PRKCBl, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-181b-2, Hcd417, Hcd440_HPR257, hsa-mir-019b-2-prec, hsa-mir-213-prec, hsa-mir-033-prec, hsa-mir- 092-prec- 13=092- 1, hsa-mir- 18 lb-prec, hsa-mir-128b-prec, hsa-mir-526a-2, MPR95, HPR220, hsa-mir- 133a- 1, hsa-mir- 148a, hsa-mir- 142-prec, HPRl 69, hsa-mir-223-prec, hsa-mir-018-prec, hsa-mir-020-prec, and hsa-mir-484, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Ifosfamide.
59. The method of claim 1, wherein said at least one gene is selected from the group consisting of MLP, GLUL, SLC9A3R1, ZFP36L2, INSIGl, TBLlX, NDUFABl, EBP, TRIM14, SRPK2, PMM2, CLDN3, GCHl, IDIl, TTFl, MYB, RASGRPl, HIST1H3H, CBFA2T3, SRRM2, ANAPC5, MBD4, GATA3, HIST1H2BG, RAB14, PIK3R1, MGC50853, ELFl, ZRFl, ZNF394, S100A14, SLC6A14, GALNT6, SPDEF, TPRT, and CALML4, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of EIF4A1 , TFFl, TFFl, MYBBPlA, AKAPl, DGKZ, EIF4A1, KIAA0182, SLC19A1, ATP2A3, MYBLl , EIF4EBP2, Gl P2, and MANlAl , or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-092-prec-X=092-2, Hcd547, Hcd257, hsa-mir- 148-prec, HUMTRS, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1, hsa-mir-375, hsa-mir-095- prec-4, hsa-mir-025-prec, hsa-mir-202-prec, hsa-mir-007-l-prec, hsa-mir-093-prec- 7.1=093-1 , hsa-mir-106-prec-X, hsa-mir-142-prec, hsa-mir-223-prec, and hsa-mir-018- prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Tamoxifen.
60. The method of claim 1, wherein said at least one gene is selected from the group consisting of CSDA, F8A1 , KYNU, PHF 14, SERPINB2, OPHNl, HRMTl L2, TNFRSFlA, PPP4C, CESl, TP53AP1, TM4SF4, RPL5, BC008967, TLK2, COL4A6, PAK3, RECK, LOC51321, MST4, DERP6, SCD4, and FLJ22800, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of STC2, BAX, CDKNlA, DDB2, RGS2, BAX, BAX, RPL 13, RPLl 3, CDKNlA, and GABPB2, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of HUMTRF, HUMTRN, hsa-mir-124a-l-precl, hsa-mir-150-prec, Hcd923, HPRl 81, Hcd569, hsa-mir-199a-2-prec, Hcd754, and hsa-mir-4323p, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Floxuridine.
61. The method of claim 1, wherein said at least one gene is selected from the group consisting of CSDA, UBE2L6, TAPl, RPS 19, SERPINAl, ClQRl, SLA, GPSM3, PSMB9, EDGl, FMNLl, PTPN7, ZNFNlAl, CENTBl , BATF, MAP4K1, PDE4C, SPl 10, HLA-DRA, IFI 16, HLA-DRBl, ARHGEF6, SELPLG, SEC31L2, CD3Z, PRKCQ, SH2D1A, GZMB, TRB@, HLA-DPAl, AIMl, DOCK2, CD3D, IFITMl, ZAP70, PRFl, Clorf24, ARHGAPl 5, C13orfl8, and TM6SF1, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of PTPRC, TRIM22, PSME2, LAT, METAPl, CD53, FARSLA, RPLl 3, RAC2, RPLl 3, PTMA, CD53, COROlA, PTPRCAP, PTPRC, GMFG, ITK, GMFG, PTPRCAP, PTPRC, CD53, COROlA, ITGB2, PTPRC, HCLSl , and FARSLA, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of HUMTRF, hsa-mir-380- 5p, hsa-mir-342, hsa-mir-142-prec, and Hcd200, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Irinotecan.
62. The method of claim 1, wherein said at least one gene is selected from the group consisting of STATl, HSBPl , IFI30, RI0K3, TNFSFlO, ALOX5AP, ADFP, IRS2, EFEMP2, RIPK2, DKFZp564I1922, MTl K, RNASET2, EFHD2, TRIB3, ACSL5, IFIHl, and DNAPTP6, or wherein the method further comprises measuring a level of expression of at least one gene selected from the group consisting of IFI27, OPTN, C20orfl8, FNl, LOC51123, FNl, OPTN, and OPTN, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of Hcd289, Hcd939, Hcd330, HPR76, Hcdl 11, Hcd976, hsa-mir-15a, hsa-mir-OOlb-1-precl, hsa-mir-450-1, hsa-mir-200b, Hcd578, and hsa-mir-200a-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to Satraplatin.
63. The method of any of claims 1-62, wherein said level of expression of said gene is determined by detecting the level of mRNA transcribed from said gene.
64. The method of any of claims 1-62, wherein said level of expression of said gene is determined by detecting the level of a protein product of said gene.
65. The method of any of claims 1-62, wherein said level of expression of said gene is determined by detecting the level of the biological activity of a protein product of said gene. '
66. The method of any of claims 1-62, wherein an increase in the level of expression of said gene or microRNA indicates increased sensitivity of said cell to said treatment.
67. The method of any of claims 1-62, wherein said cell is a cancer cell.
68. The method of any of claims 1-62, wherein a decrease in the level of expression of said gene or microRNA indicates increased sensitivity of said cell to said treatment.
69. The method of claim 1 , wherein said level of expression of said gene or microRNA is measured using a quantitative reverse transcription-polymerase chain reaction (qRT-PCR).
70. A method for determining the development of resistance of a cell in a patient to a treatment to which said cell in said patient has previously been sensitive, said method comprising measuring a level of expression of at least one gene or microRNA of any one of claims 1-62 of said cell, wherein a decrease in said level of expression of said gene or microRNA in said cell relative to the level of expression of said gene or microRNA in a control cell sensitive to said treatment indicates resistance or a propensity to develop resistance to the treatment by said patient.
71. A method for determining the development of resistance of a cell in a patient to a treatment to which said cell in said patient has previously been sensitive, said method comprising measuring a level of expression of at least one gene or microRNA of any one of claims 1-62 in said cell, wherein an increase in said level of expression of said gene or microRNA in said cell relative to the level of expression of said gene or microRNA in a control cell sensitive to said treatment indicates resistance or a propensity to develop resistance to the treatment by said patient.
72. A method of determining sensitivity of a cancer patient to a treatment for cancer comprising measuring a level of expression of at least one microRNA in a cell of said patient, said microRNA selected from the group consisting of ath-MIR180aNo2, HcdlO2 left, Hcdl 1 1 left, Hcdl 15 left, Hcdl20 left, Hcdl42 right, Hcdl45 left, Hcdl48_HPR225 left, Hcdl 81 left, Hcdl 81 right, Hcd210_HPR205 right, Hcd213_HPR182 left, Hcd230 left, Hcd243 right, Hcd246 right, Hcd248 right, Hcd249 right, Hcd250 left, Hcd255 left, Hcd257 left, Hcd257 right, Hcd263 left, Hcd266 left, Hcd270 right, Hcd279 left, Hcd279 right, , Hcd28_HPR391eft, Hcd28_HPR39right, Hcd282PO right, Hcd289 left, Hcd294 left, Hcd318 right, Hcd323 left, Hcd330 right, Hcd338 left, Hcd340 left, Hcd350 right, Hcd355_HPR190 left, Hcd361 right, Hcd366 left, Hcd373 right, Hcd383 left, Hcd383 right, Hcd384 left, Hcd397 left, Hcd404 left, Hcd412 left, Hcd413 right, Hcd415 right, Hcd417 right, Hcd421 right, Hcd425 left, Hcd43 8right, Hcd434 right, Hcd438 left, Hcd440_HPR257 right, Hcd444 right, Hcd447 right, Hcd448 left, Hcd498 right, Hcd503 left, Hcd51 1 right, Hcd512 left, Hcd514 right, Hcd517 left, Hcd517 right, Hcd530 right, Hcd536_HPR104 right, Hcd542 left, Hcd544 left, Hcd547 left, Hcd559 right, Hcd562 right, Hcd569 right, Hcd570 right, Hcd578 right, Hcd581 right, Hcd586 left, Hcd586 right, Hcd587 right, Hcd605 left, Hcd605 left, Hcd605 right, Hcd608 right, Hcd627 left, Hcd631 left, Hcd631 right, Hcd634 left, Hcd642 right, Hcd649 right, Hcd654 left, Hcd658 right, Hcd669 right, Hcd674 left, Hcd678 right, Hcd683 left, Hcd684 right, Hcd689 right, Hcd690 right, Hcd691 right, Hcd693 right, Hcd697 right, Hcd704 left, Hcd704 left, Hcd712 right, Hcd716 right, Hcd731 left, Hcd738 left, Hcd739 right, Hcd739 right, Hcd749 right, Hcd753 left, Hcd754 left, Hcd755 left, Hcd760 left, Hcd763 right, Hcd768 left ,Hcd768 right, Hcd770 left, Hcd773 left, Hcd777 left, Hcd778 right, Hcd781 left, Hcd781 right, Hcd782 left, Hcd783 left, Hcd788 left, Hcd794 right, Hcd796 left, Hcd799 left, Hcd807 right, Hcd812 left, Hcd817 left, Hcd817 right, Hcd829 right, Hcd852 right, Hcd861 right, Hcd863PO right, Hcd866 right, Hcd869 left, Hcd873 left, Hcd886 right, Hcd889 right, Hcd891 right, Hcd892 left, Hcd913 right, Hcd923 left, Hcd923 right, Hcd938 left, Hcd938 right, Hcd939 right, Hcd946 left, Hcd948 right, Hcd960 left, Hcd965 left, Hcd970 left, Hcd975 left, Hcd976 right, Hcd99 right, HPRlOO right, HPRl 29 left, HPRl 54 left, HPRl 59 left, HPRl 63 left, HPRl 69 right, HPR172 right, HPR181 left, HPR187 left, HPR199 right, HPR206 left, HPR213 right, HPR214 right, HPR220 left , HPR220 right, HPR227 right, HPR232 right, HPR233 right, HPR244 right, HPR262 left, HPR264 right, HPR266 right, HPR271 right, HPR76 right, hsa_mir_490_Hcd20 right, HSHELAOl , HSTRNL, HUMTRAB, HUMTRF, HUMTRN, HUMTRS, HUMTRVlA, let-7f-2-prec2, mir-OOlb-1-precl , mir-OOlb-2-prec, mir-007-l-prec, mir-007-2-precNo2, mir-Ol Oa-precNol , mir-015b- precNo2, mir-016a-chrl3, mir-016b-chr3, mir-017-precNol, mir-017-precNo2, mir- 018-prec, mir-019a-prec, mir-019b-l-prec, mir-019b-2-prec, mir-020-prec, mir-022- prec, mir-023a-prec, mir-023b-prec, mir-024-2-prec, mir-025-prec, mir-027b-prec, mir- 029c-prec, mir-032-precNo2, mir-033b-prec, mir-O33-prec, mir-034-precNol, mir-034- precNo2, mir-092-prec-l 3=092- 1NO2, mir-092-prec-X=092-2, mir-093-prec-7.1=093- 1, mir-095-prec-4 ,mir-096-prec-7Nol ,mir-096-prec-7No2, mir-098-prec-X, mir-099b- prec-19Nol, mir-lOO-l/2-prec, mir-100Nol, mir-lOl-prec-9, mir-102-prec-l, mir- 103- 2-prec, mir-103-prec-5= 103-1 , mir-106aNol, mir-106-prec-X,mir-107Nol , mir-107- prec-10, mir-122a-prec, mir-123-precNol , mir-123-precNo2, mir-124a-l-precl, mir- 124a-2-prec, mir-124a-3-prec, mir-125b-l, mir-125b-2-precNo2, mir-127-prec, mir- 128b-precNol, mir-128b-precNo2, mir-133a-l, mir-135-2-prec, mir-136-precNo2, mir- 138-1-prec, mir-140No2, mir-142-prec, mir-143-prec, mir-144-precNo2, mir-145-prec, mir-146bNol, mir- 146-prec, mir-147-prec, mir-148aNol, mir-148-prec, mir-149-prec, mir-150-prec, mir-153-l-precl, mir-154-preclNol , mir-155-prec, mir-15aNol, mir- 16- INoI, mir-16-2Nol , mir-181a-precNol, mir-181b-lNol, mir-181b-2Nol, mir-181b- precNo 1 , mir- 181 b-precNo2, mir- 181 c-precNo 1 , mir- 181 dNo 1 , mir- 188-prec, mir- 18bNo2, mir-191-prec, mir-192No2, mir-193bNo2, mir- 194-2NoI, mir- 195 -prec, mir- 196-2-precNo2, mir-197-prec, mir-198-prec, mir- 199a- 1 -prec, mir-199a-2-prec, mir- 199b-precNol , mir-200a-prec, mir-200bNol, mir-200bNo2, mir-202*, mir-202-prec, mir-204-precNo2, mir-205-prec, mir-208-prec, mir-20bNol, mir-212-precNol, mir- 212-precNo2, mir-213-precNol, mir-214-prec, mir-215-precNo2, mir-216-precNol , mir-219-2Nol, mir-219-prec, mir-223-prec, mir-29b-lNol, mir-29b-2=102prec7.1=7.2, mir-321Nol, mir-321No2, mir-324Nol, mir-324No2, mir-328Nol, mir-342Nol, mir- 361NoI, mir-367Nol, mir-370Nol, mir-371Nol , miR-373*Nol , mir-375, mir- 376aNol, mir-379Nol, mir-380-5p, mir-382, mir-384, mir-409-3p, mir-423Nol , mir- 424No2, mir-429Nol , mir-429No2, mir-4323p, mir-4325p, mir-449Nol, mir-450-1, mir-450-2Nol, mir-483Nol , mir-484, mir-487Nol, mir-495Nol, mir-499No2, mir- 501No2, mir-503Nol, mir-509Nol, mir-514-lNo2, mir-515-15p, mir-515-23p, mir- 516-33p, mir-516-43p, mir-518e/526c, mir-519a- 1/52, mir-519a-2No2, mir-519b, mir- 519c/52, mir-520c/52, mir-526a-2Nol, mir-526a-2No2, MPR103 right, MPR121 left, MPR121 left, MPR130 left, MPR130 right, MPR133 right, MPR141 left, MPR151 left, MPRl 56 left, MPRl 62 left, MPRl 74 left, MPRl 74 right, MPRl 85 right, MPRl 97 right, MPR203 left, MPR207 right, MPR215 left, MPR216 left, MPR224 left, MPR224 right, MPR228 left, MPR234 right, MPR237 left, MPR243 left, MPR244 right, MPR249 left, MPR254 right, MPR74 left, MPR88 right, and MPR95 left, wherein said level of expression of said microRNA indicates said cell is sensitive to said treatment.
73. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd892, Hcd678, hsa-mir-007-l-prec, MPR243, Hcd654, hsa- mir-487, Hcd794, Hcd739, and Hcd562, wherein said level of expression of said microRNA indicates that said cell is sensitive to Vincristine.
74. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of HUMTRF, HPRl 87, hsa-mir-450-1, hsa-mir-155-prec, hsa-mir- 515-15p, hsa-mir-181b-prec, hsa-mir-124a-l-precl, hsa-mir-450-2, Hcd923, hsa-mir- 342, hsa-mir-142-prec, hsa-mir-223-prec, Hcd754, and Hcd213_HPR182, wherein said level of expression of said microRNA indicates that said cell is sensitive to Cisplatin.
75. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of MPR121 , HUMTRS, hsa-mir-213-prec, hsa-mir-155-prec, hsa- mir-147-prec, hsa-mir-100, hsa-mir-138-l-prec, hsa-mir-140, hsa-mir-146-prec, hsa- mir-509, hsa-mir-146b, Hcd514, Hcd397, Hcd731 , hsa-mir-034-prec, and hsa-mir-100- 1/2-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Azaguanine.
76. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd415, Hcd768, HUMTRF, Hcd866, Hcdl45, HUMTRAB, Hcd913, HPR163, Hcd697, Hcd755, Hcd716, MPR207, HSTRNL, HPR206, MPR243, Hcd654, MPR130, Hcd782, Hcd794, Hcd739, hsa-mir-142-prec, HSHELAOl, HUMTRVlA, and Hcd754, wherein said level of expression of said microRNA indicates that said cell is sensitive to Etoposide.
77. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd768, hsa-mir-483, Hcdl45, hsa-mir-197-prec, hsa-mir-212- prec, HPRl 63, Hcd654, hsa-mir-342, Hcd794, hsa-mir-142-prec, and Hcd754, wherein said level of expression of said microRNA indicates that said cell is sensitive to Adriamycin.
78. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-096-prec-7, Hcd605, hsa- mir-007-2-prec, hsa-mir-019b-2-prec, MPR216, hsa-mir-019b-l-prec, hsa-mir- 135-2- prec, HSTRNL, hsa-mir-025-prec, hsa-mir-007-l-prec, hsa-mir-019a-prec, hsa-mir- 380-5p, hsa-mir-093-prec-7.1=093-1, hsa-mir- 106-prec-X, hsa-mir- 142-prec, hsa-mir- 018-prec, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Aclarubicin.
79. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd768, HUMTRF, hsa-mir-213-prec, hsa-mir-181b-prec, MPR244, hsa-mir-409-3p, HSTRNL, hsa-mir-382, hsa-mir-342, hsa-mir- 142-prec, and Hcd200, wherein said level of expression of said microRNA indicates that said cell is sensitive to Mitoxantrone.
80. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of HUMTRF, Hcdl48_HPR2251eft, Hcd938, MPRl 74, and hsa- mir-4323p, wherein said level of expression of said microRNA indicates that said cell is sensitive to Mitomycin.
81. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-096-prec-7, hsa-mir- 101- prec-9, hsa-mir-20b, hsa-mir-019b-2-prec, hsa-mir-032-prec, MPR156, hsa-mir-019b-l- prec, hsa-mir- 135-2-prec, hsa-mir-025-prec, hsa-mir-007-l-prec, hsa-mir-361, hsa-mir- 093-prec-7.1=093-1, hsa-mir- 106-prec-X, hsa-mir-098-prec-X, hsa-mir- 142-prec, HPRl 69, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Paclitaxel.
82. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir- 123 -prec, Hcd257, hsa-mir- 155-prec, ath-MIR180a, Hcd448, HSTRNL, MPRl 74, Hcd200, hsa-mir-4323p, and HPR244, wherein said level of expression of said microRNA indicates that said cell is sensitive to Gemcitabine.
83. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-096-prec-7, hsa-mir-095-prec-4, HSTRNL, and hsa- mir-007-l-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Taxotere.
84. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of MPR141 , hsa-mir-424, Hcd690, Hcd783, hsa-mir-150-prec, Hcd266, hsa-mir-503, hsa-mir-128b-prec, Hcd397, and hsa-mir-484, wherein said level of expression of said microRNA indicates that said cell is sensitive to Dexamethasone.
85. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of HUMTRF, hsa-mir-155-prec, hsa-mir-515-15p, Hcd938, Hcd642, Hcdl20, hsa-mir-380-5p, hsa-mir-342, hsa-mir-142-prec, hsa-mir-223-prec, and hsa-mir-4323p, wherein said level of expression of said microRNA indicates that said cell is sensitive to Ara-C.
86. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd544, hsa-mir-181c-prec, Hcd517, MPRl 51, hsa-mir-213- prec, hsa-mir- 181 b-prec, hsa-mir-150-prec, hsa-mir-153-l-precl, hsa-mir-128b-prec, Hcd812, hsa-mir- 195 -prec, hsa-mir-342, hsa-mir-370, hsa-mir-142-prec, hsa-mir-223- prec, and hsa-mir-484, wherein said level of expression of said microRNA indicates that said cell is sensitive to Methylprednisolone.
87. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-096-prec-7, hsa-mir- 123- prec, Hcd250, hsa-mir-518e, HPR232, Hcd263, hsa-mir-516-33p, Hcd605, Hcd373, MPR254, MPR215, HUMTRF, hsa-mir-106a, hsa-mir-20b, Hcd361, Hcd412, Hcd78L hsa-mir-019b-2-prec, HPR214, Hcd807, Hcd817, Hcd788, Hcd970, Hcdl48_HPR2251eft, HcdlO2, Hcd246, HPR199, HPR233, Hcd383, MPR224, HPR172, MPR216, hsa-mir-321 , Hcd586, Hcd587, Hcd249, Hcd279, HPR159, Hcd689, Hcd691, hsa-mir-019b-l-prec, Hcd413, Hcd581 , Hcd536_HPR104, Hcd230, HPRl 54, Hcd270, Hcd649, Hcd889, Hcd938, HPR266, hsa-mir-025-prec, Hcd355_HPR190, MPRl 62, Hcd923, MPR237, MPRl 74, hsa-mir-019a-prec, hsa_mir_490_Hcd20, hsa-mir-380-5p, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec- X, Hcd627, hsa-mir-142-prec, HPRl 69, hsa-mir-OOlb-2-prec, hsa-mir-018-prec, hsa- mir-020-prec, Hcd404, hsa-mir-384, and hsa-mir-4323p, wherein said level of expression of said microRNA indicates that said cell is sensitive to Methotrexate.
88. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-376a, hsa-mir-155-prec, hsa-mir-409-3p, hsa-mir-495, Hcd498, hsa-mir-199a-2-prec, hsa-mir-382, HPR271, hsa-mir-145-prec, and hsa-mir- 199a-l-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Bleomycin.
89. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-lOl-prec-9, hsa-mir-144- prec, hsa-mir-519a-l, hsa-mir-519b, hsa-mir-015b-prec, hsa-mir-106a, hsa-mir-16-1, hsa-mir-181d, hsa-mir-017-prec, hsa-mir-019b-2-prec, hsa-mir-192, hsa-mir-213-prec, hsa-mir-215-prec, hsa-mir-107, hsa-mir-200b, hsa-mir-103-prec-5=103-l, hsa-mir- 519a-l/526c, MPR216, hsa-mir-019b- l-prec, hsa-mir-107-prec-lO, hsa-mir-135-2-prec, hsa-mir-103-2-prec, hsa-mir-519a-2, hsa-mir-025-prec, hsa-mir-16-2, MPR95, hsa-mir- 016b-chr3, Hcd948, hsa-mir-195-prec, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec- X, hsa-mir-142-prec, hsa-mir-519c/526c, hsa-mir-200a-prec, hsa-mir-016a-chrl3, hsa- mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Methyl-GAG.
90. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd829, HUMTRF, HPRl 87, Hcd210_HPR205, hsa-mir-379, hsa-mir-213-prec, hsa-mir-4325p, hsa-mir-450-1 , hsa-mir-155-prec, Hcd28_HPR39right, MPR244, hsa-mir-409-3p, hsa-mir-124a-l-precl, hsa-mir- 154- precl, hsa-mir-495, hsa-mir-515-23p, Hcd43 δright, Hcd770, hsa-mir-382, hsa-mir- 223-prec, Hcd754, and Hcd213_HPR182, wherein said level of expression of said microRNA indicates that said cell is sensitive to Carboplatin.
91. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-096-prec-7, hsa-mir-429, Hcd693, HPR214, Hcd586, Hcd249, Hcd689, hsa-mir- 194-2, Hcd581, Hcd270, hsa-mir-025-prec, Hcd340, hsa- mir-007-l-prec, hsa-mir-093-prec-7.1=093-1, hsa-mir- 106-prec-X, Hcd794, hsa-mir- 020-prec, and hsa-mir-4323p, wherein said level of expression of said microRNA indicates that said cell is sensitive to 5-FU (5-Fluorouracil).
92. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir- 136-prec, Hcd570, Hcd873, Hcd282PO, Hcd799, Hcd829, Hcd210_HPR205, hsa-mir-219-prec, hsa-mir-202, hsa-mir-429, Hcd693, hsa- mir-022-prec, MPR88, hsa-mir- 198-prec, hsa-mir- 199b-prec, Hcdl45, hsa-mir- 124a-2- prec, hsa-mir- 138-2-prec, Hcd960, Hcd869, Hcd384, hsa-mir-027b-prec, Hcd444, hsa- mir-194-2, hsa-mir- 197-prec, Hcd913, HPR163, hsa-mir- 138-1 -prec, hsa-mir-OlOa- prec, hsa-mir-023b-prec, hsa-mir- 193b, Hcd654, Hcd542, hsa-mir- 199a-2-prec, hsa- mir-214-prec, Hcd608, Hcd684, hsa-mir- 145-prec, hsa-mir-023a-prec, hsa-mir-024-2- prec, and hsa-mir- 199a- 1 -prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to radiation therapy.
93. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir- 123 -prec, hsa-mir- 106a, hsa-mir-20b, hsa-mir-017-prec, hsa-mir-019b-2-prec, hsa-mir-033-prec, hsa-mir-092- prec- 13=092-1, hsa-mir- 122a-prec, Hcd783, MPR216, hsa-mir-019b-l-prec, hsa-mir- 135-2-prec, hsa-mir- 128b-prec, hsa-mir-025-prec, Hcd51 1, hsa-mir-093-prec-7.1=093 - 1, hsa-mir- 106-prec-X, hsa-mir- 142-prec, HPRl 69, hsa-mir-223-prec, hsa-mir-018- prec, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to PXDlOl (belinostat).
94. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-096-prec-7, Hcd605, hsa-mir-20b, hsa-miR-373*, HUMTRAB, hsa-mir-019b-l-prec, HPR163, hsa-mir-371 , hsa-mir-025-prec, hsa-mir- 18b, hsa-mir-093-prec-7.1=093-1 , hsa-mir-106-prec-X, hsa-mir-142-prec, and hsa-mir- 020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to 5-Aza-2'-deoxycytidine (Decitabine).
95. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of HUMTRF, hsa-mir-483, MPR74, hsa-mir-122a-prec, ath- MIRl 80a, hsa-mir-128b-prec, Hcd923, hsa-mir-106-prec-X, hsa-mir-342, hsa-mir-142- prec, HPRl 69, hsa-mir-223-prec, Hcd754, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Idarubicin.
96. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-124a-3-prec, hsa-mir-181a-prec, Hcd773, Hcd683, Hcd796, HUMTRF, HUMTRS, hsa-mir-181b-2, Hcd294, hsa-mir-20b, hsa-mir-181d, hsa-mir-213-prec, Hcdl48_HPR2251eft, hsa-mir-515-15p, hsa-mir-181b-prec, Hcd783, HUMTRAB, HUMTRN, hsa-mir-181b-l, hsa-mir-124a-l-precl, hsa-mir-367, hsa-mir- 128b-prec, Hcd43 8right, hsa-mir-025-prec, hsa-mir-216-prec, Hcd731, hsa-mir-093- prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir-342, hsa-mir-142-prec, HSHELAOl, HUMTRVlA, hsa-mir-223-prec, Hcd754, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Melphalan.
97. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd829, hsa-mir-197-prec, HPR163, and hsa-mir-150-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to IL4-PE38 fusion protein.
98. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd829, hsa-mir-197-prec, HPRl 63, and hsa-mir-150-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to IL13-PE38QQR fusion protein (cintredekin besudotox).
99. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-034prec, Hcd255, Hcd712, Hcd965, Hcd891 , Hcd210_HPR205, hsa-mir-429, Hcd753, Hcd693, MPR203, Hcd704, Hcd863PO, hsa- mir-122a-prec, Hcd760, Hcd338, HPR213, Hcd852, Hcd366, MPR103, Hcd669, and hsa-mir-188-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Valproic acid (VPA).
100. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd257, hsa-mir-148-prec, Hcd512, HPR227, Hcd421, MPR203, hsa-mir-017-prec, hsa-mir-219-2, hsa-mir-328, Hcd783, Hcdl 81 , HPR213, hsa-mir-191-prec, hsa-mir-375, hsa-mir-212-prec, Hcd913, Hcd716, MPR207, HPR206, hsa-mir-016b-chr3, Hcd654, hsa-mir-195-prec, Hcd425, hsa-mir-148a, hsa- mir-142-prec, and hsa-mir-016a-chrl3, wherein said level of expression of said microRNA indicates that said cell is sensitive to All-trans retinoic acid (ATRA).
101. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd99, hsa-mir-520c/526a, hsa-mir-191-prec, hsa-mir-205-prec, hsa-mir-375, hsa-mir-423, hsa-mir-449, and hsa-mir-196-2-prec, wherein said level of expression of said micrRNA indicates that said cell is sensitive to Cytoxan.
102. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of HUMTRF, MPR74, hsa-mir-213-prec, hsa-mir-155-prec, hsa- mir-181b-prec, hsa-mir-342, and hsa-mir-4323p, wherein said level of expression of said microRNA indicates that said cell is sensitive to Topotecan (Hycamtin).
103. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-123 -prec, hsa-mir-514-1 , hsa-mir-1 Ol-prec-9, hsa-mir-148-prec, hsa-mir-106a, hsa-mir-20b, Hcd781 , hsa-mir- 017-prec, hsa-mir-019b-2-prec, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1, hsa-mir- 107, hsa-mir-103-prec-5=103-l , MPR216, hsa-mir-29b-2=102prec7.1=7.2, hsa-mir- 019b-l-prec, hsa-mir-107-prec-lO, hsa-mir-135-2-prec, Hcd581 , hsa-mir-103-2-prec, Hcd230, hsa-mir-025-prec, hsa-mir-208-prec, hsa-mir-18b, hsa-mir-093-prec-7.1=093- 1, hsa-mir-106-prec-X, hsa-mir-142-prec, HPRl 69, hsa-mir-018-prec, and hsa-mir-020- prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Suberoylanilide hydroxamic acid (SAHA, vorinostat, Zolinza).
104. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd415, hsa-mir-147-prec, hsa-mir-033b-prec, Hcd778, hsa- mir-127-prec, hsa-mir-324, Hcd794, and Hcd634, wherein said level of expression of said microRNA indicates that said cell is sensitive to Depsipeptide (FR901228).
105. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of MPR121, Hcdl 15, Hcd693, Hcd704, HPRlOO, Hcd760, hsa- mir-147-prec, hsa-mir-033b-prec, hsa-mir-146-prec, Hcdl42, hsa-mir-501 , Hcd716, MPR207, Hcd777, hsa-mir-204-prec, hsa-mir-146b, Hcd51 1, Hcd397, MPR130, Hcd782, hsa-mir-324, Hcd794, and Hcd739, wherein said level of expression of said microRNA indicates that said cell is sensitive to Bortezomib.
106. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-096-prec-7, hsa-mir-123- prec, MPR249, HPR232, hsa-mir-lOl-prec-9, hsa-mir-106a, hsa-mir-20b, Hcd861, hsa- mir-017-prec, hsa-mir-019b-2-prec, hsa-mir-033-prec, Hcdl 02, MPR216, Hcd975, hsa- mir-019b-l-prec, hsa-mir-135-2-prec, Hcd581, Hcd536_HPR104, hsa-mir-128b-prec, HSTRNL, hsa-mir-025-prec, hsa-mir-18b, HPR262, Hcd923, Hcd434, Hcd658, HPR129, hsa-mir-380-5p, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, Hcd627, hsa-mir-142-prec, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Leukeran.
107. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd773, Hcd248, hsa-mir-181d, MPR74, hsa-mir-213-prec, hsa-mir-155-prec, MPR197, hsa-mir-181b-prec, hsa-mir-29b-2=102prec7.1=7.2, hsa- mir-029c-prec, Hcd318, hsa-mir-128b-prec, hsa-mir-130a-prec, hsa-mir-140, hsa-mir- 16-2, hsa-mir-526a-2, hsa-mir-016b-chr3, hsa-mir-195-prec, hsa-mir-216-prec, hsa-mir- 342, hsa-mir-29b-l, Hcd627, hsa-mir-102-prec-l, hsa-mir-142-prec, hsa-mir-223-prec, hsa-let-7f-2-prec2, and hsa-mir-016a-chrl3, wherein said level of expression of said microRNA indicates that said cell is sensitive to Fludarabine.
108. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd794 and Hcd754, wherein said level of expression of said microRNA indicates that said cell is sensitive to Vinblastine.
109. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-096-prec-7, hsa-mir-124a-3-prec, hsa-mir-lOl-prec-9, Hcd712, Hcd693, hsa-mir-219-2, Hcdl45, hsa-mir-155-prec, HPR213, hsa-mir-212- prec, Hcd913, Hcd716, MPR207, Hcd559, Hcd654, Hcd739, and hsa-mir-142-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Busulfan.
110. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-123-prec, hsa-mir-101- prec-9, Hcd517, Hcd796, Hcd749, Hcd674, hsa-mir-019b-2-prec, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1, hsa-mir- 124a-2-prec, hsa-mir-143-prec, hsa-mir-516-43p, hsa-mir-216-prec, Hcd731, hsa-mir- 106-prec-X, hsa-mir-142-prec, hsa-mir-223-prec, Hcd754, and hsa-mir-018-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Dacarbazine.
1 1 1. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir- 148-prec, hsa-mir-20b, hsa- mir-007-2-prec, hsa-mir-017-prec, hsa-mir-019b-2-prec, Hcd760, Hcd783, MPR216, hsa-mir-375, hsa-mir-019b- 1 -prec, hsa-mir-135-2-prec, hsa-mir- 150-prec, hsa-mir- 128b-prec, hsa-mir-499, hsa-mir-025-prec, hsa-mir-007-l-prec, hsa-mir-019a-prec, hsa- mir-093-prec-7.1=093-1 , hsa-mir-106-prec-X, hsa-mir-142-prec, HPR169, hsa-mir-018- prec, hsa-mir-020-prec, and hsa-mir-484, wherein said level of expression of said microRNA indicates that said cell is sensitive to Oxaliplatin.
1 12. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd257, Hcd768, Hcd796, HUMTRF, HUMTRS, MPR74, hsa- mir-213-prec, hsa-mir-155-prec, Hcd763, hsa-mir-181b-prec, ath-MIR180a, hsa-mir- 216-prec, hsa-mir-342, hsa-mir-142-prec, HSHELAOl , HUMTRVlA, hsa-mir-223- prec, Hcd754, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Hydroxyurea.
1 13. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd257, Hcd946, Hcd503, hsa-mir-429, Hcd693, hsa-miR- 373*, Hcd738, hsa-mir-328, Hcd783, Hcdl 81, Hcd631, Hcd279, hsa-mir- 194-2, hsa- mir-197-prec, HPR163, hsa-mir- 150-prec, Hcd323, hsa-mir- 103-2-prec, Hcd243, Hcd938, hsa-mir-025-prec, hsa-mir-007-l-prec, MPR243, Hcd51 1 , Hcd654, hsa-mir- 199a-2-prec, hsa-mir-214-prec, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, Hcd794, Hcd530, HSHELAOl, Hcd754, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Tegafur.
1 14. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd768, HUMTRF, Hcdl45, Hcd923, hsa-mir-216-prec, hsa- mir-093-prec-7.1=093-1 , hsa-mir-342, Hcd794, hsa-mir-142-prec, HSHELAOl, hsa- mir-223-prec, and Hcd754, wherein said level of expression of said microRNA indicates that said cell is sensitive to Daunorubicin.
1 15. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir- 125b-2-prec, hsa-mir-022-prec, hsa-mir- 125b- 1 , hsa- mir- 155-prec, hsa-mir- 100, hsa-mir-409-3p, hsa-mir-495, hsa-mir- 199a-2-prec, hsa-mir- 382, and hsa-mir- 100- 1/2-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Bleomycin.
1 16. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd338, hsa-mir-099b-prec-19, and hsa-mir-149-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Estramustine.
117. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-181a-prec, hsa-mir-181c-prec, HUMTRF, hsa-mir- 18Id 9 MPR74, Hcd817, hsa-mir-213-prec, hsa-mir-155-prec, Hcdl48_HPR2251eft, hsa- mir-515-15p, hsa-mir-181b-prec, HUMTRN, hsa-mir-128b-prec, hsa-mir-450-2, hsa- mir-216-prec, hsa-mir-342, hsa-mir-142-prec, hsa-mir-223-prec, Hcd754, and hsa-mir- 020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Chlorambucil.
1 18. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-124a-3-prec, Hcd946, Hcd683, HPR264, MPRl 85, HUMTRF, Hcd294, Hcd503, hsa-mir-20b, MPR74, MPR234, Hcd447, Hcd817, Hcdl48_HPR2251eft, hsa-mir-515-15p, Hcd383, hsa-mir-181b-prec, Hcd783, MPR224, HPR172, MPR216, HUMTRN, hsa-mir-321, HPR159, MPR228, ath-MIR180a, hsa- mir-197-prec, hsa-mir-124a-l-precl, hsa-mir-128b-prec, Hcd28_HPR391eft, Hcd889, Hcd350, hsa-mir-025-prec, hsa-mir-208-prec, hsa-mir-450-2, Hcd923, Hcd434, HPR129, HPR220, hsa-mir-380-5p, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir-342, hsa-mir-142-prec, HSHELAOl, hsa-mir-223-prec, Hcd754, hsa-mir-020- prec, and hsa-mir-4323p, wherein said level of expression of said microRNA indicates that said cell is sensitive to Mechlorethamine.
1 19. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-483, Hcd631 , hsa-mir-212-prec, Hcd938, MPR133, Hcd794, Hcd438, and Hcd886, wherein said level of expression of said microRNA indicates that said cell is sensitive to Streptozocin.
120. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, Hcd517, Hcd796, HUMTRF, hsa- mir-20b, hsa-mir-019b-2-prec, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1, Hcdl48_HPR2251eft, HUMTRAB, Hcd975, hsa-mir-135-2-prec, hsa-mir-128b-prec, hsa-mir-143-prec, hsa-mir-025-prec, hsa-mir-216-prec, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir-142-prec, HSHELAOl , HUMTRVlA, hsa-mir-223-prec, Hcd754, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Carmustine.
121. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-lOl-prec-9, Hcd796, hsa-mir-20b, HUMTRAB, hsa- mir-135-2-prec, hsa-mir-153-l-precl, hsa-mir-025-prec, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir-142-prec, HUMTRVlA, Hcd754, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Lomustine.
122. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-096-prec-7, hsa-mir-123- prec, MPR249, HPR232, hsa-mir-101-prec-9, hsa-mir-106a, hsa-mir-20b, Hcd861 , hsa- mir-017-prec, hsa-mir-019b-2-prec, hsa-mir-033-prec, HcdlO2, MPR216, Hcd975, hsa- mir-019b-l-prec, hsa-mir-135-2-prec, Hcd581, Hcd536_HPR104, hsa-mir-128b-prec, HSTRNL, hsa-mir-025-prec, hsa-mir-18b, HPR262, Hcd923, Hcd434, Hcd658, HPR129, hsa-mir-380-5p, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, Hcd627, hsa-mir-142-prec, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Mercaptopurine.
123. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-124a-3-prec, Hcd768, HUMTRF, hsa-mir-213-prec, hsa-mir-181b-prec, Hcd783, hsa-mir-212-prec, hsa-mir-124a-l-precl, hsa-mir-342, hsa- mir-142-prec, HSHELAOl , hsa-mir-223-prec, and Hcd754, wherein said level of expression of said microRNA indicates that said cell is sensitive to Teniposide.
124. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-025-prec, hsa-mir-007-l-prec, hsa-mir-093-prec- 7.1=093-1, Hcd794, and hsa-mir-142-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Dactinomycin.
125. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd257, hsa-mir-148-prec, Hcd512, HPR227, Hcd421, MPR203, hsa-mir-017-prec, hsa-mir-219-2, hsa-mir-328, Hcd783, Hcdl δl , HPR213, hsa-mir-191-prec, hsa-mir-375, hsa-mir-212-prec, Hcd913, Hcd716, MPR207, HPR206, hsa-mir-016b-chr3, Hcd654, hsa-mir-195-prec, Hcd425, hsa-mir-148a, hsa- mir-142-prec, and hsa-mir-016a-chrl3, wherein said level of expression of said microRNA indicates that said cell is sensitive to Tretinoin.
126. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-181b-2, Hcd417, Hcd440_HPR257, hsa-mir-019b-2-prec, hsa-mir-213 -prec, hsa-mir-O33-prec, hsa-mir- 092-prec- 13=092-1, hsa-mir-181b-prec, hsa-mir-128b-prec, hsa-mir-526a-2, MPR95, HPR220, hsa-mir-133a-l, hsa-mir-148a, hsa-mir-142-prec, HPR169, hsa-mir-223-prec, hsa-mir-018-prec, hsa-mir-020-prec, and hsa-mir-484, wherein said level of expression of said microRNA indicates that said cell is sensitive to Ifosfamide.
127. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, Hcd547, Hcd257, hsa-mir-148-prec, HUMTRS, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1, hsa-mir-375, hsa-mir-095- prec-4, hsa-mir-025-prec, hsa-mir-202-prec, hsa-mir-007-l-prec, hsa-mir-093-prec- 7.1=093-1, hsa-mir-106-prec-X, hsa-mir-142-prec, hsa-mir-223-prec, and hsa-mir-018- prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Tamoxifen.
128. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of HUMTRF, HUMTRN, hsa-mir-124a-l-precl, hsa-mir-150-prec, Hcd923, HPR181 , Hcd569, hsa-mir-199a-2-prec, Hcd754, and hsa-mir-4323p, wherein said level of expression of said microRNA indicates that said cell is sensitive to Floxuridine.
129. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of HUMTRF, hsa-mir-380-5p, hsa-mir-342, hsa-mir-142-prec, and Hcd200, wherein said level of expression of said microRNA indicates that said cell is sensitive to Irinotecan.
130. The method of claim 72, wherein said at least one microRNA is selected from the group consisting of Hcd289, Hcd939, Hcd330, HPR76, Hcdl 1 1, Hcd976, hsa-mir- 15a, hsa-mir-OOlb-1-precl, hsa-mir-450-1, hsa-mir-200b, Hcd578, and hsa-mir-200a- prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to Satraplatin.
131. The method of any of claims 72-130, wherein an increase in the level of expression of said microRNA indicates increased sensitivity of said cell to said treatment.
132. The method of any of claims 72-130, wherein said cell is a cancer cell.
133. The method of any of claims 72-130, wherein a decrease in the level of expression of said microRNA indicates increased sensitivity of said cell to said treatment.
134. The method of claim 72, wherein said level of expression of said microRNA is measured using a quantitative reverse transcription-polymerase chain reaction (qRT- PCR).
135. A method for determining the development of resistance of a cell in a patient to a treatment to which said cell in said patient has previously been sensitive, said method comprising measuring a level of expression of at least one microRNA of any one of claims 72-130 of said cell, wherein a decrease in said level of expression of said microRNA in said cell relative to the level of expression of said microRNA in a control cell sensitive to said treatment indicates resistance or a propensity to develop resistance to the treatment by said patient.
136. A method for determining the development of resistance of a cell in a patient to a treatment to which said cell in said patient has previously been sensitive, said method comprising measuring a level of expression of at least one microRNA of any one of claims 72-130 in said cell, wherein an increase in said level of expression of said microRNA in said cell relative to the level of expression of said microRNA in a control cell sensitive to said treatment indicates resistance or a propensity to develop resistance to the treatment by said patient.
137. A kit comprising a single-stranded nucleic acid molecule that is substantially complementary to or substantially identical to at least 5 consecutive nucleotides of at least one gene selected from the group consisting of ACTB, ACTN4, ADA, ADAM9, ADAMTSl, ADDl, AFlQ, AIFl, AKAPl , AKAP13, AKRlCl, AKTl, ALDH2, ALDOC, ALG5, ALMSl, ALOXl 5B, AMIG02, AMPD2, AMPD3, ANAPC5, ANP32A, ANP32B, ANXAl, AP1G2, APOBEC3B, APRT, ARHE, ARHGAP15, ARHGAP25, ARHGDIB, ARHGEF6, ARL7, ASAHl, ASPH, ATF3, ATIC, ATP2A2, ATP2A3, ATP5D, ATP5G2, ATP6V1B2, BC008967, BCATl , BCHE, BCLl IB, BDNF, BHLHB2, BIN2, BLMH, BMIl , BNIP3, BRDT, BRRNl , BTN3A3, Cl Iorf2, C14orfl39, C15orf25, C18orflO, Clorf24, Clorf29, Clorf38, ClQRl, C22orfl 8, C6orf32, CACNAlG, CACNB3, CALMl, CALML4, CALU, CAP350, CASP2, CASP6, CASP7, CAST, CBLB, CCNA2, CCNBlIPl, CCND3, CCR7, CCR9, CDlA, CDlC, CDlD, CDlE, CD2, CD28, CD3D, CD3E, CD3G, CD3Z, CD44, CD47, CD59, CD6, CD63, CD8A, CD8B1, CD99, CDClO, CDC14B, CDHl 1 , CDH2, CDKL5, CDKN2A, CDW52, CECRl, CENPB, CENTBl , CENTG2, CEPl, CG018, CHRNA3, CHSl , CIAPINl , CKAP4, CKIP-I, CNP, COL4A1, COL5A2, COL6A1, COROlC, CRABPl , CRK, CRYl , CSDA, CTBPl , CTSC, CTSL, CUGBP2, CUTC, CXCLl , CXCR4, CXorf9, CYFIP2, CYLD, CYR61, DATFl , DAZAPl , DBNl, DBT, DCTNl , DDX 18, DDX5, DGKA, DIAPHl , DKCl, DKFZP434J154, DKFZP564C186, DKFZP564G2022, DKFZp564J157, DKFZP564K0822, DNAJClO, DNAJC7, DNAPTP6, DOCKlO, DOCK2, DPAGTl, DPEP2, DPYSL3, DSIPI, DUSPl , DXS9879E, EEF1B2, EFNB2, EHD2, EIF5A, ELK3, ENO2, EPASl, EPB41L4B, ERCC2, ERG, ERP70, EVERl, EVI2A, EVL, EXTl, EZH2, F2R, FABP5, FAD 104, FAM46A, FAU, FCGR2A, FCGR2C, FER 1L3, FHLl, FHODl, FKBPlA, FKBP9, FLJ10350, FLJ10539, FLJ10774, FLJ12270, FLJ13373, FLJ20859, FLJ21 159, FLJ22457, FLJ35036, FLJ46603, FLNC, FLOTl, FMNLl, FNBPl, FOLHl, FOXF2, FSCNl, FTL, FYB, FYN, G0S2, G6PD, GALIG, GALNT6, GAT A2, GATA3, GFPTl, GIMAP5, GIT2, GJAl, GLRB, GLTSCR2, GLUL, GMDS, GNAQ, GNB2, GNB5, GOT2, GPR65, GPRASPl, GPSM3, GRP58, GSTM2, GTF3A, GTSEl , GZMA, GZMB, HlFO, HlFX, H2AFX, H3F3A, HA-I, HEXB, HIC, HIST1H4C, HKl, HLA- A, HLA-B, HLA-DRA, HMGAl, HMGN2, HMMR, HNRPAl, HNRPD, HNRPM, HOXA9, HRMTlLl , HSA9761, HSPA5, HSU79274, HTATSFl, ICAMl, ICAM2, IER3, IFIl 6, IFI44, IFITM2, IFITM3, IFRG28, IGFBP2, IGSF4, IL13RA2, IL21R, IL2RG, IL4R, IL6, IL6R, IL6ST, IL8, IMPDH2, INPP5D, INSIGl, IQGAPl, IQGAP2, IRS2, ITGA5, ITM2A, JARID2, JUNB, K-ALPHA-I, KHDRBSl , KIAA0355, KIAA0802, KIAA0877, KIAA0922, KIAA1078, KIAAl 128, KIAA1393, KIFCl, LAIRl, LAMBl, LAMB3, LAT, LBR, LCK, LCPl, LCP2, LEFl, LEPREl , LGALSl , LGALS9, LHFPL2, LNK, LOC54103, LOC55831 , LOC81558, LOC94105, LONP, LOX, LOXL2, LPHN2, LPXN, LRMP, LRP12, LRRC5, LRRN3, LSTl, LTB, LUM, LY9, LY96, MAGEB2, MAL, MAPlB, MAP1LC3B, MAP4K1, MAPKl, MARCKS, MAZ, MCAM, MCLl , MCM5, MCM7, MDH2, MDNl, MEF2C, MFNG, MGC17330, MGC21654, MGC2744, MGC4083, MGC8721, MGC8902, MGLL, MLPH, MPH0SPH6, MPPl , MPZLl, MRP63, MRPS2, MTlE, MTlK, MUFl, MVP, MYB, MYL9, MYOlB, NAPlLl , NAPl L2, NARF, NASP, NCOR2, NDN, NDUFABl, NDUFS6, NFKBIA, NID2, NIPA2, NME4, NME7, NNMT, NOL5A, NOL8, NOMO2, NOTCHl, NPCl, NQOl , NRl D2, NUDC, NUP210, NUP88, NVL, NXFl, OBFCl , OCRL, OGT, OXAlL, P2RX5, P4HA1, PACAP, PAF53, PAFAH1B3, PALM2- AKAP2, PAX6, PCBP2, PCCB, PFDN5, PFNl, PFN2, PGAMl, PHEMX, PHLDAl, PIM2, PITPNCl, PLAC8, PLAGLl, PLAUR, PLCBl , PLEK2, PLEKHCl , PLOD2, PLSCRl , PNAS-4, PNMA2, POLR2F, PPAP2B, PRFl, PRGl , PRIMl , PRKCH, PRKCQ, PRKD2, PRNP, PRP19, PRPF8, PRSS23, PSCDBP, PSMB9, PSMC3, PSME2, PTGER4, PTGES2, PTOVl, PTP4A3, PTPN7, PTPNSl , PTRF, PURA, PWPl , PYGL, QKI, RAB3GAP, RAB7L1, RAB9P40, RAC2, RAFTLIN, RAG2, RAPlB, RASGRP2, RBPMS, RCNl, RFC3, RFC5, RGC32, RGS3, RHOH, RIMS3, RIOK3, RIPK2, RISl , RNASE6, RNF144, RPLlO, RPLlOA, RPL12, RPL13A, RPL17, RPLl 8, RPL36A, RPLPO, RPLP2, RPS 15, RPS 19, RPS2, RPS4X, RPS4Y1, RRAS, RRAS2, RRBPl, RRM2, RUNXl, RUNX3, S100A4, SART3, SATBl, SCAPl, SCARBl , SCN3A, SEC31L2, SEC61G, SELL, SELPLG, SEMA4G, SEPTlO, SEPT6, SERPINAl, SERPINBl, SERPINB6, SFRS5, SFRS6, SFRS7, SH2D1A, SH3GL3, SH3TC1, SHDl, SHMT2, SIATl, SKBl , SKP2, SLA, SLC 1A4, SLC20A1, SLC25A15, SLC25A5, SLC39A14, SLC39A6, SLC43A3, SLC4A2, SLC7A1 1, SLC7A6, SMAD3, SMOX, SNRPA, SNRPB, SOD2, SOX4, SP 140, SPANXC, SPIl, SRF, SRM, SSA2, SSBP2, SSRPl, SSSCAl, STAG3, STATl, STAT4, STAT5A, STCl , STC2, STOML2, T3JAM, TACCl, TACC3, TAF5, TALI , TAPl, TARP, TBCA, TCF12, TCF4, TFDP2, TFPI, TIMM17A, TIMPl, TJPl, TK2, TM4SF1, TM4SF2, TM4SF8, TM6SF1, TMEM2, TMEM22, TMSBlO, TMSNB, TNFAIP3, TNFAIP8, TNFRSFlOB, TNFRSFlA, TNFRSF7, TNIK, TNPOl, TOBl, TOMM20, TOX, TPKl , TPM2, TRA@, TRAl , TRAM2, TRB@, TRD@, TRIM, TRIM 14, TRIM22, TRIM28, TRIPl 3, TRPV2, TUBGCP3, TUSC3, TXN, TXNDC5, UBASH3A, UBE2A, UBE2L6, UBE2S, UCHLl, UCK2, UCP2, UFDlL, UGDH, ULK2, UMPS, UNG, USP34, USP4, VASP, VAVl, VLDLR, VWF, WASPIP, WBSCR20A, WBSCR20C, WHSCl , WNT5A, ZAP70, ZFP36L1 , ZNF32, ZNF335, ZNF593, ZNFNlAl, and ZYX, wherein said single-stranded nucleic acid molecule allows detection of a level of expression of said gene when said single-stranded nucleic acid molecule is contacted with a nucleic acid molecule expressed from said gene, or its complement, under conditions allowing hybridization to occur between said single- stranded nucleic acid molecule and said nucleic acid molecule expressed from said gene, said kit further comprising instructions for applying nucleic acids collected from a sample from a cancer patient, instructions for measuring the level of expression of said gene, and instructions for determining said cell's sensitivity to a treatment for cancer.
138. The kit of claim 137, wherein said instructions further indicate that a change in said level of expression of said gene relative to the level of expression of said gene in a control cell sensitive to said treatment indicates a change in sensitivity of said cell to said treatment.
139. The kit of claim 137, wherein said gene is selected from the group consisting of RPS4X, S100A4, NDUFS6, C14orfl39, SLC25A5, RPLlO, RPL12, EIF5A, RPL36A, BLMH, CTBPl, TBCA, MDH2, and DXS9879E, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of UBB, B2M, MANlAl, and SUIl, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd892, Hcd678, hsa-mir-007-l-prec, MPR243, Hcd654, hsa-mir-487, Hcd794, Hcd739, and Hcd562, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Vincristine.
140. The kit of claim 137, wherein said gene is selected from the group consisting of ClQRl, SLA, PTPN7, ZNFNlAl, CENTBl , IFI 16, ARHGEF6, SEC31L2, CD3Z, GZMB, CD3D, MAP4K1, GPR65, PRFl, ARHGAP15, TM6SF1 , and TCF4, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of HCLSl, CD53, PTPRCAP, and PTPRC, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of HUMTRF, HPRl 87, hsa-mir-450-1 , hsa-mir-155-prec, hsa-mir-515-15p, hsa-mir-181b-prec, hsa-mir-124a-l-precl , hsa-mir-450-2, Hcd923, hsa-mir-342, hsa- mir-142-prec, hsa-mir-223-prec, Hcd754, and Hcd213_HPR182, wherein said level of expression of said gene or microRN A indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Cisplatin.
141. The kit of claim 137, wherein said gene is selected from the group consisting of SRM, SCARBl, SlATl, CUGBP2, ICAMl, WASPIP, ITM2A, PALM2-AKAP2, PTPNSl , MPPl , LNK, FCGR2A, RUNX3, EVI2A, BTN3A3, LCP2, BCHE, LY96, LCPl, IFIl 6, MCAM, MEF2C, SLC 1A4, FYN, Clorf38, CHSl, FCGR2C, TNIK, AMPD2, SEPT6, RAFTLIN, SLC43A3, RAC2, LPXN, CKIP-I, FLJl 0539, FLJ35036, DOCKlO, TRPV2, IFRG28, LEFl, and ADAMTSl, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of MSN, SPARC, VIM, GAS7, ANPEP, EMP3, BTN3A2, FNl , and CAPN3, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of MPRl 21 , HUMTRS, hsa-mir-213-prec, hsa-mir-155-prec, hsa-mir-147- prec, hsa-mir-100, hsa-mir-138-l-prec, hsa-mir-140, hsa-mir-146-prec, hsa-mir-509, hsa-mir-146b, Hcd514, Hcd397, Hcd731, hsa-mir-034-prec, and hsa-mir-lOO-l/2-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Azaguanine.
142. The kit of claim 137, wherein said gene is selected from the group consisting of CD99, INSIGl , PRGl, MUFl, SLA, SSBP2, GNB5, MFNG, PSMB9, EVI2A, PTPN7, PTGER4, CXorf9, ZNFNlAl , CENTBl, NAPl Ll, HLA-DRA, IFIl 6, ARHGEF6, PSCDBP, SELPLG, LAT, SEC31L2, CD3Z, SH2D1A, GZMB, SCN3A, RAFTLIN, DOCK2, CD3D, RAC2, ZAP70, GPR65, PRFl , ARHG AP 15, NOTCHl, and UBASH3A, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of LAPTM5, HCLSl , CD53, GMFG, PTPRCAP, PTPRC, COROlA, and ITK, or wherein said kit further comprises one or more single- stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd415, Hcd768, HUMTRF, Hcd866, Hcdl45, HUMTRAB, Hcd913, HPR163, Hcd697, Hcd755, Hcd716, MPR207, HSTRNL, HPR206, MPR243, Hcd654, MPRl 30, Hcd782, Hcd794, Hcd739, hsa-mir-142-prec, HSHELAOl, HUMTRVlA, and Hcd754, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Etoposide.
143. The kit of claim 137, wherein said gene is selected from the group consisting of CD99, ALDOC, SLA, SSBP2, IL2RG, CXorf9, RHOH, ZNFNlAl, CENTBl, CDlC, MAP4K1, CD3G, CCR9, CXCR4, ARHGEF6, SELPLG, LAT, SEC31L2, CD3Z, SH2D1A, CDlA, LAIRl, TRB@, CD3D, WBSCR20C, ZAP70, IFI44, GPR65, AIFl, ARHGAPl 5, NARF, and PACAP, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of LAPTM5, HCLSl, CD53, GMFG, PTPRCAP, TCF7, CDlB, PTPRC, COROlA, HEMl, and ITK, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd768, hsa-mir-483, Hcdl45, hsa-mir-197-prec, hsa-mir-212-prec, HPRl 63, Hcd654, hsa-mir-342, Hcd794, hsa-mir-142-prec, and Hcd754, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Adriamycin.
144. The kit of claim 137, wherein said gene is selected from the group consisting of RPL 12, RPLP2, MYB, ZNFNlAl, SCAPl, STAT4, SP 140, AMPD3, TNFAIP8, DDXl 8, TAF5, RPS2, D0CK2, GPR65, H0XA9, FLJ 12270, and HNRPD, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of RPL32, FBL, and PTPRC, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir- 092-prec-X=092-2, hsa-mir-096-prec-7, Hcd605, hsa-mir-007-2-prec, hsa-mir-019b-2- prec, MPR216, hsa-mir-019b-l-prec, hsa-mir-135-2-prec, HSTRNL, hsa-mir-025-prec, hsa-mir-007-l-prec, hsa-mir-019a-prec, hsa-mir-380-5p, hsa-mir-093-prec-7.1=093-1 , hsa-mir-106-prec-X, hsa-mir- 142-prec, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Aclarubicin.
145. The kit of claim 137, wherein said gene is selected from the group consisting of PGAMl, DPYSL3, INSIGl, GJAl, BNIP3, PRGl, G6PD, PLOD2, LOXL2, SSBP2, Clorf29, TOX, STCl, TNFRSFlA, NC0R2, NAPlLl, LOC94105, ARHGEF6, GATA3, TFPI, LAT, CD3Z, AFlQ, MAPlB, TRIM22, CD3D, BCATl , IFI44, CUTC, NAP1L2, NME7, FLJ21 159, and COL5A2, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of BASPl, COL6A2, PTPRC, PRKCA, CCL2, and RAB31, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd768, HUMTRF, hsa-mir-213-prec, hsa-mir-181b-prec, MPR244, hsa-mir-409-3p, HSTRNL, hsa-mir-382, hsa-mir-342, hsa-mir- 142-prec, and Hcd200, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Mitoxantrone.
146. The kit of claim 137, wherein said gene is selected from the group consisting of STCl, GPR65, DOCKlO, COL5A2, FAM46A, and LOC54103, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of HUMTRF, Hcdl48_HPR2251eft, Hcd938, MPR174, and hsa-mir-4323p, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Mitomycin.
147. The kit of claim 137, wherein said gene is selected from the group consisting of RPLlO, RPS4X, NUDC, DKCl , DKFZP564C186, PRP19, RAB9P40, HSA9761 , GMDS, CEPl, IL13RA2, MAGEB2, HMGN2, ALMSl , GPR65, FLJ10774, NOL8, DAZAPl , SLC25A15, PAF53, DXS9879E, PITPNCl , SPANXC, and KIAAl 393, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of RALY, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRN A selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-096-prec-7, hsa-mir-lOl-prec-9, hsa-mir-20b, hsa-mir-019b-2-prec, hsa-mir-032-prec, MPRl 56, hsa-mir-019b-l-prec, hsa-mir-135-2-prec, hsa-mir-025-prec, hsa-mir-007-l-prec, hsa- mir-361, hsa-mir-093-prec-7.1=093-1 , hsa-mir-106-prec-X, hsa-mir-098-prec-X, hsa- mir-142-prec, HPR 169, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Paclitaxel.
148. The kit of claim 137, wherein said gene is selected from the group consisting of PFNl , PGAMl , K-ALPHA-I, CSDA, UCHLl, PWPl, PALM2-AKAP2, TNFRSFlA, ATP5G2, AFlQ, NME4, and FHODl, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir- 096-prec-7, hsa-mir-095-prec-4, HSTRNL, and hsa-mir-007-l-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Taxotere.
149. The kit of claim 137, wherein said gene is selected from the group consisting of IFITM2, UBE2L6, USP4, ITM2A, IL2RG, GPRASPl, PTPN7, CXorf9, RHOH, GIT2, ZNFNlAl, CEPl , TNFRSF7, MAP4K1, CCR7, CD3G, ATP2A3, UCP2, GATA3, CDKN2A, TARP, LAIRl , SH2D1A, SEPT6, HA-I, ERCC2, CD3D, LSTl, AIFl, ADA, DATFl, ARHGAP15, PLAC8, CECRl , LOC81558, and EHD2, and COL5A2, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of LAPTM5, ITGB2, ANPEP, CD53, CD37, AD0RA2A, GNA15, PTPRC, COROlA, HEMl , FLII, and CREB3L1 , or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of MPR141, hsa-mir-424, Hcd690, Hcd783, hsa-mir-150-prec, Hcd266, hsa-mir-503, hsa- mir-128b-prec, Hcd397, and hsa-mir-484, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Dexamethasone.
150. The kit of claim 137, wherein said gene is selected from the group consisting of ITM2A, RHOH, PRIMl , CENTBl, NAPlLl, ATP5G2, GATA3, PRKCQ, SH2D1A, SEPT6, NME4, CD3D, CDlE, ADA, and FHODl, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of GNA 15, PTPRC, and RPLl 3, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of HUMTRF, hsa-mir-155-prec, hsa-mir- 515-15p, Hcd938, Hcd642, Hcdl20, hsa-mir-380-5p, hsa-mir-342, hsa-mir- 142-prec, hsa-mir-223-prec, and hsa-mir-4323p, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Ara-C.
151. The kit of claim 137, wherein said gene is selected from the group consisting of CD99, ARHGDIB, VWF, ITM2A, LGALS9, INPP5D, SATBl, TFDP2, SLA, IL2RG, MFNG, SELL, CDW52, LRMP, ICAM2, RIMS3, PTPN7, ARHGAP25, LCK, CXorf9, RHOH, GIT2, ZNFNlAl, CENTBl , LCP2, SPIl , GZMA, CEPl, CD8A, SCAPl, CD2, CDlC, TNFRSF7, VAVl , MAP4K1, CCR7, C6orf32, ALOXl 5B, BRDT, CD3G, LTB, ATP2A3, NVL, RASGRP2, LCPl, CXCR4, PRKD2, GATA3, TRA@, KIAA0922, TARP, SEC31 L2, PRKCQ, SH2D1A, CHRNA3, CDlA, LSTl, LAIRl , CACNAlG, TRB@, SEPT6, HA-I, D0CK2, CD3D, TRD@, T3JAM, FNBPl , CD6, AIFl, FOLHl, CDlE, LY9, ADA, CDKL5, TRIM, EVL, DATFl, RGC32, PRKCH, ARHGAPl 5, NOTCHl, BIN2, SEMA4G, DPEP2, CECRl, BCLl IB, STAG3, GALNT6, UBASH3A, PHEMX, FLJ13373, LEFl, IL21R, MGC17330, AKAP13, ZNF335, and GIMAP5, or wherein said kit further comprises one or more single- stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of SRRMl, LAPTM5, ITGB2, CD53, CD37, GMFG, PTPRCAP, GNA15, BLM, PTPRC, COROlA, PRKCBl , HEMl , and UGT2B17, or wherein said kit further comprises one or more single- stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd544, hsa-mir- 181c-prec, Hcd517, MPR151, hsa-mir-213-prec, hsa-mir-181b-prec, hsa-mir-150-prec, hsa-mir-153-l-precl, hsa-mir-128b-prec, Hcd812, hsa-mir-195-prec, hsa-mir-342, hsa- mir-370, hsa-mir-142-prec, hsa-mir-223-prec, and hsa-mir-484, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Methylprednisolone.
152. The kit of claim 137, wherein said gene is selected from the group consisting of PRPF8, RPL18, G0T2, RPL13A, RPS15, RPLP2, CSDA, KHDRBSl, SNRPA, IMPDH2, RPS19, NUP88, ATP5D, PCBP2, ZNF593, HSU79274, PRIMl, PFDN5, OXAlL, H3F3A, ATIC, CIAPINl, RPS2, PCCB, SHMT2, RPLPO, HNRPAl, ST0ML2, SKBl, GLTSCR2, CCNBlIPl, MRPS2, FLJ20859, and FLJ 12270, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of RNPSl , RPL32, EEFlG, PTMA, RPLl 3, FBL, RBMX, and RPS9, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir- 096-prec-7, hsa-mir-123-prec, Hcd250, hsa-mir-518e, HPR232, Hcd263, hsa-mir-516- 33p, Hcd605, Hcd373, MPR254, MPR215, HUMTRF, hsa-mir- 106a, hsa-mir-20b, Hcd361, Hcd412, Hcd781 , hsa-mir-019b-2-prec, HPR214, Hcd807, Hcd817, Hcd788, Hcd970, Hcdl48_HPR2251eft, HcdlO2, Hcd246, HPRl 99, HPR233, Hcd383, MPR224, HPRl 72, MPR216, hsa-mir-321 , Hcd586, Hcd587, Hcd249, Hcd279, HPR159, Hcd689, Hcd691 , hsa-mir-019b-l-prec, Hcd413, Hcd581, Hcd536_HPR104, Hcd230, HPRl 54, Hcd270, Hcd649, Hcd889, Hcd938, HPR266, hsa-mir-025-prec, Hcd355_HPR190, MPRl 62, Hcd923, MPR237, MPRl 74, hsa-mir-019a-prec, hsa_mir_490_Hcd20, hsa-mir-380-5p, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec- X, Hcd627, hsa-mir-142-prec, HPR169, hsa-mir-OOlb-2-prec, hsa-mir-018-prec, hsa- mir-020-prec, Hcd404, hsa-mir-384, and hsa-mir-4323p, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Methotrexate.
153. The kit of claim 137, wherein said gene is selected from the group consisting of PFNl, HKl , MCLl, ZYX, RAPlB, GNB2, EPASl, PGAMl, CKAP4, DUSPl, MYL9, K-ALPHA-I , LGALSl, CSDA, IFITM2, ITGA5, DPYSL3, JUNB, NFKBIA, LAMBl , FHLl, INSIGl , TIMPl , GJAl, PSME2, PRGl , EXTl, DKFZP434J154, MVP, VASP, ARL7, NNMT, TAPl, PLOD2, ATF3, PALM2-AKAP2, IL8, LOXL2, IL4R, DGKA, STC2, SEC61G, RGS3, F2R, TPM2, PSMB9, LOX, STCl, PTGER4, IL6, SMAD3, WNT5A, BDNF, TNFRSFlA, FLNC, DKFZP564K0822, FLOTl, PTRF, HLA-B, MGC4083, TNFRSFlOB, PLAGLl, PNMA2, TFPI, LAT, GZMB, CYR61, PLAUR, FSCNl , ERP70, AFlQ, HIC, COL6A1, IFITM3, MAPlB, FLJ46603, RAFTLIN, RRAS, FTL, KIAA0877, MTlE, CDClO, D0CK2, TRIM22, RISl, BCATl, PRFl, DBNl, MTlK, TMSBlO, FLJ10350, Clorf24, NME7, TMEM22, TPKl, COL5A2, ELK3, CYLD, ADAMTSl , EHD2, and ACTB, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of MSN, ACTR2, AKRlBl, VIM, ITGA3, OPTN, M6PRBP1, COLlAl, BASPl, ANPEP, TGFBl , NFIL3, NK4, CSPG2, PLAU, COL6A2, UBC, FGFRl, BAX, COL4A2, and RAB31, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-376a, hsa-mir-155-prec, hsa-mir-409-3p, hsa-mir-495, Hcd498, hsa-mir-199a-2-prec, hsa-mir-382, HPR271, hsa-mir-145-prec, and hsa-mir-199a-l-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Bleomycin.
154. The kit of claim 137, wherein said gene is selected from the group consisting of SSRPl, NUDC, CTSC, AP1G2, PSME2, LBR, EFNB2, SERPINAl , SSSCAl, EZH2, MYB, PRIMl , H2AFX, HMGAl , HMMR, TK2, WHSCl , DIAPHl , LAMB3, DPAGTl, UCK2, SERPINBl, MDNl, BRRNl , G0S2, RAC2, MGC21654, GTSEl , TACC3, PLEK2, PLAC8, HNRPD, and PNAS-4, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of PTMA, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-092-prec- X=092-2, hsa-mir-lOl-prec-9, hsa-mir-144-prec, hsa-mir-519a-l, hsa-mir-519b, hsa- mir-015b-prec, hsa-mir-106a, hsa-mir-16-1, hsa-mir-181d, hsa-mir-017-prec, hsa-mir- 019b-2-prec, hsa-mir-192, hsa-mir-213-prec, hsa-mir-215-prec, hsa-mir-107, hsa-mir- 200b, hsa-mir-103-prec-5=103-l, hsa-mir-519a-l/526c, MPR216, hsa-mir-019b-l-prec, hsa-mir-107-prec-lO, hsa-mir-135-2-prec, hsa-mir-103-2-prec, hsa-mir-519a-2, hsa-mir- 025-prec, hsa-mir-16-2, MPR95, hsa-mir-016b-chr3, Hcd948, hsa-mir-195-prec, hsa- mir-093-prec-7.1=093-1, hsa-mir- 106-prec-X, hsa-mir-142-prec, hsa-mir-519c/526c, hsa-mir-200a-prec, hsa-mir-016a-chrl3, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Methyl-GAG.
155. The kit of claim 137, wherein said gene is selected from the group consisting of ITGA5, TNFAIP3, WNT5A, FOXF2, LOC94105, IFI16, LRRN3, DOCKlO, LEPREl , COL5A2, and ADAMTSl , or wherein said kit further comprises one or more single- stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of MSN, VIM, CSPG2, and FGFRl, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd829, HUMTRF, HPRl 87, Hcd210_HPR205, hsa-mir-379, hsa-mir-213-prec, hsa-mir-4325p, hsa-mir-450-1, hsa-mir- 155-prec, Hcd28_HPR39right, MPR244, hsa-mir-409-3p, hsa-mir- 124a- 1-precl, hsa-mir- 154- precl , hsa-mir-495, hsa-mir-515-23p, Hcd43 8right, Hcd770, hsa-mir-382, hsa-mir- 223-prec, Hcd754, and Hcd213_HPR182, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Carboplatin.
156. The kit of claim 137, wherein said gene is selected from the group consisting of RPLl 8, RPLlOA, ANAPC5, EEF1B2, RPL13A, RPSl 5, AKAPl , NDUFABl, APRT, ZNF593, MRP63, IL6R, SART3, UCK2, RPLl 7, RPS2, PCCB, TOMM20, SHMT2, RPLPO, GTF3A, STOML2, DKFZp564J157, MRPS2, ALG5, and CALML4, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of RNPSl , RPL13, RPS6, and RPL3, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-096-prec-7, hsa-mir-429, Hcd693, HPR214, Hcd586, Hcd249, Hcd689, hsa-mir- 194-2, Hcd581, Hcd270, hsa-mir-025-prec, Hcd340, hsa-mir-007-1- prec, hsa-mir-093-prec-7.1=093-1, hsa-mir- 106-prec-X, Hcd794, hsa-mir-020-prec, and hsa-mir-4323p, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with 5-FU (5-Fluorouracil).
157. The kit of claim 137, wherein said gene is selected from the group consisting of KIFCl, VLDLR, RUNXl , P AF AHl B3, HlFX, RNF 144, TMSNB, CRYl , MAZ, SLA, SRF, UMPS, CD3Z, PRKCQ, HNRPM, ZAP70, ADDl , RFC5, TM4SF2, PFN2, BMIl, TUBGCP3, ATP6V1B2, CDlD, ADA, CD99, CD2, CNP, ERG, CD3E, CDlA, PSMC3, RPS4Y1, AKTl, TALI, UBE2A, TCF 12, UBE2S, CCND3, PAX6, RAG2, GSTM2, SATBl 5 NASP, IGFBP2, CDH2, CRABPl , DBNl, AKRlCl, CACNB3, CASP2, CASP2, LCP2, CASP6, MYB, SFRS6, GLRB, NDN, GNAQ, TUSC3, GNAQ, JARID2, OCRL, FHLl , EZH2, SMOX, SLC4A2, UFDlL, ZNF32, HTATSFl, SHDl, PTOVI 5 NXFl , FYB, TRIM28, BC008967, TRB@, HlFO, CD3D, CD3G, CENPB, ALDH2, ANXAl, H2AFX, CDlE, DDX5, CCNA2, ENO2, SNRPB, GATA3, RRM2, GLUL, SOX4, MAL, UNG, ARHGDIB, RUNXl , MPHOSPH6, DCTNl , SH3GL3, PLEKHCl , CD47, POLR2F, RHOH, and ADDl, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of ITK, RALY, PSMC5, MYL6, CDlB, STMNl , GNA15, MDK, CAPG, ACTNl , CTNNAl , FARSLA, E2F4, CPSFl, SEPWl, TFRC, ABLl, TCF7, FGFRl, NUCB2, SMA3, FAT, VIM, and ATP2A3, wherein said level of expression of said gene indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Rituximab.
158. The kit of claim 137, wherein said gene is selected from the group consisting of TRAl, ACTN4, CALMl, CD63, FKBPlA, CALU, IQGAPl , MGC8721, STATl, TACCl, TM4SF8, CD59, CKAP4, DUSPl , RCNl, MGC8902, LGALSl, BHLHB2, RRBPl, PRNP, IER3, MARCKS, LUM, FER1L3, SLC20A1, HEXB, EXTl, TJPl, CTSL, SLC39A6, RI0K3, CRK, NNMT, TRAM2, ADAM9, DNAJC7, PLSCRl, PRSS23, PLOD2, NPCl, TOBl, GFPTl , IL8, PYGL, LOXL2, KIAA0355, UGDH, PURA, ULK2, CENTG2, NID2, CAP350, CXCLl, BTN3A3, IL6, WNT5A, FOXF2, LPHN2, CDHl 1 , P4HA1, GRP58, DSIPI, MAP1LC3B, GALIG, IGSF4, IRS2, ATP2A2, OGT, TNFRSFlOB, KIAAl 128, TM4SF1 , RBPMS, RIPK2, CBLB, NR1D2, SLC7A1 1, MPZLl, SSA2, NQOl, ASPH, ASAHl, MGLL, SERPINB6, HSPA5, ZFP36L1 , COL4A1, CD44, SLC39A14, NIPA2, FKBP9, IL6ST, DKFZP564G2022, PPAP2B, MAPlB, MAPKl, MYOlB, CAST, RRAS2, QKI, LHFPL2, 38970, ARHE, KIAA1078, FTL, KIAA0877, PLCBl , KI AA0802, RAB3GAP, SERPINBl , TIMM 17A, SOD2, HLA-A, N0M02, LOC55831, PHLDAl , TMEM2, MLPH, FAD104, LRRC5, RAB7L1, FLJ35036, DOCKlO, LRP12, TXNDC5, CDC14B, HRMTlLl, COROlC, DNAJClO, TNPOl, LONP, AMIG02, DNAPTP6, and ADAMTSl, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of WARS, CD81 , CTSB, PKM2, PPP2CB, CNN3, ANXA2, JAKl, EIF4G3, COLlAl, DYRK2, NFIL3, ACTNl , CAPN2, BTN3A2, IGFBP3, FNl, COL4A2, and KPNBl, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir- 136-prec, Hcd570, Hcd873, Hcd282PO, Hcd799, Hcd829, Hcd210_HPR205, hsa-mir- 219-prec, hsa-mir-202, hsa-mir-429, Hcd693, hsa-mir-022-prec, MPR88, hsa-mir-198- prec, hsa-mir-199b-prec, Hcdl45, hsa-mir-124a-2-prec, hsa-mir-138-2-prec, Hcd960, Hcd869, Hcd384, hsa-mir-027b-prec, Hcd444, hsa-mir- 194-2, hsa-mir-197-prec, Hcd913, HPR163, hsa-mir- 138- 1-prec, hsa-mir-010a-prec, hsa-mir-023b-prec, hsa-mir- 193b, Hcd654, Hcd542, hsa-mir- 199a-2-prec, hsa-mir-214-prec, Hcd608, Hcd684, hsa- mir- 145-prec, hsa-mir-023a-prec, hsa-mir-024-2-prec, and hsa-mir- 199a- 1-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with radiation therapy.
159. The kit of claim 137, wherein said gene is selected from the group consisting of FAU, NOL5A, ANP32A, ARHGDIB, LBR, FABP5, ITM2A, SFRS5, IQGAP2, SLC7A6, SLA, IL2RG, MFNG, GPSM3, PIM2, EVERl , LRMP, ICAM2, RIMS3, FMNLl , MYB, PTPN7, LCK, CXorf9, RHOH, ZNFNlAl, CENTBl, LCP2, DBT, CEPl, IL6R, VAVl, MAP4K1, CD28, PTP4A3, CD3G, LTB, USP34, NVL, CD8B1 , SFRS6, LCPl, CXCR4, PSCDBP, SELPLG, CD3Z, PRKCQ, CDlA, GATA2, P2RX5, LAIRl, ClorD8, SH2D1A, TRB@, SEPT6, HA-I, DOCK2, WBSCR20C, CD3D, RNASE6, SFRS7, WBSCR20A, NUP210, CD6, HNRPAl, AIFl , CYFIP2, GLTSCR2, Cl lorf2, ARHGAPl 5, BIN2, SH3TC1, STAG3, TM6SF1 , C15orf25, FLJ22457, PACAP, and MGC2744, or wherein said kit further comprises one or more single- stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-092-prec- X=092-2, hsa-mir- 123-prec, hsa-mir- 106a, hsa-mir-20b, hsa-mir-017-prec, hsa-mir- 019b-2-prec, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1, hsa-mir- 122a-prec, Hcd783, MPR216, hsa-mir-019b- 1-prec, hsa-mir- 135-2-prec, hsa-mir- 128b-prec, hsa- mir-025-prec, Hcd51 1, hsa-mir-093-prec-7.1=093-1, hsa-mir- 106-prec-X, hsa-mir- 142- prec, HPRl 69, hsa-mir-223-prec, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with PXDlOl (belinostat).
160. The kit of claim 137, wherein said gene is selected from the group consisting of CD99, SNRPA, CUGBP2, STAT5A, SLA, IL2RG, GTSEl, MYB, PTPN7, CXorf9, RHOH, ZNFNlAl, CENTBl, LCP2, HIST1H4C, CCR7, APOBEC3B, MCM7, LCPl, SELPLG, CD3Z, PRKCQ, GZMB, SCN3A, LAIRl, SH2D1A, SEPT6, CG018, CD3D, ClδorflO, PRFl, AIFl , MCM5, LPXN, C22orfl8, ARHGAPl 5, and LEFl, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-096-prec-7, Hcd605, hsa-mir-20b, hsa-miR-373*, HUMTRAB, hsa-mir-019b-l-prec, HPR163, hsa-mir-371, hsa-mir-025-prec, hsa-mir-18b, hsa-mir- 093-prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir-142-prec, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with 5-Aza-2'- deoxycytidine (Decitabine).
161. The kit of claim 137, wherein said gene is selected from the group consisting of SLC9A3R1 , RPS 19, ITM2A, SSBP2, CXorf9, RHOH, ZNFNlAl , FXYD2, CCR9, NAPlLl, CXCR4, SH2D1 A, CDlA, TRB@, SEPT6, RPS2, D0CK2, CD3D, CD6, ZAP70, AIFl , CDlE, CYFIP2, ADA, TRIM, GLTSCR2, FLJ10858, BCLl IB, GIMAP6, STAG3, and UBASH3A, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of MRPS24, TRIM22, TRIM41, LAT, CDlC, MRPS22, ADAMI l , RPLl 3, RPS27, RPLl 3, RPS25, RPLl 8A, COROlA, PTPRCAP, GMFG, ITK, CDlB, GMFG, PTPRCAP, COROlA, ITGB2, HCLSl, and ATP2A3, or wherein said kit further comprises one or more single- stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of HUMTRF, hsa-mir- 483, MPR74, hsa-mir-122a-prec, ath-MIR180a, hsa-mir-128b-prec, Hcd923, hsa-mir- 106-prec-X, hsa-mir-342, hsa-mir-142-prec, HPR169, hsa-mir-223-prec, Hcd754, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Idarubicin.
162. The kit of claim 137, wherein said gene is selected from the group consisting of CD99, HLA-DPBl, ARHGDIB, IFITMl, UBE2L6, ITM2A, SERPINAl, STAT5A, INPP5D, DGKA, SATBl, SEMA4D, TFDP2, SLA, IL2RG, CD48, MFNG, AL0X5AP, GPSM3, PSMB9, KIAA071 1, SELL, ADA, EDGl, RIMS3, FMNLl, MYB, PTPN7, LCK, CXorf9, RHOH, ZNFNlAl, CENTBl, LCP2, FXYD2, CDlD, BATF, STAT4, VAVl, MAP4K1, CCR7, PDE4C, CD3G, CCR9, SPl 10, LCPl, IFIl 6, CXCR4, ARHGEF6, GATA3, SELPLG, SEC31L2, CD3Z, PRKCQ, SH2D1A, GZMB, CDlA, SCN3A, LAIRl, FYB, TRB@, SEPT6, HA-I, D0CK2, CGOl 8, CD3D, T3JAM, FNBPl, CD6, ZAP70, LSTl, GPR65, PRFl, AIFl, FLJ20331, RAG2, WDR45, CDlE, CYFIP2, TARP, TRIM, RPLlOL, GLTSCR2, GIMAP5, ARHGAP15, NOTCHl, BIN2, C13orfl 8, CECRl, BCLI lB, GIMAP6, STAG3, TM6SF1, HSD17B7, UBASH3A, MGC5566, FLJ22457, TPKl, PHFl 1, and DKFZP434B0335, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of FLJ 10534, PTPRC, TRIM22, C18orfl, EVL, TRIM41, PSME2, LAT, CDlC, MYBBPlA, ICAM3, ADAMI l, CD53, FARSLA, RPL13, RAC2, RPL13, GNA15, PGF, LAPTM5, RPL18A, CD53, COROlA, PTPRCAP, PTPRC, HEMl, GMFG, GNAl 5, ITK, CDlB, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl, GNA15, TCF7, ITGB2, PTPRC, HCLSl, ATP2A3, MYBLl, and FARSLA, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-124a-3-prec, hsa-mir-181a- prec, Hcd773, Hcd683, Hcd796, HUMTRF, HUMTRS, hsa-mir-181b-2, Hcd294, hsa- mir-20b, hsa-mir-181d, hsa-mir-213-prec, Hcdl48_HPR2251eft, hsa-mir-515-15p, hsa- mir-181b-prec, Hcd783, HUMTRAB, HUMTRN, hsa-mir-181b-l, hsa-mir-124a-l- precl, hsa-mir-367, hsa-mir-128b-prec, Hcd43 8right, hsa-mir-025-prec, hsa-mir-216- prec, Hcd731 , hsa-mir-093-prec-7.1=093-1 , hsa-mir-106-prec-X, hsa-mir-342, hsa-mir- 142-prec, HSHELAOl , HUMTRVlA, hsa-mir-223-prec, Hcd754, and hsa-mir-020- prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Melphalan.
163. The kit of claim 137, wherein said gene is selected from the group consisting of MCLl, DDX23, JUNB, ZFP36, IFITMl , CKSlB, SERPINAl, IL4R, CLDN3, ARL4A, HMMR, FLJ 12671, ANKHDl, KIF2C, RPA3, MCCC2, CDH17, LSM5, PRFl , RODl, FLJ 12666, SUV420H1, MUCl 3, C13orfl8, and CDCA8, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of ETS2, ARIDlA, IDl, DDC, NID2, CCT3, ID2, NFIL3, and AREG, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd829, hsa-mir-197-prec, HPR 163, and hsa-mir-150-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with IL4-PE38 fusion protein.
164. The kit of claim 137, wherein said gene is selected from the group consisting of MCLl , DDX23, JUNB, ZFP36, IFITMl, CKSlB, SERPINAl, IL13R, CLDN3, ARL4A, HMMR, FLJ 12671 , ANKHDl, KIF2C, RP A3, MCCC2, CDH17, LSM5, PRFl, RODl, FLJ12666, SUV420H1 , MUC13, C13orfl8, and CDCA8, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of ETS2, ARIDlA, IDl, DDC, NID2, CCT3, ID2, NFIL3, and AREG, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd829, hsa-mir-197-prec, HPRl 63, and hsa-mir- 150-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with ILl 3- PE38QQR fusion protein (cintredekin besudotox).
165. The kit of claim 137, wherein said gene is selected from the group consisting of STOM, TNFAIP3, ASNS, GARS, CXCR4, EGLN3, LBH, and GDFl 5, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of STOMLl and KIAA0746, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a micro RN A selected from the group consisting of hsa-mir- 034prec, Hcd255, Hcd712, Hcd965, Hcd891, Hcd210_HPR205, hsa-mir-429, Hcd753, Hcd693, MPR203, Hcd704, Hcd863PO, hsa-mir-122a-prec, Hcd760, Hcd338, HPR213, Hcd852, Hcd366, MPRl 03, Hcd669, and hsa-mir-188-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Valproic acid (VPA).
166. The kit of claim 137, wherein said gene is selected from the group consisting of PPIB, ZFP36L2, IFI30, USP7, SRM, SH3BP5, ALDOC, FADS2, GUSB, PSCDl, IQGAP2, STS, MFNG, FLIl, PIM2, INPP4A, LRMP, ICAM2, EVI2A, MAL, BTN3A3, PTPN7, ILlORA, SPIl, TRAFl, ITGB7, ARHGAP6, MAP4K1, CD28, PTP4A3, LTB, Clorf38, WBSCR22, CD8B1, LCPl, FLJ13052, MEF2C, PSCDBP, IL 16, SELPLG, MAGEA9, LAIRl, TNFRSF25, EVI2B, IGJ, PDCD4, RASA4, HA-I, PLCL2, RNASE6, WBSCR20C, NUP210, RPLlOL, Cl Iorf2, CABCl, ARHGEF3, TAPBPL, CHST12, FKBPl 1, FLJ35036, MYLIP, TXNDC5, PACAP, TOSO, PNAS-4, IL21 R, and TCF4, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of CLTB, BTN3A2, BCL2, SETBPl , ICAM3, BCL2, BCL2, BCL2, CD53, CCND2, CLTB, CLTB, BCL2L1 1, BTN3A2, CD37, MYCL2, CTSS, LAPTM5, CD53, COROlA, HEMl , CD53, COROlA, HEMl, HCLSl, BCL2L1 1 , MYCLl, MYC, and MANlAl, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd257, hsa-mir-148-prec, Hcd512, HPR227, Hcd421, MPR203, hsa-mir-017-prec, hsa-mir-219-2, hsa-mir-328, Hcd783, Hcdlδl , HPR213, hsa-mir-191-prec, hsa-mir- 375, hsa-mir-212-prec, Hcd913, Hcd716, MPR207, HPR206, hsa-mir-016b-chr3, Hcd654, hsa-mir-195-prec, Hcd425, hsa-mir-148a, hsa-mir-142-prec, and hsa-mir- 016a-chrl3, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with All- trans retinoic acid (ATRA).
167. The kit of claim 137, wherein said gene is selected from the group consisting of C6orf29, TRIM31, CD69, LRRN3, GPR35, and CDW52, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd99, hsa-mir-520c/526a, hsa-mir-191-prec, hsa-mir-205-prec, hsa-mir-375, hsa-mir- 423, hsa-mir-449, and hsa-mir-196-2-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Cytoxan.
168. The kit of claim 137, wherein said gene is selected from the group consisting of K-ALPHA-I, CSDA, UCHLl, NAPlLl, ATP5G2, HDGFRP3, and IFI44, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of HUMTRF, MPR74, hsa-mir-213 -prec, hsa-mir- 155 -prec, hsa-mir- 181b- prec, hsa-mir-342, and hsa-mir-4323p, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Topotecan (Hycamtin).
169. The kit of claim 137, wherein said gene is selected from the group consisting of N0L5A, STOM, SIATl , CUGBP2, GUSB, ITM2A, JARID2, RUNX3, ICAM2, PTPN7, VAVl , PTP4A3, MCAM, MEF2C, IDH3B, RFP, SEPT6, SLC43A3, WBSCR20C, SHMT2, GLTSCR2, CABCl, FLJ20859, FLJ20010, MGC10993, and FKBPl 1, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of STOMLl, EIF4A1, PDE3B, BCLl IA, INPP4B, HLA-DMA, TRFP, EIF4A1 , GAS7, MYCL2, HCLSl , MYCLl, and MYC, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-123-prec, hsa-mir-514-1, hsa-mir- 101-prec-9, hsa-mir-148-prec, hsa-mir-106a, hsa-mir-20b, Hcd781 , hsa-mir-017-prec, hsa-mir-019b-2-prec, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1, hsa-mir-107, hsa- mir-103-prec-5=103-l , MPR216, hsa-mir-29b-2=102prec7.1=7.2, hsa-mir-019b-l-prec, hsa-mir-107-prec-lO, hsa-mir-135-2-prec, Hcd581, hsa-mir-103-2-prec, Hcd230, hsa- mir-025-prec, hsa-mir-208-prec, hsa-mir-18b, hsa-mir-093-prec-7.1=093-1, hsa-mir- 106-prec-X, hsa-mir-142-prec, HPR 169, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Suberoylanilide hydroxamic acid.
170. The kit of claim 137, wherein said gene is selected from the group consisting of ZFP36L2, TRIB2, LCP2, C6orf32, IL16, CACNAlG, SPDEF, HABl, TOSO, and ARHGAP25, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of SGCD and CAPN3, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd415, hsa-mir-147-prec, hsa-mir-033b-prec, Hcd778, hsa-mir-127-prec, hsa-mir-324, Hcd794, and Hcd634, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Depsipeptide.
171. The kit of claim 137, wherein said gene is selected from the group consisting of PLEKHB2, ARPClB, MXl , CUGBP2, IFI 16, TNFRSF 14, SPI lO, ELFl , LPXN, IFRG28, LEFl , and PYCARD, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of HMXl, or wherein said kit further comprises one or more single- stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of MPR121 , Hcdl 15, Hcd693, Hcd704, HPRlOO, Hcd760, hsa-mir-147-prec, hsa-mir-033b-prec, hsa-mir- 146-prec, Hcdl 42, hsa-mir-501 , Hcd716, MPR207, Hcd777, hsa-mir-204-prec, hsa- mir-146b, Hcd51 1 , Hcd397, MPR130, Hcd782, hsa-mir-324, Hcd794, and Hcd739, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Bortezomib.
172. The kit of claim 137, wherein said gene is selected from the group consisting of SSRPl, ALDOC, ClQRl, TTFl, PRIMl, USP34, TK2, GOLGIN-67, NPD014, KIAA0220, SLC43A3, WBSCR20C, ICAM2, TEXlO, CHD7, SAMSNl, and TPRT, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of PTPRC, CD53, RNPSl , H3F3A, NUDC, SMARCA4, RPL32, PTMA, CD53, PTPRCAP, PTPRC, RPL32, PTPRCAP, PTPRC, CD53, PTPRC, HCLSl, and SLCl 9Al, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-092-prec- X=092-2, hsa-mir-096-prec-7, hsa-mir-123-prec, MPR249, HPR232, hsa-mir-101-prec- 9, hsa-mir-106a, hsa-mir-20b, Hcd861 , hsa-mir-017-prec, hsa-mir-019b-2-prec, hsa- mir-033-prec, HcdlO2, MPR216, Hcd975, hsa-mir-019b-l-prec, hsa-mir-135-2-prec, Hcd581 , Hcd536_HPR104, hsa-mir-128b-prec, HSTRNL, hsa-mir-025-prec, hsa-mir- 18b, HPR262, Hcd923, Hcd434, Hcd658, HPRl 29, hsa-mir-380-5p, hsa-mir-093-prec- 7.1=093-1 , hsa-mir- 106-prec-X, Hcd627, hsa-mir-142-prec, hsa-mir-018-prec, and hsa- mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Leukeran.
173. The kit of claim 137, wherein said gene is selected from the group consisting of HLA-E, BAT3, ENO2, UBE2L6, CUGBP2, ITM2A, PALM2-AKAP2, JARID2, DGKA, SLC7A6, TFDP2, ADA, EDGl, ICAM2, PTPN7, CXorf9, RHOH, MX2, ZNFNlAl, COCH, LCP2, CLGN, BNCl, FLNC, HLA-DRB3, UCP2, HLA-DRBl, GATA3, PRKCQ, SH2D1 A, NFATC3, TRB@, FNBPl , SEPT6, NME4, DKFZP434C171, ZC3HAV1, SLC43A3, CD3D, AIFl, SPTANl, CDlE, TRIM, DATFl , FHODl, ARHGAPl 5, STAG3, SAPl 30, and CYLD, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of PTPRC, MX2004PA1 1424, TRIM22, TRIM41 , CDlC, CHD8, ADAMl 1, ANPEP, RBMX2, RAC2, GNA15, LAPTM5, PTPRCAP, PTPRC, GNA15, CDlB, PTPRCAP, PTPRC, GNAl 5, PTPRC, and ATP2A3, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd773, Hcd248, hsa-mir-181d, MPR74, hsa-mir-213-prec, hsa-mir-155-prec, MPR197, hsa-mir-181b-prec, hsa-mir-29b-2=102prec7.1=7.2, hsa-mir-029c-prec, Hcd318, hsa-mir-128b-prec, hsa-mir-130a-prec, hsa-mir-140, hsa-mir-16-2, hsa-mir- 526a-2, hsa-mir-016b-chr3, hsa-mir-195-prec, hsa-mir-216-prec, hsa-mir-342, hsa-mir- 29b- 1 , Hcd627, hsa-mir-102-prec-l, hsa-mir-142-prec, hsa-mir-223-prec, hsa-let-7f-2- prec2, and hsa-mir-016a-chrl3, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Fludarabine.
174. The kit of claim 137, wherein said gene is CD99, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd794, and Hcd754, wherein said level expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Vinblastine.
175. The kit of claim 137, wherein said gene is selected from the group consisting of RPLP2, BTGl, CSDA, ARHGDIB, INSIGl, ALDOC, WASPIP, ClQRl, EDEMl , SLA, MFNG, GPSM3, ADA, LRMP, EVI2A, FMNLl , PTPN7, RHOH, ZNFNlAl , CENTBl , MAP4K1 , CD28, SPl 10, NAPlLl, IFI 16, ARHGEF6, SELPLG, CD3Z, SH2D1A, LAIRl, RAFTLIN, HA-I , D0CK2, CD3D, T3JAM, ZAP70, GPR65, CYFIP2, LPXN, RPLlOL, GLTSCR2, ARHGAPl 5, BCLI lB, TM6SF1, PACAP, and TCF4, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of PTPRC, BCL2, LAT, ICAM3, BCL2, BCL2, BCL2, ADAMl 1 , CD53, FARSLA, BCL2L1 1 , RPLl 3, RAC2, RPLl 3, MYCL2, LAPTM5, RPL18A, CD53, COROlA, PTPRCAP, PTPRC, HEMl, GMFG, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl, PTPRC, HCLSl, BCL2L1 1, MYCLl, FARSLA, and MYC, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-096-prec-7, hsa-mir-124a-3- prec, hsa-mir-lOl-prec-9, Hcd712, Hcd693, hsa-mir-219-2, Hcdl45, hsa-mir-155-prec, HPR213, hsa-mir-212-prec, Hcd913, Hcd716, MPR207, Hcd559, Hcd654, Hcd739, and hsa-mir-142-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Busulfan.
176. The kit of claim 137, wherein said gene is selected from the group consisting of ARHGDIB, ITM2A, SSBP2, PIM2, SELL, ICAM2, EVI2A, MAL, PTPN7, ZNFNlAl , LCP2, ARHGAP6, CD28, CD8B1, LCPl, NPDO 14, CD69, NFATC3, TRB@, IGJ, SLC43A3, D0CK2, FHODl, and PACAP, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of ICAM3, CD53, SMARCA4, CD37, LAPTM5, CD53, COROlA, HEMl, GMFG, GMFG, CD53, COROlA, HEMl, and HCLSl , or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-092-prec- X=092-2, hsa-mir-123-prec, hsa-mir-101-prec-9, Hcd517, Hcd796, Hcd749, Hcd674, hsa-mir-019b-2-prec, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1, hsa-mir-124a-2- prec, hsa-mir-143-prec, hsa-mir-516-43p, hsa-mir-216-prec, Hcd731, hsa-mir-106-prec- X, hsa-mir-142-prec, hsa-mir-223-prec, Hcd754, and hsa-mir-018-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Dacarbazine.
177. The kit of claim 137, wherein said gene is selected from the group consisting of RPL18, RPLlOA, RPS3A, EEF1B2, GOT2, RPL13A, RPS15, NOL5A, RPLP2, SLC9A3R1, EIF3S3, MTHFD2, IMPDH2, ALDOC, FABP5, ITM2A, PCK2, MFNG, GCHl, PIM2, ADA, ICAM2, TTFl, MYB, PTPN7, RHOH, ZNFNlAl, PRlMl, FHIT, ASS, SYK, OXAlL, LCPl , DDXl 8, N0LA2, KIAA0922, PRKCQ, NFATC3, ANAPC5, TRB@, CXCR4, FNBP4, SEPT6, RPS2, MDNl, PCCB, RAS A4, WBSCR20C, SFRS7, WBSCR20A, NUP210, SHMT2, RPLPO, MAP4K1, HNRPAl , CYFIP2, RPLlOL, GLTSCR2, MRPLl 6, MRPS2, FLJ 12270, CDK5RAP3, ARHGAP15, CUTC, FKBPl 1 , ADPGK, FLJ22457, PUS3, PACAP, and CALML4, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of MRPS24, DUSP2, EIF4A1, BRD2, BCLl IA, RASSF2, MRPL37, MRPL30, RASSFl , MYBBPlA, LASS2, MRPS22, ADAMI l , CD53, RPS6KB1, RNPSl, BRD2, EIF4A1 , FBL, BRD2, RPL36A, RPL13, RPL38, H3F3A, KIAAO 182, RPS27, RPS6, EEFlG, RPLl 3, MYCL2, FBLNl, RPS25, RPL32, PTMA, RPLl 8A, RPL3, CD53, COROlA, HEMl , GMFG, RPL32, GMFG, CD53, COROlA, HEMl , HCLSl , ATP2A3, RASSF7, MYCLl, MYBLl, MYC, RPS15A, RASSF2, and LASS6, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-148-prec, hsa-mir-20b, hsa-mir-007-2-prec, hsa-mir-017-prec, hsa-mir-019b-2-prec, Hcd760, Hcd783, MPR216, hsa-mir-375, hsa-mir-019b-l-prec, hsa-mir-135-2-prec, hsa-mir- 150-prec, hsa-mir-128b-prec, hsa-mir-499, hsa-mir-025-prec, hsa-mir-007-l-prec, hsa- mir-019a-prec, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir-142-prec, HPR 169, hsa-mir-018-prec, hsa-mir-020-prec, and hsa-mir-484, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Oxaliplatin.
178. The kit of claim 137, wherein said gene is selected from the group consisting of CSDA, INSIGl , UBE2L6, PRGl, ITM2A, DGKA, SLA, PCBP2, IL2RG, ALOX5AP, PSMB9, LRMP, ICAM2, PTPN7, CXorf9, RHOH, ZNFNlAl , CENTBl , LCP2, STAT4, CCR7, CD3G, SPl 10, TNFAIP8, IFI 16, CXCR4, ARHGEF6, SELPLG, CD3Z, PRKCQ, SH2D1A, CDlA, NFATC3, LAIRl, TRB@, SEPT6, RAFTLIN, DOCK2, CD3D, CD6, AIFl , CDlE, CYFIP2, TARP, ADA, ARHGAP15, GIMAP6, STAG3, FLJ22457, PACAP, and TCF4, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of PTPRC, TRIM22, PSME2, LAT, CDlC, ICAM3, ADAMl 1, CD53, FARSLA, RPL13, RAC2, RPL13, NK4, LAPTM5, CD53, COROlA, PTPRCAP, PTPRC, HEMl , GMFG, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl, ITGB2, PTPRC, HCLSl, ATP2A3, and FARSLA, or wherein said kit further comprises one or more single- stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd257, Hcd768, Hcd796, HUMTRF, HUMTRS, MPR74, hsa-mir-213-prec, hsa-mir-155-prec, Hcd763, hsa-mir-181b-prec, ath-MIR180a, hsa-mir-216-prec, hsa-mir-342, hsa-mir-142-prec, HSHELAOl, HUMTRVlA, hsa-mir-223-prec, Hcd754, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Hydroxyurea.
179. The kit of claim 137, wherein said gene is selected from the group consisting of RPLl 1 , RPL17, ANAPC5, RPL13A, STOM, TUFM, SCARBl, FABP5, KIAA071 1, IL6R, WBSCR22, UCK2, GZMB, ClorG8, PCBP2, GPR65, GLTSCR2, and FKBPl 1, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of STOMLl, MRPL37, MRPL30, RPL36A, RPL38, HSPDl , MIF, RPL32, RPL3, and RPL32, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd257, Hcd946, Hcd503, hsa-mir-429, Hcd693, hsa-miR-373*, Hcd738, hsa-mir-328, Hcd783, Hcdl 81, Hcd631 , Hcd279, hsa-mir- 194-2, hsa-mir-197-prec, HPR 163, hsa-mir-150-prec, Hcd323, hsa-mir-103-2-prec, Hcd243, Hcd938, hsa-mir-025-prec, hsa-mir-007-l-prec, MPR243, Hcd51 1, Hcd654, hsa-mir-199a-2-prec, hsa-mir-214-prec, hsa-mir-093-prec- 7.1=093-1, hsa-mir-106-prec-X, Hcd794, Hcd530, HSHELAOl, Hcd754, and hsa-mir- 020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Tegafur.
180. The kit of claim 137, wherein said gene is selected from the group consisting of ALDOC, ITM2A, SLA, SSBP2, IL2RG, MFNG, SELL, STCl, LRMP, MYB, PTPN7, CXorf9, RHOH, ZNFNlAl, CENTBl , MAP4K1, CCR7, CD3G, CCR9, CBFA2T3, CXCR4, ARHGEF6, SELPLG, SEC31L2, CD3Z, SH2D1A, CDlA, SCN3A, LAIRl, TRB@, DOCK2, WBSCR20C, CD3D, T3JAM, CD6, ZAP70, GPR65, AIFl, WDR45, CDlE, CYFIP2, TARP, TRIM, ARHGAP 15, NOTCHl, STAG3, UBASH3A, MGC5566, and PACAP, or wherein said kit further comprises one or more single- stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of PTPRC, TRIM22, TRIM41, LAT, CDlC, MYBBPlA, CD53, FARSLA, PPP2CA, LAPTM5, CD53, COROlA, PTPRCAP, PTPRC, HEMl , GMFG, ITK, CDlB, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl, TCF7, PTPRC, HCLSl, ATP2A3, MYBLl, and FARSLA, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd768, HUMTRF, Hcdl45, Hcd923, hsa-mir- 216-prec, hsa-mir-093-prec-7.1=093-l, hsa-mir-342, Hcd794, hsa-mir-142-prec, HSHELAOl, hsa-mir-223-prec, and Hcd754, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Daunorubicin.
181. The kit of claim 137, wherein said gene is selected from the group consisting of PFNl , CALU, ZYX, PSMD2, RAPlB, EPASl, PGAMl, STATl, CKAP4, DUSPl, RCNl , UCHLl, ITGA5, NFKBIA, LAMBl, TGFBI, FHLl , GJAl, PRGl , EXTl, MVP, NNMT, TAPl , CRIMl, PLOD2, RPS 19, AXL, PALM2-AKAP2, IL8, LOXL2, PAPSS2, CAVl, F2R, PSMB9, LOX, Clorf29, STCl, LIF, KCNJ8, SMAD3, HPCALl , WNT5A, BDNF, TNFRSFlA, NCOR2, FLNC, HMGA2, HLA-B, FLOTl , PTRF, IFI16, MGC4083, TNFRSFlOB, PNMA2, TFPI, CLECSF2, SPl 10, PLAUR, ASPH, FSCNl , HIC, HLA-C, COL6A1, IL6ST, IFITM3, MAPlB, FLJ46603, RAFTLIN, FTL, KIAA0877, MTlE, CDClO, ZNF258, BCATl, IFI44, SOD2, TMSBlO, FLJ10350, Clorf24, EFHD2, RPS27L, TNFRSF12A, FAD104, RAB7L1, NME7, TMEM22, TPKl, ELK3, CYLD, AMIGO2, ADAMTSl, and ACTB, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of ACLY, MPZLl, STC2, BAX, RAB31, RAB31,, (UBC 12, LOXLl , EMP3, FGFRlOP, IL6, TRIM22, OPTN, CYR61, METAPl, SHCl, FNl, EMP3, RAB31 , LOXLl , BAX, BAX, RAB31, FNl , CD44, ANXAl , COL5A2, LGALSl, FGFRl, PLAU, TFPI2, TFPI2, VCAMl, SHCl , CSF2RA, EMP3, COLlAl, TGFBl, COL6A2, FGFRl, ITGA3, AKRlBl, MSN, EMP3, VIM, EMP3, COL6A2, MSN, PSMC5, UBC, FGFRl, BASPl, ANXAl 1, CSPG2, M6PRBP1 , PRKCA, OPTN, OPTN, SPARC, CCL2, and ITGA3, or wherein the method further comprises measuring a level of expression of at least one microRNA selected from the group consisting of hsa-mir-125b-2-prec, hsa-mir-022-prec, hsa-mir-125b-l , hsa-mir- 155- prec, hsa-mir-100, hsa-mir-409-3p, hsa-mir-495, hsa-mir- 199a-2-prec, hsa-mir-382, and hsa-mir-lOO-l/2-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Bleomycin.
182. The kit of claim 137, wherein said gene is selected from the group consisting of HSPCB, LDHA, and TM4SF7, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of LY6E, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd338, hsa-mir-099b-prec-19, and hsa-mir- 149-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Estramustine.
183. The kit of claim 137, wherein said gene is selected from the group consisting of CSDA, INSlGl , UBE2L6, PRGl , ITM2A, DGKA, TFDP2, SLA, IL2RG, ALOX5AP, GPSM3, PSMB9, SELL, ADA, EDGl , FMNLl , PTPN7, CXorf9, RHOH, ZNFNlAl , CENTBl, LCP2, CDlD, STAT4, VAVl, MAP4K1 , CCR7, PDE4C, CD3G, CCR9, SPl 10, TNFAIP8, LCPl, IFI 16, CXCR4, ARHGEF6, SELPLG, SEC31L2, CD3Z, PRKCQ, SH2D1A, GZMB, CDlA, LAIRl, AFlQ, TRB@, SEPT6, DOCK2, RPS 19, CD3D, T3JAM, FNBPl , CD6, ZAP70, LSTl, BCATl , PRFl, AIFl, RAG2, CDlE, CYFIP2, TARP, TRIM, GLTSCR2, GIMAP5, ARHGAPl 5, NOTCHl, BCLl IB, GIMAP6, STAG3, TM6SF1, UBASH3A, MGC5566, FLJ22457, and TPKl, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of PTPRC, TRIM22, EVL, TRIM41, PSME2, LAT, CDlC, ADAMl 1, CD53, FARSLA, RPLl 3, RAC2, RPLl 3, GNAl 5, LAPTM5, RPLl 8A, CD53, COROlA, PTPRCAP, PTPRC, HEMl, GMFG, GNAl 5, ITK, CDlB, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl , GNA15, ITGB2, PTPRC, HCLSl, ATP2A3, and FARSLA, or wherein said kit further comprises one or more single- stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-181a-prec, hsa-mir-181c-prec, HUMTRF, hsa-mir-181d, MPR74, Hcd817, hsa-mir-213-prec, hsa- mir-155-prec, Hcdl48_HPR2251eft, hsa-mir-515-15p, hsa-mir-181b-prec, HUMTRN, hsa-mir-128b-prec, hsa-mir-450-2, hsa-mir-216-prec, hsa-mir-342, hsa-mir-142-prec, hsa-mir-223-prec, Hcd754, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Chlorambucil.
184. The kit of claim 137, wherein said gene is selected from the group consisting of PRGl , SLC2A3, RPS19, PSMBlO, ITM2A, DGKA, SEMA4D, SLA, IL2RG, MFNG, AL0X5AP, GPSM3, PSMB9, SELL, ADA, FMNLl, MYB, PTPN7, CXorf9, RHOH, ZNFNlAl, CENTBl, FXYD2, CDlD, STAT4, MAP4K1, CCR7, PDE4C, CD3G, CCR9, SPl 10, TK2, TNFAIP8, NAPlLl, SELPLG, SEC31L2, CD3Z, PRKCQ, SH2D1A, GZMB, CDlA, LAIRl , TRB@, SEPT6, DOCK2, CGOl 8, WBSCR20C, CD3D, CD6, LSTl , GPR65, PRFl, ALMSl , AIFl , CDlE, CYFIP2, TARP, GLTSCR2, FLJ12270, ARHGAP15, NAP1 L2, CECRl, GIMAP6, STAG3, TM6SF1 , C15orf25, MGC5566, FLJ22457, ET, TPKl , and PHFl 1 , or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of ETS2, PTPRC, PETER, SETBPl , LAT, MYBBPlA, ETV5, METAPl, ETSl, ADAMI l , CD53, FARSLA, RPLl 3, ARMET, TETRAN, BETl, RPLl 3, MET, LAPTM5, CD53, COROlA, PTPRCAP, PTPRC, HEMl, GMFG, CDlB, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl, ETV4, ITGB2, PTPRC, HCLSl , MYBLl, FARSLA, and METAP2, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-124a-3-prec, Hcd946, Hcd683, HPR264, MPRl 85, HUMTRF, Hcd294, Hcd503, hsa-mir-20b, MPR74, MPR234, Hcd447, Hcd817, Hcdl48_HPR2251eft, hsa-mir-515-15p, Hcd383, hsa-mir- 181b-prec, Hcd783, MPR224, HPR172, MPR216, HUMTRN, hsa-mir-321 , HPR159, MPR228, ath-MIR180a, hsa-mir-197-prec, hsa-mir-124a-l-precl , hsa-mir-128b-prec, Hcd28_HPR391eft, Hcd889, Hcd350, hsa-mir-025-prec, hsa-mir-208-prec, hsa-mir- 450-2, Hcd923, Hcd434, HPR129, HPR220, hsa-mir-380-5p, hsa-mir-093-prec- 7.1=093-1, hsa-mir-106-prec-X, hsa-mir-342, hsa-mir-142-prec, HSHELAOl, hsa-mir- 223-prec, Hcd754, hsa-mir-020-prec, and hsa-mir-4323p, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Mechlorethamine.
185. The kit of claim 137, wherein said gene is selected from the group consisting of PGKl, SCD, INSIGl , IGBPl, TNFAIP3, TNFSFlO, ABCAl, AGA, ABCA8, DBCl , PTGER2, UGTl A3, ClOorflO, TM4SF13, CGI-90, LXN, DNAJC 12, HIPK2, and C9orf95, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of FGFRlOP, PLXNAl, PSCD2L, TUBB, FGFRl , TUBB2, PAGA, TUBB2, UBB, TUBB2, FGFRl , FGFRl , and TUBB-P ARALOG, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-483, Hcd631, hsa-mir-212-prec, Hcd938, MPR133, Hcd794, Hcd438, and Hcd886, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Streptozocin.
186. The kit of claim 137, wherein said gene is selected from the group consisting of RPLP2, CD99, IFITMl , INSIGl 5 ALDOC, ITM2A, SERPINAl, ClQRl , STAT5A, INPP5D, SATBl, VPS 16, SLA, IL2RG, MFNG, SELL, LRMP, ICAM2, MYB, PTPN7, ARHGAP25, LCK, CXorf9, RHOH, ZNFNlAl, CENTBl, ADD2, LCP2, SPIl, DBT, GZMA, CD2, BATF, HISTl H4C, ARHGAP6, VAVl, MAP4K1, CCR7, PDE4C, CD3G, CCR9, SP140, TK2, LCPl, IFIl 6, CXCR4, ARHGEF6, PSCDBP, SELPLG, SEC31L2, CD3Z, PRKCQ, SH2D1A, GZMB, CDlA, GATA2, LY9, LAIRl, TRB@, SEPT6, HA-I, SLC43A3, D0CK2, CGOl 8, MLCl , CD3D, T3JAM, CD6, ZAP70, D0K2, LSTl, GPR65, PRFl, ALMSl, AIFl, PRDX2, FLJ12151, FBXW12, CDlE, CYFIP2, TARP, TRIM, RPLlOL, GLTSCR2, CKIP-I, NRNl, ARHG AP 15, NOTCHl, PSCD4, C13orfl8, BCLl IB, GIMAP6, STAG3, NARF, TM6SF1, C15orf25, FLJl 1795, SAMSNl, UBASH3A, PACAP, LEFl , IL21R, TCF4, and DKFZP434B0335, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of FLJ10534, PTPRC, CD27BP, TRIM22, TRIM41, PSCD2L, CDlC, MYBBPlA, ICAM3, CD53, FARSLA, GAS7, ABCD2, CD24, CD29, RAC2, CD37, GNA15, PGF, LAPTM5, RPL18A, CD53, COROlA, PTPRCAP, PTPRC, HEMl, GMFG, GNAl 5, ITK, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl , GNA15, TCF7, ITGB2, PTPRC, HCLSl, PRKCBl, ATP2A3, PRKCBl, MYBLl, and FARSLA, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-092-prec- X=092-2, Hcd517, Hcd796, HUMTRF, hsa-mir-20b, hsa-mir-019b-2-prec, hsa-mir- 033-prec, hsa-mir-092-prec- 13=092-1, Hcdl48_HPR2251eft, HUMTRAB, Hcd975, hsa-mir-135-2-prec, hsa-mir-128b-prec, hsa-mir-143-prec, hsa-mir-025-prec, hsa-mir- 216-prec, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir-142-prec, HSHELAOl , HUMTRVlA, hsa-mir-223-prec, Hcd754, hsa-mir-018-prec, and hsa-mir- 020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Carmustine.
187. The kit of claim 137, wherein said gene is selected from the group consisting of RPS 15, INSIGl , ALDOC, ITM2A, ClQRl, STAT5A, INPP5D, VPS 16, SLA, USP20, IL2RG, MFNG, LRMP, EVI2A, PTPN7, ARHGAP25, RHOH, ZNFNlAl, CENTBl, LCP2, SPIl, ARHGAP6, MAP4K1, CCR7, LY96, C6orf32, MAGEAl, SP140, LCPl, IFI 16, ARHGEF6, PSCDBP, SELPLG, CD3Z, PRKCQ, GZMB, LAIRl , SH2D1A, TRB@, RFP, SEPT6, HA-I , SLC43A3, CD3D, T3JAM, GPR65, PRFl , AIFl, LPXN, RPLlOL, SITPEC, ARHGAP15, C13orfl 8, NARF, TM6SF1, PACAP, and TCF4, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of PTPRC, ICAM3, TRFP, CD53, FARSLA, RAC2, MAGEAl 1, LAPTM5, CD53, COROlA, PTPRCAP, PTPRC, HEMl, GMFG, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl , PTPRC, HCLSl, SLC 19Al, FARSLA, and RPS 15 A, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-lOl-prec-9, Hcd796, hsa-mir- 20b, HUMTRAB, hsa-mir-135-2-prec, hsa-mir-153-l-precl, hsa-mir-025-prec, hsa-mir- 093-prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir-142-prec, HUMTRVlA, Hcd754, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Lomustine.
188. The kit of claim 137, wherein said gene is selected from the group consisting of SSRPl, ALDOC, ClQRl , TTFl, PRIMl , USP34, TK2, GOLGIN-67, NPD014, K1AA0220, SLC43A3, WBSCR20C, ICAM2, TEXlO, CHD7, SAMSNl, and TPRT, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of PTPRC, CD53, RNPSl, H3F3A, NUDC, SMARCA4, RPL32, PTMA, CD53, PTPRCAP, PTPRC, RPL32, PTPRCAP, PTPRC, CD53, PTPRC, HCLSl , and SLC 19Al, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-092-prec- X=092-2, hsa-mir-096-prec-7, hsa-mir-123-prec, MPR249, HPR232, hsa-mir-101-prec- 9, hsa-mir-106a, hsa-mir-20b, Hcd861, hsa-mir-017-prec, hsa-mir-019b-2-prec, hsa- mir-033-prec, HcdlO2, MPR216, Hcd975, hsa-mir-019b-l-prec, hsa-mir-135-2-prec, Hcd581, Hcd536_HPR104, hsa-mir-128b-prec, HSTRNL, hsa-mir-025-prec, hsa-mir- 18b, HPR262, Hcd923, Hcd434, Hcd658, HPRl 29, hsa-mir-380-5p, hsa-mir-093-prec- 7.1=093-1, hsa-mir-106-prec-X, Hcd627, hsa-mir-142-prec, hsa-mir-018-prec, and hsa- mir-020-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Mercaptopurine.
189. The kit of claim 137, wherein said gene is selected from the group consisting of CD99, INSIGl, PRGl, ALDOC, ITM2A, SLA, SSBP2, IL2RG, MFNG, ALOX5AP, Clorf29, SELL, STCl, LRMP, MYB, PTPN7, CXorf9, RHOH, ZNFNlAl , CENTBl, ADD2, CDlD, BATF, MAP4K1, CCR7, PDE4C, CD3G, CCR9, SPl 10, TNFAIP8, NAPlLl, CXCR4, ARHGEF6, GATA3, SELPLG, SEC31L2, CD3Z, SH2D1A, GZMB, CDlA, SCN3A, LAIRl , AFlQ, TRB@, D0CK2, MLCl , CD3D, T3JAM, CD6, ZAP70, IFI44, GPR65, PRFl, AIFl, WDR45, CDlE, CYFIP2, TARP, TRIM, ARHGAPl 5, NOTCHl, STAG3, NARF, TM6SF1, UBASH3A, and MGC5566, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of FLJl 0534, PTPRC, TRIM22, C18orfl , TRIM41, LAT, CDlC, MYBBPlA, CD53, FARSLA, PPP2CA, COL5A2, LAPTM5, CD53, COROlA, PTPRCAP, PTPRC, HEMl , GMFG, ITK, CDlB, GMFG, PTPRCAP, PTPRC, CD53, COROlA, HEMl , TCF7, PTPRC, HCLSl, ATP2A3, MYBLl, and FARSLA, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-124a-3-prec, Hcd771, HUMTRF, hsa- mir-213-prec, hsa-mir-181b-prec, Hcd783, hsa-mir-212-prec, hsa-mir-124a-l -precl , hsa-mir-342, hsa-mir-142-prec, HSHELAOl , hsa-mir-223-prec, and Hcd754, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Teniposide.
190. The kit of claim 137, wherein said gene is selected from the group consisting of ALDOC, ClQRl, SLA, WBSCR20A, MFNG, SELL, MYB, RHOH 3 ZNFNlAl , LCP2, MAP4K1, CBFA2T3, LCPl , SELPLG, CD3Z, LAIRl, WBSCR20C, CD3D, GPR65, ARHGAPl 5, FLJlOl 78, NARF, and PUS3, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of PTPRC, MYBBPlA, ICAM3, CD53, FARSLA, CD53, PTPRCAP, PTPRC, HEMl , GMFG, GMFG, PTPRCAP, PTPRC, CD53, HEMl, PTPRC, HCLSl, PRKCBl, PRKCBl , MYBLl, and FARSLA, or wherein said kit further comprises one or more single- stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-025-prec, hsa-mir-007-l-prec, hsa-mir-093-prec-7.1=093-1, Hcd794, and hsa-mir-142-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Dactinomycin.
191. The kit of claim 137, wherein said gene is selected from the group consisting of PPIB, ZFP36L2, IFI30, USP7, SRM, SH3BP5, ALDOC, FADS2, GUSB, PSCDl, IQGAP2, STS, MFNG, FLIl , PIM2, INPP4A, LRMP, ICAM2, EVI2A, MAL, BTN3A3, PTPN7, ILlORA, SPIl, TRAFl , ITGB7, ARHGAP6, MAP4K1 , CD28, PTP4A3, LTB, Clorβ8, WBSCR22, CD8B1 , LCPl , FLJ 13052, MEF2C, PSCDBP, ILl 6, SELPLG, MAGEA9, LAIRl, TNFRSF25, EVI2B, IGJ, PDCD4, RASA4, HA-I, PLCL2, RNASE6, WBSCR20C, NUP210, RPLlOL, Cl Iorf2, CABCl , ARHGEF3, TAPBPL, CHST12, FKBPl 1 , FLJ35036, MYLIP, TXNDC5, PACAP, TOSO, PNAS-4, IL21 R, and TCF4, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of CLTB, BTN3A2, BCL2, SETBPl , ICAM3, BCL2, BCL2, BCL2, CD53, CCND2, CLTB, CLTB, BCL2L1 1 , BTN3A2, CD37, MYCL2, CTSS, LAPTM5, CD53, COROlA, HEMl , CD53, COROlA, HEMl , HCLSl , BCL2L11 , MYCLl, MYC, and MANlAl, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd257, hsa-mir-148-prec, Hcd512, HPR227, Hcd421 , MPR203, hsa-mir-017-prec, hsa-mir-219-2, hsa-mir-328, Hcd783, Hcdl81, HPR213, hsa-mir-191-prec, hsa-mir- 375, hsa-mir-212-prec, Hcd913, Hcd716, MPR207, HPR206, hsa-mir-016b-chr3, Hcd654, hsa-mir-195-prec, Hcd425, hsa-mir-148a, hsa-mir-142-prec, and hsa-mir- 016a-chrl3, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Tretinoin.
192. The kit of claim 137, wherein said gene is selected from the group consisting of PDGFRB, KDR, KIT, and FLT3, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of FLTl, FLT4, PDGFRA, and CSFlR, wherein said level of expression of said gene indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with sunitinib.
193. The kit of claim 137, wherein said gene is BCL2, wherein said level of expression of said gene indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with SPC2996.
194. The kit of claim 137, wherein said gene is selected from the group consisting of ARHGDlB, ZFP36L2, ITM2A, LGALS9, INPP5D, SATBl , TFDP2, IL2RG, CD48, SELL, ADA, LRMP, RIMS3, LCK, CXorf9, RHOH, ZNFNlAl, LCP2, CDlD, CD2, ZNF91, MAP4K1 , CCR7, IGLLl, CD3G, ZNF430, CCR9, CXCR4, KIAA0922, TARP, FYN, SH2D1A, CDl A, LSTl , LAIRl, TRB@, SEPT6, CD3D, CD6, AIFl , CD 1 E, TRIM, GLTSCR2, ARHGAP 15, BIN2, SH3TC 1 , CECR 1 , BCL 1 1 B, GIM AP6, STAG3, GALNT6, MGC5566, PACAP, and LEFl , or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of CD27BP, TRIM22, TRA@, C18orfl , EVL, PRKCH, TRIM41, PSCD2L, CDlC, ADAMl 1 , ABCD2, CD24, CD29, CD37, GNA15, LAPTM5, COROlA, HEMl, GMFG, GNA15, CDlB, GMFG, COROlA, HEMl, GNA15, ITGB2, PRKCBl, ATP2A3, and PRKCBl , or wherein said kit further comprises one or more single- stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-092-prec- X=092-2, hsa-mir-181b-2, Hcd417, Hcd440_HPR257, hsa-mir-019b-2-prec, hsa-mir- 213-prec, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1 , hsa-mir-181b-prec, hsa-mir- 128b-prec, hsa-mir-526a-2, MPR95, HPR220, hsa-mir-133a-l, hsa-mir-148a, hsa-mir- 142-prec, HPR169, hsa-mir-223-prec, hsa-mir-018-prec, hsa-mir-020-prec, and hsa- mir-484, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Ifosfamide.
195. The kit of claim 137, wherein said gene is selected from the group consisting of MLP, GLUL, SLC9A3R1, ZFP36L2, INSIGl, TBLlX, NDUFABl, EBP, TRIMl 4, SRPK2, PMM2, CLDN3, GCHl, IDIl, TTFl, MYB, RASGRPl, HIST1H3H, CBFA2T3, SRRM2, ANAPC5, MBD4, GAT A3, HISTl H2BG, RAB14, PIK3R1, MGC50853, ELFl , ZRFl , ZNF394, S100A14, SLC6A14, GALNT6, SPDEF, TPRT, and CALML4, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of EIF4A1 , TFFl , TFFl , MYBBPlA, AKAPl , DGKZ, EIF4A1, KIAAOl 82, SLC19A1 , ATP2A3, MYBLl , EIF4EBP2, Gl P2, and MANlAl, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of hsa-mir-092-prec-X=092-2, Hcd547, Hcd257, hsa-mir-148-prec, HUMTRS, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1, hsa-mir-375, hsa-mir-095-prec-4, hsa-mir-025-prec, hsa-mir-202-prec, hsa-mir-007-1- prec, hsa-mir-093-prec-7.1=093-1 , hsa-mir-106-prec-X, hsa-mir-142-prec, hsa-mir-223- prec, and hsa-mir-018-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Tamoxifen.
196. The kit of claim 137, wherein said gene is selected from the group consisting of CSDA, F8A1 , KYNU, PHF14, SERPINB2, OPHNl, HRMT1L2, TNFRSFlA, PPP4C, CESl, TP53AP1, TM4SF4, RPL5, BC008967, TLK2, COL4A6, PAK3, RECK, LOC51321, MST4, DERP6, SCD4, and FLJ22800, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of STC2, BAX, CDKNlA, DDB2, RGS2, BAX, BAX, RPL13, RPL13, CDKNlA, and GABPB2, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of HUMTRF, HUMTRN, hsa-mir-124a- 1-precl, hsa-mir-150-prec, Hcd923, HPR181, Hcd569, hsa-mir-199a-2-prec, Hcd754, and hsa-mir-4323p, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Floxuridine.
197. The kit of claim 137, wherein said gene is selected from the group consisting of CSDA, UBE2L6, TAPl , RPS19, SERPINAl, ClQRl, SLA, GPSM3, PSMB9, EDGl, FMNLl, PTPN7, ZNFNlAl, CENTBl, BATF, MAP4K1, PDE4C, SPl 10, HLA-DRA, IFI 16, HLA-DRBl , ARHGEF6, SELPLG, SEC31L2, CD3Z, PRKCQ, SH2D1A, GZMB, TRB@, HLA-DPAl, AIMl, D0CK2, CD3D, IFITMl, ZAP70, PRFl , Clorf24, ARHGAPl 5, C13orfl 8, and TM6SF1, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of PTPRC, TRIM22, PSME2, LAT 5 METAPl , CD53, FARSLA, RPLl 3, RAC2, RPLl 3, PTMA, CD53, COROlA, PTPRCAP, PTPRC, GMFG, ITK, GMFG, PTPRCAP, PTPRC, CD53, COROlA, ITGB2, PTPRC, HCLSl , and FARSLA, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of HUMTRF, hsa-mir-380-5p, hsa-mir-342, hsa-mir-142-prec, and Hcd200, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Irinotecan.
198. The kit of claim 137, wherein said gene is selected from the group consisting of STATl, HSBPl, IFI30, RI0K3, TNFSFlO, ALOX5AP, ADFP, IRS2, EFEMP2, RIPK2, DKFZp564I1922, MTlK, RNASET2, EFHD2, TRIB3, ACSL5, IFIHl, and DNAPTP6, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a gene selected from the group consisting of IFI27, OPTN, C20orfl 8, FNl, LOC51 123, FNl, OPTN, and OPTN, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRNA selected from the group consisting of Hcd289, Hcd939, Hcd330, HPR76, Hcdl 1 1 , Hcd976, hsa-mir-15a, hsa-mir-OOlb-1-precl, hsa-mir-450-1 , hsa-mir-200b, Hcd578, and hsa-mir-200a-prec, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Satraplatin.
199. The method of any one of claims 1-136, wherein said measuring comprises measuring said level of expression of said gene or microRNA by using a kit of any one of claims 137-198 and 300.
200. The kit of claim 137, wherein said treatment comprises administering a chemotherapeutic agent.
201. The kit of claim 137, wherein said single-stranded nucleic acid is characterized by the ability to specifically identify the presence or absence of a nucleic acid complementary to said gene or microRNA in a sample collected from said cancer patient.
202. The kit of any one of claims 137-198 and 300, wherein said single-stranded nucleic acid is at least 15 nucleotides long.
203. The kit of claim 137, wherein said single-stranded nucleic acid is at least 25 nucleotides long.
204. The kit of any one of claims 137-198 and 300, wherein said single-stranded nucleic acid is a deoxyribonucleic acid (DNA).
205. A kit comprising a single-stranded nucleic acid molecule that is substantially complementary to or substantially identical to at least 5 consecutive nucleotides of at least one microRNA selected from the group consisting of ath-MIR180aNo2, HcdlO2 left, Hcdl 11 left, Hcdl 15 left, Hcdl20 left, Hcdl42 right, Hcdl45 left, Hcdl48_HPR225 left, Hcdl 81 left, Hcdl 81 right, Hcd210 HPR205 right, Hcd213_HPR182 left, Hcd230 left, Hcd243 right, Hcd246 right, Hcd248 right, Hcd249 right, Hcd250 left, Hcd255 left, Hcd257 left, Hcd257 right, Hcd263 left, Hcd266 left, Hcd270 right, Hcd279 left, Hcd279 right, , Hcd28_HPR391eft, Hcd28_HPR39right, Hcd282PO right, Hcd289 left, Hcd294 left, Hcd318 right, Hcd323 left, Hcd330 right, Hcd338 left, Hcd340 left, Hcd350 right, Hcd355_HPR190 left, Hcd361 right, Hcd366 left, Hcd373 right, Hcd383 left, Hcd383 right, Hcd384 left, Hcd397 left, Hcd404 left, Hcd412 left, Hcd413 right, Hcd415 right, Hcd417 right, Hcd421 right, Hcd425 left, Hcd43 8right, Hcd434 right, Hcd438 left, Hcd440_HPR257 right, Hcd444 right, Hcd447 right, Hcd448 left, Hcd498 right, Hcd503 left, Hcd51 1 right, Hcd512 left, Hcd514 right, Hcd517 left, Hcd517 right, Hcd530 right, Hcd536_HPR104 right, Hcd542 left, Hcd544 left, Hcd547 left, Hcd559 right, Hcd562 right, Hcd569 right, Hcd570 right, Hcd578 right, Hcd581 right, Hcd586 left, Hcd586 right, Hcd587 right, Hcd605 left, Hcd605 left, Hcd605 right, Hcd608 right, Hcd627 left, Hcd631 left, Hcd631 right, Hcd634 left, Hcd642 right, Hcd649 right, Hcd654 left, Hcd658 right, Hcd669 right, Hcd674 left, Hcd678 right, Hcd683 left, Hcd684 right, Hcd689 right, Hcd690 right, Hcd691 right, Hcd693 right, Hcd697 right, Hcd704 left, Hcd704 left, Hcd712 right, Hcd716 right, Hcd731 left, Hcd738 left, Hcd739 right, Hcd739 right, Hcd749 right, Hcd753 left, Hcd754 left, Hcd755 left, Hcd760 left, Hcd763 right, Hcd768 left ,Hcd768 right, Hcd770 left, Hcd773 left, Hcd777 left, Hcd778 right, Hcd781 left, Hcd781 right, Hcd782 left, Hcd783 left, Hcd788 left, Hcd794 right, Hcd796 left, Hcd799 left, Hcd807 right, Hcd812 left, Hcd817 left, Hcd817 right, Hcd829 right, Hcd852 right, Hcd861 right, Hcd863PO right, Hcd866 right, Hcd869 left, Hcd873 left, Hcd886 right, Hcd889 right, Hcd891 right, Hcd892 left, Hcd913 right, Hcd923 left, Hcd923 right, Hcd938 left, Hcd938 right, Hcd939 right, Hcd946 left, Hcd948 right, Hcd960 left, Hcd965 left, Hcd970 left, Hcd975 left, Hcd976 right, Hcd99 right, HPRlOO right, HPRl 29 left, HPRl 54 left, HPRl 59 left, HPRl 63 left, HPRl 69 right, HPR172 right, HPR181 left, HPR187 left, HPR199 right, HPR206 left, HPR213 right, HPR214 right, HPR220 left , HPR220 right, HPR227 right, HPR232 right, HPR233 right, HPR244 right, HPR262 left, HPR264 right, HPR266 right, HPR271 right, HPR76 right, hsa_mir_490_Hcd20 right, HSHELAOl , HSTRNL, HUMTRAB, HUMTRF, HUMTRN, HUMTRS, HUMTRVlA, let-7f-2-prec2, mir-OOlb-1-precl, mir-OOlb-2-prec, mir-007-l-prec, mir-007-2-precNo2, mir-OlOa-precNol, mir-015b- precNo2, mir-016a-chrl3, mir-016b-chr3, mir-017-precNol, mir-017-precNo2, mir- 018-prec, mir-019a-prec, mir-019b-l-prec, mir-019b-2-prec, mir-020-prec, mir-022- prec, mir-023a-prec, mir-023b-prec, mir-024-2-prec, mir-025-prec, mir-027b-prec, mir- 029c-prec, mir-032-precNo2, mir-033b-prec, mir-033-prec, mir-034-precNol , mir-034- precNo2, mir-092-prec-l 3=092- 1NO2, mir-092-prec-X=092-2, mir-093-prec-7.1=093- 1, mir-095-prec-4 ,mir-096-prec-7Nol ,mir-096-prec-7No2, mir-098-prec-X, mir-099b- prec-19Nol, mir-lOO-l/2-prec, mir-100Nol, mir-lOl-prec-9, mir-102-prec-l , mir-103- 2-prec, mir-103-prec-5=103-l, mir-106aNol, mir-106-prec-X,mir-107Nol , mir-107- prec-10, mir- 122a-prec, mir-123-precNol , mir-123-precNo2, mir-124a-l-precl , mir- 124a-2-prec, mir-124a-3-prec, mir- 125b- 1, mir-125b-2-precNo2, mir-127-prec, mir- 128b-precNol , mir-128b-precNo2, mir- 133a- 1, mir-135-2-prec, mir-136-precNo2, mir- 138-1-prec, mir-140No2, mir-142-prec, mir-143-prec, mir-144-precNo2, mir-145-prec, mir-146bNol , mir-146-prec, mir- 147-prec, mir-148aNol , mir-148-prec, mir-149-prec, mir-150-prec, mir-153-l-precl, mir-154-preclNol, mir-155-prec, mir-15aNol, mir-16- INoI , mir-16-2Nol, mir-181a-precNol , mir-181b-lNol, mir-181b-2Nol, mir-181b- precNol, mir-181b-precNo2, mir-181c-precNol, mir-18IdNoI, mir-188-prec, mir- 18bNo2, mir-191-prec, mir-192No2, mir-193bNo2, mir-194-2NoI, mir-195-prec, mir- 196-2-precNo2, mir-197-prec, mir-198-prec, mir-199a- 1-prec, mir-199a-2-prec, mir- 199b-precNol , mir-200a-prec, mir-200bNol, mir-200bNo2, mir-202*, mir-202-prec, mir-204-precNo2, mir-205-prec, mir-208-prec, mir-20bNol, mir-212-precNol, mir- 212-precNo2, mir-213-precNol, mir-214-prec, mir-215-precNo2, mir-216-precNol, mir-219-2Nol, mir-219-prec, mir-223-prec, mir-29b-lNol, mir-29b-2=102prec7.1=7.2, mir-321Nol, mir-321No2, mir-324Nol, mir-324No2, mir-328Nol, mir-342Nol, mir- 361NoI, mir-367Nol , mir-370Nol, mir-371Nol, miR-373*Nol , mir-375, mir- 376aNol, mir-379Nol, mir-380-5p, mir-382, mir-384, mir-409-3p, mir-423Nol, mir- 424No2, mir-429Nol, mir-429No2, mir-4323p, mir-4325p, mir-449Nol, mir-450-1, mir-450-2Nol, mir-483Nol, mir-484, mir-487Nol, mir-495Nol, mir-499No2, mir- 501No2, mir-503Nol , mir-509Nol, mir-514-lNo2, mir-515-15p, mir-515-23p, mir- 516-33p, mir-516-43p, mir-518e/526c, mir-519a- 1/52, mir-519a-2No2, mir-519b, mir- 519c/52, mir-520c/52, mir-526a-2Nol, mir-526a-2No2, MPR103 right, MPR121 left, MPR121 left, MPR130 left, MPR130 right, MPR133 right, MPR141 left, MPR151 left, MPRl 56 left, MPRl 62 left, MPRl 74 left, MPRl 74 right, MPRl 85 right, MPRl 97 right, MPR203 left, MPR207 right, MPR215 left, MPR216 left, MPR224 left, MPR224 right, MPR228 left, MPR234 right, MPR237 left, MPR243 left, MPR244 right, MPR249 left, MPR254 right, MPR74 left, MPR88 right, and MPR95 left, wherein said single-stranded nucleic acid molecule allows detection of a level of expression of said microRNA when said single-stranded nucleic acid molecule is contacted with said microRNA, or its complement, under conditions allowing hybridization to occur between said single-stranded nucleic acid molecule and said microRNA, said kit further comprising instructions for applying nucleic acids collected from a sample from a cancer patient, instructions for measuring the level of expression of said microRNA, and instructions for determining said cell's sensitivity to a treatment for cancer.
206. The kit of claim 205, wherein said instructions further indicate that a change in said level of expression of said microRNA relative to the level of expression of said microRNA in a control cell sensitive to said treatment indicates a change in sensitivity of said cell to said treatment.
207. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd892, Hcd678, hsa-mir-007-l-prec, MPR243, Hcd654, hsa-mir-487, Hcd794, Hcd739, and Hcd562, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Vincristine.
208. The kit of claim 205, wherein said microRNA is selected from the group consisting of HUMTRF, HPR187, hsa-mir-450-1 , hsa-mir-155-prec, hsa-mir-515-15p, hsa-mir-181b-prec, hsa-mir-124a-l-precl, hsa-mir-450-2, Hcd923, hsa-mir-342, hsa- mir-142-prec, hsa-mir-223-prec, Hcd754, and Hcd213_HPR182, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Cisplatin.
209. The kit of claim 205, wherein said microRNA is selected from the group consisting of MPR121, HUMTRS, hsa-mir-213-prec, hsa-mir-155-prec, hsa-mir-147- prec, hsa-mir-100, hsa-mir-138-l-prec, hsa-mir-140, hsa-mir-146-prec, hsa-mir-509, hsa-mir-146b, Hcd514, Hcd397, Hcd731, hsa-mir-034-prec, and hsa-mir-lOO-l/2-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Azaguanine.
210. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd415, Hcd768, HUMTRF, Hcd866, Hcdl45, HUMTRAB, Hcd913, HPR163, Hcd697, Hcd755, Hcd716, MPR207, HSTRNL, HPR206, MPR243, Hcd654, MPRl 30, Hcd782, Hcd794, Hcd739, hsa-mir-142-prec, HSHELAOl , HUMTRVlA, and Hcd754, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Etoposide.
21 1. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd768, hsa-mir-483, Hcdl45, hsa-mir-197-prec, hsa-mir-212-prec, HPR 163, Hcd654, hsa-mir-342, Hcd794, hsa-mir-142-prec, and Hcd754, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Adriamycin.
212. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-096-prec-7, Hcd605, hsa-mir-007-2- prec, hsa-mir-019b-2-prec, MPR216, hsa-mir-019b-l-prec, hsa-mir-135-2-prec, HSTRNL, hsa-mir-025-prec, hsa-mir-007-l-prec, hsa-mir-019a-prec, hsa-mir-380-5p, hsa-mir-093-prec-7.1=093-1 , hsa-mir-106-prec-X, hsa-mir-142-prec, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Aclarubicin.
213. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd768, HUMTRF, hsa-mir-213-prec, hsa-mir-181b-prec, MPR244, hsa- mir-409-3p, HSTRNL, hsa-mir-382, hsa-mir-342, hsa-mir-142-prec, and Hcd200, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Mitoxantrone.
214. The kit of claim 205, wherein said microRNA is selected from the group consisting of HUMTRF, Hcdl48_HPR2251eft, Hcd938, MPRl 74, and hsa-mir-4323p, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Mitomycin.
215. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-096-prec-7, hsa-mir-l Ol-prec-9, hsa- mir-20b, hsa-mir-019b-2-prec, hsa-mir-032-prec, MPRl 56, hsa-mir-019b- 1-prec, hsa- mir-135-2-prec, hsa-mir-025-prec, hsa-mir-007-l-prec, hsa-mir-361, hsa-mir-093-prec- 7.1=093-1 , hsa-mir-106-prec-X, hsa-mir-098-prec-X, hsa-mir-142-prec, HPR169, hsa- mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Paclitaxel.
216. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-096-prec-7, hsa-mir-095-prec-4, HSTRNL, and hsa-mir-007-1- prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Taxotere.
217. The kit of claim 205, wherein said microRNA is selected from the group consisting of MPRl 41, hsa-mir-424, Hcd690, Hcd783, hsa-mir-150-prec, Hcd266, hsa- mir-503, hsa-mir-128b-prec, Hcd397, and hsa-mir-484, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Dexamethasone.
218. The kit of claim 205, wherein said microRNA is selected from the group consisting of HUMTRF, hsa-mir-155-prec, hsa-mir-515-15p, Hcd938, Hcd642, Hcdl20, hsa-mir-380-5p, hsa-mir-342, hsa-mir-142-prec, hsa-mir-223-prec, and hsa- mir-4323p, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Ara-C.
219. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd544, hsa-mir- 181 c-prec, Hcd517, MPR151, hsa-mir-213-prec, hsa- mir-181b-prec, hsa-mir-150-prec, hsa-mir- 153- 1-precl , hsa-mir- 128b-prec, Hcd812, hsa-mir- 195-prec, hsa-mir-342, hsa-mir-370, hsa-mir-142-prec, hsa-mir-223-prec, and hsa-mir-484, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Methylprednisolone.
220. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-096-prec-7, hsa-mir- 123 -prec, Hcd250, hsa-mir-518e, HPR232, Hcd263, hsa-mir-516-33p, Hcd605, Hcd373, MPR254, MPR215, HUMTRF, hsa-mir-106a, hsa-mir-20b, Hcd361, Hcd412, Hcd781 , hsa-mir-019b-2-prec, HPR214, Hcd807, Hcd817, Hcd788, Hcd970, Hcdl48_HPR2251eft, HcdlO2, Hcd246, HPR199, HPR233, Hcd383, MPR224, HPRl 72, MPR216, hsa-mir-321 , Hcd586, Hcd587, Hcd249, Hcd279, HPRl 59, Hcd689, Hcd691, hsa-mir-019b-l-prec, Hcd413, Hcd581 , Hcd536_HPR104, Hcd230, HPRl 54, Hcd270, Hcd649, Hcd889, Hcd938, HPR266, hsa-mir-025-prec, Hcd355_HPR190, MPRl 62, Hcd923, MPR237, MPRl 74, hsa-mir-019a-prec, hsa_mir_490_Hcd20, hsa-mir-380-5p, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec- X, Hcd627, hsa-mir-142-prec, HPRl 69, hsa-mir-OOlb-2-prec, hsa-mir-018-prec, hsa- mir-020-prec, Hcd404, hsa-mir-384, and hsa-mir-4323p, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Methotrexate.
221. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-376a, hsa-mir-155-prec, hsa-mir-409-3p, hsa-mir-495, Hcd498, hsa-mir-199a-2-prec, hsa-mir-382, HPR271, hsa-mir-145-prec, and hsa-mir-199a-l- prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Bleomycin.
222. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-lOl-prec-9, hsa-mir-144-prec, hsa- mir-519a-l, hsa-mir-519b, hsa-mir-015b-prec, hsa-mir-106a, hsa-mir-16-l, hsa-mir- 181d, hsa-mir-017-prec, hsa-mir-019b-2-prec, hsa-mir-192, hsa-mir-213-prec, hsa-mir- 215-prec, hsa-mir-107, hsa-mir-200b, hsa-mir-103-prec-5= 103-1, hsa-mir-519a- 1 /526c, MPR216, hsa-mir-019b- 1-prec, hsa-mir-107-prec-lO, hsa-mir-135-2-prec, hsa-mir-103- 2-prec, hsa-mir-519a-2, hsa-mir-025-prec, hsa-mir-16-2, MPR95, hsa-mir-016b-chr3, Hcd948, hsa-mir-195-prec, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir- 142-prec, hsa-mir-519c/526c, hsa-mir-200a-prec, hsa-mir-016a-chrl 3, hsa-mir-018- prec, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Methyl-GAG.
223. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd829, HUMTRF, HPRl 87, Hcd210_HPR205, hsa-mir-379, hsa-mir- 213-prec, hsa-mir-4325p, hsa-mir-450-1, hsa-mir-155-prec, Hcd28_HPR39right, MPR244, hsa-mir-409-3p, hsa-mir-124a-l-precl, hsa-mir-154-precl, hsa-mir-495, hsa- mir-515-23p, Hcd43 8right, Hcd770, hsa-mir-382, hsa-mir-223-prec, Hcd754, and Hcd213_HPR182, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Carboplatin.
224. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-096-prec-7, hsa-mir-429, Hcd693, HPR214, Hcd586, Hcd249, Hcd689, hsa-mir- 194-2, Hcd581, Hcd270, hsa-mir-025-prec, Hcd340, hsa-mir-007-1- prec, hsa-mir-093-prec-7.1=093-1, hsa-mir- 106-prec-X, Hcd794, hsa-mir-020-prec, and hsa-mir-4323p, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with 5-FU (5- Fluorouracil).
225. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir- 136-prec, Hcd570, Hcd873, Hcd282PO, Hcd799, Hcd829, Hcd210_HPR205, hsa-mir-219-prec, hsa-mir-202, hsa-mir-429, Hcd693, hsa-mir-022- prec, MPR88, hsa-mir- 198-prec, hsa-mir- 199b-prec, Hcdl45, hsa-mir- 124a-2-prec, hsa- mir- 138-2-prec, Hcd960, Hcd869, Hcd384, hsa-mir-027b-prec, Hcd444, hsa-mir- 194-2, hsa-mir- 197-prec, Hcd913, HPR 163, hsa-mir- 138- 1-prec, hsa-mir-010a-prec, hsa-mir- 023b-prec, hsa-mir- 193b, Hcd654, Hcd542, hsa-mir- 199a-2-prec, hsa-mir-214-prec, Hcd608, Hcd684, hsa-mir- 145-prec, hsa-mir-023a-prec, hsa-mir-024-2-prec, and hsa- mir- 199a- 1-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with radiation therapy.
226. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-123-prec, hsa-mir-106a, hsa-mir-20b, hsa-mir-017-prec, hsa-mir-019b-2-prec, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1 , hsa-mir-122a-prec, Hcd783, MPR216, hsa-mir-019b-l-prec, hsa-mir-135-2-prec, hsa- mir-128b-prec, hsa-mir-025-prec, Hcd51 1, hsa-mir-093-prec-7.1=093-1, hsa-mir- 106- prec-X, hsa-mir-142-prec, HPR169, hsa-mir-223-prec, hsa-mir-018-prec, and hsa-mir- 020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with PXDlOl (belinostat).
227. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-096-prec-7, Hcd605, hsa-mir-20b, hsa-miR-373*, HUMTRAB, hsa-mir-019b-l-prec, HPR163, hsa-mir-371, hsa-mir-025-prec, hsa-mir-18b, hsa-mir- 093-prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir-142-prec, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with 5-Aza-2'-deoxycytidine (Decitabine).
228. The kit of claim 205, wherein said microRNA is selected from the group consisting of HUMTRF, hsa-mir-483, MPR74, hsa-mir- 122a-prec, ath-MIR180a, hsa- mir-128b-prec, Hcd923, hsa-mir-106-prec-X, hsa-mir-342, hsa-mir-142-prec, HPRl 69, hsa-mir-223-prec, Hcd754, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Idarubicin.
229. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir- 124a-3-prec, hsa-mir-181a-prec, Hcd773, Hcd683, Hcd796, HUMTRF, HUMTRS, hsa-mir-181b-2, Hcd294, hsa-mir-20b, hsa-mir-181d, hsa-mir- 213-prec, Hcdl48_HPR2251eft, hsa-mir-515-15p, hsa-mir-181b-prec, Hcd783, HUMTRAB, HUMTRN, hsa-mir-181b-l, hsa-mir- 124a- 1-precl , hsa-mir-367, hsa-mir- 128b-prec, Hcd43 8right, hsa-mir-025-prec, hsa-mir-216-prec, Hcd731, hsa-mir-093- prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir-342, hsa-mir-142-prec, HSHELAOl, HUMTRVlA, hsa-mir-223-prec, Hcd754, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Melphalan.
230. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd829, hsa-mir-197-prec, HPR163, and hsa-mir-150-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with IL4-PE38 fusion protein.
231. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd829, hsa-mir-197-prec, HPR163, and hsa-mir-150-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with IL13-PE38QQR fusion protein (cintredekin besudotox).
232. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-034prec, Hcd255, Hcd712, Hcd965, Hcd891, Hcd210_HPR205, hsa-mir-429, Hcd753, Hcd693, MPR203, Hcd704, Hcd863PO, hsa-mir-122a-prec, Hcd760, Hcd338, HPR213, Hcd852, Hcd366, MPR103, Hcd669, and hsa-mir-188-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Valproic acid (VPA).
233. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd257, hsa-mir-148-prec, Hcd512, HPR227, Hcd421, MPR203, hsa-mir- 017-prec, hsa-mir-219-2, hsa-mir-328, Hcd783, Hcdlδl, HPR213, hsa-mir-191-prec, hsa-mir-375, hsa-mir-212-prec, Hcd913, Hcd716, MPR207, HPR206, hsa-mir-016b- chr3, Hcd654, hsa-mir-195-prec, Hcd425, hsa-mir-148a, hsa-mir-142-prec, and hsa- mir-016a-chrl3, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with All-trans retinoic acid (ATRA).
234. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd99, hsa-mir-520c/526a, hsa-mir-191-prec, hsa-mir-205-prec, hsa-mir- 375, hsa-mir-423, hsa-mir-449, and hsa-mir-196-2-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Cytoxan.
235. The kit of claim 205, wherein said microRNA is selected from the group consisting of HUMTRF, MPR74, hsa-mir-213-prec, hsa-mir-155-prec, hsa-mir-181b- prec, hsa-mir-342, and hsa-mir-4323p, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Topotecan (Hycamtin).
236. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-123-prec, hsa-mir-514-1, hsa-mir- 101-prec-9, hsa-mir-148-prec, hsa-mir-106a, hsa-mir-20b, Hcd781, hsa-mir-017-prec, hsa-mir-019b-2-prec, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1, hsa-mir-107, hsa- mir-103-prec-5=103-l, MPR216, hsa-mir-29b-2=102prec7.1=7.2, hsa-mir-019b-l-prec, hsa-mir-107-prec-lO, hsa-mir-135-2-prec, Hcd581, hsa-mir-103-2-prec, Hcd230, hsa- mir-025-prec, hsa-mir-208-prec, hsa-mir-18b, hsa-mir-093-prec-7.1=093-1 , hsa-mir- 106-prec-X, hsa-mir-142-prec, HPR 169, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Suberoylanilide hydroxamic acid.
237. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd415, hsa-mir-147-prec, hsa-mir-O33b-prec, Hcd778, hsa-mir-127-prec, hsa-mir-324, Hcd794, and Hcd634, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Depsipeptide.
238. The kit of claim 205, wherein said microRNA is selected from the group consisting of MPR121, Hcdl 15, Hcd693, Hcd704, HPRlOO, Hcd760, hsa-mir-147-prec, hsa-mir-033b-prec, hsa-mir-146-prec, Hcdl42, hsa-mir-501 , Hcd716, MPR207, Hcd777, hsa-mir-204-prec, hsa-mir-146b, Hcd51 1 , Hcd397, MPR130, Hcd782, hsa- mir-324, Hcd794, and Hcd739, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Bortezomib.
239. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-096-prec-7, hsa-mir-123-prec, MPR249, HPR232, hsa-mir-lOl-prec-9, hsa-mir- 106a, hsa-mir-20b, Hcd861, hsa-mir- 017-prec, hsa-mir-019b-2-prec, hsa-mir-033-prec, HcdlO2, MPR216, Hcd975, hsa-mir- 019b-l-prec, hsa-mir-135-2-prec, Hcd581, Hcd536_HPR104, hsa-mir- 128b-prec, HSTRNL, hsa-mir-025-prec, hsa-mir-18b, HPR262, Hcd923, Hcd434, Hcd658, HPR129, hsa-mir-380-5p, hsa-mir-093-prec-7.1=093-1, hsa-mir- 106-prec-X, Hcd627, hsa-mir- 142-prec, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Leukeran.
240. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd773, Hcd248, hsa-mir-181d, MPR74, hsa-mir-213-prec, hsa-mir-155- prec, MPR197, hsa-mir-181b-prec, hsa-mir-29b-2=102prec7.1=7.2, hsa-mir-029c-prec, Hcd318, hsa-mir- 128b-prec, hsa-mir- 130a-prec, hsa-mir- 140, hsa-mir- 16-2, hsa-mir- 526a-2, hsa-mir-016b-chr3, hsa-mir- 195 -prec, hsa-mir-216-prec, hsa-mir-342, hsa-mir- 29b- 1, Hcd627, hsa-mir- 102-prec-l, hsa-mir- 142-prec, hsa-mir-223-prec, hsa-let-7f-2- prec2, and hsa-mir-016a-chrl3, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Fludarabine.
241. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd794, and Hcd754, wherein said level expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Vinblastine.
242. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-096-prec-7, hsa-mir-124a-3-prec, hsa-mir-lOl-prec-9, Hcd712, Hcd693, hsa-mir-219-2, Hcdl45, hsa-mir-155-prec, HPR213, hsa-mir-212-prec, Hcd913, Hcd716, MPR207, Hcd559, Hcd654, Hcd739, and hsa-mir-142-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Busulfan.
243. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-123-prec, hsa-mir-101-prec-9, Hcd517, Hcd796, Hcd749, Hcd674, hsa-mir-019b-2-prec, hsa-mir-033-prec, hsa-mir- 092-prec- 13=092-1, hsa-mir-124a-2-prec, hsa-mir-143-prec, hsa-mir-516-43p, hsa-mir- 216-prec, Hcd731, hsa-mir-106-prec-X, hsa-mir-142-prec, hsa-mir-223-prec, Hcd754, and hsa-mir-018-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Dacarbazine.
244. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-148-prec, hsa-mir-20b, hsa-mir-007- 2-prec, hsa-mir-017-prec, hsa-mir-019b-2-prec, Hcd760, Hcd783, MPR216, hsa-mir- 375, hsa-mir-019b-l-prec, hsa-mir-135-2-prec, hsa-mir-150-prec, hsa-mir-128b-prec, hsa-mir-499, hsa-mir-025-prec, hsa-mir-007-l-prec, hsa-mir-019a-prec, hsa-mir-093- prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir-142-prec, HPR 169, hsa-mir-018-prec, hsa-mir-020-prec, and hsa-mir-484, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Oxaliplatin.
245. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd257, Hcd768, Hcd796, HUMTRF, HUMTRS, MPR74, hsa-mir-213- prec, hsa-mir-155-prec, Hcd763, hsa-mir-181b-prec, ath-MIR180a, hsa-mir-216-prec, hsa-mir-342, hsa-mir-142-prec, HSHELAOl , HUMTRVlA, hsa-mir-223-prec, Hcd754, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Hydroxyurea.
246. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd257, Hcd946, Hcd503, hsa-mir-429, Hcd693, hsa-miR-373*, Hcd738, hsa-mir-328, Hcd783, Hcdl 81, Hcd631, Hcd279, hsa-mir- 194-2, hsa-mir-197-prec, HPRl 63, hsa-mir- 150-prec, Hcd323, hsa-mir- 103 -2-prec, Hcd243, Hcd938, hsa-mir- 025-prec, hsa-mir-007-l-prec, MPR243, Hcd51 1, Hcd654, hsa-mir- 199a-2-prec, hsa- mir-214-prec, hsa-mir-093-prec-7.1=093-1, hsa-mir- 106-prec-X, Hcd794, Hcd530, HSHELAOl, Hcd754, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Tegafur.
247. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd768, HUMTRF, Hcdl45, Hcd923, hsa-mir-216-prec, hsa-mir-093- prec-7.1=093-1, hsa-mir-342, Hcd794, hsa-mir-142-prec, HSHELAOl, hsa-mir-223- prec, and Hcd754, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Daunorubicin.
248. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir- 125b-2-prec, hsa-mir-022-prec, hsa-mir- 125b- 1, hsa-mir- 155- prec, hsa-mir-100, hsa-mir-409-3p, hsa-mir-495, hsa-mir- 199a-2-prec, hsa-mir-382, and hsa-mir- 100-1 /2-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Bleomycin.
249. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd338, hsa-mir-099b-prec- 19, and hsa-mir-149-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Estramustine.
250. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-181a-prec, hsa-mir-181c-prec, HUMTRF, hsa-mir-181d, MPR74, Hcd817, hsa-mir-213-prec, hsa-mir-155-prec, Hcdl48_HPR2251eft, hsa-mir-515-15p, hsa-mir-181b-prec, HUMTRN, hsa-mir-128b-prec, hsa-mir-450-2, hsa-mir-216-prec, hsa-mir-342, hsa-mir-142-prec, hsa-mir-223-prec, Hcd754, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Chlorambucil.
251. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-124a-3-prec, Hcd946, Hcd683, HPR264, MPRl 85, HUMTRF, Hcd294, Hcd503, hsa-mir-20b, MPR74, MPR234, Hcd447, Hcd817, Hcdl48_HPR2251eft, hsa-mir-515-15p, Hcd383, hsa-mir-181b-prec, Hcd783, MPR224, HPR172, MPR216, HUMTRN, hsa-mir-321, HPR159, MPR228, ath-MIR180a, hsa- mir-197-prec, hsa-mir-124a-l-precl, hsa-mir-128b-prec, Hcd28_HPR391eft, Hcd889, Hcd350, hsa-mir-025-prec, hsa-mir-208-prec, hsa-mir-450-2, Hcd923, Hcd434, HPR129, HPR220, hsa-mir-380-5p, hsa-mir-093-prec-7.1=093-1 , hsa-mir-106-prec-X, hsa-mir-342, hsa-mir-142-prec, HSHELAOl , hsa-mir-223-prec, Hcd754, hsa-mir-020- prec, and hsa-mir-4323p, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Mechlorethamine.
252. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-483, Hcd631 , hsa-mir-212-prec, Hcd938, MPR133, Hcd794, Hcd438, and Hcd886, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Streptozocin.
253. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, Hcd517, Hcd796, HUMTRF, hsa-mir-20b, hsa-mir-019b-2-prec, hsa-mir-033-prec, hsa-mir-092-prec- 13=092- 1 , Hcdl48_HPR2251eft, HUMTRAB, Hcd975, hsa-mir-135-2-prec, hsa-mir-128b-prec, hsa-mir-143-prec, hsa-mir-025-prec, hsa-mir-216-prec, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, hsa-mir-142-prec, HSHELAOl, HUMTRVlA, hsa-mir-223-prec, Hcd754, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Carmustine.
254. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-101-ρrec-9, Hcd796, hsa-mir-20b, HUMTRAB, hsa-mir- 135-2- prec, hsa-mir-153-l-precl, hsa-mir-025-prec, hsa-mir-093-prec-7.1=093-1, hsa-mir- 106-prec-X, hsa-mir-142-prec, HUMTRVlA, Hcd754, hsa-mir-018-prec, and hsa-mir- 020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Lomustine.
255. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-096-prec-7, hsa-mir-123-prec, MPR249, HPR232, hsa-mir-lOl-prec-9, hsa-mir-106a, hsa-mir-20b, Hcd861 , hsa-mir- 017-prec, hsa-mir-019b-2-prec, hsa-mir-033-prec, HcdlO2, MPR216, Hcd975, hsa-mir- 019b-l-prec, hsa-mir-135-2-prec, Hcd581, Hcd536_HPR104, hsa-mir-128b-prec, HSTRNL, hsa-mir-025-prec, hsa-mir-18b, HPR262, Hcd923, Hcd434, Hcd658, HPR129, hsa-mir-380-5p, hsa-mir-093-prec-7.1=093-1, hsa-mir-106-prec-X, Hcd627, hsa-mir-142-prec, hsa-mir-018-prec, and hsa-mir-020-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Mercaptopurine.
256. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-124a-3-prec, Hcd771, HUMTRF, hsa-mir-213-prec, hsa-mir- 181b-prec, Hcd783, hsa-mir-212-prec, hsa-mir-124a-l-precl, hsa-mir-342, hsa-mir- 142-prec, HSHELAOl , hsa-mir-223-prec, and Hcd754, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Teniposide.
257. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-025-prec, hsa-mir-007-l-prec, hsa-mir-093-prec-7.1=093-1, Hcd794, and hsa-mir- 142-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Dactinomycin.
258. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd257, hsa-mir- 148-prec, Hcd512, HPR227, Hcd421, MPR203, hsa-mir- 017-prec, hsa-mir-219-2, hsa-mir-328, Hcd783, Hcdl81, HPR213, hsa-mir- 191 -prec, hsa-mir-375, hsa-mir-212-prec, Hcd913, Hcd716, MPR207, HPR206, hsa-mir-016b- chr3, Hcd654, hsa-mir- 195 -prec, Hcd425, hsa-mir-148a, hsa-mir- 142-prec, and hsa- mir-016a-chrl3, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Tretinoin.
259. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, hsa-mir-181b-2, Hcd417, Hcd440_HPR257, hsa-mir-019b-2-prec, hsa-mir-213-prec, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1, hsa-mir-181b-prec, hsa-mir- 128b-prec, hsa-mir-526a-2, MPR95, HPR220, hsa-mir- 133a-l , hsa-mir-148a, hsa-mir- 142-prec, HPR169, hsa-mir-223-prec, hsa-mir-018-prec, hsa-mir-020-prec, and hsa-mir-484, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Ifosfamide.
260. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-092-prec-X=092-2, Hcd547, Hcd257, hsa-mir- 148-prec, HUMTRS, hsa-mir-033-prec, hsa-mir-092-prec- 13=092-1 , hsa-mir-375, hsa-mir-095- prec-4, hsa-mir-025-prec, hsa-mir-202-prec, hsa-mir-007-l-prec, hsa-mir-093-prec-
7.1=093-1, hsa-mir- 106-prec-X, hsa-mir-142-prec, hsa-mir-223-prec, and hsa-mir-018- prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Tamoxifen.
261. The kit of claim 205, wherein said microRNA is selected from the group consisting of HUMTRF, HUMTRN, hsa-mir- 124a- 1-precl, hsa-mir- 150-prec, Hcd923, HPRl 81, Hcd569, hsa-mir- 199a-2-prec, Hcd754, and hsa-mir-4323p, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Floxuridine.
262. The kit of claim 205, wherein said microRNA is selected from the group consisting of HUMTRF, hsa-mir-380-5p, hsa-mir-342, hsa-mir-142-prec, and Hcd200, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Irinotecan.
263. The kit of claim 205, wherein said microRNA is selected from the group consisting of Hcd289, Hcd939, Hcd330, HPR76, Hcdl 1 1, Hcd976, hsa-mir-15a, hsa- mir-00 Ib- 1-precl, hsa-mir-450-l , hsa-mir-200b, Hcd578, and hsa-mir-200a-prec, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Satraplatin.
264. The method of any one of claims 72-130, wherein said measuring comprises detecting said level of expression of said microRNA by using a kit of any one of claims 205-263 and 301.
265. The kit of claim 205, wherein said treatment comprises administering a chemotherapeutic agent.
266. The kit of claim 205, wherein said single-stranded nucleic acid is characterized by the ability to specifically identify the presence or absence of a nucleic acid complementary to said microRNA in a sample collected from said cancer patient.
267. The kit of any one of claims 205-263 and 301 , wherein said single-stranded nucleic acid is at least 15 nucleotides long.
268. The kit of claim 205, wherein said single-stranded nucleic acid is at least 25 nucleotides long. •
269. The kit of any one of claims 205-263 and 301, wherein said single-stranded nucleic acid is a deoxyribonucleic acid (DNA).
270. A method of identifying biomarkers useful for the determination of sensitivity of a cancer patient to a treatment for cancer comprising: a. obtaining pluralities of measurements of the level of expression of a gene or microRNA in different cell types and measurements of the growth of said cell types in the presence of a treatment for cancer relative to the growth of said cell types in the absence of said treatment for cancer; b. correlating each plurality of measurements of the level of expression of said gene or microRNA in said cells with the growth of said cells to obtain a correlation coefficient; c. selecting the median correlation coefficient calculated for said gene or microRNA; and d. identifying said gene or microRNA as a biomarker for use in determining the sensitivity of a cancer patient to said treatment for cancer if said median correlation coefficient exceeds 0.3.
271. The method of claim 270, wherein said correlation coefficient exceeds 0.4.
272. The method of claim 270, wherein the measurement of step a) includes measurements of growth in the presence of a second treatment.
273. The method of claim 270, wherein said treatment comprises administering a compound, a protein, an antibody, an oligonucleotide, a chemotherapeutic agent, or radiation to a patient.
274. The method of claim 273, wherein said chemotherapeutic agent is selected from the group consisting of Vincristine, Cisplatin, Adriamycin, Etoposide, Azaguanine, Aclarubicin, Mitoxantrone, Paclitaxel, Mitomycin, Gemcitabine, Taxotere, Dexamethasone, Methylprednisolone, Ara-C, Methotrexate, Bleomycin, Methyl-GAG, Rituximab, PXDlOl, 5-Aza-2'-deoxycytidine (Decitabine Melphalan, IL4-PE38 fusion protein, IL13-PE38QQR fusion protein (cintredekin besudotox), Valproic acid (VPA), All-trans retinoic acid (ATRA), Cytoxan, Topotecan (Hycamtin), Suberoylanilide hydroxamic acid (SAHA, vorinostat, Zolinza), Depsipeptide (FR901229), Bortezomib, Leukeran, Fludarabine, Vinblastine, Busulfan, Dacarbazine, Oxaliplatin, Hydroxyurea, Tegafur, Daunorubicin, Bleomycin, Estramustine, Chlorambucil, Mechlorethamine, Streptozocin, Carmustine, Lomustine, Mercaptopurine, Teniposide, Dactinomycin, Tretinoin, Sunitinib, SPC2996, Ifosfamide, Tamoxifen, Floxuridine, Irinotecan, and Satraplatin.
275. The method of claim 270, wherein said treatment has previously failed to show an effect in said cancer patient.
276. The method of claim 270, wherein said cancer patient is selected from a subpopulation determined to be sensitive to said treatment.
277. The method of claim 270, wherein said cancer patient is selected from a subpopulation predicted to die without treatment.
278. The method of claim 270, wherein said cancer patient is selected from a subpopulation predicted to have disease symptoms without treatment.
279. The method of claim 270, wherein said cancer patient is selected from a subpopulation predicted to be cured without treatment.
280. The methods of claim 1, 72, or 270, wherein said measurements of the level of expression are made using a quantitative reverse transcription-polymerase chain reaction (qRT-PCR).
281. A method of determining sensitivity of a cancer patient to a treatment for cancer comprising: a. obtaining a measurement of the level of expression of a gene or microRNA in a sample from said cancer patient; b. applying a model predictive of sensitivity to a treatment for cancer to said measurement, wherein said model is developed using an algorithm selected from the group consisting of linear sums, nearest neighbor, nearest centroid, linear discriminant analysis, support vector machines, and neural networks; and c. predicting whether or not said cancer patient will be responsive to said treatment for cancer.
282. The method of claim 281, wherein said gene is selected from the group consisting of ACTB, ACTN4, ADA, ADAM9, ADAMTSl, ADDl, AFlQ, AIFl, AKAPl , AKAPl 3, AKRlCl, AKTl , ALDH2, ALDOC, ALG5, ALMSl, ALOXl 5B, AMIG02, AMPD2, AMPD3, ANAPC5, ANP32A, ANP32B, ANXAl, AP1G2, APOBEC3B, APRT, ARHE, ARHGAP 15, ARHGAP25, ARHGDIB, ARHGEF6, ARL7, ASAHl, ASPH, ATF3, ATIC, ATP2A2, ATP2A3, ATP5D, ATP5G2, ATP6V1B2, BC008967, BCATl, BCHE, BCLl IB, BDNF, BHLHB2, BIN2, BLMH, BMIl, BNIP3, BRDT, BRRNl, BTN3A3, Cl Iorf2, C14orfl39, C15orf25, C18orflO, Clorf24, Clorf29, Clorf38, ClQRl , C22orfl 8, C6orf32, CACNAlG, CACNB3, CALMl, CALML4, CALU, CAP350, CASP2, CASP6, CASP7, CAST, CBLB, CCNA2, CCNBlIPl , CCND3, CCR7, CCR9, CDlA, CDlC, CDlD, CDlE, CD2, CD28, CD3D, CD3E, CD3G, CD3Z, CD44, CD47, CD59, CD6, CD63, CD8A, CD8B1 , CD99, CDClO, CDC 14B, CDHI l, CDH2, CDKL5, CDKN2A, CDW52, CECRl , CENPB, CENTBl, CENTG2, CEPl , CGO 18, CHRN A3, CHSl, CIAPINl, CKAP4, CKIP-I, CNP, COL4A1, COL5A2, COL6A1 , COROlC, CRABPl, CRK, CRYl, CSDA, CTBPl , CTSC, CTSL, CUGBP2, CUTC, CXCLl, CXCR4, CXorf9, CYF1P2, CYLD, CYR61 , DATFl , DAZAPl, DBNl, DBT, DCTNl, DDX 18, DDX5, DGKA, DIAPHl , DKCl , DKFZP434J154, DKFZP564C186, DKFZP564G2022, DKFZp564J157, DKFZP564K0822, DNAJClO, DNAJC7, DNAPTP6, DOCKlO, DOCK2, DPAGTl, DPEP2, DPYSL3, DSIPI, DUSPl , DXS9879E, EEF1B2, EFNB2, EHD2, EIF5A, ELK3, ENO2, EPASl, EPB41L4B, ERCC2, ERG, ERP70, EVERl , EVI2A, EVL, EXTl, EZH2, F2R, FABP5, FADl 04, FAM46A, FAU, FCGR2A, FCGR2C, FER1L3, FHLl, FHODl, FKBPlA, FKBP9, FLJ10350, FLJ10539, FLJ10774, FLJ12270, FLJ13373, FLJ20859, FLJ21159, FLJ22457, FLJ35036, FLJ46603, FLNC, FLOTl, FMNLl, FNBPl, FOLHl, FOXF2, FSCNl, FTL, FYB, FYN, G0S2, G6PD, GALIG, GALNT6, GATA2, GATA3, GFPTl , GIM AP5, GIT2, GJAl, GLRB, GLTSCR2, GLUL, GMDS, GNAQ, GNB2, GNB5, GOT2, GPR65, GPRASPl, GPSM3, GRP58, GSTM2, GTF3A, GTSEl, GZMA, GZMB, HlFO, HlFX, H2AFX, H3F3A, HA-I, HEXB, HIC, HIST1H4C, HKl, HLA-A, HLA-B, HLA-DRA, HMGAl, HMGN2, HMMR, HNRPAl, HNRPD, HNRPM, HOXA9, HRMTlLl, HSA9761, HSPA5, HSU79274, HTATSFl, ICAMl, ICAM2, IER3, IFI16, IFI44, IFITM2, IFITM3, IFRG28, IGFBP2, IGSF4, IL13RA2, IL21R, IL2RG, IL4R, IL6, IL6R, IL6ST, IL8, IMPDH2, INPP5D, INSIGl, IQGAPl, IQGAP2, IRS2, ITG A5, ITM2A, JARID2, JUNB, K-ALPHA-I, KHDRBSl, KIAA0355, KIAA0802, KIAA0877, KIAA0922, KIAA1078, KIAAl 128, KIAA1393, KIFCl , LAIRl , LAMBl, LAMB3, LAT, LBR, LCK, LCPl, LCP2, LEFl, LEPREl, LGALSl, LGALS9, LHFPL2, LNK, LOC54103, LOC55831 , LOC81558, LOC94105, LONP, LOX, LOXL2, LPHN2, LPXN, LRMP, LRP12, LRRC5, LRRN3, LSTl, LTB, LUM, LY9, LY96, MAGEB2, MAL, MAPlB, MAP1LC3B, MAP4K1, MAPKl , MARCKS, MAZ, MCAM, MCLl, MCM5, MCM7, MDH2, MDNl, MEF2C, MFNG, MGC 17330, MGC21654, MGC2744, MGC4083, MGC8721, MGC8902, MGLL, MLPH, MPHOSPH6, MPPl, MPZLl, MRP63, MRPS2, MTlE, MTlK, MUFl, MVP, MYB, MYL9, MYOlB, NAPlLl, NAP1L2, NARF, NASP, NCOR2, NDN, NDUFABl, NDUFS6, NFKBIA, NID2, NIPA2, NME4, NME7, NNMT, NOL5A, NOL8, NOMO2, NOTCH 1 , NPC 1 , NQO 1 , NRl D2, NUDC, NUP210, NUP88, NVL, NXF 1 , OBFC 1 , OCRL, OGT, OXAlL, P2RX5, P4HA1, PACAP, PAF53, PAFAH1B3, PALM2- AKAP2, PAX6, PCBP2, PCCB, PFDN5, PFNl , PFN2, PGAMl , PHEMX, PHLDAl, PIM2, PITPNCl , PLAC8, PLAGLl , PLAUR, PLCBl, PLEK2, PLEKHCl , PLOD2, PLSCRl , PNAS-4, PNM A2, POLR2F, PPAP2B, PRFl , PRGl, PRIMl, PRKCH, PRKCQ, PRKD2, PRNP, PRPl 9, PRPF8, PRSS23, PSCDBP, PSMB9, PSMC3, PSME2, PTGER4, PTGES2, PTOVl , PTP4A3, PTPN7, PTPNSl, PTRF, PURA, PWPl, PYGL, QKI, RAB3GAP, RAB7L1, RAB9P40, RAC2, RAFTLIN, RAG2, RAPlB, RASGRP2, RBPMS, RCNl, RFC3, RFC5, RGC32, RGS3, RHOH, RIMS3, RI0K3, RIPK2, RISl, RNASE6, RNF144, RPLlO, RPLlOA, RPL12, RPL13A, RPL17, RPL18, RPL36A, RPLPO, RPLP2, RPS15, RPS19, RPS2, RPS4X, RPS4Y1, RRAS, RRAS2, RRBPl, RRM2, RUNXl, RUNX3, S100A4, SART3, SATBl, SCAPl, SCARBl, SCN3A, SEC31L2, SEC61G, SELL, SELPLG, SEMA4G, SEPTlO, SEPT6, SERPINAl , SERPINBl, SERPINB6, SFRS5, SFRS6, SFRS7, SH2D1A, SH3GL3, SH3TC1, SHDl, SHMT2, SIATl, SKBl, SKP2, SLA, SLC1A4, SLC20A1, SLC25A15, SLC25A5, SLC39A14, SLC39A6, SLC43A3, SLC4A2, SLC7A1 1, SLC7A6, SMAD3, SMOX, SNRPA, SNRPB, SOD2, SOX4, SP 140, SPANXC, SPIl, SRF, SRM, SSA2, SSBP2, SSRPl, SSSCAl, STAG3, STATl, STAT4, STAT5A, STCl, STC2, STOML2, T3JAM, TACCl, TACC3, TAF5, TALI, TAPl, TARP, TBCA, TCF 12, TCF4, TFDP2, TFPI, TIMM 17 A, TIMPl, TJPl, TK2, TM4SF1, TM4SF2, TM4SF8, TM6SF1, TMEM2, TMEM22, TMSBlO, TMSNB, TNFAIP3, TNFAIP8, TNFRSFlOB, TNFRSFlA, TNFRSF7, TNIK, TNPOl, TOBl, TOMM20, TOX, TPKl, TPM2, TRA@, TRAl, TRAM2, TRB@, TRD@, TRIM, TRIM 14, TRIM22, TRIM28, TRIP13, TRPV2, TUBGCP3, TUSC3, TXN, TXNDC5, UBASH3A, UBE2A, UBE2L6, UBE2S, UCHLl, UCK2, UCP2, UFDlL, UGDH, ULK2, UMPS, UNG, USP34, USP4, VASP, VAVl, VLDLR, VWF, WASPIP, WBSCR20A, WBSCR20C, WHSCl, WNT5A, ZAP70, ZFP36L1, ZNF32, ZNF335, ZNF593, ZNFNlAl, and ZYX.
283. The method of claim 281, wherein said microRNA is selected from the group consisting of ath-MIR180aNo2, HcdlO2 left, Hcdl 11 left, Hcdl 15 left, Hcdl20 left, Hcdl42 right, Hcdl 45 left, Hcdl48_HPR225 left, Hcdl 81 left, Hcdl 81 right, Hcd210_HPR205 right, Hcd213_HPR182 left, Hcd230 left, Hcd243 right, Hcd246 right, Hcd248 right, Hcd249 right, Hcd250 left, Hcd255 left, Hcd257 left, Hcd257 right, Hcd263 left, Hcd266 left, Hcd270 right, Hcd279 left, Hcd279 right, , Hcd28_HPR391eft, Hcd28_HPR39right, Hcd282PO right, Hcd289 left, Hcd294 left, Hcd318 right, Hcd323 left, Hcd330 right, Hcd338 left, Hcd340 left, Hcd350 right, Hcd355_HPR190 left, Hcd361 right, Hcd366 left, Hcd373 right, Hcd383 left, Hcd383 right, Hcd384 left, Hcd397 left, Hcd404 left, Hcd412 left, Hcd413 right, Hcd415 right, Hcd417 right, Hcd421 right, Hcd425 left, Hcd43 8right, Hcd434 right, Hcd438 left, Hcd440_HPR257 right, Hcd444 right, Hcd447 right, Hcd448 left, Hcd498 right, Hcd503 left, Hcd51 1 right, Hcd512 left, Hcd514 right, Hcd517 left, Hcd517 right, Hcd530 right, Hcd536_HPR104 right, Hcd542 left, Hcd544 left, Hcd547 left, Hcd559 right, Hcd562 right, Hcd569 right, Hcd570 right, Hcd578 right, Hcd581 right, Hcd586 left, Hcd586 right, Hcd587 right, Hcd605 left, Hcd605 left, Hcd605 right, Hcd608 right, Hcd627 left, Hcd631 left, Hcd631 right, Hcd634 left, Hcd642 right, Hcd649 right, Hcd654 left, Hcd658 right, Hcd669 right, Hcd674 left, Hcd678 right, Hcd683 left, Hcd684 right, Hcd689 right, Hcd690 right, Hcd691 right, Hcd693 right, Hcd697 right, Hcd704 left, Hcd704 left, Hcd712 right, Hcd716 right, Hcd731 left, Hcd738 left, Hcd739 right, Hcd739 right, Hcd749 right, Hcd753 left, Hcd754 left, Hcd755 left, Hcd760 left, Hcd763 right, Hcd768 left ,Hcd768 right, Hcd770 left, Hcd773 left, Hcd777 left, Hcd778 right, Hcd781 left, Hcd781 right, Hcd782 left, Hcd783 left, Hcd788 left, Hcd794 right, Hcd796 left, Hcd799 left, Hcd807 right, Hcd812 left, Hcd817 left, Hcd817 right, Hcd829 right, Hcd852 right, Hcd861 right, Hcd863PO right, Hcd866 right, Hcd869 left, Hcd873 left, Hcd886 right, Hcd889 right, Hcd891 right, Hcd892 left, Hcd913 right, Hcd923 left, Hcd923 right, Hcd938 left, Hcd938 right, Hcd939 right, Hcd946 left, Hcd948 right, Hcd960 left, Hcd965 left, Hcd970 left, Hcd975 left, Hcd976 right, Hcd99 right, HPRlOO right, HPRl 29 left, HPRl 54 left, HPRl 59 left, HPRl 63 left, HPRl 69 right, HPRl 72 right, HPRl 81 left, HPRl 87 left, HPR 199 right, HPR206 left, HPR213 right, HPR214 right, HPR220 left , HPR220 right, HPR227 right, HPR232 right, HPR233 right, HPR244 right, HPR262 left, HPR264 right, HPR266 right, HPR271 right, HPR76 right, hsa_mir_490_Hcd20 right, HSHELAOl , HSTRNL, HUMTRAB, HUMTRF, HUMTRN, HUMTRS, HUMTRVlA, let-7f-2-prec2, mir-OOlb-1-precl, mir-OOlb-2-prec, mir-007-l-prec, mir-007-2- precNo2, mir-OlOa-precNol , mir-015b-precNo2, mir-016a-chrl3, mir-016b-chr3, mir- 017-precNol , mir-017-precNo2, mir-018-prec, mir-019a-prec, mir-019b-l-prec, mir- 019b-2-prec, mir-020-prec, mir-022-prec, mir-023a-prec, mir-023b-prec, mir-024-2- prec, mir-025-prec, mir-027b-prec, mir-029c-prec, mir-032-precNo2, mir-033b-prec, mir-033-prec, mir-034-precNol, mir-034-precNo2, mir-092-prec-l 3=092- 1NO2, mir- 092-prec-X=092-2, mir-093-prec-7.1=093-1, mir-095-prec-4 ,mir-096-prec-7Nol ,mir- 096-prec-7No2, mir-098-prec-X, mir-099b-prec-19Nol, mir-lOO-l/2-prec, mir-lOONol, mir-lOl-prec-9, mir-102-prec-l, mir-103-2-prec, mir-103-prec-5= 103-1, mir-106aNol, mir-106-prec-X,mir-107Nol , mir-107-prec-lO, mir-122a-prec, mir-123-precNol, mir- 123-precNo2, mir-124a-l-precl , mir- 124a-2-prec, mir-124a-3-prec, mir-125b-l, mir- 125b-2-precNo2, mir-127-prec, mir-128b-precNol, mir-128b-precNo2, mir-133a-l, mir-135-2-prec, mir-136-precNo2, mir- 138-1 -prec, mir-140No2, mir-142-prec, mir- 143-prec, mir-144-precNo2, mir- 145 -prec, mir-146bNol, mir-146-prec, mir-147-prec, mir-148aNol, mir-148-prec, mir-149-prec, mir-150-prec, mir- 153-1 -prec 1, mir- 154- preclNol, mir-155-prec, mir-15aNol, mir- 16-1 NoI, mir- 16-2NoI, mir-181a-precNol , mir- 18Ib-INoI, mir- 181 b-2No 1 , mir- 181 b-precNo 1 , mir- 181 b-precNo2, mir- 181c- precNol, mir- 18IdNoI, mir-188-prec, mir-18bNo2, mir- 191 -prec, mir-192No2, mir- 193bNo2, mir- 194-2NoI , mir-195-prec, mir-196-2-precNo2, mir-197-prec, mir- 198- prec, mir- 199a- 1 -prec, mir-199a-2-prec, mir-199b-precNol, mir-200a-prec, mir- 20ObNoI, mir-200bNo2, mir-202*, mir-202-prec, mir-204-precNo2, mir-205-prec, mir- 208-prec, mir-20bNol , mir-212-precNol, mir-212-precNo2, mir-213-precNol , mir- 214-prec, mir-215-precNo2, mir-216-precNol, mir-219-2Nol, mir-219-prec, mir-223- prec, mir-29b-lNol, mir-29b-2=102prec7.1=7.2, mir-321Nol, mir-321No2, mir- 324NoI , mir-324No2, mir-328Nol, mir-342Nol, mir-361Nol, mir-367Nol, mir- 370NoI , mir-371Nol, miR-373*Nol , mir-375, mir-376aNol, mir-379Nol , mir-380-5p, mir-382, mir-384, mir-409-3p, mir-423Nol, mir-424No2, mir-429Nol, mir-429No2, mir-4323p, mir-4325p, mir-449Nol, mir-450-1, mir-450-2Nol , mir-483Nol , mir-484, mir-487Nol, mir-495Nol , mir-499No2, mir-501No2, mir-503Nol , mir-509Nol , mir- 514-lNo2, mir-515-15p, mir-515-23p, mir-516-33p, mir-516-43p, mir-518e/526c, mir- 519a- 1/52, mir-519a-2No2, mir-519b, mir-519c/52, mir-520c/52, mir-526a-2Nol, mir- 526a-2No2, MPRl 03 right, MPRl 21 left, MPRl 21 left, MPRl 30 left, MPRl 30 right, MPR133 right, MPR141 left, MPR151 left, MPR156 left, MPR162 left, MPR174 left, MPRl 74 right, MPRl 85 right, MPRl 97 right, MPR203 left, MPR207 right, MPR215 left, MPR216 left, MPR224 left, MPR224 right, MPR228 left, MPR234 right, MPR237 left, MPR243 left, MPR244 right, MPR249 left, MPR254 right, MPR74 left, MPR88 right, and MPR95 left.
284. The method of claim 281, wherein said model combines the outcomes of linear sums, linear discriminant analysis, support vector machines, neural networks, k-nearest neighbors, and nearest centroids.
285. The method of claim 281, wherein said model is cross-validated using a random sample of said measurements.
286. The method of claim 281, wherein a second treatment is present.
287. The method of claim 281, wherein said treatment comprises administering a compound, a protein, an antibody, an oligonucleotide, a chemotherapeutic agent, or radiation to a patient.
288. The method of claim 287, wherein said chemotherapeutic agent is selected from the group consisting of Vincristine, Cisplatin, Adriamycin, Etoposide, Azaguanine, Aclarubicin, Mitoxantrone, Paclitaxel, Mitomycin, Gemcitabine, Taxotere, Dexamethasone, Methylprednisolone, Ara-C, Methotrexate, Bleomycin, Methyl-GAG, Rituximab, PXDlOl , 5-Aza-2'-deoxycytidine (Decitabine), Melphalan, IL4-PE38 fusion protein, IL13-PE38QQR fusion protein (cintredekin besudotox), Valproic acid (VPA), All-trans retinoic acid (ATRA), Cytoxan, Topotecan (Hycamtin), Suberoylanilide hydroxamic acid (SAHA, vorinostat, Zolinza), Depsipeptide (FR901229), Bortezomib, Leukeran, Fludarabine, Vinblastine, Busulfan, Dacarbazine, Oxaliplatin, Hydroxyurea, Tegafur, Daunorubicin, Bleomycin, Estramustine, Chlorambucil, Mechlorethamine, Streptozocin, Carmustine, Lomustine, Mercaptopurine, Teniposide, Dactinomycin, Tretinoin, Sunitinib, SPC2996, Ifosfamide, Tamoxifen, Floxuridine, Irinotecan, and Satraplatin..
289. The method of claim 281 , wherein said treatment has previously failed to show effect on patients.
290. The method of claim 281 , wherein said linear sum is compared to a sum of a reference population with known sensitivity.
291. The method of claim 281 , wherein said sum of a reference population is the median of the sums derived from the population members' biomarker gene expression.
292. The method of claim 281, wherein said model is derived from the components of a data set obtained by independent component analysis.
293. The method of claim 281 , wherein said model is derived from the components of a data set obtained by principal component analysis.
294. The method of claim 281, wherein said cancer patient is selected from a subpopulation determined to be sensitive to said treatment.
295. The method of claim 281, wherein said cancer patient is selected from a subpopulation predicted to die without treatment.
296. The method of claim 281, wherein said cancer patient is selected from a subpopulation predicted to have disease symptoms without treatment.
297. The method of claim 281, wherein said cancer patient is selected from a subpopulation predicted to be cured without treatment.
298. The method of claim 281, wherein said measurements of the level of expression of said gene or microRNA are made using a quantitative reverse transcription- polymerase chain reaction (qRT-PCR).
299. A kit, apparatus, and software used to implement the method of claim 281.
300. The kit of claim 137, wherein said gene is selected from the group consisting of PFNl, PGAMl, K-ALPHA-I, CSDA, UCHLl, PWPl , PALM2-AKAP2, TNFRSFlA, ATP5G2, AFlQ, NME4, and FHODl, or wherein said kit further comprises one or more single-stranded nucleic acids complementary to or identical to at least 5 consecutive nucleotides of a microRN A selected from the group consisting of hsa-mir- 123-prec, Hcd257, hsa-mir-155-prec, ath-MIR180a, Hcd448, HSTRNL, MPRl 74, Hcd200, hsa-mir-4323p, and HPR244, wherein said level of expression of said gene or microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Gemcitabine.
301. The kit of claim 205, wherein said microRNA is selected from the group consisting of hsa-mir-123-prec, Hcd257, hsa-mir-155-prec, ath-MIR180a, Hcd448, HSTRNL, MPRl 74, Hcd200, hsa-mir-4323p, and HPR244, wherein said level of expression of said microRNA indicates that said cell is sensitive to said treatment and wherein said treatment is treatment with Gemcitabine. |
METHODS, KITS, AND DEVICES FOR IDENTIFYING BIOMARKERS OF TREATMENT RESPONSE AND USE THEREOF TO PREDICT TREATMENT
EFFICACY
FIELD OF THE INVENTION
The invention features methods, kits, and devices for identifying biomarkers of patient sensitivity to medical treatments, e.g., sensitivity to chemotherapeutic agents, and predicting treatment efficacy using the biomarkers.
BACKGROUND OF THE INVENTION
DNA microarrays have been used to measure gene expression in tumor samples from patients and to facilitate diagnosis. Gene expression can reveal the presence of cancer in a patient, its type, stage, and origin, and whether genetic mutations are involved. Gene expression may even have a role in predicting the efficacy of chemotherapy. Over recent decades, the National Cancer Institute (NCI) has tested compounds, including chemotherapy agents, for their effect in limiting the growth of 60 human cancer cell lines. The NCI has also measured gene expression in these 60 cancer cell lines using DNA microarrays. Various studies have explored the relationship between gene expression and compound effect using the NCI datasets. Critical time is often lost due to a trial and error approach to finding an effective chemotherapy for patients with cancer. In addition, cancer cells often develop resistance to a previously effective therapy. In such situations, patient outcome could be greatly improved by early detection of such resistance.
There remains a need for proven methods and devices that predict the sensitivity or resistance of cancer patients to a medical treatment.
SUMMARY OF THE INVENTION
The invention features methods, kits, and devices for determining the sensitivity or resistance of a patient, e.g., a cancer patient, to a treatment, e.g., treatment with a
compound, such as a chemotherapeutic agent, or radiation. In particular, the methods, kits, and devices can be used to determine the sensitivity or resistance of a cancer patient to any medical treatment, including, e.g., treatment with a compound, drug, or radiation. The methods, kits, and devices of the invention have been used to accurately determine treatment efficacy in cancer patients (e.g., patients with lung, lymphoma, and brain cancer) and can be used to determine treatment efficacy in patients diagnosed with any cancer.
Methods, kits, and devices for detecting the level of expression of biomarkers (e.g., genes and microRNAs) that indicate sensitivity or resistance to radiation therapy or the chemotherapy agents Vincristine, Cisplatin, Azaguanine, Etoposide, Adriamycin, Aclarubicin, Mitoxantrone, Mitomycin, Paclitaxel, Gemcitabine, Taxotere, Dexamethasone, Ara-C, Methylprednisolone, Methotrexate, Bleomycin, Methyl-GAG, Carboplatin, 5-FU (5-Fluorouracil), Rituximab, , PXDlOl, (a histone deacetylase (HDAC) inhibitor), 5-Aza-2'-deoxycytidine (Decitabine), Melphalan, IL4-PE38 fusion protein, IL13-PE38QQR fusion protein (cintredekin besudotox), Valproic acid (VPA), All-trans retinoic acid (ATRA), Cytoxan, Topotecan (Hycamtin), Suberoylanilide hydroxamic acid (SAHA, vorinostat, Zolinza), Depsipeptide (FR901229), Bortezomib, Leukeran, Fludarabine, Vinblastine, Busulfan, Dacarbazine, Oxaliplatin, Hydroxyurea, Tegafur, Daunorubicin, Bleomycin, Estramustine, Chlorambucil, Mechlorethamine, Streptozocin, Carmustine, Lomustine, Mercaptopurine, Teniposide, Dactinomycin, Tretinoin, Sunitinib, SPC2996, Ifosfamide, Tamoxifen, Floxuridine, Irinotecan, and Satraplatin are also provided. The methods, kits, and devices can be used to predict the sensitivity or resistance of a subject (e.g., a cancer patient) diagnosed with a disease condition, e.g., cancer (e.g., cancers of the breast, prostate, lung and bronchus, colon and rectum, urinary bladder, skin, kidney, pancreas, oral cavity and pharynx, ovary, thyroid, parathyroid, stomach, brain, esophagus, liver and intrahepatic bile duct, cervix larynx, heart, testis, small and large intestine, anus, anal canal and anorectum, vulva, gallbladder, pleura, bones and joints, hypopharynx, eye and orbit, nose, nasal cavity and middle ear, nasopharynx, ureter, peritoneum, omentum and mesentery, or gastrointestines, as well as any form of cancer including, e.g., chronic myeloid leukemia, acute lymphocytic leukemia, non-Hodgkin's lymphoma, melanoma,
carcinoma, basal cell carcinoma, malignant mesothelioma, neuroblastoma, multiple myeloma, leukemia, retinoblastoma, acute myeloid leukemia, chronic lymphocytic leukemia, Hodgkin's lymphoma, carcinoid tumors, acute tumor, or soft tissue sarcoma) to a treatment, e.g., treatment with a compound or drug, e.g., a chemotherapeutic agent, or radiation.
In a first aspect, the invention features a method of determining sensitivity of a cancer in a patient to a treatment for cancer by measuring the level of expression of at least one gene in a cell (e.g., a cancer cell) of the patient, in which the gene is selected from the group consisting of ACTB, ACTN4, ADA, ADAM9, ADAMTS 1 , ADD 1 , AFlQ, AIFl, AKAPl , AKAP13, AKRlCl, AKTl , ALDH2, ALDOC, ALG5, ALMSl, ALOXl 5B, AMIG02, AMPD2, AMPD3, ANAPC5, ANP32A, ANP32B, ANXAl, AP1G2, APOBEC3B, APRT, ARHE, ARHGAPl 5, ARHGAP25, ARHGDIB, ARHGEF6, ARL7, ASAHl, ASPH, ATF3, ATIC, ATP2A2, ATP2A3, ATP5D, ATP5G2, ATP6V1B2, BC008967, BCATl, BCHE, BCLl IB, BDNF, BHLHB2, BIN2, BLMH, BMIl, BNIP3, BRDT, BRRNl, BTN3A3, Cl lorf2, C14orfl39, C15orf25, C18orflO, Clorf24, Clorf29, Clorf38, ClQRl, C22orfl 8, C6or02, CACNAlG, CACNB3, CALMl, CALML4, CALU, CAP350, CASP2, CASP6, CASP7, CAST, CBLB, CCNA2, CCNBlIPl , CCND3, CCR7, CCR9, CDlA, CDlC, CDlD, CDlE, CD2, CD28, CD3D, CD3E, CD3G, CD3Z, CD44, CD47, CD59, CD6, CD63, CD8A, CD8B1, CD99, CDClO, CDC 14B, CDHI l, CDH2, CDKL5, CDKN2A, CDW52, CECRl, CENPB, CENTBl, CENTG2, CEPl, CG018, CHRNA3, CHSl, CIAPINl , CKAP4, CKIP-I , CNP, COL4A1, COL5A2, COL6A1, COROlC, CRABPl , CRK, CRYl , CSDA, CTBPl, CTSC, CTSL, CUGBP2, CUTC, CXCLl , CXCR4, CXorf9, CYFIP2, CYLD, CYR61, DATFl, DAZAPl, DBNl, DBT, DCTNl , DDXl 8, DDX5, DGKA, DIAPHl, DKCl , DKFZP434J154, DKFZP564C186, DKFZP564G2022, DKFZp564J157, DKFZP564K0822, DNAJClO, DNAJC7, DNAPTP6, DOCKlO, DOCK2, DPAGTl , DPEP2, DPYSL3, DSIPI, DUSPl, DXS9879E, EEF 1 B2, EFNB2, EHD2, EIF5A, ELK3, ENO2, EPASl, EPB41L4B, ERCC2, ERG, ERP70, EVERl , EVI2A, EVL, EXTl, EZH2, F2R, FABP5, FADl 04, FAM46A, FAU, FCGR2A, FCGR2C, FER1L3, FHLl , FHODl , FKBPlA, FKBP9, FLJ1O35O, FLJ10539, FLJ 10774, FLJ 12270, FLJ 13373, FLJ20859, FLJ21 159, FLJ22457, FLJ35036,
FU46603, FLNC, FLOTl, FMNLl , FNBPl, FOLHl , FOXF2, FSCNl, FTL, FYB, FYN, G0S2, G6PD, GALIG, GALNT6, GATA2, GATA3, GFPTl, GIMAP5, GIT2, GJAl , GLRB, GLTSCR2, GLUL, GMDS, GNAQ, GNB2, GNB5, G0T2, GPR65, GPRASPl, GPSM3, GRP58, GSTM2, GTF3A, GTSEl, GZMA, GZMB, HlFO, HlFX, H2AFX, H3F3A, HA-I, HEXB, HIC, HIST1H4C, HKl, HLA-A, HLA-B, HLA-DRA, HMGAl, HMGN2, HMMR, HNRPAl, HNRPD, HNRPM, HOXA9, HRMTlLl, HSA9761, HSPA5, HSU79274, HTATSFl, ICAMl, ICAM2, IER3, IFIl 6, IFI44, IFITM2, IFITM3, IFRG28, IGFBP2, IGSF4, IL13RA2, IL21R, IL2RG, IL4R, IL6, IL6R, IL6ST, IL8, IMPDH2, INPP5D, INSIGl , IQGAPl, IQGAP2, IRS2, ITGA5, ITM2A, JARID2, JUNB, K-ALPHA-I, KHDRBSl, KIAA0355, KIAA0802, KIAA0877, KIAA0922, KIAA1078, KIAAl 128, KIAA1393, KIFCl, LAIRl, LAMBl, LAMB3, LAT, LBR, LCK, LCPl, LCP2, LEFl, LEPREl, LGALSl, LGALS9, LHFPL2, LNK, LOC54103, LOC55831, LOC81558, LOC94105, LONP, LOX, LOXL2, LPHN2, LPXN, LRMP, LRP12, LRRC5, LRRN3, LSTl, LTB, LUM, LY9, LY96, MAGEB2, MAL, MAPlB, MAP1LC3B, MAP4K1, MAPKl, MARCKS, MAZ, MCAM, MCLl, MCM5, MCM7, MDH2, MDNl, MEF2C, MFNG, MGC17330, MGC21654, MGC2744, MGC4083, MGC8721, MGC8902, MGLL, MLPH, MPHOSPH6, MPPl, MPZLl, MRP63, MRPS2, MTlE, MTlK, MUFl, MVP, MYB, MYL9, MYOlB, NAPlLl, NAPl L2, NARF, NASP, NCOR2, NDN, NDUFABl, NDUFS6, NFKBIA, NID2, NIPA2, NME4, NME7, NNMT, NOL5A, N0L8, N0M02, NOTCHl, NPCl, NQOl, NRl D2, NUDC, NUP210, NUP88, NVL, NXFl, OBFCl, OCRL, OGT, OXAlL, P2RX5, P4HA1, PACAP, PAF53, PAFAH1B3, PALM2- AKAP2, PAX6, PCBP2, PCCB, PFDN5, PFNl, PFN2, PGAMl, PHEMX, PHLDAl, PIM2, PITPNCl , PLAC8, PLAGLl, PLAUR, PLCBl, PLEK2, PLEKHCl, PL0D2, PLSCRl, PNAS-4, PNMA2, P0LR2F, PPAP2B, PRFl, PRGl, PRIMl, PRKCH, PRKCQ, PRKD2, PRNP, PRP19, PRPF8, PRSS23, PSCDBP, PSMB9, PSMC3, PSME2, PTGER4, PTGES2, PTOVl, PTP4A3, PTPN7, PTPNSl , PTRF, PURA, PWPl, PYGL, QKI, RAB3GAP, RAB7L1, RAB9P40, RAC2, RAFTLIN, RAG2, RAPlB, RASGRP2, RBPMS, RCNl, RFC3, RFC5, RGC32, RGS3, RHOH, RIMS3, RI0K3, RIPK2, RISl , RNASE6, RNF 144, RPLlO, RPLlOA, RPLl 2, RPLl 3 A, RPLl 7, RPL18, RPL36A, RPLPO, RPLP2, RPS15, RPS19, RPS2, RPS4X, RPS4Y1, RRAS,
RRAS2, RRBPl , RRM2, RUNXl , RUNX3, S100A4, SART3, SATBl , SCAPl , SCARBl , SCN3A, SEC31L2, SEC61G, SELL, SELPLG, SEMA4G, SEPTlO, SEPT6, SERPINAl , SERPINBl , SERPINB6, SFRS5, SFRS6, SFRS7, SH2D1A, SH3GL3, SH3TC1, SHDl , SHMT2, SIATl , SKBl, SKP2, SLA, SLC1A4, SLC20A1, SLC25A15, SLC25A5, SLC39A14, SLC39A6, SLC43A3, SLC4A2, SLC7A1 1 , SLC7A6, SMAD3, SMOX, SNRPA, SNRPB, SOD2, SOX4, SP140, SPANXC, SPIl, SRF, SRM, SSA2, SSBP2, SSRPl, SSSCAl, STAG3, STATl, STAT4, STAT5A, STCl, STC2, STOML2, T3JAM, TACCl, TACC3, TAF5, TALI, TAPl, TARP, TBCA, TCF 12, TCF4, TFDP2, TFPI, TIMM 17 A, TIMPl , TJPl , TK2, TM4SF1, TM4SF2, TM4SF8, TM6SF1, TMEM2, TMEM22, TMSBlO, TMSNB, TNFAIP3, TNFAIP8, TNFRSFlOB, TNFRSFlA, TNFRSF7, TNIK, TNPOl, TOBl , TOMM20, TOX, TPKl, TPM2, TRA@, TRAl, TRAM2, TRB@, TRD@, TRIM, TRIM 14, TRIM22, TRIM28, TRIPl 3, TRPV2, TUBGCP3, TUSC3, TXN, TXNDC5, UBASH3A, UBE2A, UBE2L6, UBE2S, UCHLl, UCK2, UCP2, UFDlL, UGDH, ULK2, UMPS, UNG, USP34, USP4, VASP, VAVl, VLDLR, VWF, WASPIP, WBSCR20A, WBSCR20C, WHSCl , WNT5A, ZAP70, ZFP36L1 , ZNF32, ZNF335, ZNF593, ZNFNlAl , and ZYX; in which change in the level of expression of the gene indicates the cell is sensitive or resistant to the treatment.
In an embodiment, the method further includes determining a patient's resistance or sensitivity to radiation therapy or the chemotherapy agents Vincristine, Cisplatin, Adriamycin, Etoposide, Azaguanine, Aclarubicin, Mitoxantrone, Paclitaxel, Mitomycin, Gemcitabine, Taxotere, Dexamethasone, Methylprednisolone, Ara-C, Methotrexate, Bleomycin, Methyl-GAG, Rituximab, PXDlOl (a histone deacetylase (HDAC) inhibitor), 5-Aza-2'-deoxycytidine (Decitabine), Melphalan, IL4-PE38 fusion protein, IL13-PE38QQR fusion protein (cintredekin besudotox), Valproic acid (VPA), All-trans retinoic acid (ATRA), Cytoxan, Topotecan (Hycamtin), Suberoylanilide hydroxamic acid (SAHA, vorinostat, Zolinza), Depsipeptide (FR901229), Bortezomib, Leukeran, Fludarabine, Vinblastine, Busulfan, Dacarbazine, Oxaliplatin, Hydroxyurea, Tegafur, Daunorubicin, Bleomycin, Estramustine, Chlorambucil, Mechlorethamine, Streptozocin, Carmustine, Lomustine, Mercaptopurine, Teniposide, Dactinomycin, Tretinoin, Sunitinib, SPC2996, Ifosfamide, Tamoxifen, Floxuridine, Irinotecan, and
Satraplatin by measuring the level of expression of one or more of the genes known to change (e.g., to increase or decrease) in a patient sensitive to treatment with these agents (e.g., a patient is determined to be sensitive, or likely to be sensitive, to the indicated treatment if the level of expression of one or more of the gene(s) increases or decreases relative to the level of expression of the gene(s) in a control sample (e.g., a cell or tissue) in which increased or decreased expression of the gene(s) indicates sensitivity to the treatment, and vice versa). Alternatively, a patient's resistance or sensitivity to radiation therapy or any of the chemotherapy agents listed above can be determined by measuring the level of expression of at least one microRNA in a cell (e.g., a cancer cell) known to change (e.g., the level of expression is increased or decreased) in a patient sensitive to a treatment with these agents, in which the microRNA is selected from the group consisting of ath-MIR180aNo2, HcdlO2 left, Hcdl 1 1 left, Hcdl 15 left, Hcdl20 left, Hcdl 42 right, Hcdl 45 left, Hcdl48_HPR225 left, Hcdl 81 left, Hcdl 81 right, Hcd210_HPR205 right, Hcd213_HPR182 left, Hcd230 left, Hcd243 right, Hcd246 right, Hcd248 right, Hcd249 right, Hcd250 left, Hcd255 left, Hcd257 left, Hcd257 right, Hcd263 left, Hcd266 left, Hcd270 right, Hcd279 left, Hcd279 right, , Hcd28_HPR391eft, Hcd28_HPR39right, Hcd282PO right, Hcd289 left, Hcd294 left, Hcd318 right, Hcd323 left, Hcd330 right, Hcd338 left, Hcd340 left, Hcd35O right, Hcd355_HPR190 left, Hcd361 right, Hcd366 left, Hcd373 right, Hcd383 left, Hcd383 right, Hcd384 left, Hcd397 left, Hcd404 left, Hcd412 left, Hcd413 right, Hcd415 right, Hcd417 right, Hcd421 right, Hcd425 left, Hcd43 8right, Hcd434 right, Hcd438 left, Hcd440_HPR257 right, Hcd444 right, Hcd447 right, Hcd448 left, Hcd498 right, Hcd503 left, Hcd51 1 right, Hcd512 left, Hcd514 right, Hcd517 left, Hcd517 right, Hcd530 right, Hcd536_HPR104 right, Hcd542 left, Hcd544 left, Hcd547 left, Hcd559 right, Hcd562 right, Hcd569 right, Hcd570 right, Hcd578 right, Hcd581 right, Hcd586 left, Hcd586 right, Hcd587 right, Hcd605 left, Hcd605 left, Hcd605 right, Hcd608 right, Hcd627 left, Hcd631 left, Hcd631 right, Hcd634 left, Hcd642 right, Hcd649 right, Hcd654 left, Hcd658 right, Hcd669 right, Hcd674 left, Hcd678 right, Hcd683 left, Hcd684 right, Hcd689 right, Hcd690 right, Hcd691 right, Hcd693 right, Hcd697 right, Hcd704 left, Hcd704 left, Hcd712 right, Hcd716 right, Hcd731 left, Hcd738 left, Hcd739 right, Hcd739 right, Hcd749 right, Hcd753 left, Hcd754 left, Hcd755 left,
Hcd760 left, Hcd763 right, Hcd768 left ,Hcd768 right, Hcd770 left, Hcd773 left, Hcd777 left, Hcd778 right, Hcd781 left, Hcd781 right, Hcd782 left, Hcd783 left, Hcd788 left, Hcd794 right, Hcd796 left, Hcd799 left, Hcd807 right, Hcd812 left, Hcd817 left, Hcd817 right, Hcd829 right, Hcd852 right, Hcd861 right, Hcd863PO right, Hcd866 right, Hcd869 left, Hcd873 left, Hcd886 right, Hcd889 right, Hcd891 right, Hcd892 left, Hcd913 right, Hcd923 left, Hcd923 right, Hcd938 left, Hcd938 right, Hcd939 right, Hcd946 left, Hcd948 right, Hcd960 left, Hcd965 left, Hcd970 left, Hcd975 left, Hcd976 right, Hcd99 right, HPRlOO right, HPR129 left, HPR154 left, HPRl 59 left, HPRl 63 left, HPRl 69 right, HPRl 72 right, HPRl 81 left, HPRl 87 left, HPR 199 right, HPR206 left, HPR213 right, HPR214 right, HPR220 left , HPR220 right, HPR227 right, HPR232 right, HPR233 right, HPR244 right, HPR262 left, HPR264 right, HPR266 right, HPR271 right, HPR76 right, hsa_mir_490_Hcd20 right, HSHELAOl, HSTRNL, HUMTRAB, HUMTRF, HUMTRN, HUMTRS, HUMTRVlA, let-7f-2-prec2, mir-OOlb-1-precl , mir-OOlb-2-prec, mir-007-l-prec, mir-007-2- precNo2, mir-OlOa-precNol, mir-015b-precNo2, mir-016a-chrl3, mir-016b-chr3, mir- 017-precNol , mir-017-precNo2, mir-018-prec, mir-019a-prec, mir-019b-l-prec, mir- 019b-2-prec, mir-020-prec, mir-022-prec, mir-023a-prec, mir-023b-prec, mir-024-2- prec, mir-025-prec, mir-027b-prec, mir-029c-prec, mir-032-precNo2, mir-033b-prec, mir-033-prec, mir-034-precNol, mir-034-precNo2, mir-092-prec-l 3=092- 1NO2, mir- 092-prec-X=092-2, mir-093-prec-7.1=093-l, mir-095-prec-4 ,mir-096-prec-7Nol ,mir- 096-prec-7No2, mir-098-prec-X, mir-099b-prec-19Nol, mir-lOO-l/2-prec, mir-lOONol, mir-lOl-prec-9, mir-102-prec-l, mir-103-2-prec, mir-103-prec-5=103-l , mir-106aNol, mir-106-prec-X,mir-107Nol , mir-107-prec-lO, mir-122a-prec, mir-123-precNol, mir- 123-precNo2, mir-124a-l-precl, mir-124a-2-prec, mir-124a-3-prec, mir-125b-l, mir- 125b-2-precNo2, mir-127-prec, mir-128b-precNol, mir-128b-precNo2, mir-133a-l , mir-135-2-prec, mir-136-precNo2, mir-138-l-prec, mir-140No2, mir-142-prec, mir- 143-prec, mir-144-precNo2, mir-145-prec, mir-146bNol , mir-146-prec, mir-147-prec, mir-148aNol, mir-148-prec, mir-149-prec, mir-150-prec, mir-153-l-precl, mir-154- preclNol, mir-155-prec, mir-15aNol , mir-16-lNol, mir-16-2Nol , mir-181a-precNol , mir- 18Ib-INoI, mir- 181 b-2No 1 , mir- 181 b-precNo 1 , mir- 181 b-precNo2, mir- 181 c- precNol , mir-181dNol , mir-188-prec, mir-18bNo2, mir-191 -prec, mir-192No2, mir-
193bNo2, mir-194-2Nol, mir-195-prec, mir-196-2-precNo2, mir- 197-prec, mir-198- prec, mir-199a-l-prec, mir-199a-2-prec, mir-199b-precNol, mir-200a-prec, mir- 20ObNoI , mir-200bNo2, mir-202*, mir-202-prec, mir-204-precNo2, mir-205-prec, mir- 208-prec, mir-20bNol , mir-212-precNol, mir-212-precNo2, mir-213-precNol , mir- 214-prec, mir-215-precNo2, mir-216-precNol , mir-219-2Nol , mir-219-prec, mir-223- prec, mir-29b-lNol, mir-29b-2=102prec7.1=7.2, mir-321Nol , mir-321No2, mir- 324NoI, mir-324No2, mir-328Nol, mir-342Nol , mir-361Nol, mir-367Nol , mir- 370NoI, mir-371Nol, miR-373*Nol, mir-375, mir-376aNol, mir-379Nol, mir-380-5p, mir-382, mir-384, mir-409-3p, mir-423Nol, mir-424No2, mir-429Nol , mir-429No2, mir-4323p, mir-4325p, mir-449Nol, mir-450-1, mir-450-2Nol , mir-483Nol, mir-484, mir-487Nol, mir-495Nol, mir-499No2, mir-501No2, mir-503Nol, mir-509Nol , mir- 514-lNo2, mir-515-15p, mir-515-23p, mir-516-33p, mir-516-43p, mir-518e/526c, mir- 519a- 1/52, mir-519a-2No2, mir-519b, mir-519c/52, mir-520c/52, mir-526a-2Nol, mir- 526a-2No2, MPRl 03 right, MPRl 21 left, MPRl 21 left, MPRl 30 left, MPRl 30 right, MPR133 right, MPR141 left, MPR151 left, MPR156 left, MPR162 left, MPR174 left, MPRl 74 right, MPRl 85 right, MPRl 97 right, MPR203 left, MPR207 right, MPR215 left, MPR216 left, MPR224 left, MPR224 right, MPR228 left, MPR234 right, MPR237 left, MPR243 left, MPR244 right, MPR249 left, MPR254 right, MPR74 left, MPR88 right, and MPR95 left.
In an embodiment, the method includes determining the expression of two of the listed genes or microRNAs, more preferably three, four, five, six, seven, eight, nine, or ten of the listed genes, and most preferably twenty, thirty, forty, fifty, sixty, seventy, eighty, ninety, or one hundred or more of the listed genes. In another embodiment, the change in the level of gene or microRNA expression (e.g., an increase or decrease) is determined relative to the level of gene or microRNA expression in a cell or tissue known to be sensitive to the treatment, such that a similar level of gene or microRNA expression exhibited by a cell or tissue of the patient indicates the patient is sensitive to the treatment. In another embodiment, the change in the level of gene or microRNA expression (e.g., an increase or decrease) is determined relative to the level of gene or microRNA expression in a cell or tissue known to be resistant to the treatment, such that a similar level of gene or microRNA expression exhibited by a cell or tissue of the
patient indicates the patient is resistant to the treatment.
In a second aspect, the invention features a method of determining sensitivity of a cancer in a patient to a treatment for cancer by measuring the level of expression of at least one microRNA in a cell (e.g., a cancer cell) of the patient, in which the microRNA is selected from the group set forth in the first aspect of the invention. In an embodiment, the method further includes determining a patient's resistance or sensitivity to radiation therapy or any of the chemotherapy agents set forth in the first aspect of the invention by measuring the level of expression of one or more of the microRNAs known to change (e.g., to increase or decrease) in a patient sensitive to treatment with these agents (e.g., a patient is determined to be sensitive, or likely to be sensitive, to the indicated treatment if the level of expression of one or more of the microRNA(s) increases or decreases relative to the level of expression of the microRNA(s) in a control sample (e.g., a cell or tissue) in which increased or decreased expression of the microRNA(s) indicates sensitivity to the treatment, and vice versa). In an embodiment, the method includes determining the expression of two of the listed genes or microRNAs, more preferably three, four, five, six, seven, eight, nine, or ten of the listed genes, and most preferably twenty, thirty, forty, fifty, sixty, seventy, eighty, ninety, or one hundred or more of the listed genes. In another embodiment, the change in the level of microRNA expression (e.g., an increase or decrease) is determined relative to the level of microRNA expression in a cell or tissue known to be sensitive to the treatment, such that a similar level of microRNA expression exhibited by a cell or tissue of the patient indicates the patient is sensitive to the treatment. In another embodiment, the change in the level of microRNA expression (e.g., an increase or decrease) is determined relative to the level of microRNA expression in a cell or tissue known to be resistant to the treatment, such that a similar level of microRNA expression exhibited by a cell or tissue of the patient indicates the patient is resistant to the treatment.
In another embodiment, the invention features a method for determining the development of resistance by a patient (e.g., resistance of a cell, such as a cancer cell, in the patient) to a treatment to which the patient was previously sensitive. The method includes measuring the level of expression of one or more of the microRNAs set forth
in the first aspect of the invention, such that the level of expression of a micro RN A which is decreased in a cell or tissue known to be sensitive to the treatment indicates that the patient is resistant to or has a propensity to become resistant to the treatment. Alternatively, a decrease in the expression level of a microRNA which is increased in a cell or tissue known to be sensitive to the treatment indicates that the patient is resistant to or has a propensity to become resistant to the treatment.
In a third aspect, the invention features a kit that includes a single-stranded nucleic acid molecule (e.g., one or a plurality thereof; e.g., a deoxyribonucleic acid molecule or a ribonucleic acid molecule) that is substantially complementary to (e.g., that has at least 80%, 90%, 95% 97%, 99%, or 100% identical to the complement of) or that is substantially identical to (e.g., that has at least 80%, 90%, 95% 97%, 99%, or 100% identity to) at least 5 consecutive nucleotides (more preferably at least 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 150, 200, 250, 300, or more consecutive nucleotides; the nucleic acid can also be 5-20, 25, 5-50, 50-100, or over 100 consecutive nucleotides long) of at least one of the genes (e.g., at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, or more of the genes) set forth in the first aspect of the invention, such that the single-stranded nucleic acid molecule is sufficient for measuring the level of expression of the gene(s) by allowing specific hybridization between the single-stranded nucleic acid molecule and a nucleic acid molecule encoded by the gene, or a complement thereof. Alternatively, the kit includes one or more single-stranded nucleic acid molecules that are substantially complementary to or substantially identical to at least 5 consecutive nucleotides of at least one of the microRNAs set forth in the first aspect of the invention, such that the single-stranded nucleic acid molecule is sufficient for measuring the level of expression of the microRNA(s) by allowing specific hybridization between the single-stranded nucleic acid molecule and the microRNA, or a complement thereof. The kit further includes instructions for applying nucleic acid molecules collected from a sample from a cancer patient (e.g., from a cell of the patient), determining the level of expression of the gene(s) or microRNA(s) hybridized to the single-stranded nucleic acid, and determining the patient's sensitivity to a treatment for cancer when use of the kit indicates that the level of expression of the gene(s) or microRNA(s) changes (e.g.,
increases or decreases relative to a control sample (e.g., tissue or cell) known to be sensitive or resistant to the treatment, as is discussed above in connection with the first aspect of the invention). In an embodiment, the instructions further indicate that a change in the level of expression of the gene(s) or microRNA(s) relative to the expression of the gene(s) or microRNA(s) in a control sample (e.g., a cell or tissue known to be sensitive or resistant to the treatment) indicates a change in sensitivity of the patient to the treatment (e.g., a decrease in the level of expression of a gene or microRNA known to be expressed in cells sensitive to the treatment indicates that the patient is becoming resistant to the treatment or is likely to become resistant to the treatment, and vice versa).
In another embodiment, the kit can be utilized to determine a patient's resistance or sensitivity to radiation therapy or the chemotherapy agents Vincristine, Cisplatin, Adriamycin, Etoposide, Azaguanine, Aclarubicin, Mitoxantrone, Paclitaxel, Mitomycin, Gemcitabine, Taxotere, Dexamethasone, Methylprednisolone, Ara-C, Methotrexate, Bleomycin, Methyl-GAG, Rituximab, PXDlOl (a histone deacetylase (HDAC) inhibitor), 5-Aza-2'-deoxycytidine (Decitabine), Melphalan, IL4-PE38 fusion protein, IL13-PE38QQR fusion protein (cintredekin besudotox), Valproic acid (VPA), All-trans retinoic acid (ATRA), Cytoxan, Topotecan (Hycamtin), Suberoylanilide hydroxamic acid (SAHA, vorinostat, Zolinza), Depsipeptide (FR901229), Bortezomib, Leukeran, Fludarabine, Vinblastine, Busulfan, Dacarbazine, Oxaliplatin, Hydroxyurea, Tegafur, Daunorubicin, Bleomycin, Estramustine, Chlorambucil, Mechlorethamine, Streptozocin, Carmustine, Lomustine, Mercaptopurine, Teniposide, Dactinomycin, Tretinoin, Sunitinib, SPC2996, Ifosfamide, Tamoxifen, Floxuridine, Irinotecan, and Satraplatin by measuring the level of expression of one or more of the genes or microRNAs set forth in the first aspect of the invention and known to change (e.g., to increase or decrease) in a patient sensitive to treatment with these agents (e.g., a patient is determined to be sensitive, or likely to be sensitive, to the indicated treatment if the level of expression of one or more of the gene(s) or micro RN A(s) increases or decreases relative to the level of expression of the gene(s) or microRNA(s) in a control sample (e.g., a cell or tissue) in which increased or decreased expression of the gene(s) or microRNA(s) indicates sensitivity to the treatment, and vice versa).
In another embodiment, the nucleic acid molecules are characterized by their ability to specifically identity nucleic acid molecules complementary to the genes or microRNAs in a sample collected from a cancer patient.
In a fourth aspect, the invention features a kit that includes a single-stranded nucleic acid molecule (e.g., one or a plurality thereof; e.g., a deoxyribonucleic acid molecule or a ribonucleic acid molecule) that is substantially complementary to (e.g., that has at least 80%, 90%, 95% 97%, 99%, or 100% identical to the complement of) or that is substantially identical to (e.g., that has at least 80%, 90%, 95% 97%, 99%, or 100% identity to) at least 5 consecutive nucleotides (more preferably at least 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 150, 200, 250, 300, or more consecutive nucleotides; the nucleic acid can also be 5-20, 25, 5-50, 50-100, or over 100 consecutive nucleotides long) of at least one of the microRNAs (e.g., at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, or more of the microRNAs) set forth in the first aspect of the invention, such that the single-stranded nucleic acid molecule is sufficient for measuring the level of expression of the microRNA(s) by allowing specific hybridization between the single-stranded nucleic acid molecule and a microRNA, or a complement thereof. The kit further includes instructions for applying nucleic acid molecules collected from a sample from a cancer patient (e.g., from a cell of the patient), determining the level of expression of the micro RNA(s) hybridized to the single-stranded nucleic acid, and determining the patient's sensitivity to a treatment for cancer when use of the kit indicates that the level of expression of microRNA(s) changes (e.g., increases or decreases relative to a control sample (e.g., tissue or cell) known to be sensitive or resistant to the treatment, as is discussed above in connection with the first aspect of the invention). In an embodiment, the instructions further indicate that a change in the level of expression of microRNA(s) relative to the expression of microRNA(s) in a control sample (e.g., a cell or tissue known to be sensitive or resistant to the treatment) indicates a change in sensitivity of the patient to the treatment (e.g., a decrease in the level of expression of a microRNA known to be expressed in cells sensitive to the treatment indicates that the patient is becoming resistant to the treatment or is likely to become resistant to the treatment, and vice versa).
In another embodiment, the kit can be utilized to determine a patient's resistance or sensitivity to radiation therapy or the chemotherapy agents Vincristine, Cisplatin, Adriamycin, Etoposide, Azaguanine, Aclarubicin, Mitoxantrone, Paclitaxel, Mitomycin, Gemcitabine, Taxotere, Dexamethasone, Methylprednisolone, Ara-C, Methotrexate, Bleomycin, Methyl-GAG, Rituximab, PXDlOl (a histone deacetylase (HDAC) inhibitor), 5-Aza-2'-deoxycytidine (Decitabine), Melphalan, IL4-PE38 fusion protein, IL13-PE38QQR fusion protein (cintredekin besudotox), Valproic acid (VPA), All-trans retinoic acid (ATRA), Cytoxan, Topotecan (Hycamtin), Suberoylanilide hydroxamic acid (SAHA 5 vorinostat, Zolinza), Depsipeptide (FR901229), Bortezomib, Leukeran, Fludarabine, Vinblastine, Busulfan, Dacarbazine, Oxaliplatin, Hydroxyurea, Tegafur, Daunorubicin, Bleomycin, Estramustine, Chlorambucil, Mechlorethamine, Streptozocin, Carmustine, Lomustine, Mercaptopurine, Teniposide, Dactinomycin, Tretinoin, Sunitinib, SPC2996, Ifosfamide, Tamoxifen, Floxuridine, Irinotecan, and Satraplatin by measuring the level of expression of one or more of the microRNAs set forth in the first aspect of the invention and known to change (e.g., to increase or decrease) in a patient sensitive to treatment with these agents (e.g., a patient is determined to be sensitive, or likely to be sensitive, to the indicated treatment if the level of expression of one or more of the microRNA(s) increases or decreases relative to the level of expression of the microRNA(s) in a control sample (e.g., a cell or tissue) in which increased or decreased expression of the or micro RN A(s) indicates sensitivity to the treatment, and vice versa).
In another embodiment, the nucleic acid molecules are characterized by their ability to specifically identify nucleic acid molecules complementary to the microRNAs in a sample collected from a cancer patient.
In a fifth aspect, the invention features a method of identifying biomarkers (e.g., genes and microRNAs) indicative of sensitivity of a cancer patient to a treatment for cancer by obtaining pluralities of measurements of the expression level of a gene or microRNA (e.g., by detection of the expression of a gene or microRNA using a single probe or by using multiple probes directed to a single gene or microRNA) in different cell types and measurements of the growth of those cell types in the presence of a treatment for cancer relative to the growth of the cell types in the absence of the
treatment for cancer; correlating each plurality of measurements of the expression level of the gene or microRNA in cells with the growth of the cells to obtain a correlation coefficient; selecting the median correlation coefficient calculated for the gene or microRNA; and identifying the gene or microRNA as a biomarker for use in determining the sensitivity of a cancer patient to said treatment for cancer if said median correlation coefficient exceeds 0.3 (preferably the gene or microRNA is identified as a biomarker for a patient's sensitivity to a treatment if the correlation coefficient exceeds 0.4, 0.5, 0.6, 0.7, 0.8. 0.9, 0.95, or 0.99 or more). In an embodiment, the method is performed in the presence of a second treatment.
In a sixth aspect, the invention features a method of determining sensitivity of a patient (e.g., a cancer patient) to a treatment for cancer by obtaining a measurement of the level of expression of a gene or microRNA in a sample (e.g., a cell or tissue) from the patient; applying a model predictive of sensitivity to a treatment for cancer to the measurement, in which the model is developed using an algorithm selected from the group consisting of linear sums, nearest neighbor, nearest centroid, linear discriminant analysis, support vector machines, and neural networks; and determining whether or not the patient will be responsive to the treatment for cancer. In an embodiment, the measurement is obtained by measuring the level of expression of any of the genes or microRNAs set forth in the first aspect of the invention in a cell known to be sensitive or resistant to the treatment. In another embodiment, the method is performed in the presence of a second treatment. In another embodiment, the model combines the outcomes of linear sums, linear discriminant analysis, support vector machines, neural networks, k-nearest neighbors, and nearest centroids, or the model is cross-validated using a random sample of multiple measurements. In another embodiment, treatment, e.g., a compound, has previously failed to show efficacy in a patient. In several embodiments, the linear sum is compared to a sum of a reference population with known sensitivity; the sum of a reference population is the median of the sums derived from the population members' biomarker gene expression. In another embodiment, the model is derived from the components of a data set obtained by independent component analysis or is derived from the components of a data set obtained by principal component analysis. In another embodiment, the invention features a kit, apparatus,
and software used to implement the method of the sixth aspect of the invention.
In several embodiments of all aspects of the invention, the level of expression of the gene(s) is determined by measuring the level of mRNA transcribed from the gene(s), by detecting the level of a protein product of the gene(s), or by detecting the level of the biological activity of a protein product of the gene(s). In further embodiments of all aspects of the invention, an increase or decrease in the expression level of the gene(s) or microRNA(s), relative to the expression level of the gene(s) or microRNA(s) in a cell or tissue sensitive to the treatment, indicates increased sensitivity of the cancer patient to the treatment. Alternatively, an increase or decrease in the expression level of the gene(s) or microRNA(s), relative to the expression level of the gene(s) or microRNA(s) in a cell or tissue resistant to the treatment, indicates increased resistance of the cancer patient to the treatment. In another embodiment of all aspects of the invention, the cell is a cancer cell. In another embodiment of all aspects of the invention, the expression level of the gene(s) is measured using a quantitative reverse transcription-polymerase chain reaction (qRT-PCR). In an embodiment of all aspects of the invention, the level of expression of two of the listed genes or microRNAs is measured, more preferably the level of expression of three, four, five, six, seven, eight, nine, or ten of the listed genes or microRNAs is measured, and most preferably twenty, thirty, forty, fifty, sixty, seventy, eighty, ninety, or one hundred or more of the listed genes or microRNAs is measured. In another embodiment of all aspects of the invention, the expression level of the gene(s) or microRNA(s) is determined using the kit of the third or fourth aspects of the invention.
In another embodiment of all aspects of the invention, the treatment is radiation therapy or a compound, such as a chemotherapy agent selected from the group consisting of Vincristine, Cisplatin, Adriamycin, Etoposide, Azaguanine, Aclarubicin, Mitoxantrone, Paclitaxel, Mitomycin, Gemcitabine, Taxotere, Dexamethasone, Methylprednisolone, Ara-C, Methotrexate, Bleomycin, Methyl-GAG, Rituximab, PXDl Ol (a histone deacetylase (HDAC) inhibitor), 5-Aza-2'-deoxycytidine (Decitabine), Melphalan, IL4-PE38 fusion protein, IL13-PE38QQR fusion protein (cintredekin besudotox), Valproic acid (VPA), All-trans retinoic acid (ATRA), Cytoxan, Topotecan (Hycamtin), Suberoylanilide hydroxamic acid (SAHA, vorinostat,
Zolinza), Depsipeptide (FR901229), Bortezomib, Leukeran, Fludarabine, Vinblastine, Busulfan, Dacarbazine, Oxaliplatin, Hydroxyurea, Tegafur, Daunorubicin, Bleomycin, Estramustine, Chlorambucil, Mechlorethamine, Streptozocin, Carmustine, Lomustine, Mercaptopurine, Teniposide, Dactinomycin, Tretinoin, Sunitinib, SPC2996, Ifosfamide, Tamoxifen, Floxuridine, Irinotecan, and Satraplatin. In another embodiment of all aspects of the invention, the treatment has previously failed to show effect in a subject (e.g., a subject selected from a subpopulation determined to be sensitive to the treatment, a subject selected from a subpopulation predicted to die without treatment, a subject selected from a subpopulation predicted to have disease symptoms without treatment, a subject selected from a subpopulation predicted to be cured without treatment.
In another embodiment of all aspects of the invention, the treatment is, e.g., administration of a compound, a protein, an antibody, an oligonucleotide, a chemotherapeutic agent, or radiation to a patient. In an emobodiment of all aspects of the invention, the treatment is, e.g., a chemotherapeutic agent, such as, e.g., Vincristine, Cisplatin, Azaguanine, Etoposide, Adriamycin, Aclarubicin, Mitoxantrone, Mitomycin, Paclitaxel, Gemcitabine, Taxotere, Dexamethasone, Ara-C, Methylprednisolone, Methotrexate, Bleomycin, Methyl-GAG, Carboplatin, 5-FU (5-Fluorouracil), a histone deacetylase (HDAC) inhibitor such as PXDlOl, 5-Aza-2'-deoxycytidine (Decitabine), alpha emitters such as astatine-211 , bismuth-212, bismuth-213, lead-212, radium-223, actinium-225, and thorium-227, beta emitters such as tritium, strontium-90, cesium- 137, carbon-1 1, nitrogen-13, oxygen-15, fluorine-18, iron-52, cobalt-55, cobalt-60, copper-61, copper-62, copper-64, zinc-62, zinc-63, arsenic-70, arsenic-71 , arsenic-74, bromine-76, bromine-79, rubidium-82, yttrium-86, zirconium-89, indium- 1 10, iodine- 120, iodine- 124, iodine- 129, iodine-131, iodine- 125, xenon- 122, technetium-94m, technetium-94, technetium-99m, and technetium-99, gamma emitters such as cobalt-60, cesium-137, and technetium-99m, Alemtuzumab, Daclizumab, Rituximab (e.g., MABTHERA™), Trastuzumab (e.g., HERCEPTIN™), Gemtuzumab, Ibritumomab, Edrecolomab, Tositumomab, CeaVac, Epratuzumab, Mitumomab, Bevacizumab, Cetuximab, Edrecolomab, Lintuzumab, MDX-210, IGN-101 , MDX-010, MAb, AME, ABX-EGF, EMD 72 000, Apolizumab, Labetuzumab, ior-tl , MDX-220, MRA, H-1 1
scFv, Oregovomab, huJ591 MAb, BZL, Visilizumab, TriGem, TriAb, R3, MT-201, G- 250, unconjugated, ACA- 125, Onyvax-105, CDP-860, BrevaRex MAb, AR54, IMC- ICl 1 , GHoMAb-H, ING-I 5 Anti-LCG MAbs, MT-103, KSB-303, Therex, KW-2871 , Anti-HMI.24, Anti-PTHrP, 2C4 antibody, SGN-30, TRAIL-RI MAb, CAT, Prostate cancer antibody, H22xKi-4, ABX-MAl , Imuteran, Monopharm-C, Acivicin, Aclarubicin, Acodazole Hydrochloride, Acronine, Adozelesin, Adriamycin, Aldesleukin, Altretamine, Ambomycin, A. metantrone Acetate, Aminoglutethimide, Amsacrine, Anastrozole, Anthramycin, Asparaginase, Asperlin, Azacitidine, Azetepa, Azotomycin, Batimastat, Benzodepa, Bicalutamide, Bisantrene Hydrochloride, Bisnafide Dimesylate, Bizelesin, Bleomycin Sulfate, Brequinar Sodium, Bropirimine, Busulfan, Cactinomycin, Calusterone, Camptothecin, Caracemide, Carbetimer, Carboplatin, Carmustine, Carubicin Hydrochloride, Carzelesin, Cedefingol, Chlorambucil, Cirolemycin, Cisplatin, Cladribine, Combretestatin A-4, Crisnatol Mesylate, Cyclophosphamide, Cytarabine, Dacarbazine, DACA (N- [2- (Dimethyl- amino) ethyl] acridine-4-carboxamide), Dactinomycin, Daunorubicin Hydrochloride, Daunomycin, Decitabine, Dexormaplatin, Dezaguanine, Dezaguanine Mesylate, Diaziquone, Docetaxel, Dolasatins, Doxorubicin, Doxorubicin Hydrochloride, Droloxifene, Droloxifene Citrate, Dromostanolone Propionate, Duazomycin, Edatrexate, Eflornithine Hydrochloride, Ellipticine, Elsamitrucin, Enloplatin, Enpromate, Epipropidine, Epirubicin Hydrochloride, Erbulozole, Esorubicin Hydrochloride, Estramustine, Estramustine Phosphate Sodium, Etanidazole, Ethiodized Oil 1 131, Etoposide, Etoposide Phosphate, Etoprine, Fadrozole Hydrochloride, Fazarabine, Fenretinide, Floxuridine, Fludarabine Phosphate, Fluorouracil, 5-FdUMP, Flurocitabine, Fosquidone, Fostriecin Sodium, Gemcitabine, Gemcitabine Hydrochloride, Gold Au 198, Homocamptothecin, Hydroxyurea, Idarubicin Hydrochloride, Ifosfamide, Ilmofosine, Interferon Alfa-2a, Interferon Alfa-2b, Interferon Alfa-nl, Interferon Alfa-n3, Interferon Beta-I a, Interferon Gamma-I b, Iproplatin, Irinotecan Hydrochloride, Lanreotide Acetate, Letrozole, Leuprolide Acetate, Liarozole Hydrochloride, Lometrexol Sodium, Lomustine, Losoxantrone Hydrochloride, Masoprocol, Maytansine, Mechlorethamine Hydrochloride, Megestrol Acetate, Melengestrol Acetate, Melphalan, Menogaril, Mercaptopurine, Methotrexate,
Methotrexate Sodium, Metoprine, Meturedepa, Mitindomide, Mitocarcin, Mitocromin, Mitogillin, Mitomalcin, Mitomycin, Mitosper, Mitotane, Mitoxantrone Hydrochloride, Mycophenolic Acid, Nocodazole, Nogalamycin,Ormaplatin, Oxisuran, Paclitaxel, Pegaspargase, Peliomycin, Pentamustine, PeploycinSulfate, Perfosfamide, Pipobroman, Piposulfan, Piroxantrone Hydrochloride, Plicamycin, Plomestane, Porfimer Sodium, Porfiromycin, Prednimustine, Procarbazine Hydrochloride, Puromycin, Puromycin Hydrochloride, Pyrazofurin, Rhizoxin, Rhizoxin D, Riboprine, Rogletimide, Safingol, Safingol Hydrochloride, Semustine, Simtrazene, Sparfosate Sodium, Sparsomycin, Spirogermanium Hydrochloride, Spiromustine, Spiroplatin, Streptonigrin, Streptozocin, Strontium Chloride Sr 89, Sulofenur, Talisomycin, Taxane, Taxoid, Tecogalan Sodium, Tegafur, Teloxantrone Hydrochloride, Temoporfin, Teniposide, Teroxirone, Testolactone, Thiamiprine, Thioguanine, Thiotepa, Thymitaq, Tiazofurin, Tirapazamine, Tomudex, TOP53, Topotecan Hydrochloride, Toremifene Citrate, Trestolone Acetate, Triciribine Phosphate, Trimetrexate, Trimetrexate Glucuronate, Triptorelin, Tubulozole Hydrochloride, Uracil Mustard, Uredepa, Vapreotide, Verteporfin, Vinblastine, Vinblastine Sulfate, Vincristine, Vincristine Sulfate, Vindesine, Vindesine Sulfate, Vinepidine Sulfate, Vinglycinate Sulfate, Vinleurosine Sulfate, Vinorelbine Tartrate, Vinrosidine Sulfate, Vinzolidine Sulfate, Vorozole, Zeniplatin, Zinostatin, Zorubicin Hydrochloride, 2-Chlorodeoxyadenosine, 2' Deoxyformycin, 9-aminocamptothecin, raltitrexed, N-propargyl-5,8-dideazafolic acid, 2chloro-2'-arabino-fluoro-2'-deoxyadenosine, 2-chloro-2'-deoxyadenosine, anisomycin, trichostatin A, hPRL-G129R, CEP-751, linomide, sulfur mustard, nitrogen mustard (mechlor ethamine), cyclophosphamide, melphalan, chlorambucil, ifosfamide, busulfan, N-methyl-Nnitrosourea (MNU), N, N'-Bis (2-chloroethyl)-N-nitrosourea (BCNU), N- (2-chloroethyl)-N' cyclohexyl-N-nitrosourea (CCNU), N- (2-chloroethyl)-N'- (trans-4- methylcyclohexyl-N-nitrosourea (MeCCNU), N- (2-chloroethyl)-N- (diethyl) ethylphosphonate-N-nitrosourea (fotemustine), streptozotocin, diacarbazine (DTIC), mitozolomide, temozolomide, thiotepa, mitomycin C, AZQ, adozelesin, Cisplatin, Carboplatin, Ormaplatin, Oxaliplatin,C 1-973, DWA 21 14R, JM216, JM335, Bis (platinum), tomudex, azacitidine, cytarabine, gemcitabine, 6-Mercaptopurine, 6- Thioguanine, Hypoxanthine, teniposide 9-amino camptothecin, Topotecan, CPT-1 1 ,
Doxorubicin, Daunomycin, Epirubicin, darubicin, mitoxantrone, losoxantrone, Dactinomycin (Actinomycin D), amsacrine, pyrazoloacridine, all-trans retinol, 14- hydroxy-retro-retinol, all-trans retinoic acid, N- (4- Hydroxyphenyl) retinamide, 13-cis retinoic acid, 3-Methyl TTNEB, 9-cis retinoic acid, fludarabine (2-F-ara-AMP), 2- chlorodeoxyadenosine (2-Cda), 20-pi-l,25 dihydroxyvitamin D3, 5-ethynyluracil, abiraterone, aclarubicin, acylfulvene, adecypenol, adozelesin, aldesleukin, ALL-TK antagonists, altretamine, ambamustine, amidox, amifostine, aminolevulinic acid, amrubicin, amsacrine, anagrelide, anastrozole, andrographolide, angiogenesis inhibitors, antagonist D, antagonist G, antarelix, anti-dorsalizing morphogenetic protein- 1, antiandrogen, prostatic carcinoma, antiestrogen, antineoplaston, antisense oligonucleotides, aphidicolin glycinate, apoptosis gene modulators, apoptosis regulators, apurinic acid, ara-CDP-DL-PTBA, argininedeaminase, asulacrine, atamestane, atrimustine, axinastatin 1, axinastatin 2, axinastatin 3, azasetron, azatoxin, azatyrosine, baccatin III derivatives, balanol, batimastat, BCR/ ABL antagonists, benzochlorins, benzoylstaurosporine, beta lactam derivatives, beta-alethine, betaclamycin B, betulinic acid, bFGF inhibitor, bicalutamide, bisantrene, bisaziridinylspermine, bisnafide, bistratene A, bizelesin, breflate, bleomycin A2, bleomycin B2, bropirimine, budotitane, buthionine sulfoximine, calcipotriol, calphostin C, camptothecin derivatives (e.g., 10-hydroxy-camptothecin), canarypox IL-2, capecitabine, carboxamide-amino-triazole, carboxyamidotriazole, CaRest M3, CARN 700, cartilage derived inhibitor, carzelesin, casein kinase inhibitors (ICOS), castanospermine, cecropin B, cetrorelix, chlorins, chloroquinoxaline sulfonamide, cicaprost, cis-porphyrin, cladribine, clomifene analogues, clotrimazole, collismycin A, collismycin B, combretastatin A4, combretastatin analogue, conagenin, crambescidin 816 , crisnatol, cryptophycin 8, cryptophycin A derivatives, curacin A, cyclopentanthraquinones, cycloplatam, cypemycin, cytarabine ocfosfate, cytolytic factor, cytostatin, dacliximab, decitabine, dehydrodidemnin B, 2'deoxycoformycin (DCF), deslorelin, dexifosfamide, dexrazoxane, dexverapamil, diaziquone, didemnin B, didox, diethylnorspermine, dihydro-5-azacytidine, 9-dihydrotaxol, dioxamycin, diphenyl spiromustine, discodermolide, docosanol, dolasetron, doxifluridine, droloxifene, dronabinol, duocarmycin SA, ebselen, ecomustine, edelfosine,
edrecolomab, eflornithine, elemene, emitefur, epirubicin, epothilones (A, R = H, B, R = Me), epithilones, epristeride, estramustine analogue, estrogen agonists, estrogen antagonists, etanidazole, etoposide, etoposide 4'-phosphate (etopofos), exemestane, fadrozole, fazarabine, fenretinide, filgrastim, finasteride, flavopiridol, flezelastine, fluasterone, fludarabine, fluorodaunorunicin hydrochloride, forfenimex, formestane, fostriecin, fotemustine, gadolinium texaphyrin, gallium nitrate, galocitabine, ganirelix, gelatinase inhibitors, gemcitabine, glutathione inhibitors, hepsulfam, heregulin, hexamethylene bisacetamide, homoharringtonine (HHT), hypericin, ibandronic acid, idarubicin, idoxifene, idramantone, ilmofosine, ilomastat, imidazoacridones, imiquimod, immunostimulant peptides, insulin-like growth factor- 1 receptor inhibitor, interferon agonists, interferons, interleukins, iobenguane, iododoxorubicin, 4- ipomeanol, irinotecan, iroplact, irsogladine, isobengazole, isohomohalicondrin B, itasetron, jasplakinolide, kahalalide F, lamellarin-N triacetate, lanreotide, leinamycin, lenograstim, lentinan sulfate, leptolstatin, letrozole, leukemia inhibiting factor, leukocyte alpha interferon, leuprolide, estrogen, and progesterone combinations, leuprorelin, levamisole, liarozole, linear polyamine analogue, lipophilic disaccharide peptide, lipophilic platinum compounds, lissoclinamide 7, lobaplatin, lombricine, lometrexol, lonidamine, losoxantrone, lovastatin, loxoribine, lurtotecan, lutetium texaphyrin, lysofylline, lytic peptides, maytansine, mannostatin A, marimastat, masoprocol, maspin, matrilysin inhibitors, matrix metalloproteinase inhibitors, menogaril, merbarone, meterelin, methioninase, metoclopramide, MIF inhibitor, ifepristone, miltefosine, mirimostim, mismatched double stranded RNA, mithracin, mitoguazone, mitolactol, mitomycin analogues, mitonafide, mitotoxin fibroblast growth factor-saporin, mitoxantrone, mofarotene, molgramostim, monoclonal antibody, human chorionic gonadotrophin, monophosphoryl lipid A and myobacterium cell wall skeleton combinations, mopidamol, multiple drug resistance gene inhibitor, multiple tumor suppressor 1 -based therapy, mustard anticancer agent, mycaperoxide B, mycobacterial cell wall extract, myriaporone, N-acetyldinaline, N-substituted benzamides, nafarelin, nagrestip, naloxone and pentazocine combinations, napavin, naphterpin, nartograstim, nedaplatin, nemorubicin, neridronic acid, neutral endopeptidase, nilutamide, nisamycin, nitric oxide modulators, nitroxide antioxidant, nitrullyn, 06-benzylguanine, octreotide,
okicenone, oligonucleotides, onapristone, ondansetron, ondansetron, oracin, oral cytokine inducer, ormaplatin, osaterone, oxaliplatin, oxaunomycin, paclitaxel analogues, paclitaxel derivatives, palauamine, palmitoylrhizoxin, pamidronic acid, panaxytriol, panomifene, parabactin, pazelliptine, pegaspargase, peldesine, pentosan polysulfate sodium, pentostatin, pentrozole, perflubron, perfosfamide, perillyl alcohol, phenazinomycin, phenylacetate, phosphatase inhibitors, picibanil, pilocarpine hydrochloride, pirarubicin, piritrexim, placetin A, placetin B, plasminogen activator inhibitor, platinum complex, platinum compounds, platinum-triamine complex, podophyllotoxin, porfimer sodium, porfiromycin, propyl bis-acridone, prostaglandin 32, proteasome inhibitors, protein A-based immune modulator, protein kinase C inhibitor, protein kinase C inhibitors, microalgal, protein tyrosine phosphatase inhibitors, purine nucleoside phosphorylase inhibitors, purpurins, pyrazoloacridine, pyridoxylated hemoglobin polyoxyethylene conjugate, raf antagonists, raltitrexed, ramosetron, ras farnesyl protein transferase inhibitors, ras inhibitors, ras-GAP inhibitor, retelliptine demethylated, rhenium Re 186 etidronate, rhizoxin, ribozymes, RII retinamide, rogletimide, rohitukine, romurtide, roquinimex, rubiginone B 1 , ruboxyl, safingol, saintopin, SarCNU, sarcophytol A, sargramostim, Sdi 1 mimetics, semustine, senescence derived inhibitor 1 , sense oligonucleotides, signal transduction inhibitors, signal transduction modulators, single chain antigen binding protein, sizofiran, sobuzoxane, sodium borocaptate, sodium phenylacetate, solverol, somatomedin binding protein, sonermin, sparfosic acid, spicamycin D, spiromustine, splenopentin, spongistatin 1, squalamine, stem cell inhibitor, stem-cell division inhibitors, stipiamide, stromelysin inhibitors, sulfinosine, superactive vasoactive intestinal peptide antagonist, suradista, suramin, swainsonine, synthetic glycosaminoglycans, tallimustine, tamoxifen methiodide, tauromustine, tazarotene, tecogalan sodium, tegafur, tellurapyrylium, telomerase inhibitors, temoporfin, temozolomide, teniposide, tetrachlorodecaoxide, tetrazomine, thaliblastine, thalidomide, thiocoraline, thrombopoietin, thrombopoietin mimetic, thymalfasin, thymopoietin receptor agonist, thymotrinan, thyroid stimulating hormone, tin ethyl etiopurpurin, tirapazamine, titanocene dichloride, topotecan, topsentin, toremifene, totipotent stem cell factor, translation inhibitors, tretinoin, triacetyluridine, triciribine, trimetrexate, triptorelin, tropisetron, turosteride, tyrosine
kinase inhibitors, tyrphostins, UBC inhibitors, ubenimex, urogenital sinus-derived growth inhibitory factor, urokinase receptor antagonists, vapreotide, variolin B, vector system, erythrocyte gene therapy, velaresol, veramine, verdins, verteporfin, vinorelbine, vinxaltine, vitaxin, vorozole, zanoterone, zeniplatin, zilascorb, or zinostatin stimalamer. In another embodiment of all aspects of the invention, a second treatment is utilized to determine gene expression in a sample from the patient.
In another embodiment of all aspects of the invention, the gene is selected from the group consisting of ABLl, ACTB, ACTNl, ACTN4, ACTR2, ADA, ADAM9, ADAMTSl , ADDl, AD0RA2A, AFlQ, AIFl, AKAPl, AKAP13, AKRlBl , AKRlCl, AKTl , ALDH2, ALDH3 Al, ALDOC, ALG5, ALMSl, ALOX15B, AMIG02, AMPD2, AMPD3, ANAPC5, ANP32A, ANP32B, ANPEP, ANXAl, ANXA2, AP1G2, APOBEC3B, APRT, ARHE, ARHGAP15, ARHGAP25, ARHGDIB, ARHGEF6, ARL7, ASAHl, ASPH, ATF3, ATIC, ATOXl , ATPl B3, ATP2A2, ATP2A3, ATP5D, ATP5G2, ATP6V1B2, B2M, BASPl , BAX, BC008967, BCATl, BCHE, BCLl IB, BDNF, BHLHB2, BIN2, BLM, BLMH, BLVRA, BMIl, BNIP3, BRDT, BRRNl, BTN3A2, BTN3A3, Cl Iorf2, C14orfl39, C15orf25, C18orflO, Clorf24, Clorf29, Clorf38, ClQRl, C22orfl8, C5orω3, C6orf32, CACNAlG, CACNB3, CALDl, CALMl , CALML4, CALU, CAP35O, CAPG, CAPN2, CAPN3, CASP2, CASP6, CASP7, CAST, CBFB, CBLB, CBRl, CBX3, CCL2, CCL21, CCNA2, CCNBlIPl , CCND3, CCR7, CCR9, CCT5, CD151, CDlA, CDlB, CDlC, CDlD, CDlE, CD2, CD28, CD37, CD3D, CD3E, CD3G, CD3Z, CD44, CD47, CD53, CD59, CD6, CD63, CD81, CD8A, CD8B1, CD99, CDClO, CDC14B, CDHl 1, CDH2, CDKL5, CDKN2A, CDW52, CECRl, CENPB, CENTBl, CENTG2, CEPl, CGOl 8, CHRNA3, CHSl , CIAPINl , CKAP4, CKIP-I, CNN3, CNP, COLlAl, COL4A1, COL4A2, COL5A2, COL6A1 , COL6A2, COPA, COPEB, COROlA, COROlC, C0X7B, CPSFl, CRABPl , CREB3L1 , CRIP2, CRK, CRYl, CSDA, CSPG2, CSRPl , CST3, CTBPl, CTGF, CTNNAl, CTSB, CTSC, CTSD, CTSL, CUGBP2, CUTC, CXCLl , CXCR4, CXorf9, CYFIP2, CYLD, CYR61, DATFl, DAZAPl, DBNl , DBT, DCTNl, DDOST, DDX18, DDX5, DGKA, DIAPHl, DIPA, DKCl, DKFZP434J154, DKFZP564C186, DKFZP564G2022, DKFZp564J157, DKFZP564K0822, DNAJClO, DNAPTP6, DOCKlO, D0CK2, DPAGTl, DPEP2, DPYSL3, DSIPI, DUSPl , DUSP3,
DXS9879E, DYRK2, E2F4, ECEl, ECMl , EEFlAl , EEF1B2, EEFlG, EFNB2, EHD2, EIF2S2, EIF3S2, EIF4B, EIF4G3, EIF5A, ELA2B, ELK3, EMP3, ENO2, EPASl , EPB41L4B, ERCC2, ERG, ERP70, EVERl, EVI2A, EVL, EXTl , EZH2, F2R, FABP5, FAD 104, FAM46A, FARSLA, FAT, FAU, FBL, FCGR2A, FCGR2C, FER1L3, FGFRl, FHLl , FHODl , FKBPlA, FKBP9, FLII, FLJ10350, FLJ10539, FLJ10774, FLJ12270, FLJ13373, FLJ20859, FLJ21159, FLJ22457, FLJ35036, FLJ46603, FLNC, FLOTl , FMNLl, FNl, FNBPl, FOLHl, FOXF2, FSCNl, FSTLl, FTHl, FTL, FYB, FYN, G0S2, G6PD, GALIG, GALNT6, GAPD, GAS7, GATA2, GATA3, GFPTl, GIMAP5, GIT2, GJAl, GLRB, GLTSCR2, GLUL, GMDS, GMFG, GNAl 5, GNAI2, GNAQ, GNB2, GNB5, GOT2, GPNMB, GPR65, GPRASPl, GPSM3, GRP58, GSTM2, GTF3A, GTSEl, GYPC, GZMA, GZMB, HlFO, HlFX, H2AFX, H3F3A, HA-I, HCLSl, HEMl, HEXB, HIC, HIST1H4C, HKl, HLA-A, HLA-B, HLA-DRA, HMGAl, HMGB2, HMGN2, HMMR, HNRPAl, HNRPD, HNRPM, HOXA9, HPRTl, HRMTlLl, HSA9761, HSPA5, HSU79274, HTATSFl, HU6800, ICAMl, ICAM2, IER3, IFI16, IFI44, IFITM2, IFITM3, IFRG28, IGFBP2, IGFBP3, IGSF4, IL13RA2, IL21R, IL2RG, IL4R, IL6, IL6R, IL6ST, IL8, IMPDH2, INPP5D, INSIGl , IQGAPl, IQGAP2, IRS2, ITGA3, ITGA5, ITGB2, ITK, ITM2A, JAKl, JARID2, JUNB, K-ALPHA-I , KHDRBSl , KIAA0220, KIAA0355, KIAA0802, KIAA0877, KIAA0922, KIAA1078, KIAAl 128, KIAA1393, KIFCl, KPNBl, LAIRl, LAMBl , LAMB3, LAMRl, LAPTM5, LAT, LBR, LCK, LCPl, LCP2, LDHB, LEFl, LEPREl, LGALSl, LGALS9, LHFPL2, LMNBl, LNK, LOC54103, LOC55831, LOC81558, LOC94105, LONP, LOX, LOXL2, LPHN2, LPXN, LRMP, LRP12, LRRC5, LRRN3, LSTl, LTB, LUM, LY9, LY96, M6PRBP1, MAD2L1BP, MAGEB2, MAL, MANlAl , MAPlB, MAP1LC3B, MAP4K1 , MAPKl, MAPREl, MARCKS, MAZ, MCAM, MCLl, MCM5, MCM7, MDH2, MDK, MDNl , MEF2C, MFNG, MGC17330, MGC21654, MGC2744, MGC4083, MGC8721, MGC8902, MGLL, MIA, MICA, MLPH, MME, MMP2, MPHOSPH6, MPPl, MPZLl, MRP63, MRPL12, MRPS2, MSN, MTlE, MTlK, MUFl, MVP, MYB, MYC, MYL6, MYL9, MYOlB, NAPlLl , NAPl L2, NARF, NARS, NASP, NBLl , NCL, NCOR2, NDN, NDUFABl, NDUFS6, NFIL3, NFKBIA, NID2, NIPA2, NK4, NME4, NME7, NNMT, NOL5A, NOL8, NOMO2, NOTCHl, NPCl, NQOl , NRl D2, NUCB2, NUDC, NUP210,
NUP88, NVL, NXFl , OBFCl , OCRL, OGT, OK/SW-cl.56, OPTN, OXAlL, P2RX5, P4HA1 , PACAP, PAF53, PAFAHl B3, PALM2-AKAP2, PAX6, PBEFl , PCBP2, PCCB, PEAl 5, PFDN5, PFNl , PFN2, PGAMl , PGKl , PHEMX, PHLDAl , PIM2, PITPNCl, PKM2, PLAC8, PLAGLl, PLAU, PLAUR, PLCBl , PLEK2, PLEKHCl , PLOD2, PLSCRl, PNAS-4, PNMA2, P0LR2F, PON2, PPAP2B, PPIA, PPIF, PPPlRl 1, PPP2CB, PRFl, PRGl, PRIMl, PRKCA, PRKCBl, PRKCH, PRKCQ, PRKD2, PRNP, PRP 19, PRPF8, PRPSl, PRSSI l, PRSS23, PSCDBP, PSMB9, PSMC3, PSMC5, PSME2, PTGER4, PTGES2, PTMA, PTOVl , PTP4A3, PTPN7, PTPNSl , PTPRC, PTPRCAP, PTRF, PTS, PURA, PWPl, PYGL, QKI, RAB31, RAB3GAP, RAB7, RAB7L1, RAB9P40, RAC2, RAFTLIN, RAG2, RALY, RAPlB, RASGRP2, RBMX, RBPMS, RCNl, REA, RFC3, RFC5, RGC32, RGS3, RHOC, RHOH, RIMS3, RI0K3, RIPK2, RISl , RNASE6, RNF 144, RNPSl, RPLlO, RPLlOA, RPLl 1, RPL12, RPLl 3, RPLl 3A, RPLl 7, RPLl 8, RPLl 8A, RPL24, RPL3, RPL32, RPL36A, RPL39, RPL7, RPL9, RPLPO, RPLP2, RPSlO, RPSl 1, RPS 15, RPS 15 A, RPS19, RPS2, RPS23, RPS24, RPS25, RPS27, RPS28, RPS4X, RPS4Y1, RPS6, RPS7, RPS9, RRAS, RRAS2, RRBPl, RRM2, RUNXl, RUNX3, S100A13, S100A4, SART3, SATBl, SCAPl , SCARBl, SCARB2, SCN3A, SCTR, SEC31L2, SEC61G, SELL, SELPLG, SEMA4G, SEPT6, SEPTlO, SEPWl, SERPINAl, SERPINBl , SERPINB6, SFRS3, SFRS5, SFRS6, SFRS7, SH2D1A, SH3GL3, SH3TC1, SHDl, SHFMl, SHMT2, SIATl , SKBl, SKP2, SLA, SLC 1A4, SLC20A1, SLC25A15, SLC25A5, SLC39A14, SLC39A6, SLC43A3, SLC4A2, SLC7A11, SLC7A6, SMA3, SMAD3, SMARCD3, SMOX, SMS, SNDl, SNRPA, SNRPB, SNRPB2, SNRPE, SNRPF, SOD2, SOX4, SP 140, SPANXC, SPARC, SPIl, SRF, SRM, SRRMl, SSA2, SSBP2, SSRPl, SSSCAl , STAG3, STATl, STAT4, STAT5A, STCl, STC2, STMNl, STOML2, SUIl, T3JAM, TACCl, TACC3, TAF5, TAGLN, TALI, TAPl , TARP, TBCA, TCF 12, TCF4, TCF7, TFDP2, TFPI, TFRC, TGFBl, TIMM 17A, TIMPl, TJPl, TK2, TM4SF1, TM4SF2, TM4SF8, TM6SF1 , TMEM2, TMEM22, TMSBlO, TMSNB, TNFAIP3, TNFAIP8, TNFRSFlOB, TNFRSFlA, TNFRSF7, TNIK, TNPOl , TOBl, TOMM20, TOP2A, TOX, TPKl, TPM2, TRA@, TRAl, TRAM2, TRB@, TRD@, TRIM, TRIM14, TRIM22, TRIM28, TRIP13, TRPV2, TUBA3, TUBGCP3, TUFM, TUSC3, TXN, TXNDC5, UBASH3A, UBB, UBC, UBE2A, UBE2L6, UBE2S,
UCHLl, UCK2, UCP2, UFDlL, UGCG, UGDH, UGT2B17, ULK2, UMPS, UNG, UROD, USP34, USP4, USP7, VASP, VAVl , VIM, VLDLR, VWF, WARS, WASPIP, WBSCR20A, WBSCR20C, WHSCl , WNT5A, XPOl, ZAP128, ZAP70, ZFP36L1, ZNF32, ZNF335, ZNF593, ZNFNlAl, or ZYX.
The nucleic acid sequence of each listed genes is publicly available through the GenBank or RefSeq database (http://www.ncbi.nlm.nih.gov/sites/gquery). The gene sequences are also included as part of the HG-Ul 33A GeneChip from Affymetrix, Inc.
"Resistant" or "resistance" as used herein means that a cell, a tumor, a patient (e.g., a human), or a living organism is able to withstand treatment, e.g., with a compound, such as a chemotherapeutic agent, or radiation treatment, in that the treatment inhibits the growth of a cell, e.g., a cancer cell, in vitro or in a tumor, patient, or living organism by less than 10%, 20%, 30%, 40%, 50%, 60%, or 70% relative to the growth of a similar cell not exposed to the treatment. Resistance to treatment can be determined by a cell-based assay that measures the growth of treated cells as a function of the cells' absorbance of an incident light beam as used to perform the NCI60 assays described herein. In this example, greater absorbance indicates greater cell growth, and thus, resistance to the treatment. A reduction in growth indicates more resistance to a treatment. By "chemoresistant" or "chemoresistance" is meant resistance to a compound.
"Sensitive" or "sensitivity" as used herein means that a cell, a tumor, a patient (e.g., a human), or a living organism is responsive to treatment, e.g., with a compound, such as a chemotherapeutic agent, or radiation treatment, in that the treatment inhibits the growth of a cell, e.g., a cancer cell, in vitro or in a tumor, patient, or living organism by 70%, 80%, 90%, 95%, 99%, or 100%. Sensitivity to treatment may be determined by a cell-based assay that measures the growth of treated cells as a function of the cells' absorbance of an incident light beam as used to perform the NCI60 assays described herein. In this example, lesser absorbance indicates reduced cell growth, and thus, sensitivity to the treatment. A greater reduction in growth indicates more sensitivity to the treatment. By "chemosensitive" or "chemosensitivity" is meant sensitivity to a compound.
"Complement" of a nucleic acid sequence or a "complementary" nucleic acid
sequence as used herein refers to an oligonucleotide which is in "antiparallel association" when it is aligned with the nucleic acid sequence such that the 5' end of one sequence is paired with the 3' end of the other. Nucleotides and other bases can have complements and may be present in complementary nucleic acids. Bases not commonly found in natural nucleic acids that can be included in the nucleic acids of the present invention include, for example, inosine and 7-deazaguanine. "Complementarity" may not be perfect; stable duplexes of complementary nucleic acids can contain mismatched base pairs or unmatched bases. Skilled artisans can determine duplex stability empirically considering a number of variables including, for example, the length of the oligonucleotide, percent concentration of cytosine and guanine bases in the oligonucleotide, ionic strength, and incidence of mismatched base pairs. Typically, complementarity is determined by comparing contiguous nucleic acid sequences.
When complementary nucleic acid sequences form a stable duplex, they are said to be "hybridized" or to "hybridize" to each other or it is said that "hybridization" has occurred. Nucleic acids are referred to as being "complementary" if they contain nucleotides or nucleotide homologues that can form hydrogen bonds according to Watson-Crick base-pairing rules (e.g., G with C, A with T, or A with U) or other hydrogen bonding motifs such as, for example, diaminopurine with T, 5-methyl C with G, 2-thiothymidine with A, inosine with C, and pseudoisocytosine with G. Anti-sense RNA can be complementary to other oligonucleotides, e.g., mRNA.
"Biomarker" as used herein indicates a transcription product (e.g., RNA, such as an RNA primary transcript, mRNA, tRNA, rRNA, microRNA (miRNA), or complementary RNA or DNA (e.g., cDNA) strands thereof) or a translation product (e.g., a polypeptide or metabolite thereof) of a biomarker gene, as defined herein, whose level of expression indicates the sensitivity or resistance of a cell (e.g., a cancer cell), tissue, organism, or patient (e.g., a human) to a treatment (e.g., chemotherapy, radiation therapy, or surgery).
"Compound" as used herein means a chemical or biological substance, e.g., a drug, a protein, an antibody, or an oligonucleotide, which can be used to treat a disease or which has biological activity in vivo or in vitro. Compounds may or may not be approved by the U.S. Food and Drug Administration (FDA). Preferred compounds
include, e.g., chemotherapy agents that can inhibit cancer growth. Preferred chemotherapy agents include, e.g., Vincristine, Cisplatin, Azaguanine, Etoposide, Adriamycin, Aclarubicin, Mitoxantrone, Mitomycin, Paclitaxel, Gemcitabine, Taxotere, Dexamethasone, Ara-C, Methylprednisolone, Methotrexate, Bleomycin, Methyl-GAG, Carboplatin, 5-FU (5-Fluorouracil), Rituximab (e.g., MABTHERA™), , histone deacetylase (HDAC) inhibitors, and 5-Aza-2'-deoxycytidine (Decitabine). Exemplary radioactive chemotherapeutic agents include compounds containing alpha emitters such as astatine-211 , bismuth-212, bismuth-213, lead-212, radium-223, actinium-225, and thorium-227, beta emitters such as tritium, strontium-90, cesium-137, carbon-11 , nitrogen-13, oxygen-15, fluorine-18, iron-52, cobalt-55, cobalt-60, copper-61, copper- 62, copper-64, zinc-62, zinc-63, arsenic-70, arsenic-71 , arsenic-74, bromine-76, bromine-79, rubidium-82, yttrium-86, zirconium-89, indium- 1 10, iodine- 120, iodine- 124, iodine-129, iodine-131, iodine-125, xenon-122, technetium-94m, technetium-94, technetium-99m, and technetium-99, and gamma emitters such as cobalt-60, cesium- 137, and technetium-99m. Exemplary chemotherapeutic agents also include antibodies such as Alemtuzumab, Daclizumab, Rituximab (e.g., MABTHERA™), Trastuzumab (e.g., HERCEPTIN™), Gemtuzumab, Ibritumomab, Edrecolomab, Tositumomab, CeaVac, Epratuzumab, Mitumomab, Bevacizumab, Cetuximab, Edrecolomab, Lintuzumab, MDX-210, IGN-101, MDX-010, MAb, AME, ABX-EGF, EMD 72 000, Apolizumab, Labetuzumab, ior-tl, MDX-220, MRA, H-11 scFv, Oregovomab, huJ591 MAb, BZL, Visilizumab, TriGem, TriAb, R3, MT-201 , G-250, ACA-125, Onyvax-105, CDP-860, BrevaRex MAb, AR54, IMC-ICl 1, GlioMAb-H, ING-I, Anti-LCG MAbs, MT-103, KSB-303, Therex, KW-2871, Anti-HMI.24, Anti-PTHrP, 2C4 antibody, SGN-30, TRAIL-RI MAb, CAT, Prostate cancer antibody, H22xKi-4, ABX-MAl, Imuteran, and Monopharm-C. Exemplary chemotherapeutic agents also include Acivicin; Aclarubicin; Acodazole Hydrochloride; Acronine; Adozelesin; Adriamycin; Aldesleukin; Altretamine; Ambomycin; A. metantrone Acetate; Aminoglutethimide; Amsacrine; Anastrozole; Anthramycin; Asparaginase; Asperlin; Azacitidine; Azetepa; Azotomycin; Batimastat; Benzodepa; Bicalutamide; Bisantrene Hydrochloride; Bisnafide Dimesylate; Bizelesin; Bleomycin Sulfate; Brequinar Sodium; Bropirimine; Busulfan; Cactinomycin; Calusterone; Camptothecin; Caracemide; Carbetimer;
Carboplatin; Carmustine; Carubicin Hydrochloride; Carzelesin; Cedefingol; Chlorambucil; Cirolemycin; Cisplatin; Cladribine; Combretestatin A-4; Crisnatol Mesylate; Cyclophosphamide; Cytarabine; Dacarbazine; DACA (N- [2- (Dimethyl- amino) ethyl] acridine-4-carboxamide); Dactinomycin; Daunorubicin Hydrochloride; Daunomycin; Decitabine; Dexormaplatin; Dezaguanine; Dezaguanine Mesylate; Diaziquone; Docetaxel; Dolasatins; Doxorubicin; Doxorubicin Hydrochloride; Droloxifene; Droloxifene Citrate; Dromostanolone Propionate; Duazomycin; Edatrexate; Eflornithine Hydrochloride; Ellipticine; Elsamitrucin; Enloplatin; Enpromate; Epipropidine; Epirubicin Hydrochloride; Erbulozole; Esorubicin Hydrochloride; Estramustine; Estramustine Phosphate Sodium; Etanidazole; Ethiodized Oil I 131 ; Etoposide; Etoposide Phosphate; Etoprine; Fadrozole Hydrochloride; Fazarabine; Fenretinide; Floxuridine; Fludarabine Phosphate; Fluorouracil; 5-FdUMP; Flurocitabine; Fosquidone; Fostriecin Sodium; Gemcitabine; Gemcitabine Hydrochloride; Gold Au 198; Homocamptothecin; Hydroxyurea; Idarubicin Hydrochloride; Ifosfamide; Ilmofosine; Interferon Alfa-2a; Interferon Alfa-2b; Interferon Alfa-nl; Interferon Alfa-n3; Interferon Beta-I a; Interferon Gamma-I b; Iproplatin; Irinotecan Hydrochloride; Lanreotide Acetate; Letrozole; Leuprolide Acetate; Liarozole Hydrochloride; Lometrexol Sodium; Lomustine; Losoxantrone Hydrochloride; Masoprocol; Maytansine; Mechlorethamine Hydrochloride; Megestrol Acetate; Melengestrol Acetate; Melphalan; Menogaril; Mercaptopurine; Methotrexate; Methotrexate Sodium; Metoprine; Meturedepa; Mitindomide; Mitocarcin; Mitocromin; Mitogillin; Mitomalcin; Mitomycin; Mitosper; Mitotane; Mitoxantrone Hydrochloride; Mycophenolic Acid; Nocodazole; Nogalamycin;Ormaplatin; Oxisuran; Paclitaxel; Pegaspargase; Peliomycin; Pentamustine; PeploycinSulfate; Perfosfamide; Pipobroman; Piposulfan; Piroxantrone Hydrochloride; Plicamycin; Plomestane; Porfimer Sodium; Porfiromycin; Prednimustine; Procarbazine Hydrochloride; Puromycin; Puromycin Hydrochloride; Pyrazofurin; Rhizoxin; Rhizoxin D; Riboprine; Rogletimide; Safingol; Safingol Hydrochloride; Semustine; Simtrazene; Sparfosate Sodium; Sparsomycin; Spirogermanium Hydrochloride; Spiromustine; Spiroplatin; Streptonigrin; Streptozocin; Strontium Chloride Sr 89; Sulofenur; Talisomycin; Taxane; Taxoid; Tecogalan Sodium; Tegafur; Teloxantrone Hydrochloride; Temoporfin; Teniposide; Teroxirone;
Testolactone; Thiamiprine; Thioguanine; Thiotepa; Thymitaq; Tiazofurin; Tirapazamine; Tomudex; TOP53; Topotecan Hydrochloride; Toremifene Citrate; Trestolone Acetate; Triciribine Phosphate; Trimetrexate; Trimetrexate Glucuronate; Triptorelin; Tubulozole Hydrochloride; Uracil Mustard; Uredepa; Vapreotide; Verteporfin; Vinblastine; Vinblastine Sulfate; Vincristine; Vincristine Sulfate; Vindesine; Vindesine Sulfate; Vinepidine Sulfate; Vinglycinate Sulfate; Vinleurosine Sulfate; Vinorelbine Tartrate; Vinrosidine Sulfate; Vinzolidine Sulfate; Vorozole; Zeniplatin; Zinostatin; Zorubicin Hydrochloride; 2-Chlorodeoxyadenosine; 2' Deoxyformycin; 9-aminocamptothecin; raltitrexed; N-propargyl-5,8-dideazafolic acid; 2chloro-2'-arabino-fluoro-2'-deoxyadenosine; 2-chloro-2'-deoxyadenosine; anisomycin; trichostatin A; hPRL-G129R; CEP-751 ; linomide; sulfur mustard; nitrogen mustard (mechlor ethamine); cyclophosphamide; melphalan; chlorambucil; ifosfamide; busulfan; N-methyl-Nnitrosourea (MNU); N, N'-Bis (2-chloroethyl)-N-nitrosourea (BCNU); N- (2-chloroethyl)-N' cyclohexyl-N-nitrosourea (CCNU); N- (2-chloroethyl)- N'- (trans-4-methylcyclohexyl-N-nitrosourea (MeCCNU); N- (2-chloroethyl)-N'- (diethyl) ethylphosphonate-N-nitrosourea (fotemustine); streptozotocin; diacarbazine (DTIC); mitozolomide; temozolomide; thiotepa; mitomycin C; AZQ; adozelesin; Cisplatin; Carboplatin; Ormaplatin; Oxaliplatin;C 1-973; DWA 21 14R; JM216; JM335; Bis (platinum); tomudex; azacitidine; cytarabine; gemcitabine; 6-Mercaptopurine; 6- Thioguanine; Hypoxanthine; teniposide 9-amino camptothecin; Topotecan; CPT-1 1 ; Doxorubicin; Daunomycin; Epirubicin; darubicin; mitoxantrone; losoxantrone; Dactinomycin (Actinomycin D); amsacrine; pyrazoloacridine; all-trans retinol; 14- hydroxy-retro-retinol; all-trans retinoic acid; N- (4-Hydroxyphenyl) retinamide; 13-cis retinoic acid; 3-Methyl TTNEB; 9-cis retinoic acid; fludarabine (2-F-ara-AMP); and 2- chlorodeoxyadenosine (2-Cda).
Other chemotherapeutic agents include, but are not limited to, 20-pi-l ,25 dihydroxyvitamin D3; 5-ethynyluracil; abiraterone; aclarubicin; acylfulvene; adecypenol; adozelesin; aldesleukin; ALL-TK antagonists; altretamine; ambamustine; amidox; amifostine; aminolevulinic acid; amrubicin; amsacrine; anagrelide; anastrozole; andrographolide; angiogenesis inhibitors; antagonist D; antagonist G; antarelix; anti-dorsalizing morphogenetic protein-1 ; antiandrogen,; antiestrogen;
antineoplaston; antisense oligonucleotides; aphidicolin glycinate; apoptosis gene modulators; apoptosis regulators; apurinic acid; ara-CDP-DL-PTBA; argininedeaminase; asulacrine; atamestane; atrimustine; axinastatin 1 ; axinastatin 2; axinastatin 3; azasetron; azatoxin; azatyrosine; baccatin III derivatives; balanol; batimastat; BCR/ABL antagonists; benzochlorins; benzoylstaurosporine; beta lactam derivatives; beta-alethine; betaclamycin B; betulinic acid; bFGF inhibitor; bicalutamide; bisantrene; bisaziridinylspermine; bisnafide; bistratene A; bizelesin; breflate; bleomycin A2; bleomycin B2; bropirimine; budotitane; buthionine sulfoximine; calcipotriol; calphostin C; camptothecin derivatives (e.g., 10-hydroxy-camptothecin); canarypox IL- 2; capecitabine; carboxamide-amino-triazole; carboxyamidotriazole; CaRest M3; CARN 700; cartilage derived inhibitor; carzelesin; casein kinase inhibitors (ICOS); castanospermine; cecropin B; cetrorelix; chlorins; chloroquinoxaline sulfonamide; cicaprost; cis-porphyrin; cladribine; clomifene analogues; clotrimazole; collismycin A; collismycin B; combretastatin A4; combretastatin analogue; conagenin; crambescidin 816; crisnatol; cryptophycin 8; cryptophycin A derivatives; curacin A; cyclopentanthraquinones; cycloplatam; cypemycin; cytarabine ocfosfate; cytolytic factor; cytostatin; dacliximab; decitabine; dehydrodidemnin B; 2'deoxycoformycin (DCF); deslorelin; dexifosfamide; dexrazoxane; dexverapamil; diaziquone; didemnin B; didox; diethylnorspermine; dihydro-5-azacytidine; 9-dihydrotaxol; dioxamycin; diphenyl spiromustine; discodermolide; docosanol; dolasetron; doxifluridine; droloxifene; dronabinol; duocarmycin SA; ebselen; ecomustine; edelfosine; edrecolomab; eflornithine; elemene; emitefur; epirubicin; epothilones (A, R = H; B, R = Me); epithilones; epristeride; estramustine analogue; estrogen agonists; estrogen antagonists; etanidazole; etoposide; etoposide 4'-phosphate (etopofos); exemestane; fadrozole; fazarabine; fenretinide; filgrastim; finasteride; flavopiridol; flezelastine; fluasterone; fludarabine; fluorodaunorunicin hydrochloride; forfenimex; formestane; fostriecin; fotemustine; gadolinium texaphyrin; gallium nitrate; galocitabine; ganirelix; gelatinase inhibitors; gemcitabine; glutathione inhibitors; hepsulfam; heregulin; hexamethylene bisacetamide; homoharringtonine (HHT); hypericin; ibandronic acid; idarubicin; idoxifene; idramantone; ilmofosine; ilomastat; imidazoacridones; imiquimod; immunostimulant peptides; insulin-like growth factor- 1 receptor inhibitor;
interferon agonists; interferons; interleukins; iobenguane; iododoxorubicin; 4- ipomeanol; irinotecan; iroplact; irsogladine; isobengazole; isohomohalicondrin B; itasetron; jasplakinolide; kahalalide F; lamellarin-N triacetate; lanreotide; leinamycin; lenograstim; lentinan sulfate; leptolstatin; letrozole; leukemia inhibiting factor; leukocyte alpha interferon; leuprolide, estrogen, and progesterone combinations; leuprorelin; levamisole; liarozole; linear polyamine analogue; lipophilic disaccharide peptide; lipophilic platinum compounds; lissoclinamide 7; lobaplatin; lombricine; lometrexol; lonidamine; losoxantrone; lovastatin; loxoribine; lurtotecan; lutetium texaphyrin; lysofylline; lytic peptides; maytansine; mannostatin A; marimastat; masoprocol; maspin; matrilysin inhibitors; matrix metalloproteinase inhibitors; menogaril; merbarone; meterelin; methioninase; metoclopramide; MIF inhibitor; ifepristone; miltefosine; mirimostim; mismatched double stranded RNA; mithracin; mitoguazone; mitolactol; mitomycin analogues; mitonafide; mitotoxin fibroblast growth factor-saporin; mitoxantrone; mofarotene; molgramostim; monoclonal antibody, human chorionic gonadotrophin; monophosphoryl lipid A and myobacterium cell wall skeleton combinations; mopidamol; multiple drug resistance gene inhibitor; multiple tumor suppressor 1 -based therapy; mustard anticancer agent; mycaperoxide B; mycobacterial cell wall extract; myriaporone; N-acetyldinaline; N-substituted benzamides; nafarelin; nagrestip; naloxone and pentazocine combinations; napavin; naphterpin; nartograstim; nedaplatin; nemorubicin; neridronic acid; neutral endopeptidase; nilutamide; nisamycin; nitric oxide modulators; nitroxide antioxidant; nitrullyn; 06-benzylguanine; octreotide; okicenone; oligonucleotides; onapristone; ondansetron; ondansetron; oracin; oral cytokine inducer; ormaplatin; osaterone; oxaliplatin; oxaunomycin; paclitaxel analogues; paclitaxel derivatives; palauamine; palmitoylrhizoxin; pamidronic acid; panaxytriol; panomifene; parabactin; pazelliptine; pegaspargase; peldesine; pentosan polysulfate sodium; pentostatin; pentrozole; perflubron; perfosfamide; perillyl alcohol; phenazinomycin; phenylacetate; phosphatase inhibitors; picibanil; pilocarpine hydrochloride; pirarubicin; piritrexim; placetin A; placetin B; plasminogen activator inhibitor; platinum complex; platinum compounds; platinum-triamine complex; podophyllotoxin; porfimer sodium; porfiromycin; propyl bis-acridone; prostaglandin J2; proteasome inhibitors; protein A-based immune modulator; protein kinase C inhibitor;
protein kinase C inhibitors, microalgal; protein tyrosine phosphatase inhibitors; purine nucleoside phosphorylase inhibitors; purpurins; pyrazoloacridine; pyridoxylated hemoglobin polyoxyethylene conjugate; raf antagonists; raltitrexed; ramosetron; ras farnesyl protein transferase inhibitors; ras inhibitors; ras-GAP inhibitor; retelliptine demethylated; rhenium Re 186 etidronate; rhizoxin; ribozymes; RII retinamide; rogletimide; rohitukine; romurtide; roquinimex; rubiginone B 1; ruboxyl; safϊngol; saintopin; SarCNU; sarcophytol A; sargramostim; Sdi 1 mimetics; semustine; senescence derived inhibitor 1 ; sense oligonucleotides; signal transduction inhibitors; signal transduction modulators; single chain antigen binding protein; sizofiran; sobuzoxane; sodium borocaptate; sodium phenylacetate; solverol; somatomedin binding protein; sonermin; sparfosic acid; spicamycin D; spiromustine; splenopentin; spongistatin 1 ; squalamine; stem cell inhibitor; stem-cell division inhibitors; stipiamide; stromelysin inhibitors; sulfinosine; superactive vasoactive intestinal peptide antagonist; suradista; suramin; swainsonine; synthetic glycosaminoglycans; tallimustine; tamoxifen methiodide; tauromustine; tazarotene; tecogalan sodium; tegafur; tellurapyrylium; telomerase inhibitors; temoporfin; temozolomide; teniposide; tetrachlorodecaoxide; tetrazomine; thaliblastine; thalidomide; thiocoraline; thrombopoietin; thrombopoietin mimetic; thymalfasin; thymopoietin receptor agonist; thymotrinan; thyroid stimulating hormone; tin ethyl etiopurpurin; tirapazamine; titanocene dichloride; topotecan; topsentin; toremifene; totipotent stem cell factor; translation inhibitors; tretinoin; triacetyluridine; triciribine; trimetrexate; triptorelin; tropisetron; turosteride; tyrosine kinase inhibitors; tyrphostins; UBC inhibitors; ubenimex; urogenital sinus-derived growth inhibitory factor; urokinase receptor antagonists; vapreotide; variolin B; vector system, erythrocyte gene therapy; velaresol; veramine; verdins; verteporfin; vinorelbine; vinxaltine; vitaxin; vorozole; zanoterone; zeniplatin; zilascorb; and zinostatin stimalamer.
To "inhibit growth" as used herein means causing a reduction in cell growth in vivo or in vitro by, e.g., 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or 99% or more, as evident by a reduction in the size or number of cells exposed to a treatment (e.g., exposure to a compound), relative to the size or number of cells in the absence of the treatment. Growth inhibition can be the result of a treatment that induces
apoptosis in a cell, induces necrosis in a cell, slows cell cycle progression, disrupts cellular metabolism, induces cell lysis, or induces some other mechanism that reduces the size or number of cells.
"Biomarker gene" as used herein means a gene in a cell (e.g., a cancer cell) the expression of which, as measured by, e.g., detecting the level of one or more biomarkers produced from the gene, correlates to sensitivity or resistance of the cell, tissue, organism, or patient (e.g., a human) to a treatment (e.g., chemotherapy, radiation therapy, or surgery).
"Microarray" as used herein means a device employed by any method that quantifies one or more subject oligonucleotides, e.g., DNA or RNA, or analogues thereof, at a time. One exemplary class of microarrays consists of DNA probes attached to a glass or quartz surface. Many microarrays, e.g., those made by Affymetrix, use several probes for determining the expression of a single gene. The DNA microarray can contain oligonucleotide probes that may be, e.g., full-length cDNAs complementary to an RNA or cDNA fragments that hybridize to part of an RNA. Exemplary RNAs include mRNA, miRNA, and miRNA precursors. Exemplary microarrays also include a "nucleic acid microarray" having a substrate-bound plurality of nucleic acids, hybridization to each of the plurality of bound nucleic acids being separately detectable. The substrate can be solid or porous, planar or non-planar, unitary or distributed. Exemplary nucleic acid microarrays include all of the devices so called in Schena (ed.), DNA Microarrays: A Practical Approach (Practical Approach Series), Oxford University Press (1999); Nature Genet. 21(l)(suppl.):l-60 (1999); and Schena (ed.), Microarray Biochip: Tools and Technology, Eaton Publishing Company/BioTechniques Books Division (2000). Additionally, exemplary nucleic acid microarrays can include a substrate-bound plurality of nucleic acids in which the plurality of nucleic acids is disposed on a plurality of beads, rather than on a unitary planar substrate, as is described, inter alia, in Brenner et al., Proc. Natl. Acad. Sci. USA 97(4): 1665- 1670 (2000). Examples of nucleic acid microarrays may be found in U.S. Patent Nos. 6,391 ,623, 6,383,754, 6,383,749, 6,380,377, 6,379,897, 6,376,191, 6,372,431, 6,351,712 6,344,316, 6,316,193, 6,312,906, 6,309,828, 6,309,824, 6,306,643, 6,300,063, 6,287,850, 6,284,497, 6,284,465, 6,280,954, 6,262,216, 6,251,601,
6,245,518, 6,263,287, 6,251,601 , 6,238,866, 6,228,575, 6,214,587, 6,203,989, 6,171 ,797, 6,103,474, 6,083,726, 6,054,274, 6,040,138, 6,083,726, 6,004,755, 6,001 ,309, 5,958,342, 5,952,180, 5,936,731, 5,843,655, 5,814,454, 5,837,196, 5,436,327, 5,412,087, and 5,405,783, herein incorporated by reference.
Exemplary microarrays can also include "peptide microarrays" or "protein microarrays" having a substrate-bound plurality of polypeptides, the binding of a oligonucleotide, a peptide, or a protein to the plurality of bound polypeptides being separately detectable. Alternatively, the peptide microarray, can have a plurality of binders, including, but not limited to, monoclonal antibodies, polyclonal antibodies, phage display binders, yeast 2 hybrid binders, aptamers, that can specifically detect the binding of specific oligonucleotides, peptides, or proteins. Examples of peptide arrays may be found in International Patent Publication Nos. WO 02/31463, WO 02/25288, WO 01/94946, WO 01/88162, WO 01/68671, WO 01/57259, WO 00/61806, WO 00/54046, WO 00/47774, WO 99/40434, WO 99/39210, and WO 97/42507, and in U.S. Patent Nos. 6,268,210, 5,766,960, and 5,143,854, herein incorporated by reference.
"Gene expression" as used herein means the level of expression of a biomarker gene (e.g,. the level of a transcription product, such as an mRNA, tRNA, or microRNA, or its complement (e.g., a cDNA complement of the transcription product), or a translation product, such as a polypeptide or metabolite thereof) in a cell, tissue, organism, or patient (e.g., a human). Gene expression can be measured by detecting the presence, quantity, or activity of a DNA, RNA, or polypeptide, or modifications thereof (e.g., splicing, phosphorylation, and acetylation) associated with a given gene.
"NCI60" as used herein means a panel of 60 cancer cell lines from lung, colon, breast, ovarian, leukemia, renal, melanoma, prostate, and brain cancers including the following cancer cell lines: NSCLC_NCIH23, NSCLC_NCIH522, NSCLC_A549ATCC, NSCLC_EKVX, NSCLC_NCIH226, NSCLC_NCIH332M, NSCLC_H460, NSCLC_HOP62, NSCLC_HOP92, COLON HT29, COLON_HCC- 2998, COLON_HCT1 16, COLON_SW620, COLON_COLO205, COLON_HCT15, COLON KM 12, BREAST MCF7, BREAST_MCF7ADRr, BREAST MDAMB231 , BREAST HS578T, BREAST MDAMB435, BREAST_MDN, BREAST BT549, BREAST_T47D, OVAR_OVCAR3, OVAR_OVCAR4, 0VAR 0VCAR5,
OVAR_OVCAR8, OVARJGROV 1 , OVAR_SKOV3, LEUK_CCRFCEM, LEUK_K562, LEUK_MOLT4, LEUK_HL60, LEUK RPMI8266, LEUK SR, RENAL_UO31, RENAL_SN12C, RENAL_A498, RENAL_CAKI1 , RENAL RXF393, RENAL_7860, RENAL ACHN, RENAL_TK10, MELAN LOXIMVI, MELAN_MALME3M, MELAN_SKMEL2, MELAN_SKMEL5, MELAN_SKMEL28, MELAN_M14, MELANJJ ACC62, MELAN JJ ACC257, PR0STATE_PC3, PROSTATE_DU145, CNS_SNB19, CNS_SNB75, CNS_U251 , CNS SF268, CNS_SF295, and CNS_SF539.
"Treatment" or "medical treatment" means administering to a patient (e.g., a human) or living organism or exposing to a cell or tumor a compound (e.g., a drug, a protein, an antibody, an oligonucleotide, a chemotherapeutic agent, and a radioactive agent) or some other form of medical intervention used to treat or prevent cancer or the symptoms of cancer (e.g., cryotherapy and radiation therapy). Radiation therapy includes the administration to a patient of radiation generated from sources such as particle accelerators and related medical devices that emit X-radiation, gamma radiation, or electron (Beta radiation) beams. A treatment may further include surgery, e.g., to remove a tumor from a patient or living organism.
Other features and advantages of the invention will be apparent from the following description, drawings, and claims.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 depicts an illustration of the method of identifying biomarkers and predicting patient sensitivity to a medical treatment. The method has an in vitro component where the growth inhibition of a compound or medical treatment is measured on cell lines (6 of the 60 cell lines tested are shown). The gene expression is measured on the same cell lines without compound treatment. Those genes that have a correlation above a certain cutoff (e.g., a preffered cutoff of 0.3, in which a correlation coefficient equal to or greater than the cutoff of 0.3 is deemed statistcally significant by, e.g., cross-validation) to the growth inhibition are termed marker genes and the expression of those genes in vivo, e.g., may predict the sensitivity or resistance of a patient's cancer to a compound or other medical treatment. The in vivo component is
applied to a patient to determine whether or not the treatment will be effective in treating disease in the patient. Here, the gene expression in cells of a sample of the suspected disease tissue (e.g., a tumor) in the patient is measured before or after treatment. The activity of the marker genes in the sample is compared to a reference population of patients known to be sensitive or resistant to the treatment. The expression of marker genes in the cells of the patient known to be expressed in the cells of reference patients sensitive to the treatment indicates that the patient to be treated is sensitive to the treatment and vice versa. Based on this comparison the patient is predicted to be sensitive or resistant to treatment with the compound.
Figure 2 depicts the treatment sensitivity predictions for a 5-year-old American boy with a brain tumor. The subject had surgery to remove the tumor and, based on the analysis of gene expression in cells from a sample of the tumor, the subject was predicted to be chemosensitive to ten chemotherapy drugs. The subject received Vincristine and Cisplatin and survived.
Figure 3 depicts the treatment sensitivity predictions for a 7-month-old American girl with a brain tumor. The subject had surgery to remove the tumor, and based on the analysis of gene expression in cells from a sample of the tumor, the subject was predicted to be chemoresistant to twelve chemotheraphy drugs. The subject received Vincristine and Cisplatin, but passed away 9 months later.
Figure 4 depicts the survival rate of 60 brain cancer patients divided into a group predicted to be chemosensitive to Cisplatin and a group predicted to be chemoresistant to Cisplatin. All patients received Cisplatin after surgery.
Figure 5 depicts the survival rate of 56 lymphoma patients divided into a group predicted to be chemosensitive to Vincristine and Adriamycin and a group predicted to be chemoresistant. All patients received Vincristine and Adriamycin.
Figure 6 depicts the survial rate of 19 lung cancer patients divided into a group predicted to be chemosensitive to Cisplatin and a group predicted to be chemoresistant. All patients received Cisplatin.
Figure 7 depicts the survival rate of 14 diffuse large-B-cell lymphoma (DLBCL) patients divided into a group predicted to be chemosensitive to the drug combination R- CHOP and a group predicted to be chemoresistant. All patients were treated with R-
CHOP.
Figure 8 depicts the predictions of sensitivity or resistance to treatment of a patient diagnosed with DLBCL. Various drug combinations and radiation therapy are considered. The drug combinations (indicated by abbreviations) are those commonly used to treat DLBCL.
Figure 9 depicts the survival rate of 60 brain cancer patients divided into a group predicted to be sensitive to radiation treatment and a group predicted to be resistant. All patients were treated with radiation.
Figure 10 depicts the survival rate of 60 brain cancer patients divided into a group predicted to be sensitive to radiation treatment and a group predicted to be resistant. All patients were treated with radiation. Gene biomarkers used in predicting radiation sensitivity or resistance were obtained using the correlation of the median gene expression measurement to cancer cell growth as opposed to the median of the correlations as employed in Figure 9.
Figure 1 1 depicts the predicted sensitivity of cancer patients to sunitinib. The cancer patients are grouped according to cancer type or origin and cancer types with predicted high sensitivity are labeled.
DETAILED DESCRIPTION
The invention features methods for identifying biomarkers of treatment sensitivity, e.g., chemosensitivity to compounds, or resistance, devices that include the biomarkers, kits that include the devices, and methods for predicting treatment efficacy in a patient (e.g., a human diagnosed with cancer). The kits of the invention include microarrays having oligonucleotide probes that are biomarkers of sensitivity or resistance to treatment (e.g., treatment with a chemotherapeutic agent) that hybridize to nucleic acids derived from or obtained from a subject and instructions for using the device to predict the sensitivity or resistance of the subject to the treatment. The invention also features methods of using the microarrays to determine whether a subject, e.g., a cancer patient, will be sensitive or resistant to treatment with, e.g., a chemotherapy agent. Also featured are methods of identifying biomarkers of sensitivity or resistance to a medical treatment based on the correlation of gene or microRNA
expression to treatment efficacy, e.g., the growth inhibition of cancer cells. Gene or microRNA biomarkers that identify subjects as sensitive or resistant to a treatment can also be identified within patient populations already thought to be sensitive or resistant to that treatment. Thus, the methods, devices, and kits of the invention can be used to identify patient subpopulations that are responsive to a treatment thought to be ineffective for treating disease (e.g., cancer) in the general population. More generally, cancer patient sensitivity to a compound or other medical treatment can be predicted using biomarker expression regardless of prior knowledge about patient responsiveness to treatment. The method according to the present invention can be implemented using software that is run on an apparatus (e.g., a computer) for measuring biomarker expression in connection with a microarray. The microarray (e.g., a DNA microarray), included in a kit for processing a tumor sample from a patient, and the apparatus for reading the microarray and turning the result into a chemosensitivity profile for the patient may be used to implement the methods of the invention.
Microarrays Containing Oligonucleotide Probes
The microarrays of the invention include one or more oligonucleotide probes that have nucleotide sequences that are substantially identical to or substantially complementary to, e.g., at least 5, 8, 12, 20, 30, 40, 60, 80, 100, 150, or 200 consecutive nucleotides (or nucleotide analogues) of the biomarker genes or biomarker gene products (e.g., transcription or translation gene products, such as microRNAs) listed below. The oligonucleotide probes may be, e.g., 5-20, 25, 5-50, 50-100, or over 100 nucleotides long. The oligonucleotide probes may be deoxyribonucleic acids (DNA) or ribonucleic acids (RNA). Consecutive nucleotides within the oligonucleotide probes (e.g., 5-20, 25, 5-50, 50-100, or over 100 consecutive nucleotides), which are used as biomarkers of chemosensitivity, may also appear as consecutive nucleotides in one or more of the genes described herein beginning at or near, e.g., the first, tenth, twentieth, thirtieth, fortieth, fiftieth, sixtieth, seventieth, eightieth, ninetieth, hundredth, hundred- fiftieth, two-hundredth, five-hundredth, or one-thousandth nucleotide of the genes or microRNAs listed in Tables 1-136 below. Column List_2006 of Tables 1-21 indicates the preferred biomarker genes for the compound lists. Column List_Preferred of Tables
1-21 indicates the most preferred biomarker genes. Column List_2005 of Tables 1-21 indicates additional biomarkers employed in Examples 1-8. Column Correlation of Tables 1-21 indicates the correlation coefficient of the biomarker gene expression to cancer cell growth inhibition. Tables 80-136 indicate microRNA biomarkers that can be used to determine a patient's (e.g., a human's) sensitivity to a treatment. The following combinations of biomarkers have been used to detect a patient's sensitivity to the indicated treatment:
a) One or more of the gene sequences SFRS3, CCT5, RPL39, SLC25A5, UBE2S, EEFlAl, RPLP2, RPL24, RPS23, RPL39, RPL18, NCL, RPL9, RPLlOA, RPSlO, EIF3S2, SHFMl, RPS28, REA, RPL36A, GAPD, HNRPAl, RPSI l, HNRPAl , LDHB, RPL3, RPLl 1, MRPLl 2, RPL 18 A, COX7B, and RPS7, preferably gene sequences UBB, RPS4X, S100A4, NDUFS6, B2M, C14orfl39, MANlAl, SLC25A5, RPLlO, RPLl 2, EIF5A, RPL36A, SUIl, BLMH, CTBPl , TBCA, MDH2, and DXS9879E, and most preferably gene sequences RPS4X, S100A4, NDUFS6, C14orfl39, SLC25A5, RPLlO, RPL12, EIF5A, RPL36A, BLMH, CTBPl, TBCA, MDH2, and DXS9879E, whose expression indicates chemosensitivity to Vincristine.
b) One or more of the gene sequences B2M, ARHGDIB, FTL, NCL, MSN, SNRPF, XPOl, LDHB, SNRPF, GAPD, PTPN7, ARHGDIB, RPS27, IFI 16, C5orfl3, and HCLSl, preferably gene sequences ClQRl, HCLSl, CD53, SLA, PTPN7, PTPRCAP, ZNFNlAl, CENTBl, PTPRC, IFI 16, ARHGEF6, SEC31L2, CD3Z, GZMB, CD3D, MAP4K1 , GPR65, PRFl, ARHGAPl 5, TM6SF1, and TCF4, and most preferably gene sequences ClQRl, SLA, PTPN7, ZNFNlAl, CENTBl, IFI 16, ARHGEF6, SEC31L2, CD3Z, GZMB, CD3D, MAP4K1, GPR65, PRFl , ARHGAP 15, TM6SF1 , and TCF4, whose expression indicates chemosensitivity to Cisplatin.
c) One or more of the gene sequences PRPS 1 , DDOST, B2M, SPARC, LGALS 1 , CBFB, SNRPB2, MCAM, MCAM, EIF2S2, HPRTl, SRM, FKBPlA, GYPC, UROD, MSN, HNRPAl, SNDl , COPA, MAPREl, EIF3S2, ATP1B3, EMP3, ECMl, ATOXl , NARS, PGKl, OK/SW-cl.56, FNl, EEFlAl, GNAI2, PRPSl, RPL7, PSMB9,
GPNMB, PPPlRl 1 , MIA, RAB7, VIM, and SMS, preferably gene sequences MSN, SPARC, VIM, SRM, SCARBl , SIATl, CUGBP2, GAS7, ICAMl , WASPIP, ITM2A, PALM2-AKAP2, ANPEP, PTPNSl, MPPl, LNK, FCGR2A, EMP3, RUNX3, EVI2A, BTN3A3, LCP2, BCHE, LY96, LCPl, IFI16, MCAM, MEF2C, SLC1A4, BTN3A2, FYN, FNl, Clorf38, CHSl, CAPN3, FCGR2C, TNIK, AMPD2, SEPT6, RAFTLIN, SLC43A3, RAC2, LPXN, CKIP-I, FLJ10539, FLJ35036, DOCKlO, TRPV2, IFRG28, LEFl, and ADAMTSl, and most preferably gene sequences SRM, SCARBl, SIATl, CUGBP2, ICAMl, WASPIP, ITM2A, PALM2-AKAP2, PTPNSl, MPPl, LNK, FCGR2A, RUNX3, EVI2A, BTN3A3, LCP2, BCHE, LY96, LCPl, IFIl 6, MCAM, MEF2C, SLC 1A4, FYN, ClorOδ, CHSl, FCGR2C, TNIK, AMPD2, SEPT6, RAFTLIN, SLC43A3, RAC2, LPXN, CKIP-I, FLJ10539, FLJ35036, DOCKlO, TRPV2, IFRG28, LEFl , and ADAMTSl, whose expression indicates chemosensitivity to Azaguanine.
d) One or more of the gene sequences B2M, MYC, CD99, RPS24, PPIF, PBEF 1 , and ANP32B, preferably gene sequences CD99, INSIGl , LAPTM5, PRGl, MUFl, HCLSl , CD53, SLA, SSBP2, GNB5, MFNG, GMFG, PSMB9, EVI2A, PTPN7, PTGER4, CXorf9, PTPRCAP, ZNFNlAl, CENTBl , PTPRC, NAPlLl, HLA-DRA, IFI 16, COROlA, ARHGEF6, PSCDBP, SELPLG, LAT, SEC31L2, CD3Z, SH2D1A, GZMB, SCN3A, ITK, RAFTLIN, D0CK2, CD3D, RAC2, ZAP70, GPR65, PRFl, ARHGAPl 5, NOTCHl, and UBASH3A, and most preferably gene sequences CD99, INSIGl, PRGl, MUFl , SLA, SSBP2, GNB5, MFNG, PSMB9, EVI2A, PTPN7, PTGER4, CXorf9, ZNFNlAl , CENTBl, NAPlLl , HLA-DRA, IFI 16, ARHGEF6, PSCDBP, SELPLG, LAT, SEC31L2, CD3Z, SH2D1A, GZMB, SCN3A, RAFTLIN, D0CK2, CD3D, RAC2, ZAP70, GPR65, PRFl , ARHGAP 15, NOTCHl, and UBASH3A, whose expression indicates chemosensitivity to Etoposide.
e) One or more of the gene sequences KIAA0220, B2M, TOP2A, CD99, SNRPE, RPS27, HNRPAl, CBX3, ANP32B, HNRPAl, DDX5, PPIA, SNRPF, and USP7, preferably gene sequences CD99, LAPTM5, ALDOC, HCLSl , CD53, SLA, SSBP2, IL2RG, GMFG, CXorf9, RHOH, PTPRCAP, ZNFNlAl, CENTBl, TCF7, CDlC,
MAP4K1 , CDlB, CD3G, PTPRC, CCR9, COROlA, CXCR4, ARHGEF6, HEMl , SELPLG, LAT, SEC31L2, CD3Z, SH2D1A, CDlA, LAIRl, ITK, TRB@, CD3D, WBSCR20C, ZAP70, IFI44, GPR65, AIFl, ARHGAPl 5, NARF, and PACAP, and most preferably gene sequences CD99, ALDOC, SLA, SSBP2, IL2RG, CXorf9, RHOH, ZNFNlAl , CENTBl, CDlC, MAP4K1, CD3G, CCR9, CXCR4, ARHGEF6, SELPLG, LAT, SEC31L2, CD3Z, SH2D1A, CDlA, LAIRl, TRB@, CD3D, WBSCR20C, ZAP70, IFI44, GPR65, AIFl , ARHGAP 15, NARF, and PACAP, whose expression indicates chemosensitivity to Adriamycin.
f) One or more of the gene sequences RPLP2, LAMRl , RPS25, EIF5A, TUFM, HNRPAl, RPS9, MYB, LAMRl, ANP32B, HNRPAl, HNRPAl, EIF4B, HMGB2, RPS 15 A, and RPS7, preferably gene sequences RPLl 2, RPL32, RPLP2, MYB, ZNFNlAl, SCAPl, STAT4, SP140, AMPD3, TNFAIP8, DDX18, TAF5, FBL, RPS2, PTPRC, D0CK2, GPR65, H0XA9, FLJ 12270, and HNRPD, and most preferably gene sequences RPL 12, RPLP2, MYB, ZNFNlAl, SCAPl, STAT4,
SP 140, AMPD3, TNFAIP8, DDX 18, TAF5, RPS2, DOCK2, GPR65, HOXA9,
FLJ 12270, and HNRPD, whose expression indicates chemosensitivity to Aclarubicin.
g) One or more of the gene sequences ARHGEF6, B2M, TOP2A, TOP2A, ELA2B, PTMA, LMNBl, TNFRSFlA, NAPlLl, B2M, HNRPAl, RPL9, C5orfl3, NCOR2, ANP32B, OK/SW-cl.56, TUBA3, HMGN2, PRPSl, DDX5, PRGl, PPIA, G6PD, PSMB9, SNRPF, and MAPlB, preferably gene sequences PGAMl, DPYSL3, INSIGl , GJAl, BNIP3, PRGl, G6PD, BASPl, PLOD2, LOXL2, SSBP2, Clorf29, TOX, STCl, TNFRSFlA, NCOR2, NAPlLl, LOC94105, COL6A2, ARHGEF6, GAT A3, TFPI, LAT, CD3Z, AFlQ, MAPlB, PTPRC, PRKCA, TRIM22, CD3D, BCATl, IFI44, CCL2, RAB31 , CUTC, NAP1L2, NME7, FLJ21 159, and COL5A2, and most preferably gene sequences PGAMl , DPYSL3, INSIGl , GJAl, BNIP3, PRGl , G6PD, PLOD2, LOXL2, SSBP2, Clorf29, TOX, STCl , TNFRSFlA, NC0R2, NAPlLl, LOC94105, ARHGEF6, GATA3, TFPI, LAT, CD3Z, AFlQ, MAPlB, TRIM22, CD3D, BCATl , IFI44, CUTC, NAP1L2, NME7, FLJ21 159, and COL5A2, whose expression indicates chemosensitivity to Mitoxantrone.
h) One or more of the gene sequences GAPD, GAPD, GAPD, TOP2A, SUIl , TOP2A, FTL, HNRPC, TNFRSFlA, SHCl, CCT7, P4HB, CTSL, DDX5, G6PD, and SNRPF, preferably gene sequences STCl , GPR65, DOCKlO, COL5A2, FAM46A, and LOC54103, and most preferably gene sequences STCl, GPR65, DOCKlO, COL5A2, FAM46A, and LOC54103, whose expression indicates chemosensitivity to Mitomycin.
i) One or more of the gene sequences RPS23, SFRS3, KIAAOl 14, RPL39, SFRS3, LOC51035, RPS6, EXOSC2, RPL35, IFRD2, SMN2, EEFlAl, RPS3, RPS18, and RPS7, preferably gene sequences RPLlO, RPS4X, NUDC, RALY, DKCl , DKFZP564C186, PRP 19, RAB9P40, HSA9761, GMDS, CEPl, IL13RA2, MAGEB2, HMGN2, ALMSl, GPR65, FLJ10774, NOL8, DAZAPl, SLC25A15, PAF53, DXS9879E, PITPNCl, SPANXC, and KIAA1393, and most preferably RPLlO, RPS4X, NUDC, DKCl, DKFZP564C186, PRP 19, RAB9P40, HSA9761, GMDS, CEPl , ILl 3RA2, MAGEB2, HMGN2, ALMSl, GPR65, FLJ 10774, NOL8, DAZAPl, SLC25A15, PAF53, DXS9879E, PITPNCl , SPANXC, and KIAA1393, whose expression indicates chemosensitivity to Paclitaxel.
j) One or more of the gene sequences CSDA, LAMRl , and TUBA3, preferably gene sequences PFNl , PGAMl , K-ALPHA-I, CSDA, UCHLl, PWPl, PALM2- AKAP2, TNFRSFlA, ATP5G2, AFlQ, NME4, and FHODl, and most preferably gene sequences PFNl, PGAMl, K-ALPHA-I, CSDA, UCHLl, PWPl, PALM2-AKAP2, TNFRSFlA, ATP5G2, AFlQ, NME4, and FHODl, whose expression indicates chemosensitivity to Gemcitabine.
k) One or more of the gene sequences RPS23, SFRS3, KIAAOl 14, SFRS3, RPS6, DDX39, and RPS7, preferably gene sequences ANP32B, GTF3A, RRM2, TRIM 14, SKP2, TRIPl 3, RFC3, CASP7, TXN, MCM5, PTGES2, OBFCl , EPB41L4B, and CALML4, and most preferably gene sequences ANP32B, GTF3A, RRM2, TRIM 14, SKP2, TRIPl 3, RFC3, CASP7, TXN, MCM5, PTGES2, OBFCl, EPB41L4B, and CALML4, whose expression indicates chemosensitivity to Taxotere.
1) One or more of the gene sequences IL2RG, H 1 FX, RDBP, ZAP70, CXCR4, TM4SF2, ARHGDIB, CDA, CD3E, STMNl, GNA15, AXL, CCND3, SATBl, EIF5A, LCK, NKX2-5, LAPTM5, IQGAP2, FLII, EIF3S5, TRB, CD3D, HOXB2, GATA3, HMGB2, PSMB9, ATP5G2, COROlA, ARHGDIB, DRAPl, PTPRCAP, RHOH, and ATP2A3, preferably gene sequences IFITM2, UBE2L6, LAPTM5, USP4, ITM2A, ITGB2, ANPEP, CD53, IL2RG, CD37, GPRASPl, PTPN7, CXorf9, RHOH, GIT2, AD0RA2A, ZNFNlAl, GNA15, CEPl, TNFRSF7, MAP4K1, CCR7, CD3G, PTPRC, ATP2A3, UCP2, COROlA, GATA3, CDKN2A, HEMl, TARP, LAIRl, SH2D1A, FLII, SEPT6, HA-I, CREB3L1, ERCC2, CD3D, LSTl, AIFl, ADA, DATFl , ARHGAPl 5, PLAC8, CECRl, LOC81558, and EHD2, and most preferably gene sequences IFITM2, UBE2L6, USP4, ITM2A, IL2RG, GPRASPl, PTPN7, CXorf9, RHOH, GIT2, ZNFNlAl, CEPl, TNFRSF7, MAP4K1, CCR7, CD3G, ATP2A3, UCP2, GATA3, CDKN2A, TARP, LAIRl, SH2D1A, SEPT6, HA-I, ERCC2, CD3D, LSTl, AIFl, ADA, DATFl, ARHGAP15, PLAC8, CECRl , LOC81558, and EHD2, whose expression indicates chemosensitivity to Dexamethasone.
m) One or more of the gene sequences TM4SF2, ARHGDIB, ADA, H2 AFZ, NAPlLl , CCND3, FABP5, LAMRl, REA, MCM5, SNRPF, and USP7, preferably gene sequences ITM2A, RHOH, PRIMl , CENTBl, GNA15, NAPlLl, ATP5G2, GATA3, PRKCQ, SH2D1A, SEPT6, PTPRC, NME4, RPL13, CD3D, CDlE, ADA, and FHODl, and most preferably gene sequences ITM2A, RHOH, PRIMl, CENTBl , NAPlLl , ATP5G2, GATA3, PRKCQ, SH2D1A, SEPT6, NME4, CD3D, CDlE, ADA, and FHODl , whose expression indicates chemosensitivity to Ara-C.
n) One or more of the gene sequences LGALS9, CD7, IL2RG, PTPN7, ARHGEF6, CENTBl, SEPT6, SLA, LCPl, IFITMl, ZAP70, CXCR4, TM4SF2, ZNF91 , ARHGDIB, TFDP2, ADA, CD99, CD3E, CDlC, STMNl , CD53, CD7, GNAl 5, CCND3, MAZ, SATBl, ZNF22, AES, AIFl, MYB, LCK, C5orfl3, NKX2-5, ZNFNlAl, STAT5A, CHI3L2, LAPTM5, MAP4K1, DDXl 1, GPSM3, TRB, CD3D, CD3G, PRKCBl, CDlE, HCLSl , GATA3, TCF7, RHOG, CDW52, HMGB2, DGKA,
ITGB2, PSMB9, IDH2, AES, MCM5, NUCB2, COROlA, ARHGDIB, PTPRCAP, CD47, RHOH, LGALS9, and ATP2A3, preferably gene sequences CD99, SRRMl , ARHGDIB, LAPTM5, VWF, ITM2A, ITGB2, LGALS9, INPP5D, SATBl, CD53, TFDP2, SLA, IL2RG, MFNG, CD37, GMFG, SELL, CDW52, LRMP, ICAM2, RIMS3, PTPN7, ARHGAP25, LCK, CXorf9, RHOH, PTPRCAP, GIT2, ZNFNlAl, CENTBl, LCP2, SPIl, GNAl 5, GZMA, CEPl, BLM, CD8A, SCAPl, CD2, CDlC, TNFRSF7, VAVl, MAP4K1 , CCR7, C6or02, AL0X15B, BRDT, CD3G, PTPRC, LTB, ATP2A3, NVL, RASGRP2, LCPl, COROlA, CXCR4, PRKD2, G AT A3, TRA@, PRKCBl, HEMl, KIAA0922, TARP, SEC31L2, PRKCQ, SH2D1A, CHRNA3, CDlA, LSTl, LAIRl , CACNAlG, TRB@, SEPT6, HA-I, D0CK2, CD3D, TRD@, T3JAM, FNBPl, CD6, AIFl, FOLHl, CDlE, LY9, UGT2B17, ADA, CDKL5, TRIM, EVL, DATFl , RGC32, PRKCH, ARHGAPl 5, NOTCHl, BIN2, SEMA4G, DPEP2, CECRl , BCLl IB, STAG3, GALNT6, UBASH3A, PHEMX, FLJ13373, LEFl, IL21R, MGC17330, AKAP13, ZNF335, and GIMAP5, and most preferably gene sequences CD99, ARHGDIB, VWF, ITM2A, LGALS9, INPP5D, SATBl, TFDP2, SLA, IL2RG, MFNG, SELL, CDW52, LRMP, ICAM2, RIMS3, PTPN7, ARHGAP25, LCK, CXorf9, RHOH, GIT2, ZNFNlAl, CENTBl, LCP2, SPIl, GZMA, CEPl , CD8A, SCAPl , CD2, CDlC, TNFRSF7, VAVl, MAP4K1, CCR7, C6orf32, ALOXl 5B, BRDT, CD3G, LTB, ATP2A3, NVL, RASGRP2, LCPl, CXCR4, PRKD2, GATA3, TRA@, KIAA0922, TARP, SEC31L2, PRKCQ, SH2D1A, CHRNA3, CDlA, LSTl, LAIRl, CACNAlG, TRB@, SEPT6, HA-I, D0CK2, CD3D, TRD@, T3JAM, FNBPl , CD6, AIFl, FOLHl , CDlE, LY9, ADA, CDKL5, TRIM, EVL, DATFl , RGC32, PRKCH, ARHGAPl 5, NOTCHl , BIN2, SEMA4G, DPEP2, CECRl, BCLl IB, STAG3, GALNT6, UBASH3A, PHEMX, FLJ13373, LEFl, IL21R, MGCl 7330, AKAPl 3, ZNF335, and GIMAP5, whose expression indicates chemosensitivity to Methylprednisolone.
o) One or more of the gene sequences RPLP2, RPL4, HMGAl, RPL27, IMPDH2, LAMRl , PTMA, ATP5B, NPMl , NCL, RPS25, RPL9, TRAPl, RPL21, LAMRl , REA, HNRPAl , LDHB, RPS2, NMEl , PAICS, EEF1B2, RPS15A, RPL19, RPL6, ATP5G2, SNRPF, SNRPG, and RPS7, preferably gene sequences PRPF8, RPL 18,
RNPSl, RPL32, EEFlG, GOT2, RPL13A, PTMA, RPS15, RPLP2, CSDA, KHDRBSl, SNRPA, IMPDH2, RPS 19, NUP88, ATP5D, PCBP2, ZNF593, HSU79274, PRIMl, PFDN5, OXAlL, H3F3A, ATIC, RPL13, CIAPINl, FBL, RPS2, PCCB, RBMX, SHMT2, RPLPO, HNRPAl , STOML2, RPS9, SKBl , GLTSCR2, CCNBlIPl, MRPS2, FLJ20859, and FLJ 12270, and most preferably gene sequences PRPF8, RPLl 8, GOT2, RPLl 3 A, RPS 15, RPLP2, CSDA, KHDRBSl, SNRPA, IMPDH2, RPS 19, NUP88, ATP5D, PCBP2, ZNF593, HSU79274, PRIMl, PFDN5, OXAlL, H3F3A, ATIC, CIAPINl, RPS2, PCCB, SHMT2, RPLPO, HNRPAl, STOML2, SKBl, GLTSCR2, CCNBlIPl, MRPS2, FLJ20859, and FLJ 12270, whose expression indicates chemosensitivity to Methotrexate.
p) One or more of the gene sequences ACTB, COL5A1, MTlE, CSDA, COL4A2, MMP2, COLlAl, TNFRSFlA, CFHLl , TGFBI, FSCNl, NNMT, PLAUR, CSPG2, NFIL3, C5orfl3, NCOR2, TUBB4, MYLK, TUB A3, PLAU, COL4A2, COL6A2, COL6A3, IFITM2, PSMB9, CSDA, and COLlAl, preferably gene sequences MSN, PFNl, HKl, ACTR2, MCLl, ZYX, RAPlB, GNB2, EPASl, PGAMl, CKAP4, DUSPl, MYL9, K-ALPHA-I , LGALSl, CSDA, AKRlBl, IFITM2, ITGA5, VIM, DPYSL3, JUNB, ITGA3, NFKBIA, LAMBl, FHLl, INSIGl, TIMPl, GJAl , PSME2, PRGl, EXTl, DKFZP434J154, OPTN, M6PRBP1, MVP, VASP, ARL7, NNMT, TAPl, COLlAl , BASPl, PLOD2, ATF3, PALM2-AKAP2, IL8, ANPEP, LOXL2, TGFBl, IL4R, DGKA, STC2, SEC61G, NFIL3, RGS3, NK4, F2R, TPM2, PSMB9, LOX, STCl , CSPG2, PTGER4, IL6, SMAD3, PLAU, WNT5A, BDNF, TNFRSFlA, FLNC, DKFZP564K0822, FLOTl, PTRF, HLA-B, COL6A2, MGC4083, TNFRSFlOB, PLAGLl, PNM A2, TFPI, LAT, GZMB, CYR61, PLAUR, FSCNl, ERP70, AFlQ, UBC, FGFRl, HIC, BAX, COL4A2, COL6A1, IFITM3, MAPlB, FLJ46603, RAFTLIN, RRAS, FTL, KIAA0877, MTlE, CDClO, DOCK2, TRIM22, RISl, BCATl, PRFl , DBNl , MTlK, TMSBlO, RAB31 , FLJ10350, Clorf24, NME7, TMEM22, TPKl, COL5A2, ELK3, CYLD, ADAMTSl, EHD2, and ACTB, and most preferably gene sequences PFNl, HKl, MCLl, ZYX, RAPlB, GNB2, EPASl , PGAMl , CKAP4, DUSPl , MYL9, K-ALPHA- 1 , LGALS 1 , CSDA, IFITM2, ITGA5, DPYSL3, JUNB, NFKBIA, LAMBl, FHLl, INSIGl, TIMPl, GJAl, PSME2, PRGl,
EXTl, DKFZP434J154, MVP, VASP, ARL7, NNMT, TAPl , PLOD2, ATF3, PALM2- AKAP2, IL8, LOXL2, IL4R, DGKA, STC2, SEC61G, RGS3, F2R, TPM2, PSMB9, LOX, STCl, PTGER4, IL6, SMAD3, WNT5A, BDNF, TNFRSFlA, FLNC, DKFZP564K0822, FLOTl , PTRF, HLA-B, MGC4083, TNFRSFlOB, PLAGLl , PNMA2, TFPI, LAT, GZMB, CYR61 , PLAUR, FSCNl , ERP70, AFlQ, HIC, COL6A1, IFITM3, MAPlB, FLJ46603, RAFTLIN, RRAS, FTL, KIAA0877, MTlE, CDClO, DOCK2, TRIM22, RISl, BCATl, PRFl, DBNl , MTlK, TMSBlO, FLJ10350, Clorf24, NME7, TMEM22, TPKl, COL5A2, ELK3, CYLD, ADAMTSl, EHD2, and ACTB, whose expression indicates chemosensitivity to Bleomycin.
q) One or more of the gene sequences NOS2A, MUCl , TFF3, GPlBB, IGLLl, BATF, MYB, PTPRS, NEFL, AIP, CEL, DGKA, RUNXl, ACTRlA, and CLCNKA, preferably gene sequences PTMA, SSRPl, NUDC, CTSC, AP1G2, PSME2, LBR, EFNB2, SERPINAl, SSSCAl, EZH2, MYB, PRIMl, H2AFX, HMGAl, HMMR, TK2, WHSCl, DIAPHl, LAMB3, DPAGTl , UCK2, SERPINBl, MDNl , BRRNl, G0S2, RAC2, MGC21654, GTSEl, TACC3, PLEK2, PLAC8, HNRPD, and PNAS-4, and most preferably gene sequences SSRPl, NUDC, CTSC, AP1G2, PSME2, LBR, EFNB2, SERPINAl, SSSCAl , EZH2, MYB, PRIMl, H2AFX, HMGAl , HMMR, TK2, WHSCl, DIAPHl, LAMB3, DPAGTl , UCK2, SERPINBl , MDNl , BRRNl, G0S2, RAC2, MGC21654, GTSEl, TACC3, PLEK2, PLAC8, HNRPD, and PNAS-4, whose expression indicates chemosensitivity to Methyl-GAG.
r) One or more of the gene sequences MSN, ITGA5, VIM, TNFAIP3, CSPG2, WNT5A, FOXF2, LOC94105, IFIl 6, LRRN3, FGFRl, DOCKlO, LEPREl, COL5A2, and ADAMTSl, and most preferably gene sequences ITGA5, TNFAIP3, WNT5A, FOXF2, LOC94105, IFI16, LRRN3, DOCKlO, LEPREl, COL5A2, and ADAMTSl, whose expression indicates chemosensitivity to carboplatin.
s) One or more of the gene sequences RPLl 8, RPLlOA, RNPSl , ANAPC5, EEF1B2, RPL13A, RPS15, AKAP1 , NDUFAB1, APRT, ZNF593, MRP63, IL6R, RPLl 3, SART3, RPS6, UCK2, RPL3, RPLl 7, RPS2, PCCB, TOMM20, SHMT2,
RPLPO, GTF3A, STOML2, DKFZp564J157, MRPS2, ALG5, and CALML4, and most preferably gene sequences RPL18, RPLlOA, ANAPC5, EEF1B2, RPL13A, RPS15, AKAPl, NDUFABl , APRT, ZNF593, MRP63, IL6R, SART3, UCK2, RPL17, RPS2, PCCB, TOMM20, SHMT2, RPLPO, GTF3A, STOML2, DKFZp564J157, MRPS2, ALG5, and CALML4, whose expression indicates chemosensitivity to 5-FU(5- Fluorouracil).
t) One or more of the gene sequences ITK, KIFC 1 , VLDLR, RUNX 1 , PAFAH 1B3, HlFX, RNF 144, TMSNB, CRYl, MAZ, SLA, SRF, UMPS, CD3Z, PRKCQ, HNRPM, ZAP70, ADDl, RFC5, TM4SF2, PFN2, BMIl, TUBGCP3, ATP6V1B2, RALY, PSMC5, CDlD, ADA, CD99, CD2, CNP, ERG, MYL6, CD3E, CDlA, CDlB, STMNl, PSMC3, RPS4Y1, AKTl, TALI, GNA15, UBE2A, TCF12, UBE2S, CCND3, PAX6, MDK, CAPG, RAG2, ACTNl, GSTM2, SATBl, NASP, IGFBP2, CDH2, CRABPl, DBNl, CTNNAl, AKRlCl, CACNB3, FARSLA, CASP2, CASP2, E2F4, LCP2, CASP6, MYB, SFRS6, GLRB, NDN, CPSFl, GNAQ, TUSC3, GNAQ, JARID2, OCRL, FHLl , EZH2, SMOX, SLC4A2, UFDlL, SEPWl, ZNF32, HTATSFl, SHDl, PTOVl, NXFl , FYB, TRIM28, BC008967, TRB@, TFRC, HlFO, CD3D, CD3G, CENPB, ALDH2, ANXAl, H2AFX, CDlE, DDX5, ABLl, CCNA2, EN02, SNRPB, GATA3, RRM2, GLUL, TCF7, FGFRl, SOX4, MAL, NUCB2, SMA3, FAT, UNG, ARHGDIB, RUNXl, MPHOSPH6, DCTNl, SH3GL3, VIM, PLEKHCl, CD47, POLR2F, RHOH, ADDl, and ATP2A3, preferably gene sequences ITK, KIFCl, VLDLR, RUNXl , PAF AHl B3, HlFX, RNF 144, TMSNB, CRYl, MAZ, SLA, SRF, UMPS, CD3Z, PRKCQ, HNRPM, ZAP70, ADDl, RFC5, TM4SF2, PFN2, BMIl, TUBGCP3, ATP6V1B2, RALY, PSMC5, CDlD, ADA, CD99, CD2, CNP, ERG, MYL6, CD3E, CDlA, CDlB, STMNl , PSMC3, RPS4Y1, AKTl , TALI, GNA15, UBE2A, TCF12, UBE2S, CCND3, PAX6, MDK, CAPG, RAG2, ACTNl, GSTM2, SATBl , NASP, IGFBP2, CDH2, CRABPl , DBNl, CTNNAl, AKRlCl, CACNB3, FARSLA, CASP2, CASP2, E2F4, LCP2, CASP6, MYB, SFRS6, GLRB, NDN, CPSFl , GNAQ, TUSC3, GNAQ, JARID2, OCRL, FHLl , EZH2, SMOX, SLC4A2, UFDlL, SEPWl, ZNF32, HTATSFl, SHDl , PTOVl, NXFl, FYB, TRIM28, BC008967, TRB@, TFRC, HlFO, CD3D, CD3G, CENPB, ALDH2, ANXAl, H2AFX,
CDlE, DDX5, ABLl, CCNA2, ENO2, SNRPB, GATA3, RRM2, GLUL, TCF7, FGFRl , SOX4, MAL, NUCB2, SMA3, FAT, UNG, ARHGDIB, RUNXl , MPHOSPH6, DCTNl, SH3GL3, VIM, PLEKHCl , CD47, POLR2F, RHOH, ADDl, and ATP2A3, and most preferably gene sequences KIFCl, VLDLR, RUNXl, PAFAH 1 B3, HlFX, RNF 144, TMSNB, CRYl, MAZ, SLA, SRF, UMPS, CD3Z, PRKCQ, HNRPM, ZAP70, ADDl , RFC5, TM4SF2, PFN2, BMIl , TUBGCP3, ATP6V1B2, CDlD, ADA, CD99, CD2, CNP, ERG, CD3E, CDlA, PSMC3, RPS4Y1 , AKTl, TALI, UBE2A, TCF12, UBE2S, CCND3, PAX6, RAG2, GSTM2, SATBl, NASP, IGFBP2, CDH2, CRABPl, DBNl, AKRlCl, CACNB3, CASP2, CASP2, LCP2, CASP6, MYB, SFRS6, GLRB, NDN, GNAQ, TUSC3, GNAQ, JARID2, OCRL, FHLl, EZH2, SMOX, SLC4A2, UFDlL, ZNF32, HTATSFl, SHDl, PTOVl, NXFl, FYB, TRIM28, BC008967, TRB@, HlFO, CD3D, CD3G, CENPB, ALDH2, ANXAl , H2AFX, CDlE, DDX5, CCNA2, ENO2, SNRPB, GATA3, RRM2, GLUL, S0X4, MAL, UNG, ARHGDIB, RUNXl, MPHOSPH6, DCTNl, SH3GL3, PLEKHCl , CD47, P0LR2F, RHOH, and ADDl, whose expression indicates chemosensitivity to Rituximab (e.g., MABTHERA™).
u) One or more of the gene sequences CCL21, ANXA2, SCARB2, MAD2L1BP, CAST, PTS, NBLl, ANXA2, CD151, TRAM2, HLA-A, CRIP2, UGCG, PRSSl 1 , MME, CBRl, LGALSl , DUSP3, PFN2, MICA, FTHl, RHOC, ZAP 128, P0N2, COL5A2, CST3, MCAM, IGFBP3, MMP2, GALIG, CTSD, ALDH3A1, CSRPl , S100A4, CALDl, CTGF, CAPG, HLA-A, ACTNl, TAGLN, FSTLl, SCTR, BLVRA, COPEB, DIPA, SMARCD3, FNl , CTSL, CD63, DUSPl, CKAP4, MVP, PEA15, SlOOAl 3, and ECEl, preferably gene sequences TRAl, ACTN4, WARS, CALMl, CD63, CD81 , FKBPlA, CALU, IQGAPl , CTSB, MGC8721 , STATl, TACCl, TM4SF8, CD59, CKAP4, DUSPl , RCNl , MGC8902, LGALSl , BHLHB2, RRBPl, PKM2, PRNP, PPP2CB, CNN3, ANXA2, IER3, JAKl, MARCKS, LUM, FERl L3, SLC20A1, EIF4G3, HEXB, EXTl , TJPl , CTSL, SLC39A6, RI0K3, CRK, NNMT, COLlAl , TRAM2, ADAM9, DNAJC7, PLSCRl, PRSS23, PLOD2, NPC1, TOBl , GFPTl , IL8, DYRK2, PYGL, LOXL2, KIAA0355, UGDH, NFIL3, PURA, ULK2, CENTG2, NID2, CAP350, CXCLl, BTN3A3, IL6, WNT5A, F0XF2, LPHN2, CDHl 1 ,
P4HA1, GRP58, ACTNl , CAPN2, DSIPI, MAP1LC3B, GALIG, IGSF4, IRS2, ATP2A2, OGT, TNFRSFlOB, KIAAl 128, TM4SF1, RBPMS, RIPK2, CBLB, NRl D2, BTN3A2, SLC7A1 1 , MPZLl , IGFBP3, SS A2, FNl 5 NQOl , ASPH, ASAHl, MGLL, SERPINB6, HSPA5, ZFP36L1, COL4A2, COL4A1, CD44, SLC39A14, NIPA2, FKBP9, IL6ST, DKFZP564G2022, PPAP2B, MAPlB, MAPKl, MYOlB, CAST, RRAS2, QKI, LHFPL2, 38970, ARHE, KIAAl 078, FTL, KIAA0877, PLCBl, KIAA0802, KPNBl, RAB3GAP, SERPINBl, TIMM 17A, SOD2, HLA-A, NOMO2, LOC55831, PHLDAl, TMEM2, MLPH, FAD104, LRRC5, RAB7L1, FLJ35036, DOCKlO, LRP12, TXNDC5, CDC14B, HRMTlLl, COROlC, DNAJClO, TNPOl, LONP, AMIGO2, DNAPTP6, and ADAMTSl, and most preferably gene sequences TRAl, ACTN4, CALMl, CD63, FKBPlA, CALU, IQGAPl, MGC8721, STATl , TACCl , TM4SF8, CD59, CKAP4, DUSPl , RCNl, MGC8902, LGALSl, BHLHB2, RRBPl , PRNP, IER3, MARCKS, LUM, FER1L3, SLC20A1, HEXB, EXTl, TJPl, CTSL, SLC39A6, RIOK3, CRK, NNMT, TRAM2, ADAM9, DNAJC7, PLSCRl, PRSS23, PL0D2, NPCl , TOBl, GFPTl, IL8, PYGL, L0XL2, KIAA0355, UGDH, PURA, ULK2, CENTG2, NID2, CAP350, CXCLl, BTN3A3, IL6, WNT5A, F0XF2, LPHN2, CDHI l, P4HA1, GRP58, DSIPI, MAP1LC3B, GALIG, IGSF4, IRS2, ATP2A2, OGT, TNFRSFlOB, KIAAl 128, TM4SF1, RBPMS, RIPK2, CBLB, NRl D2, SLC7A1 1, MPZLl, SSA2, NQOl, ASPH, ASAHl, MGLL, SERPINB6, HSPA5, ZFP36L1, C0L4A1, CD44, SLC39A14, NIPA2, FKBP9, IL6ST, DKFZP564G2022, PPAP2B, MAPlB, MAPKl , MYOlB, CAST, RRAS2, QKI, LHFPL2, 38970, ARHE, KIAAl 078, FTL, KIAA0877, PLCBl, KIAA0802, RAB3GAP, SERPINBl, TIMM17A, S0D2, HLA-A, N0M02, LOC55831, PHLDAl, TMEM2, MLPH, FAD104, LRRC5, RAB7L1 , FLJ35036, DOCKlO, LRP12, TXNDC5, CDC14B, HRMTlLl , COROlC, DNAJClO, TNPOl , LONP, AMIG02, DNAPTP6, and ADAMTS 1 , whose expression indicates sensitivity to radiation therapy.
v) One or more of the gene sequences FAU, NOL5 A, ANP32A, ARHGDIB, LBR, FABP5, ITM2A, SFRS5, IQGAP2, SLC7A6, SLA, IL2RG, MFNG, GPSM3, PIM2, EVERl , LRMP, ICAM2, RIMS3, FMNLl , MYB, PTPN7, LCK, CXorf9, RHOH, ZNFNlAl , CENTBl , LCP2, DBT, CEPl , IL6R, VAVl , MAP4K1, CD28, PTP4A3,
CD3G, LTB, USP34, NVL, CD8B1, SFRS6, LCPl 5 CXCR4, PSCDBP, SELPLG, CD3Z, PRKCQ, CDlA, GATA2, P2RX5, LAIRl , Clorf38, SH2D1A, TRB@, SEPT6, HA-I , DOCK2, WBSCR20C, CD3D, RNASE6, SFRS7, WBSCR20A, NUP210, CD6, HNRPAl , AIFl, CYFIP2, GLTSCR2, Cl lorf2, ARHGAPl 5, BIN2, SH3TC1, STAG3, TM6SF1, C15orf25, FLJ22457, PACAP, and MGC2744, whose expression indicates sensitivity to an HDAC inhibitor.
w) One or more of the gene sequences CD99, SNRPA, CUGBP2, STAT5A, SLA, IL2RG, GTSEl, MYB, PTPN7, CXorf9, RHOH, ZNFNlAl, CENTBl , LCP2, HIST1H4C, CCR7, APOBEC3B, MCM7, LCPl, SELPLG, CD3Z, PRKCQ, GZMB, SCN3A, LAIRl, SH2D1A, SEPT6, CG018, CD3D, C18orflO, PRFl , AIFl, MCM5, LPXN, C22orfl8, ARHGAPl 5, and LEFl, whose expression indicates sensitivity to 5- Aza-2'-deoxycytidine (Decitabine).
Probes that may be employed on microarrays of the invention include oligonucleotide probes having sequences complementary to any of the biomarker gene or microRNA sequences described above. Additionally, probes employed on microarrays of the invention may also include proteins, peptides, or antibodies that selectively bind any of the oligonucleotide probe sequences or their complementary sequences. Exemplary probes are listed in Tables 22-44, wherein for each treatment listed, the biomarkers indicative of treatment sensitivity, the correlation of biomarker expression to growth inhibition, and the sequence of an exemplary probe (Tables 22-44) to detect biomarker (Tables 1-21) expression are shown.
Identification of Biomarker Genes
The gene expression measurements of the NCI60 cancer cell lines were obtained from the National Cancer Institute and the Massachusetts Institute of Technology (MIT). Each dataset was normalized so that sample expression measured by different chips could be compared. The preferred method of normalization is the logit transformation, which is performed for each gene y on each chip:
logit(y) = log [(y-background) I {saturation -y)],
where background is calculated as the minimum intensity measured on the chip minus 0.1% of the signal intensity range: min-0.001 *(max-min), and saturation is calculated as the maximum intensity measured on the chip plus 0.1% of the signal intensity range: max+0.001 *(max-min). The resulting logit transformed data is then z-transformed to mean zero and standard deviation 1.
Next, gene expression is correlated to cancer cell growth inhibition. Growth inhibition data (GI50) of the NCI60 cell lines in the presence of any one of thousands of tested compounds was obtained from the NCI. The correlation between the logit- transformed expression level of each gene in each cell line and the logarithm of GI50 (the concentration of a given compound that results in a 50% inhibition of growth) can be calculated, e.g., using the Pearson correlation coefficient or the Spearman Rank- Order correlation coefficient. Instead of using GI50s, any other measure of patient sensitivity to a given compound may be correlated to the patient's gene expression. Since a plurality of measurements may be available for a single gene, the most accurate determination of correlation coefficient was found to be the median of the correlation coefficients calculated for all probes measuring expression of the same gene.
The median correlation coefficient of gene expression measured on a probe to growth inhibition or patient sensitivity is calculated for all genes, and genes that have a median correlation above 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 0.95, or 0.99 are retained as biomarker genes. Preferably, the correlation coefficient of biomarker genes will exceed 0.3. This is repeated for all the compounds to be tested. The result is a list of marker genes that correlates to sensitivity for each compound tested.
Predicting Patient Sensitivity or Resistance to Medical Treatment
For a given compound, the biomarker whose expression has been shown to correlate to chemosensitivity can be used to classify a patient, e.g., a cancer patient, as sensitive to a medical treatment, e.g., administration of a chemotherapeutic agent or radiation. Using a tumor sample or a blood sample (e.g., in case of leukemia or lymphoma) from a patient, expression of the biomarker in the cells of the patient in the
presence of the treatment agent is determined (using, for example, an RNA extraction kit, a DNA microarray and a DNA microarray scanner). The biomarker expression measurements are then logit transformed as described above. The sum of the expression measurements of the biomarkers is then compared to the median of the sums derived from a training set population of patients having the same tumor. If the sum of biomarker expression in the patient is closest to the median of the sums of expression in the surviving members of the training set, the patient is predicted to be sensitive to the compound or other medical treatment. If the sum of expression in the patient is closest to the median of the sums of expression in the non-surviving members of the training set, the patient is predicted to be resistant to the compound.
Machine learning techniques such as Neural Networks, Support Vector Machines, K Nearest Neighbor, and Nearest Centroids may also be employed to develop models that discriminate patients sensitive to treatment from those resistant to treatment using biomarker expression as model variables which assign each patient a classification as resistant or sensitive. Machine learning techniques used to classify patients using various measurements are described in U.S. Patent No. 5,822,715; U.S. Patent Application Publication Nos. 2003/0073083, 2005/0227266, 2005/0208512, 2005/0123945, 2003/0129629, and 2002/0006613; and in Vapnik V N. Statistical Learning Theory, John Wiley & Sons, New York, 1998; Hastie et al., 2001, The Elements of Statistical Learning: Data Mining, Inference, and Prediction, Springer, N. Y.; Agresti, 1996, An Introduction to Categorical Data Analysis, John Wiley & Sons, New York; and V. Tresp et al., "Neural Network Modeling of Physiological Processes", in Hanson S. J. et al. (Eds.), Computational Learning Theory and Natural Learning Systems 2, MIT Press, 1994, hereby incorporated by reference.
Other variables can be used to determine relative biomarker expression between a patient (e.g., a cancer patient) and a normal subject (e.g., a control subject), including but not limited to, measurement of biomarker DNA copy number and the identification of biomarker genetic mutations.
A more compact microarray can be designed using only the oligonucleotide probes having measurements yielding the median correlation coefficients with cancer cell growth inhibition. Thus, in this embodiment, only one probe needs to be used to
measure expression of each biomarker.Biomarkers include polypeptides and metabolites thereof. A skilled artisan can use employ assays that measure changes in polypeptide biomarker expression (e.g., Western blot, immunofluorescent staining, and flow cytometry) to determine a patient's sensitivity to a treatment (e.g., chemotherapy, radiation therapy, or surgery).
Identifying a Subpopulation of Patients Sensitive to a Treatment for Cancer
The invention can also be used to identify a subpopulation of patients, e.g., cancer patients, that are sensitive to a compound or other medical treatment previously thought to be ineffective for the treatment of cancer. To this end, genes or microRNAs whose expression correlates to sensitivity to a compound or other treatment can be identified so that patients sensitive to a compound or other treatment may be identified. To identify such biomarkers, gene or microRNA expression within cell lines can be correlated to the growth of those cell lines in the presence of the same compound or other treatment. Preferably, genes or microRNAs whose expression correlates to cell growth with a correlation coefficient exceeding 0.3 may be considered possible biomarkers.
Alternatively, genes or microRNAs can be identified as biomarkers according to their ability to discriminate patients known to be sensitive to a treatment from those known to be resistant. The significance of the differences in gene or microRNA expression between the sensitive and resistant patients may be measured using, e.g., t- tests. Alternatively, naive Bayesian classifiers may be used to identify gene biomarkers that discriminate sensitive and resistant patient subpopulations given the gene expressions of the sensitive and resistant subpopulations within a treated patient population.
The patient subpopulations considered can be further divided into patients predicted to survive without treatment, patients predicted to die without treatment, and patients predicted to have symptoms without treatment. The above methodology may be similarly applied to any of these further defined patient subpopulations to identify biomarkers able to predict a subject's sensitivity to compounds or other treatments for the treatment of cancer.
Patients with elevated expression of biomarkers correlated to sensitivity to a compound or other medical treatment would be predicted to be sensitive to that compound or other medical treatment.
The invention is particularly useful for recovering compounds or other treatments that failed in clinical trials by identifying sensitive patient subpopulations using the gene or microRNA expression methodology disclosed herein to identify biomarkers that can be used to predict clinical outcome.
Kit, Apparatus, and Software for Clinical Use
This invention can also be used to predict patients who are resistant or sensitive to a particular treatment by using a kit that includes a kit for RNA extraction from tumors (e.g., Trizol from Invitrogen Inc.), a kit for RNA amplification (e.g., MessageAmp from Ambion Inc.), a microarray for measuring biomarker expression (e.g., HG-U 133 A GeneChip from Affymetrix Inc.), a microarray hybridization station and scanner (e.g., GeneChip System 3000Dx from Affymetrix Inc.), and software for analyzing the expression of marker genes as described in herein (e.g., implemented in R from R-Project or S-Plus from Insightful Corp.).
Methodology of the In Vitro Cancer Growth Inhibition Screen
The human tumor cell lines of the cancer screening panel are grown in RPMI 1640 medium containing 5% fetal bovine serum and 2 mM L-glutamine. Cells are inoculated into 96 well microtiter plates in 100 μL at plating densities ranging from 5,000 to 40,000 cells/well depending on the doubling time of individual cell lines. After cell inoculation, the microtiter plates are incubated at 37°C, 5% CO 2 , 95% air, and 100% relative humidity for 24 hrs prior to addition of experimental compounds.
After 24 hrs, two plates of each cell line are fixed in situ with TCA, to represent a measurement of the cell population for each cell line at the time of compound addition (Tz). Experimental compounds are solubilized in dimethyl sulfoxide at 400-fold the desired final maximum test concentration and stored frozen prior to use. At the time of compound addition, an aliquot of frozen concentrate is thawed and diluted to twice the desired final maximum test concentration with complete medium containing 50 μg/mL
Gentamicin. Additional four, 10-fold or 1 A log serial dilutions are made to provide a total of five compound concentrations plus control. Aliquots of 100 μL of these different compound dilutions are added to the appropriate microtiter wells already containing 100 μL of medium, resulting in the required final compound concentrations. Following compound addition, the plates are incubated for an additional 48 hrs at 37°C, 5% CO 2 , 95% air, and 100% relative humidity. For adherent cells, the assay is terminated by the addition of cold TCA. Cells are fixed in situ by the gentle addition of 50 μL of cold 50% (w/v) TCA (final concentration, 10% TCA) and incubated for 60 min at 4°C. The supernatant is discarded, and the plates are washed five times with tap water and air-dried. Sulforhodamine B (SRB) solution (100 μL) at 0.4% (w/v) in 1% acetic acid is added to each well, and plates are incubated for 10 min at room temperature. After staining, unbound dye is removed by washing five times with 1% acetic acid and the plates are air-dried. Bound stain is subsequently solubilized with 10 mM trizma base, and the absorbance is read on an automated plate reader at a wavelength of 515 nm. For suspension cells, the methodology is the same except that the assay is terminated by fixing settled cells at the bottom of the wells by gently adding 50 μL of 80% TCA (final concentration, 16 % TCA). Using the seven absorbance measurements [time zero, (Tz), control growth, (C), and test growth in the presence of compound at the five concentration levels (Ti)], the percentage growth is calculated at each of the compound concentrations levels. Percentage growth inhibition is calculated as:
[(Ti-Tz)/(C-Tz)] x 100 for concentrations for which Ti>/=Tz [(Ti-Tz)/Tz] x 100 for concentrations for which Ti<Tz
Three dose response parameters are calculated for each experimental agent. Growth inhibition of 50% (GI50) is calculated from [(Ti-Tz)/(C-Tz)] x 100 = 50, which is the compound concentration resulting in a 50% reduction in the net protein increase (as measured by SRB staining) in control cells during the compound incubation. The compound concentration resulting in total growth inhibition (TGI) is calculated from Ti = Tz. The LC50 (concentration of compound resulting in a 50% reduction in the
measured protein at the end of the compound treatment as compared to that at the beginning) indicating a net loss of cells following treatment is calculated from [(Ti- Tz)/Tz] x 100 = -50. Values are calculated for each of these three parameters if the level of activity is reached; however, if the effect is not reached or is exceeded, the value for that parameter is expressed as greater or less than the maximum or minimum concentration tested.
RNA Extraction and Gene Expression Measurement
Cell/tissue samples are snap frozen in liquid nitrogen until processing. RNA is extracted using e.g., Trizol Reagent (Invitrogen) following manufacturers instructions. RNA is amplified using e.g., MessageAmp kit (Ambion) following manufacturers instructions. Amplified RNA is quantified using e.g., HG-U 133 A GeneChip (Affymetrix) and compatible apparatus e.g., GCS3000Dx (Affymetrix), using manufacturers instructions.
The resulting gene expression measurements are further processed as described in this document. The procedures described can be implemented using R software available from R-Project and supplemented with packages available from Bioconductor.
For many drugs 10-30 biomarkers are sufficient to give an adequate response, thus, given the relatively small number of biomarkers required, procedures, such as quantitative reverse transcriptase polymerase chain reaction (qRT-PCR), can be performed to measure, with greater precision, the amount of biomarker genes expressed in a sample. This will provide an alternative to or a complement to microarrays so that a single companion test, typically more quantitative than microarrays alone, employing biomarkers of the invention can be used to predict sensitivity to a new drug. qRT-PCR can be performed alone or in combination with a microarray described herein. Procedures for performing qRT-PCR are described in, e.g., U.S. Patent No. 7,101,663 and U.S. Patent Application Nos. 2006/0177837 and 2006/0088856. The methods of the invention are readily applicable to newly discovered drugs as well as drugs described herein.
The following examples are provided so that those of ordinary skill in the art can see how to use the methods and kits of the invention. The examples are not
intended to limit the scope of what the inventor regards as their invention.
EXAMPLES
Example 1 : Identification of gene biomarkers for chemosensitivity to common chemotherapy drugs.
DNA chip measurements of the 60 cancer cell lines of the NCI60 data set were downloaded from the Broad Institute (Cambridge, Massachusetts) and logit normalized. Growth inhibition data of thousands of compounds against the same cell lines were downloaded from the National Cancer Institute. Compounds where the difference concentration to achieve 50% in growth inhibition (GI50) was less than 1 log were deemed uninformative and rejected. Each gene's expression in each cell line was correlated to its growth (-log(GI50)) in those cell lines in the presence of a given compound. The median Pearson correlation coefficient was used when multiple expression measurements were available for a given gene, and genes having a median correlation coefficient greater than 0.3 were identified as biomarkers for a given compound.
Example 2: Prediction of treatment sensitivity for brain cancer patients.
DNA chip measurements of gene expression in tumors from 60 brain cancer patients were downloaded from the Broad Institute. All data files were logit normalized. For each of the common chemotherapy drugs Cisplatin, Vincristine, Adriamycine, Etoposide, Aclarubicine, Mitoxantrone and Azaguanine, the gene expression for the marker genes was summed. The sum was normalized by dividing by the standard deviation of all patients and compared to the median of the sums of patients who survived and the median of the sums of patients who died:
Normal i zed S um(compound) = sum(marker genes for compound)/sd(sums of all patients)
Sensitivity(compound) = [NormalizedSum(compound)- median(NormalizedSumdeadpatients(compound))] 2
[NormalizedSum(compound) - median(TslormalizedSumsurvivingpatients(compound))] 2
Figures 2 and 3 show the resulting treatment sensitivity predictions for two of the 60 patients. All patients received Cisplatin and the prediction of survival amongst the 60 patients based on their Cisplatin chemosensitivity yielded the Kaplan-Meier survival curve shown in Figure 4. The expression of the 16 Cisplatin biomarker genes was first reduced to 5 components (dimensions) using Independent Component Analysis (fastICA). Five different classification methods were trained on the five components from the 60 patients: K Nearest Neighbor with K=I, K Nearest Neighbor with K=3, Nearest Centroid, Support Vector Machine, and Neural Network. Chemosensitivity or sensitivity to radiation treatment was predicted by combining the classifications of the five methods wherein each classification method was assigned a single vote: unanimous chemosensitive/treatment sensitive prediction resulted in a prediction of chemosensitive/treatment sensitive. All other predictions resulted in a prediction of chemoresistant/treatment resistant. The performance of the combined classifier was validated using leave-one-out cross validation and the survival of the two predicted groups shown in Figure 4. The survival rate of the patients predicted to be chemosensitive was higher than the patients predicted to be chemoresistant.
Example 3: Prediction of chemosensitivity for lymphoma (DLBCL) patients.
DNA chip measurements of gene expression in the tumors from 56 DLBCL (diffuse large B-cell lymphoma) patients were downloaded from the Broad Institute. All data files were logit normalized. All patients received Vincristine and Adriamycine and the prediction of survival amongst the 56 patients based on their Vincristine and Adriamycine chemosensitivity yielded the Kaplan-Meier survival curve shown in Figure 5. The expression of the 33 Vincristine genes and 16 Adriamycine genes was first reduced to 3 components (dimensions) using Independent Component Analysis (fastICA). Five different classification methods were trained on the independent components from the 56 patients: K Nearest Neighbor with K=I , K Nearest Neighbor with K=3, Nearest Centroid, Support Vector Machine, and Neural Network.
Chemosensitivity was predicted by combining the classifications of the five methods wherein each classification method was assigned a single vote: unanimous chemosensitive prediction resulted in a prediction of chemosensitive. All other predictions resulted in a prediction of chemoresistant. The performance of the combined classifier was validated using leave-one-out cross validation and the survival of the two predicted groups is shown in Figure 5. The survival rate of the patients predicted to be chemosensitive was higher than the patients predicted to be chemoresistant.
Example 4: Prediction of chemosensitivity for lung cancer patients.
DNA chip measurements of gene expression in the tumors from 86 lung cancer (adenocarcinoma) patients was downloaded from the University of Michigan, Ann Arbor. Of the 86 patients, 19 had Stage III of the disease and received adjuvant chemotherapy. Raw data was logit normalized. Instead of the combined classifier described for the brain cancer and lymphoma examples above, the sum of biomarker gene expression was calculated for each patient and used to discriminate chemosensitive and chemoresistant patients. For each patient, the gene expression of the 16 marker genes for Cisplatin sensitivity (all Stage III patients received Cisplatin after surgery) was summed. If the sum was closer to the median of the sums of the surviving patients, the patient was predicted to be sensitive to Cisplatin. If the sum was closest to the median of the sums of the non-surviving patients, the patient was predicted to be resistant to Cisplatin. The survival rates of the two predicted groups are shown in Figure 6. The survival rate of the patients predicted to be chemosensitive was higher than the patients predicted to be chemoresistant.
Example 5: Prediction of Rituximab sensitivity for lymphoma (DLBCL) patients.
The method is not limited to cytotoxic chemicals. It is also applicable to predicting the efficacy of protein therapeutics, such as monoclonal antibodies, approved for treating cancer. For example, the monoclonal antibody Rituximab (e.g., MABTHERA™ and RITUXAN™) was examined. Data for cytotoxicity of Rituximab in cell lines in vitro were obtained from published reports (Ghetie et al., Blood
97(5): 1392-1398, 2001). This cytotoxicity in each cell line was correlated to the expression of genes in these cell lines (downloaded from the NCBI Gene Expression Omnibus database using accession numbers GSE2350, GSE 1880, GDS 181). The identified marker genes were used to predict the sensitivity of DLBCL to Rituximab in a small set of 14 patients treated with Rituximab and CHOP (R-CHOP) (downloaded from NCBI Gene Expression Omnibus under accession number GSE4475). Conversion between different chip types was performed using matching tables available through Affymetrix.
The survival of patients predicted to be sensitive to be R-CHOP is compared to the survival of patients predicted to be resistant to R-CHOP in Figure 7. The survival rate of the patients predicted to be chemosensitive was higher than the patients predicted to be chemoresistant.
To predict the sensitivity toward combination therapies, such as those used to treat Diffuse Large B-cell Lymphoma (DLBCL), patient sensitivity to a particular combination therapy is predicted by combining the marker genes for the individual compounds used in the combination. An example of this is shown in Figure 8, where the predicted sensitivities of one patient towards a number of combination therapies used against DLBCL (identified by their acronyms) are shown: R-CHOP contains Rituximab (e.g., MABTHERA™), Vincristine, Doxorubicin (Adriamycin), Cyclophosphamide, and Prednisolone; R-ICE contains Rituximab, Ifosfamide, Carboplatin, and Etoposide; R-MIME contains Rituximab, Mitoguazone, Ifosfamide, Methotrexate, and Etoposide; CHOEP contains Cyclophosphamide, Doxorubicin, Etoposide, Vincristine and Prednisone; DHAP contains Dexamethasone, Cytarabine (Ara C), and Cisplatin; ESHAP contains Etoposide, Methylprednisolone (Solumedrol), Cytarabine (Ara-C) and Cisplatin; and HOAP-Bleo contains Doxorubicin, Vincristine, Ara C, Prednisone, and Bleomycin.
Example 6: Prediction of radiosensitivity for brain tumor (medulloblastoma) patients.
The method of identifying biomarkers can also be applied to other forms of treatment such as radiation therapy. For example, sensitivity to radiation therapy was predicted for brain tumor patients. Radiation therapy in the form of craniospinal irradiation yielding 2,400-3,600 centiGray (cGy) with a tumor dose of 5,300-7,200 cGy was administered to the brain tumor patients using a medical device that emits beams of radiation. Sensitivity of the 60 cancer cell lines used in the NCI60 dataset to radiation treatment was obtained from published reports. This sensitivity was correlated to the expression of genes in the cell lines as described above to identify marker genes. DNA microarray measurements of gene expression in brain tumors obtained from patients subsequently treated with radiation therapy were obtained from the Broad Institute. The identified gene biomarkers were used to classify the patients as sensitive or resistant to radiation therapy. The survival of the patients in the two predicted categories is shown in Figure 9. The survival rate of the patients predicted to be sensitive to radiation therapy was higher than the patients predicted to be resistant to radiation therapy.
Example 7: Drug rescue.
Every member of a population may not be equally responsive to a particular treatment. For example, new compounds often fail in late clinical trials because of lack of efficacy in the population tested. While such compounds may not be effective in the overall population, there may be subpopulations sensitive to those failed compounds due to various reasons, including inherent differences in gene expression. The method as described herein can be used to rescue failed compounds by identifying a patient subpopulation sensitive to a compound using their gene expression as an indicator. Subsequent clinical trials restricted to a sensitive patient subpopulation may demonstrate efficacy of a previously failed compound within that particular patient subpopulation, advancing the compound towards approval for use in that subpopulation.
To this end, in vitro measurements of the inhibitory effects of a compound on various cancer cell lines are compared to the gene expression of cells. The growth of the cancer cell samples can be correlated to gene expression measurements as described
above. This will identify marker genes that can be used to predict patient sensitivity to the failed compound. Once biomarkers are identified, the expression of biomarker genes in cells obtained from patients can be measured according to the procedure detailed above. The patients are predicted to be responsive or non-responsive to compound treatment according to their gene biomarker expression profile. Clinical effect must then be demonstrated in the group of patients that are predicted to be sensitive to the failed compound.
The method may be further refined if patients responsive to the compound treatment are further subdivided into those predicted to survive without the compound and those predicted to die or suffer a relapse without the compound. Clinical efficacy in the subpopulation that is predicted to die or suffer relapse can be further demonstrated. Briefly, the gene expression at the time of diagnosis of patients who later die from their disease is compared to gene expression at the time of diagnosis of patients who are still alive after a period of time (e.g., 5 years). Genes differentially expressed between the two groups are identified as prospective biomarkers and a model is built using those gene biomarkers to predict treatment efficacy.
Examples of compounds that have failed in clinical trials include Gefinitib (e.g., Iressa, AstraZeneca) in refractory, advanced non-small-cell lung cancer (NSCLC), Bevacizumab (e.g., Avastin, Genentech) in first-line treatment for advanced pancreatic cancer, Bevacizumab (e.g., Avastin, Genentech) in relapsed metastatic breast cancer patients, and Erlotinib (e.g., Tarceva, Genentech) in metastatic non-small cell lung cancer (NSCLC). The method of the invention may be applied to these compounds, among others, so that sensitive patient subpopulations responsive to those compounds may be identified.
Example 8: Median of the correlations versus correlation of the median.
The median of the correlations of the individual probe measurements to cancer cell growth as employed by the invention was compared to the correlation of the median probe measurements: this will determine at which step of the method a median calculation should be performed. In the former, several correlations are calculated for each gene since multiple probes measure a given gene's expression, but only the median
of the correlation coefficients is finally retained to identify biomarkers. In the latter, only one correlation is calculated for each gene because only the median gene expression measurement is considered for each gene. Figure 10 shows the results of using the correlation of the median expression measurements to identify biomarker genes of radiation sensitivity predicting the survival of 60 brain cancer patients. The difference in survival between the group predicted to be radiation sensitive and the group predicted to be radiation resistant in Figure 10 is much smaller than the difference depicted in Figure 9 which employed a median correlation coefficient suggesting that the invention's median of the correlations employed in Figure 9 outperforms the correlation of the median depicted in Figure 10.
If we look at individual marker genes like OMD, the median of the correlation to measured radiosensitivity of cell lines in vitro is 0.32. The correlation of the median, however, is 0.39. Adjusting the cutoff from 0.3 to 0.4 to compensate for the difference does not improve on Figure 10, however.
We have also compared median correlation to weighted voting as proposed by Staunton et al., PNAS 98(19): 10787- 10792, 2001). Weighted voting produced a poor result similar to that of Figure 10, with a P-value of 0.1 1.
Example 9: Other methods of identifying biomarkers.
The examples shown above all rely on the availability of measurements of inhibition by a compound or treatment of the growth of cell lines in vitro. Such measurements may not always be available or practical. In that case an alternative method of identifying biomarkers can be employed. If the target(s) of the compound is/are known, it is possible to build a model based on the gene expression of the known target(s). One example is the drug sunitinib (SUl 1248), for which eight targets are known. Sunitinib inhibits at least eight receptor protein-tyrosine kinases including vascular endothelial growth factor receptors 1-3 (VEGFRl -VEGFR3), platelet-derived growth factor receptors (PDGFRA and PDGFRB), stem cell factor receptor (Kit), Flt-3, and colony-stimulating factor- 1 receptor (CSF-IR). U.S. Patent Application Publication 2006/0040292 mentions prediction of response measuring just two targets, PDGFRA and KIT. Using the sum of the gene expression of four targets it is possible
to predict with more reliability the response to sunitinib. As an example, the predicted sunitinib sensitivity of cell lines HT29, Ul 18, 786, and H226 is 0.24, 2.3, 0.14 and 0.60, respectively, based on the sum of the four targets PDGFRB, KDR, KIT and FLT3. This correlates well with the measured response in mouse xenografts of these cells (correlation coefficient 0.86) as well as with the measured anti-angiogenetic effect measured in mouse xenografts (Potapova et al. Contribution of individual targets to the antitumor efficacy of the multitargeted receptor tyrosine kinase inhibitor SUl 1248 (MoI. Cancer Ther. 5(5): 1280-9, 2006). This is better than a model based only on two targets PDGFRA and KIT (correlaton coefficient 0.56).
This four-gene predictor of sunitinib response can be applied to a large number of tumor samples from patients with different tumors from which gene expression analysis has been performed in order to get an idea of the range of sensitivities within each cancer type as well as which cancer types are most susceptible to treatment with sunitinib. Figure 11 shows just a small fraction of the cancer samples available from www.intgen.org/expo.html. The comparison is based on normalizing the samples in such a way (e.g., logit normalization) that different cancer types become comparable. Sunitinib is currently approved by the FDA for renal cancer and gastrointestinal cancer. Both kidney and colon show a good response in this plot.
Any other drug response response predictor based on gene expression can be tested in the same manner as shown in Figure 1 1.
The approach of identifying biomarkers based on known targets can also be applied to RNA antagonists such as SPC2996 targeted against Bcl-2. A response predictor can be built based on measuring the gene expression of Bcl-2 in samples from cancer patients. The same approach can be used for the targets of all mRN A antagonists or inhibitors.
Example 10: Identifying candidate drugs for a known target.
The methods of the invention described herein can also be used for identifying candidate drugs to a known target. Basically, the method of identifying biomarkers is run backwards in order to identify candidate drugs. If one starts with a known target, the expression of its corresponding gene is determined in the NCI 60 cell lines and
correlated to the measured growth inhibition of all the thousands of drugs tested in the NCI 60 cell lines. This provides a list, ranked by correlation coefficient, of candidate drugs for the target. It is even possible to test new drugs and compare their correlation coefficient to the target gene expression to the correlation coefficients of the already tested drugs.
Example 11: Using microRNAs as biomarkers of drug response.
In recent years it has become clear that microRNAs (miRNA) play an important role in regulating the translation of mRNAs. As such, microRNAs may contain important information relevant for the prediction of drug sensitivity. This information may be complementary to the information contained in mRNA expression. Shown below is the correlation between predicted and measured chemosensitivity of the NCI 60 cell lines. The prediction is based either on mRNA measurements with DNA microarrays as described herein or predictions based on measurements of microRNA concentration (ArrayExpress accession number E-MEXP- 1029) using a microRNA specific microarray (ArrayExpress accession number A-MEXP-620). Whenever more than one probe is used to determine the concentration of a given microRNA, the median correlation procedure is used for calculating correlation between microRNA concentration and -log(GI50).
miRNA mRNA Combined cisplatin 0.16 0.02 0.21
PXDlOl 0.44 0.31 0.50 vincristine 0.06 0.11 0.26 etoposide 0.32 0.41 0.44 adriamycine 0.24 0.22 0.28
As the above table shows, the correlation (determined using leave-one-out cross- validation) is highest when using a combination (linear sum) of microRNA and mRNA predictions. These results suggest that a more accurate drug response predictor can be built using a combination of microRNA and mRNA. It is possible to measure both in
the same experiment, as long as one takes into consideration that microRNAs in general do not have a polyA tail as mRNA does. Only slight modifications to the amplification and labeling methods used for mRNA may be needed to incorporate microRNAs into the analysis. Commercial kits for microRNA extraction, amplification, and labeling are available from suppliers (e.g., Ambion Inc.).
Tables 22A-76A list the microRNA probes that are useful for detection of sensitivity to individual drugs, as determined by their median correlation to -log(GI50) for the indicated drug.
Other Embodiments
All publications and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each independent publication or patent application was specifically and individually indicated to be incorporated by reference. While the invention has been described in connection with specific embodiments thereof, it will be understood that it is capable of further modifications and this application is intended to cover any variations, uses, or adaptations of the invention following, in general, the principles of the invention and including such departures from the present disclosure that come within known or customary practice within the art to which the invention pertains and may be applied to the essential features hereinbefore set forth.
Legend:
List_2006: biomarkers identified in 2006 using the new U133A chip measurements
List_2005: biomarkers listed in 2005 patent filing
HU6800: biomarkers obtained with old HU6800 chip measurements
List_Prior: matching biomakrers in prior art
List_Preferr : Prederred list of biomarkers
Correlation: The correlation of the biomarker to sensitivity to the compound
Table 1. Vincristine biomarkers
List 2006 List_2005 List Prior List Preferr Correlation
[1,1 UBB UBB ~ 0.39
[2,] RPS4X RPS4X 0.34
[3,] S100A4 S100A4 0.32
[4,] NDUFS6 NDUFS6 0.31
[5,] B2M B2M 0.35
[6,] C14orfl39 C14orfl39 0.3
[7,] MANlAl MANlAl 0.33
[8,] SLC25A5 SLC25A5 SLC25A5 0.32
[9,] RPLlO RPLlO 0.38
[10,] RPL12 RPL12 0.31
[12,] RPL36A RPL36A RPL36A 0.3
[13,] SUIl SUIl 0.33
[14,] BLMH BLMH 0.32
[15,] CTBPl CTBPl 0.32
[16,] TBCA TBCA 0.3
[17,] MDH2 MDH2 0.34
[18,] DXS9879E DXS9879E 0.35
[19,] SFRS3
[20,] CCT5
[21,] RPL39
[22,] UBE2S
[23,] EEFlAl
[24,] COX7B
[25,] RPLP2
[26,] RPL24
[27,] RPS23
[28,] RPL18
[29,] NCL
[30,] RPL9
[31,] RPLlOA
[32,] RPSlO
[33,] EIF3S2
[34,] SHFMl
[35,] RPS28
[36,] REA
[37,] GAPD
[38,] HNRPAl
[39,] RPSIl
[40,] LDHB
[41,] RPL3
[42,] RPLIl
[43,] MRPL12
[44,] RPL18A
[45,] RPS7
Fable 2. Cisplatin biomarkers
List 2006 List_2005 List Prior List Preferr Correlation
[1,] ClQRl ClQRl 0.3
[2,] HCLSl HCLSl HCLSl 0.33
[3,] CD53 CD53 0.35
[4,] SLA SLA 0.37
[5,] PTPN7 PTPN7 PTPN7 0.31
[6,] PTPRCAP PTPRCAP 0.32
[7,] ZNFNlAl ZNFNlAl 0.33
[8,] CENTBl CENTBl 0.37
[9,] PTPRC PTPRC 0.36
[10,] IFI16 IFI16 IFI16 0.31
[11,] ARHGEF6 ARHGEF6 0.35
[12,] SEC31L2 SEC31L2 0.32
[13,] CD3Z CD3Z 0.32
[14,] GZMB GZMB 0.3
[15,] CD3D CD3D 0.34
[16,] MAP4Kl MAP4K1 0.32
[17,] GPR65 GPR65 0.39
[18,] PRFl PRFl 0.31
[19,] ARHGAP15 ARHGAP15 0.35
[20,] TM6SF1 TM6SF1 0.41
[21,] TCF4 TCF4 0.4
[22,] GAPD
[23,] ARHGDIB
[24,] RPS27
[25,] C5orfl3
[26,] LDHB
[27,] SNRPF
[28,] B2M
[29,] FTL
[30,] NCL
[31,] MSN
[32,] XPOl
Table 3. Azaguanine biomarkers
List_2006 List_2005 List_Prior List_Preferr Correlation
[1,] MSN MSN MSN 0.36
[2,] SPARC SPARC SPARC 0.48
[3,] VIM VIM VIM 0.47
[4,] SRM SRM SRM 0.32
[5,] SCARBl SCARBl 0.4
[6, ] SIATl SIATl 0.31
[7, ] CUGBP2 CUGBP2 0.37
[8, ] GAS7 GAS7 0.34
[9, ] ICAMl ICAMl 0.43
[10, ] WASPIP WASPIP 0.44
[12, ] PALM2-AKAP2 PALM2-AKAP2 0.31
[13, ] ANPEP ANPEP 0.33
[14, ] PTPNSl PTPNSl 0.39
[15, ] MPPl MPPl 0.32
[16, ] LNK LNK 0.43
[17, ] FCGR2A FCGR2A 0.3
[18, ] EMP3 EMP3 EMP3 0.33
[19, ] RUNX3 RUNX3 0.43
[20, ] EVI2A EVI2A 0.4
[21, ] BTN3A3 BTN3A3 0.4
[22, ] LCP2 LCP2 0.34
[23, ] BCHE BCHE 0.35
[24, ] LY96 LY96 0.47
[25, ] LCPl LCPl 0.42
[26, ] IFI16 IFI16 0.33
[27, ] MCAM MCAM MCAM 0.37
[28, ] MEF2C MEF2C 0.41
[29, ] SLC1A4 SLC1A4 0.49
[30, ] BTN3A2 BTN3A2 0.43
[31, ] FYN FYN 0.31
[32, ] FNl FNl FNl 0.33
[33, ] Clorf38 Clorf38 0.37
[34,] CHSl CHSl 0.33
[35,] CAPN3 CAPN3 0.5
[36,] FCGR2C FCGR2C 0.34
[37,] TNIK TNIK 0.35
[38,] AMPD2 AMPD2 0.3
[39,] SEPT6 SEPT6 0.41
[40,] RAFTLIN RAFTLIN 0.39
[41,] SLC43A3 SLC43A3 0.52
[42,] RAC2 RAC2 0.33
[43,] LPXN LPXN 0.54
[44,] CKIP-I CKIP-I 0.33
[45,] FLJ10539 FLJ10539 0.33
[46,] FLJ35036 FLJ35036 0.36
[47,] DOCKlO DOCKlO 0.3
[48,] TRPV2 TRPV2 0.31
[49,] IFRG28 IFRG28 0.3
[50,] LEFl LEFl 0.31
[51,] ADAMTSl ADAMTSl 0.36
[52,] PRPSl
[53,] DDOST
[54,] B2M
[55,] LGALSl
[56,] CBFB
[57,] SNRPB2
[58,] EIF2S2
[59,] HPRTl
[60,] FKBPlA
[61,] GYPC
[62,] UROD
[63,] HNRPAl
[64,] SNDl
[65,] COPA
[66,] MAPREl
[67,] EIF3S2
[68,] ATP1B3
[69,] ECMl
[70,] ATOXl
[71,] NARS
[72,] PGKl
[73,] OK/SW-cl.56
[74,] EEFlAl
[75,] GNAI 2
[76,] RPL7
[77,] PSMB9
[78,] GPNMB
[79,] PPPlRIl
[80,] MIA
[81,] RAB 7
[82,] SMS
Table 4. Etoposide biomarkers
List_2006 List_2005 List_Prior List_Preferr Correlation
[1,] CD99 CD99 CD99 0.3
[2,] INSIGl INSIGl 0.35
[3,] LAPTM5 LAPTM5 0.32
[4,] PRGl PRGl 0.34
[5,] MUFl MUFl 0.35
[6,] HCLSl HCLSl 0.33
[7,] CD53 CD53 0.32
[8,] SLA SLA 0.37
[9,] SSBP2 SSBP2 0.37
[10,] GNB5 GNB5 0.35
[11,1 MFNG MFNG 0.33
[12,] GMFG GMFG 0.32
[13,] PSMB9 PSMB9 0.31
[14,] EVI2A EVI2A 0.41
[15,] PTPN7 PTPN7 0.3
[16,] PTGER4 PTGER4 0.3
[17,] CXorf9 CXorf9 0.3
[18,] PTPRCAP PTPRCAP 0.3
[19,] ZNFNlAl ZNFNlAl 0.35
[20,] CENTBl CENTBl 0.3
[21,] PTPRC PTPRC 0.31
[22,] NAPlLl NAPlLl 0.31
[23,] HLA-DRA HLA-DRA 0.34
[24,] IFI16 IFI16 0.38
[25,] COROlA COROlA 0.3
[26,] ARHGEF6 ARHGEF6 0.33
[27,] PSCDBP PSCDBP 0.4
[28,] SELPLG SELPLG 0.35
[29,] LAT LAT 0.3
[30,] SEC31L2 SEC31L2 0.42
[31,] CD3Z CD3Z 0.36
[32,] SH2D1A SH2D1A 0.33
[33,] GZMB GZMB 0.34
[34,] SCN3A SCN3A 0.3
[35,] ITK ITK 0.35
[36,] RAFTLIN RAFTLIN 0.39
[37,] DOCK2 DOCK2 0.33
[38,] CD3D CD3D 0.31
[39,] RAC2 RAC2 0.34
[40,] ZAP70 ZAP70 0.35
[41,] GPR65 GPR65 0.35
[42,] PRFl PRFl 0.32
[43,] ARHGAP15 ARHGAPl 5 0.32
[44,] NOTCHl NOTCHl 0.31
[45,] UBASH3A UBASH3A 0.32
[46,] B2M
[47,] MYC
[48,] RPS24
[49,] PPIF
[50,] PBEFl
[51,] ANP32B
Table 5. Adriamycin biomarkers
List 2006 List 2005 List Prior List Preferr Correlation
[1,] CD99 CD99 CD99 0.41
[2,] LAPTM5 LAPTM5 0.39
[3,] ALDOC ALDOC 0.31
[4,] HCLSl HCLSl 0.32
[5,] CD53 CD53 0.31
[6,] SLA SLA 0.35
[7,] SSBP2 SSBP2 0.34
[8,] IL2RG IL2RG 0.38
[9,] GMFG GMFG 0.32
[10,] CXorf9 CXorf9 0.32
[11,] RHOH RHOH 0.31
[12,] PTPRCAP PTPRCAP 0.32
[13,] ZNFNlAl ZNFNlAl 0.43
[14,] CENTBl CENTBl 0.36
[15,] TCF7 TCF7 0.32
[16,] CDlC CDlC 0.3
[17 < π_,] MAP4K1 MAP4K1 0.35
[18,] CDlB CDlB 0.39
[19,] CD3G CD3G 0.31
[20,] PTPRC PTPRC 0.38
[21,] CCR9 CCR9 0.34
[22,] COROlA COROlA 0.38
[23,] CXCR4 CXCR4 0.3
[24,] ARHGEF6 ARHGEF6 0.31
[25,] HEMl HEMl 0.32
[26,] SELPLG SELPLG 0.31
[27,] LAT LAT 0.31
[28,] SEC31L2 SEC31L2 0.33
[29,] CD3Z CD3Z 0.37
[30,] SH2D1A SH2D1A 0.37
[31,] CDlA CDlA 0.4
[32,] LAIRl LAIRl 0.39
[33,] ITK ITK 0.3
[34,] TRB@ TRB@ 0.34
[35,] CD3D CD3D 0.33
[36,] WBSCR20C WBSCR20C 0.34
[37,] ZAP70 ZAP70 0.33
[38,] IFI44 IFI44 0.32
[39,] GPR65 GPR65 0.31
[40,] AIFl AIFl 0.3
[41,] ARHGAP15 ARHGAP15 0.37
[42,] NARF NARF 0.3
[43,] PACAP PACAP 0.32
[44,] KIAA0220
[45,] B2M
[46,] TOP2A
[47,] SNRPE
[48,] RPS27
[49, ] HNRPAl
[50,] CBX3
[51,] ANP32B
[52,] DDX5
[53,] PPIA
[54,] SNRPF
[55,] USP7
Table 6. Aclarubicin biomarkers
List 2006 List 2005 List Prior List Preferr Correlation
[1,] RPL12 RPL12 0.3
[2,] RPL32 RPL32 0.37
[3,] RPLP2 RPLP2 RPLP2 0.37
[4,] MYB MYB MYB 0.31
ZNFNlAl ZNFNlAl 0.34
[6,] SCAPl SCAPl 0.33
[7,] STAT4 STAT4 0.31
[8,] SP140 SP140 0.4
[9,] AMPD3 AMPD3 0.3
10,] TNFAIP8 TNFAIP8 0.4
11,] DDX18 DDXl8 0.31
[12,] TAF5 TAF5 0.3
[13,] FBL FBL 0. 41
[14,] RPS2 RPS2 0. 34
[15,] PTPRC PTPRC 0. 37
[16,] DOCK2 DOCK2 0. 32
[17,] GPR65 GPR65 0. 35
[18,] HOXA9 HOXA9 0. 33
[19,] FLJ12270 FLJ12270 0. 31
[20,] HNRPD HNRPD 0. 4
[21,] LAMRl
[22,] RPS25
[23,] EIF5A
[24,] TUFM
[25,] HNRPAl
[26,] RPS9
[27,] ANP32B
[28,] EIF4B
[29,] HMGB2
[30,] RPS15A
[31,] RPS7
Table 7. Mitoxantrone biomarkers
List 2006 List 2005 List Prior List Preferr Correlation
[1,] PGAMl PGAMl 0.32
[2,] DPYSL3 DPYSL3 0.36
[3,] INSIGl INSIGl 0.32
[4,] GJAl GJAl 0.31
[5,] BNIP3 BNIP3 0.31
[6,] PRGl PRGl PRGl 0.39
[7,] G6PD G6PD G6PD 0.34
[8,] BASPl BASPl 0.31
[9,] PLOD2 PLOD2 0.34
[10,] LOXL2 LOXL2 0.31
[11,] SSBP2 SSBP2 0.36
[12,] Clorf29 Clorf29 0.35
[13,] TOX TOX 0.35
[14,] STCl STCl 0.39
[15,] TNFRSFlA TNFRSFlA TNFRSFlA 0.34
[16,] NCOR2 NCOR2 NCOR2 0.3
[17,] NAPlLl NAPlLl NAPlLl 0.32
[18,] LOC94105 LOC94105 0.34
[19,] COL6A2 COL6A2 0.3
[20,] ARHGEF6 ARHGEF6 ARHGEF6 0.34
[21,] GATA3 GATA3 0.35
[22,] TFPI TFPI 0.31
[23,] LAT LAT 0.31
[24,] CD3Z CD3Z 0.37
[25,] AFlQ AFlQ 0.33
[26,] MAPlB MAPlB MAPlB 0.34
[27,] PTPRC PTPRC 0.31
[28,] PRKCA PRKCA 0.35
[29,] TRIM22 TRIM22 0.3
[30,] CD3D CD3D 0.31
[31,] BCATl BCATl 0.32
[32,] IFI44 IFI44 0.33
[33,] CCL2 CCL2 0.37
[34,] RAB31 RAB 31 0.31
[35,] CUTC CUTC 0.33
[36,] NAP1L2 NAP1L2 0.33
[3,] NUDC NUDC 0.3
[4,] RALY RALY 0.31
[5,] DKCl DKCl 0.3
[6,] DKFZP564C186 DKFZP564C186 0.32
[7,] PRP19 PRP19 0.31
[8,] RAB9P40 RAB9P40 0.33
[9,] HSA9761 HSA9761 0.37
[10,] GMDS GMDS 0.3
[H,] CEPl CEPl 0.3
[12,] IL13RA2 IL13RA2 0.34
[13,] MAGEB2 MAGEB2 0.41
[14, ] HMGN2 HMGN2 0.35
[15,] ALMSl ALMSl 0.3
[16,] GPR65 GPR65 0.31
[17,] FLJ10774 FLJ10774 0.31
[18,] NOL8 NOL8 0.31
[19,] DAZAPl DAZAPl 0.32
[20,] SLC25A15 SLC25A15 0.31
[21,] PAF53 PAF53 0.36
[22,] DXS9879E DXS9879E 0.31
[23,] PITPNCl PITPNCl 0.33
[24,] SPANXC SPANXC 0.3
[25,] KIAA1393 KIAA1393 0.33
Table 10. Gemcitabine (Gemzar) biomarkers
List_2006 HU6800 List_Prior List_Preferr Correlation
[1,] PFNl PFNl 0.37 [2,] PGAMl PGAMl 0.35 [3,] K-ALPHA-I K-ALPHA-I 0.34 [4,] CSDA CSDA 0.31 [5,] UCHLl UCHLl 0.36 [6,] PWPl PWPl 0.37 [7,] PALM2-AKAP2 PALM2-AKAP2 0.31 [8,] TNFRSFlA TNFRSFlA 0.31
Table 11. Taxotere (docetaxel) biomarkers
List 2006 List 2005 List Prior List Preferr Correlation
[1,] ANP32B ANP32B 0, 45
[2,] GTF3A GTF3A 0, 31
[3,] RRM2 RRM2 0.31
[4,] TRIM14 TRIM14 0.31
[5,] SKP2 SKP2 0.33
[6,] TRIP13 TRIP13 0.36
[7,] RFC3 RFC3 0.45
[8,] CASP7 CASP7 0.32
[9,] TXN TXN 0.36
[10,] MCM5 MCM5 0.34
[H,] PTGES2 PTGES2 0.39
[12,] OBFCl OBFCl 0.37
[13,] EPB41L4B EPB41L4B 0.32
[14,] CALML4 CALML4 0.31
Table 12. Dexamethasone biomarkers
List_2006 HU6800 List_Prior List_Preferr Correlation
[1,] IFITM2 IFITM2 0.38 [2,] UBE2L6 UBE2L6 0.32 [3,] LAPTM5 LAPTM5 LAPTM5 0.36 [4,] USP4 USP4 0.33 [5,] ITM2A ITM2A 0.38 [6,] ITGB2 ITGB2 0.42 [7,] ANPEP ANPEP 0.31 [8,] CD53 CD53 0.34 [9,] IL2RG IL2RG IL2RG 0.36 [10,] CD37 CD37 0.34
[ H / ] GPRASPl GPRASPl 0.36 [ 12 , ] PTPN7 PTPN7 0.31 [ 13 , ] CXorf9 CXorf9 0.36 [ 14 , ] RHOH RHOH RHOH 0.33 [ 15 , ] GIT2 GIT2 0.31 [ 16 , ] ADORA2A ADORA2A 0.31 [ 17 , ] ZNFNlAl ZNFNlAl 0.35
[18,] GNAl5 GNAl5 GNAl5 0.33 [19,] CEPl CEPl 0.31 [20,] TNFRSF7 TNFRSF7 0.46 [21,] MAP4K1 MAP4K1 0.3 [22,] CCR7 CCR7 0.33 [23,] CD3G CD3G 0.35 [24,] PTPRC PTPRC 0.41 [25,] ATP2A3 ATP2A3 ATP2A3 0.4 [26,] UCP2 UCP2 0.3 [27,] COROlA COROlA COROlA 0.39 [28,] GATA3 GATA3 GATA3 0.37 [29,] CDKN2A CDKN2A 0.32 [30,] HEMl HEMl 0.3 [31,] TARP TARP 0.3 [32,] LAIRl LAIRl 0.34 [33,] SH2D1A SH2D1A 0.34 [34,] FLII FLII FLII 0.33 [35,] SEPT6 SEPT6 0.34 [36, ] HA-I HA-I 0.34 [37,] CREB3L1 CREB3L1 0.31 [38,] ERCC2 ERCC2 0.65 [39,] CD3D CD3D CD3D 0.32 [40,] LSTl LSTl 0.39 [41,] AIFl AIFl 0.35 [42,] ADA ADA 0.33 [43,] DATFl DATFl 0.41 [44,] ARHGAPl5 ARHGAP15 0.3 [45,] PLAC8 PLAC8 0.31 [46,] CECRl CECRl 0.31 [47,] LOC81558 LOC81558 0.33 [48,] EHD2 EHD2 0.37
Table 13. Ara-C (Cytarabine hydrochloride) biomarkers
List_2006 HU6800 List Prior List Preferr Correlation
[1,] ITM2A ITM2A 0.32
[2,] RHOH RHOH 0.31
[3,] PRIMl PRIMl 0.3
[4,] CENTBl CENTBl 0.31
[5,] GNAl5 GNAl5 0.32
[6,] NAPlLl NAPlLl NAPlLl 0.31
[7,] ATP5G2 ATP5G2 0.31
[8,] GATA3 GATA3 0.33
[9,] PRKCQ PRKCQ 0.32
[10,] SH2D1A SH2D1A 0.3
[11,] SEPT6 SEPT6 0.42
[12,] PTPRC PTPRC 0.35
[13,] NME4 NME4 0.33
[14,] RPL13 RPL13 0.3
[15,] CD3D CD3D 0.31
[16,] CDlE CDlE 0.32
[17,] ADA ADA ADA 0.34
[18,] FHODl FHODl 0.31
Table 14. Methylprednisolone biomarkers
List_2006 HU6800 List_Prior List_Preferr Correlation [1,] CD99 CD99 CD99 0.31
[2,] SRRMl SRRMl 0.31
[3,] ARHGDIB ARHGDIB ARHGDIB 0.31
[4,] LAPTM5 LAPTM5 LAPTM5 0.37
[5,] VWF VWF 0.45
[6,] ITM2A ITM2A 0.35
[7,] ITGB2 ITGB2 ITGB2 0.43
[8,] LGALS9 LGALS9 LGALS9 0.43
[9,] INPP5D INPP5D 0.34
[10,] SATBl SATBl SATBl 0.32
[H,] CD53 CD53 CD53 0.33
[12,] TFDP2 TFDP2 TFDP2 0.4
[13,] SLA SLA SLA 0.31
[14,] IL2RG IL2RG IL2RG 0.3
[15,] MFNG MFNG 0.3
[16,] CD37 CD37 0.37
[17,] GMFG GMFG 0.4
[18,] SELL SELL 0.33
[19,] CDW52 CDW52 CDW52 0.33
[20,] LRMP LRMP 0.32
[21,] ICAM2 ICAM2 0.38
[22,] RIMS3 RIMS3 0.36
[23,] PTPN7 PTPN7 PTPN7 0.39
[24,] ARHGAP25 ARHGAP25 0.37
[25,] LCK LCK LCK 0.3
[26,] CXorf9 CXorf9 0.3
[27,] RHOH RHOH RHOH 0.51
[28,] PTPRCAP PTPRCAP PTPRCAP 0.5
[29,] GIT2 GIT2 0.33
[30,] ZNFNlAl ZNFNlAl ZNFNlAl 0.53
[31, ] CENTBl CENTBl CENTBl 0.36
[32,] LCP2 LCP2 0.34
[33,] SPIl SPIl 0.3
[34,] GNAl 5 GNAl 5 GNAl5 0.39
[35,] GZMA GZMA 0.31
[36,] CEPl CEPl 0.37
[37,] BLM BLM 0.33
[38,] CD8A CD8A 0.38
[39,] SCAPl SCAPl 0.32
[40,] CD2 CD2 0.48
[41,] CDlC CDlC CDlC 0.37
[42,] TNFRSF7 TNFRSF7 0.31
[43,] VAVl VAVl 0.41
[44,] MAP4K1 MAP4K1 MAP4K1 0.36
[45,] CCR7 CCR7 0.37
[46,] C6orf32 C6orf32 0.38
[47,] ALOX15B AL0X15B 0.43
[48,] BRDT BRDT 0.33
[49,] CD3G CD3G CD3G 0.51
[50,] PTPRC PTPRC 0.37
[51,] LTB LTB 0.32
[52,] ATP2A3 ATP2A3 ATP2A3 0.3
[53,] NVL NVL 0.31
[54, ] RASGRP2 RASGRP2 0.35
[55,] LCPl LCPl LCPl 0.34
[56,] COROlA COROlA COROlA 0.41
[57,] CXCR4 CXCR4 CXCR4 0.3
[58,] PRKD2 PRKD2 0.33
[59,] GATA3 GATA3 GATA3 0.39
[60,] TRA@ TRAg 0.4
[61,] PRKCBl PRKCBl PRKCBl 0.35
[62,] HEMl HEMl 0.32
[63,] KIAA0922 KIAA0922 0.36
[64,] TARP TARP 0.49
[65,] SEC31L2 SEC31L2 0.32
[66,] PRKCQ PRKCQ 0.37
[67,] SH2D1A SH2D1A 0.33
[68,] CHRNA3 CHRNA3 0.5
[69,] CDlA CDlA 0.44
[70,] LSTl LSTl 0.36
[71,] LAIRl LAIRl 0.47
[72,] CACNAlG CACNAlG 0.33
[73,] TRB@ TRB@ TRB@ 0.31
[74,] SEPT6 SEPT6 SEPT6 0.33
[75,] HA-I HA-I 0.42
[76,] DOCK2 DOCK2 0.32
[77,] CD3D CD3D CD3D 0.41
[78,] TRD@ TRD@ 0.38
[79,] T3JAM T3JAM 0.37
[80,] FNBPl FNBPl 0.37
[81,] CD6 CD6 0.4
[82,] AIFl AIFl AIFl 0.31
[83,] FOLHl FOLHl 0.45
[84,] CDlE CDlE CDlE 0.58
[85,] LY9 LY9 0.39
[86,] UGT2B17 UGT2B17 0.47
[87,] ADA ADA ADA 0.39
[88,] CDKL5 CDKL5 0.44
[89,] TRIM TRIM 0.38
[90,] EVL EVL 0.39
[91,] DATFl DATFl 0.31
[92,] RGC32 RGC32 0.51
[93,] PRKCH PRKCH 0.3
[94,] ARHGAPl 5 ARHGAPl5 0.34
[95,] NOTCHl NOTCHl 0.36
[96,] BIN2 BIN2 0.31
[97,] SEMA4G SEMA4G 0.35
[98,] DPEP2 DPEP2 0.33
[99,] CECRl CECRl 0.36
[100,] BCLIlB BCLIlB 0.33
[101,] STAG3 STAG3 0.41
[102,] GALNT6 GALNT6 0.32
[103,] UBASH3A UBASH3A 0.3
[104,] PHEMX PHEMX 0.38
[105,] FLJ13373 FLJ13373 0.34
[106,] LEFl LEFl 0.49
[107,] IL21R IL21R 0.42
[108,] MGC17330 MGC17330 0.33
[109,] AKAP13 AKAP13 0.53
[110,] ZNF335 ZNF335 0.3
[in,] GIMAP5 GIMAP5 0.34
Table 15. Methotrexate biomarkers
List 2006 HU6800 List_Prior List Preferr Correlation
[1,] PRPF8 PRPF8 0.34
[2,] RPL18 RPL18 0.34
[3,] RNPSl RNPSl 0.36
[4,] RPL32 RPL32 0.39
[5,] EEFlG EEFlG 0.34
[6,] GOT2 GOT2 0.31
[7,] RPL13A RPL13A 0.31
[ 8 , ] PTMA PTMA PTMA 0.41
[9,] RPS15 RPS15 0.39
[10,] RPLP2 RPLP2 RPLP2 0.32
[11,] CSDA CSDA 0.39
[12,] KHDRBSl KHDRBSl 0.32
[13,] SNRPA SNRPA 0.31
[14,] IMPDH2 IMPDH2 IMPDH2 0.39
[15,] RPS19 RPS19 0.47
[16,] NUP88 NUP88 0.36
[17,] ATP5D ATP5D 0.33
[18,] PCBP2 PCBP2 0.32
[19,] ZNF593 ZNF593 0.4
[20,] HSU79274 HSU79274 0.32
[21,] PRIMl PRIMl 0.3
[22,] PFDN5 PFDN5 0.33
[23,] OXAlL OXAlL 0.37
[24,] H3F3A H3F3A 0.42
[25,] ATIC ATIC 0.31
[26,] RPL13 RPL13 0.36
[27,] CIAPINl CIAPINl 0.34
[28,] FBL FBL 0.33
[29,] RPS2 RPS2 RPS2 0.32
[30,] PCCB PCCB 0.36
[31,] RBMX RBMX 0.33
[32,] SHMT2 SHMT2 0.34
[33,] RPLPO RPLPO 0.35
[34,] HNRPAl HNRPAl HNRPAl 0.35
[35,] STOML2 STOML2 0.32
[36,] RPS9 RPS9 0.36
[37,] SKBl SKBl 0.33
[38,] GLTSCR2 GLTSCR2 0.37
[39,] CCNBlIPl CCNBlIPl 0.3
[40,] MRPS2 MRPS2 0.33
[41,] FLJ20859 FLJ20859 0.34
[42,] FLJ12270 FLJ12270 0.3
Table 16. Bleomycin biomarkers
List 2006 HU6800 List Prior List Preferr Correlation
[1,] MSN MSN 0. .3
[2,] PFNl PFNl 0. .45
[3,] HKl HKl 0. .33
[4,] ACTR2 ACTR2 0. .31
[5,] MCLl MCLl 0. .31
[6,] ZYX ZYX 0. .32
[7,] RAPlB RAPlB 0. .34
[8,] GNB2 GNB2 0. .32
[9,] EPASl EPASl 0. ,31
[10,] PGAMl PGAMl 0. .42
[H,] CKAP4 CKAP4 0.31
[12,] DUSPl DUSPl 0.4
[13,] MYL9 MYL9 0.4
[14,] K-ALPHA-I K-ALPHA-I 0.37
[15,] LGALSl LGALSl 0.38
[16,] CSDA CSDA CSDA 0.3
[17,] AKRlBl AKRlBl 0.32
[18,] IFITM2 IFITM2 IFITM2 0.36
[19,] ITGA5 ITGA5 0.43
[20,] VIM VIM 0.39
[21,] DPYSL3 DPYSL3 0.44
[22,] JUNB JUNB 0.32
[23,] ITGA3 ITGA3 0.38
[24,] NFKBIA NFKBIA 0.32
[25,] LAMBl LAMBl 0.37
[26,] FHLl FHLl 0.31
[27,] INSIGl INSIGl 0.31
[28,] TIMPl TIMPl 0.48
[29,] GJAl GJAl 0.54
[30,] PSME2 PSME2 0.34
[31,] PRGl PRGl 0.46
[32,] EXTl EXTl 0.35
[33,] DKFZP434J154 DKFZP434J154 0.31
[34,] OPTN OPTN 0.31
[35,] M6PRBP1 M6PRBP1 0.52
[36,] MVP MVP 0.34
[37,] VASP VASP 0.31
[38,] ARL7 ARL7 0.39
[39,] NNMT NNMT NNMT 0.34
[40,] TAPl TAPl 0.3
[41,] COLlAl COLlAl COLlAl 0.33
[42,] BASPl BASPl 0.35
[43,] PLOD2 PLOD2 0.37
[44,] ATF3 ATF3 0.42
[45,] PALM2-AKAP2 PALM2-AKAP2 0.33
[46,] IL8 IL8 0.34
[47,] ANPEP ANPEP 0.35
[48,] LOXL2 LOXL2 0.32
[49,] TGFBl TGFBl 0.31
[50,] IL4R IL4R 0.31
[51,] DGKA DGKA 0.32
[52,] STC2 STC2 0.31
[53,] SEC61G SEC61G 0.41
[54,] NFIL3 NFIL3 NFIL3 0.47
[55,] RGS3 RGS3 0.37
[56,] NK4 NK4 0.34
[57,] F2R F2R 0.34
[58,] TPM2 TPM2 0.35
[59,] PSMB9 PSMB9 PSMB9 0.34
[60,] LOX LOX 0.37
[61,] STCl STCl 0.35
[62,] CSPG2 CSPG2 CSPG2 0.35
[63,] PTGER4 PTGER4 0.31
[64,] IL6 IL6 0.34
[65,] SMAD3 SMAD3 0.38
[66,] PLAU PLAU PLAU 0.35
[67,] WNT5A WNT5A 0.44
[68,] BDNF BDNF 0.34
[69,] TNFRSFlA TNFRSFlA TNFRSFlA 0.46
[70,] FLNC FLNC 0.34
[71,] DKFZP564K0822 DKFZP564K0822 0.34
[72,] FLOTl FLOTl 0.38
[73,] PTRF PTRF 0.39
[74,] HLA-B HLA-B 0.36
[75,] COL6A2 COL6A2 COL6A2 0.32
[76,] MGC4083 MGC4083 0.32
[77,] TNFRSFlOB TNFRSFlOB 0.34
[78,] PLAGLl PLAGLl 0.31
[79,] PNMA2 PNMA2 0.38
[80,] TFPI TFPI 0.38
[81,] LAT LAT 0.46
[82,] GZMB GZMB 0.51
[83,] CYR61 CYR61 0.37
[84,] PLAUR PLAUR PLAUR 0.35
[85,] FSCNl FSCNl FSCNl 0.32
[86, ] ERP70 ERP70 0.32
[87,] AFlQ AFlQ 0.3
[88,] UBC UBC 0.37
[89,] FGFRl FGFRl 0.33
[90,] HIC HIC 0.33
[91,] BAX BAX 0.35
[92,] COL4A2 COL4A2 COL4A2 0.32
[93,] COL6A1 COL6A1 0.32
[94,] IFITM3 IFITM3 0.3
[95,] MAPlB MAPlB 0.38
[96,] FLJ46603 FLJ46603 0.37
[97,] RAFTLIN RAFTLIN 0.34
[98,] RRAS RRAS 0.31
[99,] FTL FTL 0.3
[100, ] KIAA0877 KIAA0877 0.31
[101, ] MTlE MTlE MTlE 0.31
[102, ] CDClO CDClO 0.51
[103, ] DOCK2 DOCK2 0.32
[104, ] TRIM22 TRIM22 0.36
[105, ] RISl RISl 0.37
[106, ] BCATl BCATl 0.42
[107, ] PRFl PRFl 0.34
[108, ] DBNl DBNl 0.36
[109, ] MTlK MTlK 0.3
[110, ] TMSBlO TMSBlO 0.42
[in, ] RAB31 RAB31 0.45
[112, ] FLJ10350 FLJ10350 0.4
[113, ] Clorf24 Clorf24 0.34
[114, ] NME7 NME7 0.46
[115, ] TMEM22 TMEM22 0.3
[116, ] TPKl TPKl 0.37
[117, ] COL5A2 COL5A2 0.34
[118, ] ELK3 ELK3 0.38
[119, ] CYLD CYLD 0.4
[120, ] ADAMTSl ADAMTSl 0.31
[121, ] EHD2 EHD2 0.41
[122, ] ACTB ACTB ACTB 0.33
Table 17. Methyl-GAG (Methyl glyoxal bis (amidinohydrazonel dihydrochloride)
M List 2006 HU6800 List Prior ] ist Preferr Correlation
[1,] PTMA PTMA 0.32
[2,] SSRPl SSRPl 0.37
[3,] NUDC NUDC 0.35
[4,] CTSC CTSC 0.35
[5,] AP1G2 AP1G2 0.33
[6,] PSME2 PSME2 0.3
[7,] LBR LBR 0.38
[8,] EFNB2 EFNB2 0.31
[9,] SERPINAl SERPINAl 0.34
[10,] SSSCAl SSSCAl 0.32
[H, ] EZH2 EZH2 0.36
[12,] MYB MYB MYB 0.33
[13,] PRIMl PRIMl 0.39
[14,] H2AFX H2AFX 0.33
[15,] HMGAl HMGAl 0.35
[16,] HMMR HMMR 0.33
[17,] TK2 TK2 0.42
[18,] WHSCl WHSCl 0.35
[19,] DIAPHl DIAPHl 0.34
[20,] LAMB3 LAMB3 0.31
[21,] DPAGTl DPAGTl 0.42
[22,] UCK2 UCK2 0.31
[23,] SERPINBl SERPINBl 0.31
[24,] MDNl MDNl 0.35
[25,] BRRNl BRRNl 0.33
[26,] G0S2 G0S2 0.43
[27,] RAC2 RAC2 0.35
[28,] MGC21654 MGC21654 0.36
[29,] GTSEl GTSEl 0.35
[30,] TACC3 TACC3 0.31
[31,] PLEK2 PLEK2 0.32
[32,] PLAC8 PLAC8 0.31
[33,] HNRPD HNRPD 0.35
[34,] PNAS-4 PNAS-4 0.3 rable 18. Carboplatin biomarker
List 2006 HU6800 L Liisstt Prior List Preferr Correlation
[1,] MSN MSN 0.31
ITGA5 ITGA5 0.43
[3,] VIM VIM 0.34
[4,] TNFAIP3 TNFAIP3 0.4
[5, ] CSPG2 CSPG2 0.35
[6,] WNT5A WNT5A 0.34
[7,] FOXF2 FOXF2 0.36
[8,] LOC94105 LOC94105 0.32
[9,] IFI16 IFI16 0.38
[10,] LRRN3 LRRN3 0.33
[11,] FGFRl FGFRl 0.37
[12,] DOCKlO DOCKlO 0.4
[13, ] LEPREl LEPREl 0.32
[14,] COL5A2 COL5A2 0.3
[15,] ADAMTSl ADAMTSl 0.34
Table 19. 5-FU (5-Fluorouracil) biomarkers
List 2006 HU6800 List Prior List Preferr Correlation
[1,] RPL18 RPL18 0.39
[2,] RPLlOA RPLlOA 0.36
[3,] RNPSl RNPSl 0.3
[4,] ANAPC5 ANAPC5 0.5
[5,] EEF1B2 EEF1B2 0.4
[6,] RPL13A RPL13A 0.38
[7,] RPS15 RPS15 0.34
[8,] AKAPl AKAPl 0.37
[9,] NDUFABl NDUFABl 0.3
[10,] APRT APRT 0.32
[11,] ZNF593 ZNF593 0.37
[12,] MRP63 MRP63 0.31
[13,] IL6R IL6R 0.31
[14,] RPL13 RPL13 0.31
[15,] SART3 SART3 0.35
[16,] RPS6 RPS6 0.49
[17, ] UCK2 UCK2 0.38
[18,] RPL3 RPL3 0.32
[19,] RPL17 RPL17 0.34
[20,] RPS2 RPS2 0.32
[21,] PCCB PCCB 0.31
[22, ] TOMM20 TOMM20 0.39
[23,] SHMT2 SHMT2 0.36
[24,] RPLPO RPLPO 0.3
[25,] GTF3A GTF3A 0.5
[26,] STOML2 STOML2 0.4
[27,] DKFZp564J157 DKFZp564J157 0.38
[28,] MRPS2 MRPS2 0.34
[29,] ALG5 ALG5 0.37
[30,] CALML4 CALML4 0.3 rable 20. Rituximab (e.g., Mabthera) biomarkers
List 2006 List Prior List Preferr Correlation
[1, ] ITK ITK 0.36
[2, ] KIFCl KIFCl 0.36
[3, ] VLDLR VLDLR 0.39
[4, ] RUNXl RUNXl 0.32
[5, ] PAFAH1B3 PAFAH1B3 0.32
[6, ] HlFX HlFX 0.43
[7, ] RNFl44 RNF144 0.38
[8, ] TMSNB TMSNB 0.47
[9, ] CRYl CRYl 0.37
[10, ] MAZ MAZ 0.33
[12, ] SRF SRF 0.37
[13, ] UMPS UMPS 0.41
[14, ] CD3Z CD3Z 0.33
[15, ] PRKCQ PRKCQ 0.31 '
[16, ] HNRPM HNRPM 0.45
[17, ] ZAP70 ZAP70 0.38
[18, ] ADDl ADDl 0.31
[19,] RFC5 RFC5 0.35 [20,] TM4SF2 TM4SF2 0.33 [21,] PFN2 PFN2 0.3 [22,] BMIl BMIl 0.31 [23,] TUBGCP3 TUBGCP3 0.33 [24,] δTP6V1B2 ATP6V1B2 0.42 [25,] RALY RALY 0.31 [26,] PSMC5 PSMC5 0.36 [27,] CDlD CDlD 0.32 [28,] ADA ADA 0.34 [29,] CD99 CD99 0.33 [30,] CD2 CD2 0.43 [31,] CNP CNP 0.48 [32,] ERG ERG 0.47 [33,] MYL6 MYL6 0.41 [34,] CD3E CD3E 0.36 [35,] CDlA CDlA 0.46 [36,] CDlB CDlB 0.47 [37,] STMNl STMNl 0.32 [38,] PSMC3 PSMC3 0.38 [39,] RPS4Y1 RPS4Y1 0.36 [40,] AKTl AKTl 0.38 [41,] TALI TALI 0.37 [42,] GNAl5 GNAl5 0.37 [43,] UBE2A UBE2A 0.35 [44,] TCF12 TCF12 0.35 [45,] UBE2S UBE2S 0.52 [46,] CCND3 CCND3 0.38 [47,] PAX6 PAX6 0.35 [48,] MDK MDK 0.3 [49,] CAPG CAPG 0.36 [50,] RAG2 RAG2 0.39 [51,] ACTNl ACTNl 0.37 [52,] GSTM2 GSTM2 0.47 [53,] SATBl SATBl 0.36 [54,] NASP NASP 0.3 [55,] IGFBP2 IGFBP2 0.46 [56,] CDH2 CDH2 0.49 [57, ] CRABPl CRABPl 0.36 [58,] DBNl DBNl 0.49 [59,] CTNNAl CTNNAl 0.53 [60,] AKRlCl AKRlCl 0.32 [61,] CACNB3 CACNB3 0.37 [62,] FARSLA FARSLA 0.35 [63,] CASP2 CASP2 0.42 [64,] CASP2 CASP2 0.31 [65,] E2F4 E2F4 0.36 [66,] LCP2 LCP2 0.35 [67,] CASP6 CASP6 0.32 [68,] MYB MYB 0.3 [69,] SFRS6 SFRS6 0.44 [70,] GLRB GLRB 0.34 [71,] NDN NDN 0.39 [72,] CPSFl CPSFl 0.33 [73,] GNAQ GNAQ 0.44 [74,] TUSC3 TUSC3 0.41
[75,] GNAQ GNAQ 0.54
[76,] JARI D2 JARI D2 0.44
[77,] OCRL OCRL 0.5
[78,] FHLl FHLl 0.36
[79,] EZH2 EZH2 0.4
[80,] SMOX SMOX 0.35
[81,] SLC4A2 SLC4A2 0.35
[82,] UFDlL UFDlL 0.3
[83,] SEPWl SEPWl 0.31
[84,] ZNF32 ZNF32 0.35
[85,] HTATSFl HTATSFl 0.35
[86,] SHDl SHDl 0.43
[87,] PTOVl PTOVl 0.42
[88,] NXFl NXFl 0.46
[89,] FYB FYB 0.47
[90,] TRIM28 TRIM28 0.38
[91,] BC008967 BC008967 0.4
[92,] TRB@ TRB@ 0.3
[93,] TFRC TFRC 0.31
[94,] HlFO HlFO 0.36
[95,] CD3D CD3D 0.32
[96,] CD3G CD3G 0.4
[97,] CENPB CENPB 0.36
[98,] ALDH2 ALDH2 0.33
[99,] ANXAl ANXAl 0.35
[100,] H2AFX H2AFX 0.51
[101,] CDlE CDlE 0.33
[102,] DDX5 DDX5 0.39
[103,] ABLl ABLl 0.3
[104,] CCNA2 CCNA2 0.3
[105,] ENO2 ENO2 0.35
[106,] SNRPB SNRPB 0.38
[107,] GATA3 GATA3 0.36
[108,] RRM2 RRM2 0.48
[109,] GLUL GLUL 0.4
[HO,] TCF7 TCF7 0.39
[in,] FGFRl FGFRl 0.33
[112,] SOX4 SOX4 0.3
[113,] MAL MAL 0.3
[114, ] NUCB2 NUCB2 0.38
[115,] SMA3 SMA3 0.31
[116,] FAT FAT 0.52
[117,] UNG UNG 0.31
[118,] ARHGDIB ARHGDIB 0.36
[119,] RUNXl RUNXl 0.38
[120,] MPHOSPH6 MPHOSPH6 0.5
[121,] DCTNl DCTNl 0.34
[122,] SH3GL3 SH3GL3 0.38
[123,] VIM VIM 0.41
[124,] PLEKHCl PLEKHCl 0.3
[125,] CD47 CD47 0.32
[126,] POLR2F POLR2F 0.37
[127,] RHOH RHOH 0.43
[128,] ADDl ADDl 0.46
[129, ] ATP2A3 ATP2A3 0.38
Table 21. Radiation sensitivity biomarkers
List 2006 HU6800 List Prior List Preferr
Correlation
[1,] TRAl TRAl 0.36
[2,] ACTN4 ACTN4 0.36
[3,] WARS WARS 0.39
[4,] CALMl CALMl 0.32
[5,] CD63 CD63 CD63 0.32
[6,] CD81 CD81 0.43
[7,] FKBPlA FKBPlA 0.38
[8,] CALU CALU 0.47
[9,] IQGAPl IQGAPl 0.37
[10,] CTSB CTSB 0.33
[11,] MGC8721 MGC8721 0.35
[12,] STATl STATl 0.37
[13,] TACCl TACCl 0.41
[14,] TM4SF8 TM4SF8 0.33
[15,] CD59 CD59 0.31
[16,] CKAP4 CKAP4 CKAP4 0.45
[17,] DUSPl DUSPl DUSPl 0.38
[18,] RCNl RCNl 0.31
[19,] MGC8902 MGC8902 0.35
[20,] LGALSl LGALSl LGALSl 0.33
[21,] BHLHB2 BHLHB2 0.3
[22,] RRBPl RRBPl 0.31
[23,] PKM2 PKM2 0.33
[24,] PRNP PRNP 0.42
[25,] PPP2CB PPP2CB 0.31
[26,] CNN3 CNN3 0.36
[27,] ANXA2 ANXA2 ANXA2 0.32
[28,] IER3 IER3 0.34
[29,] JAKl JAKl 0.33
[30,] MARCKS MARCKS 0.43
[31,] LUM LUM 0.48
[32,] FER1L3 FER1L3 0.47
[33,] SLC20A1 SLC20A1 0.41
[34,] EIF4G3 EIF4G3 0.36
[35,] HEXB HEXB 0.46
[36,] EXTl EXTl 0.47
[37,] TJPl TJPl 0.32
[38,] CTSL CTSL CTSL 0.38
[39,] SLC39A6 SLC39A6 0.36
[40,] RIOK3 RIOK3 0.38
[41,] CRK CRK 0.37
[42,] NNMT NNMT 0.37
[43,] COLlAl COLlAl 0.35
[44,] TRAM2 TRAM2 TRAM2 0.35
[45,] ADAM9 ADAM9 0.52
[46,] DNAJC7 DNAJC7 0.38
[47,] PLSCRl PLSCRl 0.35
[48,] PRSS23 PRSS23 0.3
[49,] PLOD2 PLOD2 0.36
[50,] NPCl NPCl 0.39
[51,] TOBl TOBl 0.37
[52,] GFPTl GFPTl 0.47
[53,] IL8 IL8 0.36
[54,] DYRK2 DYRK2 0.3
[55,] PYGL PYGL 0.46
[56,] LOXL2 LOXL2 0.49
[57,] KIAA0355 KIAA0355 0.36
[58,] UGDH UGDH 0.49
[59,] NFIL3 NFIL3 0.53
[60,] PURA PURA 0.32
[61,] ULK2 ULK2 0.37
[62,] CENTG2 CENTG2 0.35
[63,] NID2 NID2 0.42
[64, ] CAP350 CAP350 0.31
[65,] CXCLl CXCLl 0.36
[66,] BTN3A3 BTN3A3 0.35
[67,] IL6 IL6 0.32
[68, ] WNT5A WNT5A 0.3
[69,] FOXF2 FOXF2 0.44
[70,] LPHN2 LPHN2 0.34
[71,] CDHIl CDHIl 0.39
[72,] P4HAl P4HA1 0.33
[73,] GRP58 GRP58 0.44
[74,] ACTNl ACTNl ACTNl 0.41
[75,] CAPN2 CAPN2 0.54
[76,] DSIPI DSIPI 0.44
[77, ] MAP1LC3B MAP1LC3B 0.5
[78,] GALIG GALIG GALIG 0.36
[79,] IGSF4 IGSF4 0.4
[80,] IRS2 IRS2 0.35
[81,] ATP2A2 ATP2A2 0.35
[82,] OGT OGT 0.3
[83,] TNFRSFlOB TNFRSFlOB 0.31
[84,] KIAA1128 KIAA1128 0.35
[85,] TM4SF1 TM4SF1 0.35
[86,] RBPMS RBPMS 0.43
[87,] RIPK2 RIPK2 0.42
[88,] CBLB CBLB 0.46
[89,] NR1D2 NR1D2 0.47
[90,] BTN3A2 BTN3A2 0.38
[91,] SLC7A11 SLC7A11 0.4
[92,] MPZLl MPZLl 0.3
[93,] IGFBP3 IGFBP3 IGFBP3 0.31
[94,] SSA2 SSA2 0.36
[95,] FNl FNl FNl 0.32
[96,] NQOl NQOl 0.4
[97,] ASPH ASPH 0.36
[98,] ASAHl ASAHl 0.33
[99,] MGLL MGLL 0.35
[100, ] SERPINB6 SERPINB6 0.51
[101, ] HSPA5 HSPA5 0.33
[102, ] ZFP36L1 ZFP36L1 0.39
[103, ] COL4A2 COL4A2 0.3
[104, ] COL4A1 COL4A1 0.3
[105, ] CD44 CD44 0.35
[106, ] SLC39A14 SLC39A14 0.38
[107, ] NIPA2 NIPA2 0.36
[108, ] FKBP9 FKBP9 0.48
[109, ] IL6ST IL6ST 0.4
[110,] DKFZP564G2022 DKFZP564G2022 0.39
[in,] PPAP2B PPAP2B 0.33
[112,] MAPlB MAPlB 0.3
[113,] MAPKl MAPKl 0.3
[114,] MYOlB MYOlB 0.38
[115,] CAST CAST CAST 0.31
[116,] RRAS2 RRAS2 0.52
[117,] QKI QKI 0.31
[118,] LHFPL2 LHFPL2 0.36
[119,] SEPTlO SEPTlO 0.38
[120,] ARHE ARHE 0.5
[121,] KIAA1078 KIAA1078 0.34
[122,] FTL FTL 0.38
[123,] KIAA0877 KIAA0877 0.41
[124,] PLCBl PLCBl 0.3
[125,] KIAA0802 KIAA0802 0.32
[126,] KPNBl KPNBl 0.37
[127,] RAB3GAP RAB3GAP 0.43
[128,] SERPINBl SERPINBl 0.46
[129,] TIMM17A TIMM17A 0.38
[130,] SOD2 SOD2 0.35
[131,] HLA-A HLA-A HLA-A 0.33
[132,] NOMO2 NOMO2 0.43
[133,] LOC55831 LOC55831 0.32
[134,] PHLDAl PHLDAl 0.32
[135,] TMEM2 TMEM2 0.47
[136, ] MLPH MLPH 0.35
[137,] FADl04 FADl04 0.34
[138,] LRRC5 LRRC5 0.42
[139,] RAB7L1 RAB7L1 0.41
[140,] FLJ35036 FLJ35036 0.36
[141,] DOCKlO DOCKlO 0.41
[142,] LRP12 LRP12 0.36
[143,] TXNDC5 TXNDC5 0.4
[144,] CDC14B CDC14B 0.39
[145,] HRMTlLl HRMTlLl 0.38
[146,] COROlC COROlC 0.38
[147,] DNAJClO DNAJClO 0.31
[148,] TNPOl TNPOl 0.33
[149,] LONP LONP 0.32
[150,] AMIGO2 AMIGO2 0.38
[151,] DNAPTP6 DNAPTP6 0.31
[152,] ADAMTSl ADAMTSl 0.37
[153,] CCL21
[154,] SCARB2
[155,] MAD2L1BP
[156,] PTS
[157,] NBLl
[158,] CD151
[159,] CRIP2
[160,] UGCG
[161,] PRSSIl
[162,] MME
[163,] CBRl
[164,] DUSP3
[165,] PFN2
[166,] MICA
[167,] FTHl
[168, ] RHOC
[169,] ZAP128
[170,] PON2
[171,] COL5A2
[172,] CST3
[173,] MCAM
[174,] MMP2
[175,] CTSD
[176, ALDH3A1
[177, CSRPl
[178, S100A4
[179, CALDl
[180, CTGF
[181, CAPG
[182, TAGLN
[183, FSTLl
[184, SCTR
[185, BLVRA
[186, COPEB
[187, DIPA
[188, SMARCD3
[189, MVP
[190, PEAl 5
[191, ] S100A13 [192,] ECEl
Table 22. Vincristine biomarkers.
SEQIDNO Gene Correlation Medianprobe
1 SLC25A5 0 .32 TCCTGTACTTGTCCTCAGCTTGGGC
2 RPLlO 0 .38 GCCCCACTGGACAACACTGATTCCT
3 RPL12 0 .31 TGCCTGCTCCTGTACTTGTCCTCAG
4 RPS4X 0 .39 AAATGTTTCCTTGTGCCTGCTCCTG
5 EIF5A 0 .31 TCCTGTACTTGTCCTCAGCTTGGGC
6 BLMH 0 .32 AAGCCTATACGTTTCTGTGGAGTAA
7 TBCA 0 .3 ACTTGTCCTCAGCTTGGGCTTCTTC
8 MDH2 0 .34 TCCTGTACTTGTCCTCAGCTTGGGC
9 S100A4 0.32 TGGACCCCACTGGCTGAGAATCTGG
10 C14orfl39 0.3 TTGGACATCTCTAGTGTAGCTGCCA
Table 23 . Cisplatin bic
SEQIDNO Gene Corre Medianprobe
11 ClQRl 0.3 CACCCAGCTGGTCCTGTGGATGGGA
12 SLA 0.37 TGCCTGCTCCTGTACTTGTCCTCAG
13 PTPN7 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
14 ZNFNlAl 0.33 CACCCAGCTGGTCCTGTGGATGGGA
15 CENTBl 0.37 TTGGACATCTCTAGTGTAGCTGCCA
16 IFI16 0.31 TCCTCCATCACCTGAAACACTGGAC
17 ARHGEF6 0.35 TGCCTGCTCCTGTACTTGTCCTCAG
18 SEC31L2 0.32 AAGCCTATACGTTTCTGTGGAGTAA
19 CD3Z 0.32 TTGGACATCTCTAGTGTAGCTGCCA
20 GZMB 0.3 TCCTCCATCACCTGAAACACTGGAC
21 CD3D 0.34 TCCTCCATCACCTGAAACACTGGAC
22 MAP4K1 0.32 CACCCAGCTGGTCCTGTGGATGGGA
23 GPR65 0.39 CACCCAGCTGGTCCTGTGGATGGGA
24 PRFl 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
25 ARHGAPl 5 0.35 CACCCAGCTGGTCCTGTGGATGGGA
26 TM6SF1 0.41 TGCCTGCTCCTGTACTTGTCCTCAG
27 TCF4 0.4 AAATGTTTCCTTGTGCCTGCTCCTG
Table 24 . Etoposide biomarker
SEQIDNO Gene Correlation Medianprobe
28 CD99 0.3 AAGCCTATACGTTTCTGTGGAGTAA
29 INSIGl 0.35 TCCTTGTGCCTGCTCCTGTACTTGT
30 PRGl 0.34 GCCCCACTGGACAACACTGATTCCT
31 MUFl 0.35 AAGCCTATACGTTTCTGTGGAGTAA
32 SLA 0.37 CACCCAGCTGGTCCTGTGGATGGGA
33 SSBP2 0.37 TGGACCCCACTGGCTGAGAATCTGG
34 GNB5 0.35 TCCTTGTGCCTGCTCCTGTACTTGT
35 MFNG 0.33 GCCCCACTGGACAACACTGATTCCT
36 PSMB9 0.31 AAGCCTATACGTTTCTGTGGAGTAA
37 EVI2A 0.41 TCCTCCATCACCTGAAACACTGGAC
38 PTPN7 0.3 AAGCCTATACGTTTCTGTGGAGTAA
39 PTGER4 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
40 CXorf9 0.3 GCCCCACTGGACAACACTGATTCCT
41 ZNFNlAl 0.35 ACTTGTCCTCAGCTTGGGCTTCTTC
42 CENTBl 0.3 TGGACCCCACTGGCTGAGAATCTGG
43 NAPlLl 0.31 TCCTCCATCACCTGAAACACTGGAC
44 HLA-DRA 0.34 TGCCTGCTCCTGTACTTGTCCTCAG
45 IFI16 0.38 CACCCAGCTGGTCCTGTGGATGGGA
46 ARHGEF6 0.33 TGGACCCCACTGGCTGAGAATCTGG
47 PSCDBP 0.4 AAGCCTATACGTTTCTGTGGAGTAA
48 SELPLG 0.35 TTGGACATCTCTAGTGTAGCTGCCA
49 SEC31L2 0.42 AAATGTTTCCTTGTGCCTGCTCCTG
50 CD3Z 0.36 TGCCTGCTCCTGTACTTGTCCTCAG
51 SH2D1A 0.33 CACCCAGCTGGTCCTGTGGATGGGA
52 GZMB 0.34 TGGACCCCACTGGCTGAGAATCTGG
53 SCN3A 0.3 GCCCCACTGGACAACACTGATTCCT
54 RAFTLIN 0.39 TCCTCCATCACCTGAAACACTGGAC
55 DOCK2 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
56 CD3D 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
57 ZAP70 0.35 TCCTCCATCACCTGAAACACTGGAC
58 GPR65 0.35 TGGACCCCACTGGCTGAGAATCTGG
59 PRFl 0.32 TGGACCCCACTGGCTGAGAATCTGG
60 ARHGAP15 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
61 NOTCHl 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
62 UBASH3A 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
Table 25 . Azaguanme biomarkers .
SEQIDNO Gene Correlation Medianprobe
63 SRM 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
64 SCARBl 0.4 TTGGACATCTCTAGTGTAGCTGCCA
65 SIATl 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
66 CUGBP2 0.37 TGGACCCCACTGGCTGAGAATCTGG
67 WASPIP 0.44 TCCTGTACTTGTCCTCAGCTTGGGC
68 ITM2A 0.31 AAGCCTATACGTTTCTGTGGAGTAA
69 PALM2-AKAP2 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
70 LNK 0.43 TTGGACATCTCTAGTGTAGCTGCCA
71 FCGR2A 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
72 RUNX3 0.43 TCCTGTACTTGTCCTCAGCTTGGGC
73 EVI2A 0.4 AAATGTTTCCTTGTGCCTGCTCCTG
74 BTN3A3 0.4 ACTTGTCCTCAGCTTGGGCTTCTTC 75 LCP2 0.34 TCCTTGTGCCTGCTCCTGTACTTGT 76 BCHE 0.35 TCCTCCATCACCTGAAACACTGGAC 77 LY96 0.47 TGCCTGCTCCTGTACTTGTCCTCAG 78 LCPl 0.42 ACTTGTCCTCAGCTTGGGCTTCTTC 79 IFI16 0.33 CACCCAGCTGGTCCTGTGGATGGGA 80 MCAM 0.37 TTGGACATCTCTAGTGTAGCTGCCA 81 MEF2C 0.41 CACCCAGCTGGTCCTGTGGATGGGA 82 FYN 0.31 TCCTGTACTTGTCCTCAGCTTGGGC 83 Clorf38 0.37 AAGCCTATACGTTTCTGTGGAGTAA 84 FCGR2C 0.34 TGCCTGCTCCTGTACTTGTCCTCAG 85 TNIK 0.35 AAGCCTATACGTTTCTGTGGAGTAA 86 AMPD2 0.3 TCCTGTACTTGTCCTCAGCTTGGGC 87 SEPT6 0.41 AAATGTTTCCTTGTGCCTGCTCCTG 88 RAFTLIN 0.39 TCCTTGTGCCTGCTCCTGTACTTGT 89 SLC43A3 0.52 CACCCAGCTGGTCCTGTGGATGGGA 90 LPXN 0.54 AAGCCTATACGTTTCTGTGGAGTAA 91 CKIP-I 0.33 TCCTGTACTTGTCCTCAGCTTGGGC 92 FLJ10539 0.33 TCCTTGTGCCTGCTCCTGTACTTGT 93 FLJ35036 0.36 AAGCCTATACGTTTCTGTGGAGTAA 94 DOCKlO 0.3 GCCCCACTGGACAACACTGATTCCT 95 TRPV2 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC 96 IFRG28 0.3 TCCTTGTGCCTGCTCCTGTACTTGT 97 LEFl 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC 98 ADAMTSl 0.36 TGGACCCCACTGGCTGAGAATCTGG
Table 26, Carboplatin biomarkers. SEQIDNO Gene Correlation Medianprobe 99 ITGA5 0.43 A AAAAATTGGTTTTTTCCCCTTTGTGCCTGCTCCTG
100 TNFAIP3 0.4 TTGGCCCCTTGGCCTTCCCCTTGTACTTGTCCTCAG
101 WNT5A 0.34 TTCCCCTTCCCCAATTCCAACCCTGAAACACTGGAC
102 FOXF2 0.36 TTGGCCCCTTGGCCTTCCCCTTGTACTTGTCCTCAG
103 LOC94105 0.32 AAATGTTTCCTTGTGCCTGCTCCTG
104 IFI16 0.38 TCCTCCATCACCTGAAACACTGGAC
105 LRRN3 0.33 TTGGACATCTCTAGTGTAGCTGCCA
106 DOCKlO 0.4 TCCTGTACTTGTCCTCAGCTTGGGC
107 LEPREl 0.32 GCCCCACTGGACAACACTGATTCCT
108 ADAMTSl 0.34 TGGACCCCACTGGCTGAGAATCTGG
Table 27 Adriamycin biomarkers. SEQIDNO Gene Correlation Medianprobe
109 CD99 0.41 A AAAGGCCCCTTAATTAACCGGTTTCTGTGGAGTAA
110 ALDOC 0.31 TTCCCCTTTTGGTTGGCCCCTTGCTCCTGTACTTGT
111 SLA 0.35 TTGGCCCCTTGGCCTTCCCCTTGTACTTGTCCTCAG
112 SSBP2 0.34 TTCCCCTTCCCCAATTCCAACCCTGAAACACTGGAC
113 IL2RG 0.38 TTCCCCTTTTGGTTGGCCCCTTGCTCCTGTACTTGT
114 CXorf9 0.32 TTGGGGAACCCCCCCCAACCTTGGCTGAGAATCTGG
115 RHOH 0.31 AACCTTTTGGTTCCCCTTCCAAGCTTGGGCTTCTTC
116 ZNFNlAl 0.43 TTTTGGGGAACCAATTCCTTCCTAGTGTAGCTGCCA
117 CENTBl 0.36 AAAAGGCCCCTTAATTAACCGGTTTCTGTGGAGTAA
118 MAP4K1 0.35 TTCCCCTTCCCCAATTCCAACCCTGAAACACTGGAC
119 CD3G 0.31 AAAAAATTGGTTTTTTCCCCTTTGTGCCTGCTCCTG
120 CCR9 0.34 CCAACCCCCCAAGGCCTTGGGGTCCTGTGGATGGGA
121 CXCR4 0.3 TTCCCCTTTTGGTTGGCCCCTTGCTCCTGTACTTGT
122 ARHGEF6 0.31 TTCCCCTTCCCCAATTCCAACCCTGAAACACTGGAC
123 SELPLG 0.31 TTGGGGAACCCCCCCCAACCTTGGCTGAGAATCTGG
124 SEC31L2 0.33 TGCCTGCTCCTGTACTTGTCCTCAG 125 CD3Z 0.37 ACTTGTCCTCAGCTTGGGCTTCTTC 126 SH2D1A 0.37 TTGGACATCTCTAGTGTAGCTGCCA 127 CDlA 0.4 AAGCCTATACGTTTCTGTGGAGTAA 128 LAIRl 0.39 AAGCCTATACGTTTCTGTGGAGTAA 129 TRBg 0.34 TCCTCCATCACCTGAAACACTGGAC 130 CD3D 0.33 TCCTTGTGCCTGCTCCTGTACTTGT 131 WBSCR20C 0.34 ACTTGTCCTCAGCTTGGGCTTCTTC 132 ZAP70 0.33 TCCTGTACTTGTCCTCAGCTTGGGC 133 IFI44 0.32 TGCCTGCTCCTGTACTTGTCCTCAG 134 GPR65 0.31 AAGCCTATACGTTTCTGTGGAGTAA 135 AIFl 0.3 CACCCAGCTGGTCCTGTGGATGGGA 136 ARHGAPl 5 0.37 TCCTGTACTTGTCCTCAGCTTGGGC 137 NARF 0.3 TCCTCCATCACCTGAAACACTGGAC 138 PACAP 0.32 CACCCAGCTGGTCCTGTGGATGGGA
Table 28. Aclarubicin biomarkers. SEQIDNO Gene Correlation Medianprobe
139 RPL12 0.3 AAATGTTTCCTTGTGCCTGCTCCTG
140 RPLP2 0.37 TTGGACATCTCTAGTGTAGCTGCCA
141 MYB 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
142 ZNFNlAl 0.34 AAATGTTTCCTTGTGCCTGCTCCTG
143 SCAPl 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
144 STAT4 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
145 SP140 0.4 AAGCCTATACGTTTCTGTGGAGTAA
146 AMPD3 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
147 TNFAIP8 0.4 AAGCCTATACGTTTCTGTGGAGTAA
148 DDXl8 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
149 TAF5 0.3 TCCTTGTGCCTGCTCCTGTACTTGT
150 RPS2 0.34 CACCCAGCTGGTCCTGTGGATGGGA
151 DOCK2 0.32 AAGCCTATACGTTTCTGTGGAGTAA
152 GPR65 0.35 AAGCCTATACGTTTCTGTGGAGTAA
153 HOXA9 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
154 FLJ12270 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
155 HNRPD 0.4 ACTTGTCCTCAGCTTGGGCTTCTTC
Table 29. Mitoxantrone biomarkers. SEQIDNO Gene C Coorrrrelation Medianprobe
156 PGAMl 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
157 DPYSL3 0.36 AAATGTTTCCTTGTGCCTGCTCCTG
158 INSIGl 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
159 GJAl 0.31 TTGGACATCTCTAGTGTAGCTGCCA
160 BNIP3 0.31 TTGGACATCTCTAGTGTAGCTGCCA
161 PRGl 0.39 GCCCCACTGGACAACACTGATTCCT
162 G6PD 0.34 TGCCTGCTCCTGTACTTGTCCTCAG
163 PLOD2 0.34 GCCCCACTGGACAACACTGATTCCT
164 LOXL2 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
165 SSBP2 0.36 TCCTCCATCACCTGAAACACTGGAC
166 Clorf29 0.35 TCCTTGTGCCTGCTCCTGTACTTGT
167 TOX 0.35 TCCTTGTGCCTGCTCCTGTACTTGT
168 STCl 0.39 TCCTGTACTTGTCCTCAGCTTGGGC
169 TNFRSFlA 0.34 AAATGTTTCCTTGTGCCTGCTCCTG
170 NCOR2 0.3 TCCTCCATCACCTGAAACACTGGAC
171 NAPlLl 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
172 LOC94105 0.34 AAGCCTATACGTTTCTGTGGAGTAA
173 ARHGEF6 0.34 TCCTCCATCACCTGAAACACTGGAC
174 GATA3 0.35 TCCTTGTGCCTGCTCCTGTACTTGT
175 TFPI 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
176 CD3Z 0.37 AAGCCTATACGTTTCTGTGGAGTAA
177 AFlQ 0.33 GCCCCACTGGACAACACTGATTCCT
178 MAPlB 0.34 TGCCTGCTCCTGTACTTGTCCTCAG
179 CD3D 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
180 BCATl 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
181 IFI44 0.33 TGGACCCCACTGGCTGAGAATCTGG
182 CUTC 0.33 AAATGTTTCCTTGTGCCTGCTCCTG
183 NAP1L2 0.33 AAGCCTATACGTTTCTGTGGAGTAA
184 NME7 0.35 AAATGTTTCCTTGTGCCTGCTCCTG
185 FLJ21159 0.33 TCCTGTACTTGTCCTCAGCTTGGGC
Table 30. Mitomycin biomarkers.
SEQIDNO Gene Correlation Medianprobe
186 STCl 0. .34 TGCCTGCTCCTGTACTTGTCCTCAG
187 GPR65 0. .32 GCCCCACTGGACAACACTGATTCCT
188 DOCKlO 0. .35 ACTTGTCCTCAGCTTGGGCTTCTTC
189 FAM46A 0. .36 TCCTTGTGCCTGCTCCTGTACTTGT
190 LOC54103 0. .39 ACTTGTCCTCAGCTTGGGCTTCTTC
Table 31 . Paclitaxel (Taxo biomarkers .
SEQIDNO Gene C Coorrrrelation Medianprobe
191 RPLlO 0.31 TCCTCCATCACCTGAAACACTGGAC
192 RPS4X 0.31 TCCTCCATCACCTGAAACACTGGAC
193 DKCl 0.3 TCCTTGTGCCTGCTCCTGTACTTGT
194 DKFZP564C186 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
195 PRP19 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
196 RAB9P40 0.33 GCCCCACTGGACAACACTGATTCCT
197 HSA9761 0.37 AAATGTTTCCTTGTGCCTGCTCCTG
198 GMDS 0.3 AAATGTTTCCTTGTGCCTGCTCCTG
199 CEPl 0.3 AAATGTTTCCTTGTGCCTGCTCCTG
200 IL13RA2 0.34 AAATGTTTCCTTGTGCCTGCTCCTG
201 MAGEB2 0.41 ACTTGTCCTCAGCTTGGGCTTCTTC
202 HMGN2 0.35 CACCCAGCTGGTCCTGTGGATGGGA
203 ALMSl 0.3 TCCTCCATCACCTGAAACACTGGAC
204 GPR65 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
205 FLJ10774 0.31 TGGACCCCACTGGCTGAGAATCTGG
206 NOL8 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
207 DAZAPl 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
208 SLC25A15 0.31 TTGGACATCTCTAGTGTAGCTGCCA
209 PAF53 0.36 TCCTCCATCACCTGAAACACTGGAC
210 PITPNCl 0.33 TCCTCCATCACCTGAAACACTGGAC
211 SPANXC 0.3 TGGACCCCACTGGCTGAGAATCTGG
212 KIAA1393 0.33 CACCCAGCTGGTCCTGTGGATGGGA
Table 32. Gemcitabine (Gemzar) biomarkers.
SEQIDNO Gene Correlation Medianprobe
213 UBE2L6 0.38 CACCCAGCTGGTCCTGTGGATGGGA
214 TAPl 0.33 CACCCAGCTGGTCCTGTGGATGGGA
215 F2R 0.3 TCCTGTACTTGTCCTCAGCTTGGGC
216 PSMB9 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
217 IL7R 0.31 AAGCCTATACGTTTCTGTGGAGTAA
218 TNFAIP8 0.33 AAGCCTATACGTTTCTGTGGAGTAA
219 HLA-C 0.33 TGGACCCCACTGGCTGAGAATCTGG
220 IFI44 0.31 TGGACCCCACTGGCTGAGAATCTGG
Table 33 . Taxotere (docetaxel I biomarkers.
SEQIDNO Gene Correlation Medianprobe
221 ANP32B 0.45 GCCCCACTGGACAACACTGATTCCT
222 GTF3A 0.31 TTGGACATCTCTAGTGTAGCTGCCA
223 TRIM14 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
224 SKP2 0.33 GCCCCACTGGACAACACTGATTCCT
225 TRIP13 0.36 TCCTGTACTTGTCCTCAGCTTGGGC
226 RFC3 0.45 GCCCCACTGGACAACACTGATTCCT
227 CASP7 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
228 TXN 0.36 AAGCCTATACGTTTCTGTGGAGTAA
229 MCM5 0.34 AAATGTTTCCTTGTGCCTGCTCCTG
230 PTGES2 0.39 AAATGTTTCCTTGTGCCTGCTCCTG
231 OBFCl 0.37 TGGACCCCACTGGCTGAGAATCTGG
232 EPB41L4B 0.32 GCCCCACTGGACAACACTGATTCCT
233 CALML4 0.31 TCCTCCATCACCTGAAACACTGGAC
Table 34 . Dexamethasone bioma
SEQIDNO Gene Correlation
234 IFITM2 0.38 ATATATGGACCTAGCTTGAGGCAAT
235 UBE2L6 0.32 AAGCCTATACGTTTCTGTGGAGTAA
236 ITM2A 0.38 CACCCAGCTGGTCCTGTGGATGGGA
237 IL2RG 0.36 TCCTCCATCACCTGAAACACTGGAC
238 GPRASPl 0.36 TCCTGTACTTGTCCTCAGCTTGGGC
239 PTPN7 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
240 CXorf9 0.36 GCCCCACTGGACAACACTGATTCCT
241 RHOH 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
242 GIT2 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
243 ZNFNlAl 0.35 TCCTTGTGCCTGCTCCTGTACTTGT
244 CEPl 0.31 CACCCAGCTGGTCCTGTGGATGGGA
245 MAP4K1 0.3 AAGCCTATACGTTTCTGTGGAGTAA
246 CCR7 0.33 AAATGTTTCCTTGTGCCTGCTCCTG
247 CD3G 0.35 CACCCAGCTGGTCCTGTGGATGGGA
248 UCP2 0.3 AAGCCTATACGTTTCTGTGGAGTAA
249 GATA3 0.37 TGGACCCCACTGGCTGAGAATCTGG
250 CDKN2A 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
251 TARP 0.3 GCCCCACTGGACAACACTGATTCCT
252 LAIRl 0.34 TTGGACATCTCTAGTGTAGCTGCCA
253 SH2D1A 0.34 TCCTTGTGCCTGCTCCTGTACTTGT
254 SEPT6 0.34 TGCCTGCTCCTGTACTTGTCCTCAG
255 HA-I 0.34 TCCTTGTGCCTGCTCCTGTACTTGT
256 CD3D 0.32 TCCTCCATCACCTGAAACACTGGAC
257 LSTl 0.39 CACCCAGCTGGTCCTGTGGATGGGA
258 AIFl 0.35 AAGCCTATACGTTTCTGTGGAGTAA
259 ADA 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
260 DATFl 0.41 CACCCAGCTGGTCCTGTGGATGGGA
261 ARHGAP15 0.3 TCCTGTACTTGTCCTCAGCTTGGGC
262 PLAC8 0.31 CACCCAGCTGGTCCTGTGGATGGGA
263 CECRl 0.31 GCCCCACTGGACAACACTGATTCCT
264 LOC81558 0.33 TGGACCCCACTGGCTGAGAATCTGG
265 EHD2 0.37. ACTTGTCCTCAGCTTGGGCTTCTTC
Table 35. Ara-C (Cytarabine hydrochloride) biomarkers. SEQIDNO Gene Correlation Medianprobe 266 ITM2A 0.32 TGGACCCCACTGGCTGAGAATCTGG
267 RHOH 0.31 AAATGTTTCCTTGTGCCTGCTCCTG 268 PRIMl 0.3 TCCTCCATCACCTGAAACACTGGAC 269 CENTBl 0.31 TCCTTGTGCCTGCTCCTGTACTTGT 270 NAPlLl 0.31 GCCCCACTGGACAACACTGATTCCT 271 ATP5G2 0.31 TCCTCCATCACCTGAAACACTGGAC 272 GATA3 0.33 AAATGTTTCCTTGTGCCTGCTCCTG 273 PRKCQ 0.32 AAGCCTATACGTTTCTGTGGAGTAA 274 SH2D1A 0.3 GCCCCACTGGACAACACTGATTCCT 275 SEPT6 0.42 ACTTGTCCTCAGCTTGGGCTTCTTC 276 NME4 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC 277 CD3D 0.31 AAGCCTATACGTTTCTGTGGAGTAA 278 CDlE 0.32 TGGACCCCACTGGCTGAGAATCTGG 279 ADA 0.34 GCCCCACTGGACAACACTGATTCCT 280 FHODl 0.31 CACCCAGCTGGTCCTGTGGATGGGA
Table 36 Methylprednisolone biomarkers . SEQIDNO Gene Correlation Medianprobe
281 CD99 0.31 GCCCCACTGGACAACACTGATTCCT
282 ARHGDIB 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
283 ITM2A 0.35 GCCCCACTGGACAACACTGATTCCT
284 LGALS9 0.43 TCCTCCATCACCTGAAACACTGGAC
285 INPP5D 0.34 TGGACCCCACTGGCTGAGAATCTGG
286 SATBl 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
287 TFDP2 0.4 AAATGTTTCCTTGTGCCTGCTCCTG
288 SLA 0.31 TGGACCCCACTGGCTGAGAATCTGG
289 IL2RG 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
290 MFNG 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
291 SELL 0.33 AAATGTTTCCTTGTGCCTGCTCCTG
292 CDW52 0.33 TCCTCCATCACCTGAAACACTGGAC
293 LRMP 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
294 ICAM2 0.38 CACCCAGCTGGTCCTGTGGATGGGA
295 RIMS3 0.36 TGCCTGCTCCTGTACTTGTCCTCAG
296 PTPN7 0.39 TGGACCCCACTGGCTGAGAATCTGG
297 ARHGAP25 0.37 TCCTGTACTTGTCCTCAGCTTGGGC
298 LCK 0.3 TCCTCCATCACCTGAAACACTGGAC
299 CXorf9 0.3 TTGGACATCTCTAGTGTAGCTGCCA
300 RHOH 0.51 AAGCCTATACGTTTCTGTGGAGTAA
301 GIT2 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC
302 ZNFNlAl 0.53 TCCTTGTGCCTGCTCCTGTACTTGT
303 CENTBl 0.36 TCCTCCATCACCTGAAACACTGGAC
304 LCP2 0.34 TCCTGTACTTGTCCTCAGCTTGGGC
305 SPIl 0.3 TCCTGTACTTGTCCTCAGCTTGGGC
306 GZMA 0.31 AAGCCTATACGTTTCTGTGGAGTAA
307 CEPl 0.37 AAGCCTATACGTTTCTGTGGAGTAA
308 CD8A 0.38 TGGACCCCACTGGCTGAGAATCTGG
309 SCAPl 0.32 TCCTCCATCACCTGAAACACTGGAC
310 CD2 0.48 GCCCCACTGGACAACACTGATTCCT
311 VAVl 0.41 ACTTGTCCTCAGCTTGGGCTTCTTC
312 MAP4K1 0.36 TCCTGTACTTGTCCTCAGCTTGGGC
313 CCR7 0.37 ACTTGTCCTCAGCTTGGGCTTCTTC
314 C6orf32 0.38 TCCTTGTGCCTGCTCCTGTACTTGT
315 ALOX15B 0.43 TGCCTGCTCCTGTACTTGTCCTCAG
316 BRDT 0.33 AAGCCTATACGTTTCTGTGGAGTAA
317 CD3G 0.51 AAGCCTATACGTTTCTGTGGAGTAA
318 LTB 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
319 NVL 0.31 TTGGACATCTCTAGTGTAGCTGCCA
320 RASGRP2 0.35 TGCCTGCTCCTGTACTTGTCCTCAG
321 LCPl 0.34 AAATGTTTCCTTGTGCCTGCTCCTG
322 CXCR4 0.3 AAGCCTATACGTTTCTGTGGAGTAA
323 PRKD2 0.33 CACCCAGCTGGTCCTGTGGATGGGA
324 GATA3 0.39 TCCTGTACTTGTCCTCAGCTTGGGC
325 KIAA0922 0.36 GCCCCACTGGACAACACTGATTCCT
326 TARP 0.49 TCCTCCATCACCTGAAACACTGGAC
327 SEC31L2 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
328 PRKCQ 0.37 TTGGACATCTCTAGTGTAGCTGCCA
329 SH2D1A 0.33 AAGCCTATACGTTTCTGTGGAGTAA
330 CHRNA3 0.5 AAGCCTATACGTTTCTGTGGAGTAA
331 CDlA 0.44 AAGCCTATACGTTTCTGTGGAGTAA
332 LSTl 0.36 CACCCAGCTGGTCCTGTGGATGGGA
333 LAIRl 0.47 CACCCAGCTGGTCCTGTGGATGGGA
334 CACNAlG 0.33 GCCCCACTGGACAACACTGATTCCT
335 TRB@ 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
336 SEPT6 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
337 HA-I 0.42 CACCCAGCTGGTCCTGTGGATGGGA
338 DOCK2 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
339 CD3D 0.41 TCCTGTACTTGTCCTCAGCTTGGGC
340 TRD@ 0.38 TGCCTGCTCCTGTACTTGTCCTCAG
341 T3JAM 0.37 TGCCTGCTCCTGTACTTGTCCTCAG
342 FNBPl 0.37 TCCTGTACTTGTCCTCAGCTTGGGC
343 CD6 0.4 CACCCAGCTGGTCCTGTGGATGGGA
344 AIFl 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
345 FOLHl 0.45 TCCTGTACTTGTCCTCAGCTTGGGC
346 CDlE 0.58 CACCCAGCTGGTCCTGTGGATGGGA
347 LY9 0.39 TCCTTGTGCCTGCTCCTGTACTTGT
348 ADA 0.39 AAATGTTTCCTTGTGCCTGCTCCTG
349 CDKL5 0.44 GCCCCACTGGACAACACTGATTCCT
350 TRIM 0.38 AAGCCTATACGTTTCTGTGGAGTAA
351 DATFl 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
352 RGC32 0.51 TCCTTGTGCCTGCTCCTGTACTTGT
353 ARHGAPl 5 0.34 CACCCAGCTGGTCCTGTGGATGGGA
354 NOTCHl 0.36 TCCTTGTGCCTGCTCCTGTACTTGT
355 BIN2 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
356 SEMA4G 0.35 AAGCCTATACGTTTCTGTGGAGTAA
357 DPEP2 0.33 CACCCAGCTGGTCCTGTGGATGGGA
358 CECRl 0.36 TCCTGTACTTGTCCTCAGCTTGGGC
359 BCLIlB 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
360 STAG3 0.41 TTGGACATCTCTAGTGTAGCTGCCA
361 GALNT6 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
362 UBASH3A 0.3 AAATGTTTCCTTGTGCCTGCTCCTG
363 PHEMX 0.38 TCCTCCATCACCTGAAACACTGGAC
364 FLJ13373 0.34 TCCTTGTGCCTGCTCCTGTACTTGT
365 LEFl 0.49 TCCTCCATCACCTGAAACACTGGAC
366 IL21R 0.42 TTGGACATCTCTAGTGTAGCTGCCA
367 MGC17330 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
368 AKAP13 0.53 TCCTTGTGCCTGCTCCTGTACTTGT
369 GIMAP5 0.34 AAATGTTTCCTTGTGCCTGCTCCTG
Table 37. Methotrexate biomarkers.
SEQIDNO Gene Correlation Medianprobe
370 PRPF8 0.34 TCCTCCATCACCTGAAACACTGGAC
371 RPL18 0.34 AAGCCTATACGTTTCTGTGGAGTAA
372 GOT2 0.31 CACCCAGCTGGTCCTGTGGATGGGA
373 RPL13A 0.31 TCCTGTACTTGTCCTCAGCTTGGGC 374 RPS15 0.39 CACCCAGCTGGTCCTGTGGATGGGA 375 RPLP2 0.32 GCCCCACTGGACAACACTGATTCCT 376 CSDA 0.39 GCCCCACTGGACAACACTGATTCCT 377 KHDRBSl 0.32 TCCTCCATCACCTGAAACACTGGAC 378 SNRPA 0.31 TCCTGTACTTGTCCTCAGCTTGGGC 379 IMPDH2 0.39 AAATGTTTCCTTGTGCCTGCTCCTG 380 RPS19 0.47 AAATGTTTCCTTGTGCCTGCTCCTG 381 NUP88 0.36 CACCCAGCTGGTCCTGTGGATGGGA 382 ATP5D 0.33 TGCCTGCTCCTGTACTTGTCCTCAG 383 PCBP2 0.32 AAATGTTTCCTTGTGCCTGCTCCTG 384 ZNF593 0.4 AAATGTTTCCTTGTGCCTGCTCCTG 385 HSU79274 0.32 TGGACCCCACTGGCTGAGAATCTGG 386 PRIMl 0.3 CACCCAGCTGGTCCTGTGGATGGGA 387 PFDN5 0.33 TCCTCCATCACCTGAAACACTGGAC 388 OXAlL 0.37 CACCCAGCTGGTCCTGTGGATGGGA 389 ATIC 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC 390 CIAPINl 0.34 ACTTGTCCTCAGCTTGGGCTTCTTC 391 RPS2 0.32 CACCCAGCTGGTCCTGTGGATGGGA 392 PCCB 0.36 GCCCCACTGGACAACACTGATTCCT 393 SHMT2 0.34 ACTTGTCCTCAGCTTGGGCTTCTTC 394 RPLPO 0.35 AAGCCTATACGTTTCTGTGGAGTAA 395 HNRPAl 0.35 TGGACCCCACTGGCTGAGAATCTGG 396 STOML2 0.32 TGCCTGCTCCTGTACTTGTCCTCAG 397 SKBl 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC 398 GLTSCR2 0.37 AAGCCTATACGTTTCTGTGGAGTAA 399 CCNBlIPl 0.3 TCCTTGTGCCTGCTCCTGTACTTGT 400 MRPS2 0.33 TTGGACATCTCTAGTGTAGCTGCCA 401 FLJ20859 0.34 TGCCTGCTCCTGTACTTGTCCTCAG 402 FLJ12270 0.3 ACTTGTCCTCAGCTTGGGCTTCTTC
Table 38 . Bleomycin biomarkers . SEQIDNO Gene Correlation Medianprobe
403 PFNl 0.45 GCCCCACTGGACAACACTGATTCCT
404 HKl 0.33 TTGGACATCTCTAGTGTAGCTGCCA
405 MCLl 0.31 TGGACCCCACTGGCTGAGAATCTGG
406 ZYX 0.32 TGGACCCCACTGGCTGAGAATCTGG
407 RAPlB 0.34 ACTTGTCCTCAGCTTGGGCTTCTTC
408 GNB2 0.32 CACCCAGCTGGTCCTGTGGATGGGA
409 EPASl 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
410 PGAMl 0.42 TGCCTGCTCCTGTACTTGTCCTCAG
411 CKAP4 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
412 DUSPl 0.4 AAATGTTTCCTTGTGCCTGCTCCTG
413 MYL9 0.4 TTGGACATCTCTAGTGTAGCTGCCA
414 K-ALPHA-I 0.37 TTGGACATCTCTAGTGTAGCTGCCA
415 CSDA 0.3 TCCTTGTGCCTGCTCCTGTACTTGT
416 IFITM2 0.36 TTGGACATCTCTAGTGTAGCTGCCA
417 ITGA5 0.43 GCCCCACTGGACAACACTGATTCCT
418 DPYSL3 0.44 TGGACCCCACTGGCTGAGAATCTGG
419 JUNB 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
420 NFKBIA 0.32 TCCTCCATCACCTGAAACACTGGAC
421 LAMBl 0.37 AAATGTTTCCTTGTGCCTGCTCCTG
422 FHLl 0.31 TGGACCCCACTGGCTGAGAATCTGG
423 INSIGl 0.31 TGGACCCCACTGGCTGAGAATCTGG
424 TIMPl 0.48 TGGACCCCACTGGCTGAGAATCTGG
425 GJAl 0.54 AAGCCTATACGTTTCTGTGGAGTAA
426 PRGl 0.46 TCCTTGTGCCTGCTCCTGTACTTGT
427 EXTl 0.35 TCCTTGTGCCTGCTCCTGTACTTGT
428 DKFZP434J154 0.31 GCCCCACTGGACAACACTGATTCCT
429 MVP 0.34 CACCCAGCTGGTCCTGTGGATGGGA
430 VASP 0.31 TCCTCCATCACCTGAAACACTGGAC
431 ARL7 0.39 TGGACCCCACTGGCTGAGAATCTGG
432 NNMT 0.34 TCCTGTACTTGTCCTCAGCTTGGGC
433 TAPl 0.3 TCCTGTACTTGTCCTCAGCTTGGGC
434 PLOD2 0.37 GCCCCACTGGACAACACTGATTCCT
435 ATF3 0.42 CACCCAGCTGGTCCTGTGGATGGGA
436 PALM2-AKAP2 0.33 TGGACCCCACTGGCTGAGAATCTGG
437 IL8 0.34 GCCCCACTGGACAACACTGATTCCT
438 LOXL2 0.32 GCCCCACTGGACAACACTGATTCCT
439 IL4R 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
440 DGKA 0.32 GCCCCACTGGACAACACTGATTCCT
441 SEC61G 0.41 CACCCAGCTGGTCCTGTGGATGGGA
442 RGS3 0.37 TGGACCCCACTGGCTGAGAATCTGG
443 F2R 0.34 CACCCAGCTGGTCCTGTGGATGGGA
444 TPM2 0.35 CACCCAGCTGGTCCTGTGGATGGGA
445 PSMB9 0.34 CACCCAGCTGGTCCTGTGGATGGGA
446 LOX 0.37 TCCTGTACTTGTCCTCAGCTTGGGC
447 STCl 0.35 TCCTCCATCACCTGAAACACTGGAC
448 PTGER4 0.31 CACCCAGCTGGTCCTGTGGATGGGA
449 SMAD3 0.38 TTGGACATCTCTAGTGTAGCTGCCA
450 WNT5A 0.44 TGGACCCCACTGGCTGAGAATCTGG
451 BDNF 0.34 TCCTCCATCACCTGAAACACTGGAC
452 TNFRSFlA 0.46 TCCTCCATCACCTGAAACACTGGAC
453 FLNC 0.34 ACTTGTCCTCAGCTTGGGCTTCTTC
454 DKFZP564K0822 0.34 TTGGACATCTCTAGTGTAGCTGCCA
455 FLOTl 0.38 TTGGACATCTCTAGTGTAGCTGCCA
456 PTRF 0.39 TGGACCCCACTGGCTGAGAATCTGG
457 HLA-B 0.36 TTGGACATCTCTAGTGTAGCTGCCA
458 MGC4083 0.32 GCCCCACTGGACAACACTGATTCCT
459 TNFRSFlOB 0.34 TGCCTGCTCCTGTACTTGTCCTCAG
460 PLAGLl 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
461 PNMA2 0.38 GCCCCACTGGACAACACTGATTCCT
462 TFPI 0.38 TCCTGTACTTGTCCTCAGCTTGGGC
463 GZMB 0.51 TCCTCCATCACCTGAAACACTGGAC
464 PLAUR 0.35 AAGCCTATACGTTTCTGTGGAGTAA
465 FSCNl 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
466 ERP70 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
467 AFlQ 0.3 TTGGACATCTCTAGTGTAGCTGCCA
468 HIC 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
469 COL6A1 0.32 AAGCCTATACGTTTCTGTGGAGTAA
470 IFITM3 0.3 GCCCCACTGGACAACACTGATTCCT
471 MAPlB 0.38 CACCCAGCTGGTCCTGTGGATGGGA
472 FLJ46603 0.37 TCCTCCATCACCTGAAACACTGGAC
473 RAFTLIN 0.34 TGGACCCCACTGGCTGAGAATCTGG
474 RRAS 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
475 FTL 0.3 CACCCAGCTGGTCCTGTGGATGGGA
476 KIAA0877 0.31 CACCCAGCTGGTCCTGTGGATGGGA
477 MTlE 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
478 CDClO 0.51 AAATGTTTCCTTGTGCCTGCTCCTG
479 DOCK2 0.32 AAGCCTATACGTTTCTGTGGAGTAA
480 RISl 0.37 ACTTGTCCTCAGCTTGGGCTTCTTC
481 BCATl 0.42 TTGGACATCTCTAGTGTAGCTGCCA
482 PRFl 0.34 TCCTCCATCACCTGAAACACTGGAC
483 DBNl 0.36 GCCCCACTGGACAACACTGATTCCT
484 MTlK 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
485 TMSBlO 0.42 GCCCCACTGGACAACACTGATTCCT
486 FLJ10350 0.4 AAATGTTTCCTTGTGCCTGCTCCTG
487 Clorf24 0.34 TGCCTGCTCCTGTACTTGTCCTCAG
488 NME7 0.46 TCCTGTACTTGTCCTCAGCTTGGGC
489 TMEM22 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
490 TPKl 0.37 TCCTCCATCACCTGAAACACTGGAC
491 ELK3 0.38 TGCCTGCTCCTGTACTTGTCCTCAG
492 CYLD 0.4 TCCTTGTGCCTGCTCCTGTACTTGT
493 ADAMTSl 0.31 AAGCCTATACGTTTCTGTGGAGTAA
494 EHD2 0.41 TCCTCCATCACCTGAAACACTGGAC
495 ACTB 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
Table 39. Methyl-GAG (methyl glyoxal bis amidinohydrazone dihydrochloride) biomarkers.
SEQIDNO Gene Correlation Medianprobe
496 SSRPl 0.37 TGCCTGCTCCTGTACTTGTCCTCAG
497 CTSC 0.35 CACCCAGCTGGTCCTGTGGATGGGA
498 LBR 0.38 ACTTGTCCTCAGCTTGGGCTTCTTC
499 EFNB2 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
500 SERPINAl 0.34 TCCTTGTGCCTGCTCCTGTACTTGT
501 SSSCAl 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
502 EZH2 0.36 TTGGACATCTCTAGTGTAGCTGCCA
503 MYB 0.33 GCCCCACTGGACAACACTGATTCCT
504 PRIMl 0.39 TCCTCCATCACCTGAAACACTGGAC
505 H2AFX 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
506 HMGAl 0.35 TTGGACATCTCTAGTGTAGCTGCCA
507 HMMR 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
508 TK2 0.42 CACCCAGCTGGTCCTGTGGATGGGA
509 WHSCl 0.35 AAATGTTTCCTTGTGCCTGCTCCTG
510 DIAPHl 0.34 GCCCCACTGGACAACACTGATTCCT
511 LAMB3 0.31 GCCCCACTGGACAACACTGATTCCT
512 DPAGTl 0.42 TGCCTGCTCCTGTACTTGTCCTCAG
513 UCK2 0.31 GCCCCACTGGACAACACTGATTCCT
514 SERPINBl 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
515 MDNl 0.35 TGCCTGCTCCTGTACTTGTCCTCAG
516 G0S2 0.43 CACCCAGCTGGTCCTGTGGATGGGA
517 MGC21654 0.36 TGGACCCCACTGGCTGAGAATCTGG
518 GTSEl 0.35 ACTTGTCCTCAGCTTGGGCTTCTTC
519 TACC3 0.31 TCCTCCATCACCTGAAACACTGGAC
520 PLAC8 0.31 CACCCAGCTGGTCCTGTGGATGGGA
521 HNRPD 0.35 TTGGACATCTCTAGTGTAGCTGCCA
522 PNAS-4 0.3 TTGGACATCTCTAGTGTAGCTGCCA
Table 40 . HDAC inhibitors bic
SEQIDNO Gene Correlation
523 FAU 0.33 TTGGACATCTCTAGTGTAGCTGCCA
524 NOL5A 0.33 TGGACCCCACTGGCTGAGAATCTGG
525 ANP32A 0.32 CACCCAGCTGGTCCTGTGGATGGGA
526 ARHGDIB 0.3 ACTTGTCCTCAGCTTGGGCTTCTTC
527 LBR 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
528 FABP5 0.33 TCCTCCATCACCTGAAACACTGGAC
529 ITM2A 0.32 TTGGACATCTCTAGTGTAGCTGCCA
530 SFRS5 0.34 TCCTCCATCACCTGAAACACTGGAC
531 IQGAP2 0.4 CACCCAGCTGGTCCTGTGGATGGGA
532 SLC7A6 0.35 AAGCCTATACGTTTCTGTGGAGTAA
533 SLA 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
534 IL2RG 0.31 TCCTCCATCACCTGAAACACTGGAC
535 MFNG 0.39 TCCTGTACTTGTCCTCAGCTTGGGC
536 GPSM3 0.32 TTGGACATCTCTAGTGTAGCTGCCA
537 PIM2 0.3 TTGGACATCTCTAGTGTAGCTGCCA
538 EVERl 0.35 GCCCCACTGGACAACACTGATTCCT
539 LRMP 0.35 TGCCTGCTCCTGTACTTGTCCTCAG
540 ICAM2 0.44 TCCTGTACTTGTCCTCAGCTTGGGC
541 RIMS3 0.43 TGGACCCCACTGGCTGAGAATCTGG
542 FMNLl 0.35 TTGGACATCTCTAGTGTAGCTGCCA
543 MYB 0.37 TGCCTGCTCCTGTACTTGTCCTCAG
544 PTPN7 0.36 TCCTTGTGCCTGCTCCTGTACTTGT
545 LCK 0.48 CACCCAGCTGGTCCTGTGGATGGGA
546 CXorf9 0.3 ACTTGTCCTCAGCTTGGGCTTCTTC
547 RHOH 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
548 ZNFNlAl 0.33 AAATGTTTCCTTGTGCCTGCTCCTG
549 CENTBl 0.45 CACCCAGCTGGTCCTGTGGATGGGA
550 LCP2 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
551 DBT 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
552 CEPl 0.31 TTGGACATCTCTAGTGTAGCTGCCA
553 IL6R 0.31 TGGACCCCACTGGCTGAGAATCTGG
554 VAVl 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
555 MAP4K1 0.3 AAGCCTATACGTTTCTGTGGAGTAA
556 CD28 0.36 TCCTTGTGCCTGCTCCTGTACTTGT
557 PTP4A3 0.3 TTGGACATCTCTAGTGTAGCTGCCA
558 CD3G 0.33 CACCCAGCTGGTCCTGTGGATGGGA
559 LTB 0.4 TCCTGTACTTGTCCTCAGCTTGGGC
560 USP34 0.44 GCCCCACTGGACAACACTGATTCCT
561 NVL 0.41 TCCTTGTGCCTGCTCCTGTACTTGT
562 CD8B1 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC
563 SFRS6 0.31 GCCCCACTGGACAACACTGATTCCT
564 LCPl 0.34 TCCTGTACTTGTCCTCAGCTTGGGC
565 CXCR4 0.36 TGCCTGCTCCTGTACTTGTCCTCAG
566 PSCDBP 0.33 TGGACCCCACTGGCTGAGAATCTGG
567 SELPLG 0.33 TTGGACATCTCTAGTGTAGCTGCCA
568 CD3Z 0.3 TCCTTGTGCCTGCTCCTGTACTTGT
569 PRKCQ 0.33 TTGGACATCTCTAGTGTAGCTGCCA
570 CDlA 0.34 GCCCCACTGGACAACACTGATTCCT
571 GATA2 0.31 TTGGACATCTCTAGTGTAGCTGCCA
572 P2RX5 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
573 LAIRl 0.35 TGGACCCCACTGGCTGAGAATCTGG
574 Clorf38 0.4 GCCCCACTGGACAACACTGATTCCT
575 SH2D1A 0.44 TCCTTGTGCCTGCTCCTGTACTTGT
576 TRB@ 0.33 CACCCAGCTGGTCCTGTGGATGGGA
577 SEPT6 0.34 GCCCCACTGGACAACACTGATTCCT
578 HA-I 0.32 AAGCCTATACGTTTCTGTGGAGTAA
579 DOCK2 0.3 TCCTTGTGCCTGCTCCTGTACTTGT
580 WBSCR20C 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
581 CD3D 0.3 ACTTGTCCTCAGCTTGGGCTTCTTC
582 RNASE6 0.31 GCCCCACTGGACAACACTGATTCCT
583 SFRS7 0.32 AAATGTTTCCTTGTGCCTGCTCCTG
584 WBSCR20A 0.3 AAGCCTATACGTTTCTGTGGAGTAA
585 NUP210 0.31 TTGGACATCTCTAGTGTAGCTGCCA
586 CD6 0.34 TCCTTGTGCCTGCTCCTGTACTTGT
587 HNRPAl 0.3 GCCCCACTGGACAACACTGATTCCT 588 AIFl 0.34 AAGCCTATACGTTTCTGTGGAGTAA 589 CYFIP2 0.38 TGGACCCCACTGGCTGAGAATCTGG 590 GLTSCR2 0.38 TCCTTGTGCCTGCTCCTGTACTTGT 591 Cllorf2 0.31 AAGCCTATACGTTTCTGTGGAGTAA 592 ARHGAP15 0.33 TGGACCCCACTGGCTGAGAATCTGG 593 BIN2 0.35 TTGGACATCTCTAGTGTAGCTGCCA 594 SH3TC1 0.35 ACTTGTCCTCAGCTTGGGCTTCTTC 595 STAG3 0.32 AAATGTTTCCTTGTGCCTGCTCCTG 596 TM6SF1 0.34 ACTTGTCCTCAGCTTGGGCTTCTTC 597 C15orf25 0.33 TCCTCCATCACCTGAAACACTGGAC 598 FLJ22457 0.36 AAATGTTTCCTTGTGCCTGCTCCTG 599 PACAP 0.34 TGCCTGCTCCTGTACTTGTCCTCAG 600 MGC2744 0.31 GCCCCACTGGACAACACTGATTCCT
Table 41. 5-Fluorouracil biomarkers. SEQIDNO Gene Correlation Medianprobe
601 RPL18 0.38 AAATGTTTCCTTGTGCCTGCTCCTG
602 RPLlOA 0.39 TGGACCCCACTGGCTGAGAATCTGG
603 ANAPC5 0.37 ACTTGTCCTCAGCTTGGGCTTCTTC
604 EEF1B2 0.3 TCCTGTACTTGTCCTCAGCTTGGGC
605 RPL13A 0.5 TGCCTGCTCCTGTACTTGTCCTCAG
606 RPS15 0.4 ACTTGTCCTCAGCTTGGGCTTCTTC
607 NDUFABl 0.38 GCCCCACTGGACAACACTGATTCCT
608 APRT 0.32 AAATGTTTCCTTGTGCCTGCTCCTG
609 ZNF593 0.34 TCCTCCATCACCTGAAACACTGGAC
610 MRP63 0.32 AAATGTTTCCTTGTGCCTGCTCCTG
611 IL6R 0.41 TGGACCCCACTGGCTGAGAATCTGG
612 SART3 0.37 TCCTCCATCACCTGAAACACTGGAC
613 UCK2 0.32 GCCCCACTGGACAACACTGATTCCT
614 RPL17 0.31 AAGCCTATACGTTTCTGTGGAGTAA
615 RPS2 0.35 CACCCAGCTGGTCCTGTGGATGGGA
616 PCCB 0.38 TCCTTGTGCCTGCTCCTGTACTTGT
617 TOMM20 0.32 TGGACCCCACTGGCTGAGAATCTGG
618 SHMT2 0.32 TTGGACATCTCTAGTGTAGCTGCCA
619 RPLPO 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
620 GTF3A 0.32 CACCCAGCTGGTCCTGTGGATGGGA
621 STOML2 0.33 TGGACCCCACTGGCTGAGAATCTGG
622 DKFZp564J157 0.4 AAATGTTTCCTTGTGCCTGCTCCTG
623 MRPS2 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
624 ALG5 0.3 TTGGACATCTCTAGTGTAGCTGCCA
625 CALML4 0.33 CACCCAGCTGGTCCTGTGGATGGGA
Table 42 Radiation sensitivity biomarkers. SEQIDNO Gene Correlation Medianprobe
626 TRAl 0.36 TGGACCCCACTGGCTGAGAATCTGG
627 ACTN4 0.36 ACTTGTCCTCAGCTTGGGCTTCTTC
628 CALMl 0.32 TCCTCCATCACCTGAAACACTGGAC
629 CD63 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
630 FKBPlA 0.38 TGGACCCCACTGGCTGAGAATCTGG
631 CALU 0.47 ACTTGTCCTCAGCTTGGGCTTCTTC
632 IQGAPl 0.37 TTGGACATCTCTAGTGTAGCTGCCA
633 MGC8721 0.35 AAATGTTTCCTTGTGCCTGCTCCTG
634 STATl 0.37 TGGACCCCACTGGCTGAGAATCTGG
635 TACCl 0.41 ACTTGTCCTCAGCTTGGGCTTCTTC
636 TM4SF8 0.33 AAGCCTATACGTTTCTGTGGAGTAA
637 CD59 0.31 TCCTCCATCACCTGAAACACTGGAC
638 CKAP4 0.45 TCCTTGTGCCTGCTCCTGTACTTGT
639 DUSPl 0.38 TCCTGTACTTGTCCTCAGCTTGGGC
640 RCNl 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
641 MGC8902 0.35 TGCCTGCTCCTGTACTTGTCCTCAG
642 RRBPl 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
643 PRNP 0.42 TTGGACATCTCTAGTGTAGCTGCCA
644 IER3 0.34 GCCCCACTGGACAACACTGATTCCT
645 MARCKS 0.43 GCCCCACTGGACAACACTGATTCCT
646 FER1L3 0.47 TGCCTGCTCCTGTACTTGTCCTCAG
647 SLC20A1 0.41 ACTTGTCCTCAGCTTGGGCTTCTTC
648 HEXB 0.46 AAATGTTTCCTTGTGCCTGCTCCTG
649 EXTl 0.47 CACCCAGCTGGTCCTGTGGATGGGA
650 TJPl 0.32 AAATGTTTCCTTGTGCCTGCTCCTG
651 CTSL 0.38 TCCTGTACTTGTCCTCAGCTTGGGC
652 SLC39A6 0.36 TCCTGTACTTGTCCTCAGCTTGGGC
653 RIOK3 0.38 TCCTCCATCACCTGAAACACTGGAC
654 CRK 0.37 TGCCTGCTCCTGTACTTGTCCTCAG
655 NNMT 0.37 TGCCTGCTCCTGTACTTGTCCTCAG
656 TRAM2 0.35 TTGGACATCTCTAGTGTAGCTGCCA
657 ADAM9 0.52 TCCTGTACTTGTCCTCAGCTTGGGC
658 PLSCRl 0.35 TGGACCCCACTGGCTGAGAATCTGG
659 PRSS23 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
660 PLOD2 0.36 TGCCTGCTCCTGTACTTGTCCTCAG
661 NPCl 0.39 TGCCTGCTCCTGTACTTGTCCTCAG
662 TOBl 0.37 CACCCAGCTGGTCCTGTGGATGGGA
663 GFPTl 0.47 CACCCAGCTGGTCCTGTGGATGGGA
664 IL8 0.36 AAATGTTTCCTTGTGCCTGCTCCTG
665 PYGL 0.46 TCCTCCATCACCTGAAACACTGGAC
666 LOXL2 0.49 TTGGACATCTCTAGTGTAGCTGCCA
667 KIAA0355 0.36 TCCTTGTGCCTGCTCCTGTACTTGT
668 UGDH 0.49 TTGGACATCTCTAGTGTAGCTGCCA
669 PURA 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
670 ULK2 0.37 AAGCCTATACGTTTCTGTGGAGTAA
671 CENTG2 0.35 GCCCCACTGGACAACACTGATTCCT
672 CAP350 0.31 GCCCCACTGGACAACACTGATTCCT
673 CXCLl 0.36 TCCTGTACTTGTCCTCAGCTTGGGC
674 BTN3A3 0.35 AAGCCTATACGTTTCTGTGGAGTAA
675 WNT5A 0.3 AAGCCTATACGTTTCTGTGGAGTAA
676 FOXF2 0.44 AAATGTTTCCTTGTGCCTGCTCCTG
677 LPHN2 0.34 GCCCCACTGGACAACACTGATTCCT
678 CDHIl 0.39 TGGACCCCACTGGCTGAGAATCTGG
679 P4HAl 0.33 TCCTCCATCACCTGAAACACTGGAC
680 GRP58 0.44 CACCCAGCTGGTCCTGTGGATGGGA
681 DSIPI 0.44 TGGACCCCACTGGCTGAGAATCTGG
682 MAP1LC3B 0.5 AAGCCTATACGTTTCTGTGGAGTAA
683 GALIG 0.36 AAATGTTTCCTTGTGCCTGCTCCTG
684 IGSF4 0.4 TCCTCCATCACCTGAAACACTGGAC
685 IRS2 0.35 TGGACCCCACTGGCTGAGAATCTGG
686 ATP2A2 0.35 CACCCAGCTGGTCCTGTGGATGGGA
687 OGT 0.3 TCCTGTACTTGTCCTCAGCTTGGGC
688 TNFRSFlOB 0.31 AAGCCTATACGTTTCTGTGGAGTAA
689 KIAA1128 0.35 CACCCAGCTGGTCCTGTGGATGGGA
690 TM4SF1 0.35 CACCCAGCTGGTCCTGTGGATGGGA
691 RIPK2 0.42 TGCCTGCTCCTGTACTTGTCCTCAG
692 NR1D2 0.47 TTGGACATCTCTAGTGTAGCTGCCA
693 SSA2 0.36 TTGGACATCTCTAGTGTAGCTGCCA
694 NQOl 0.4 AAGCCTATACGTTTCTGTGGAGTAA
695 ASPH 0.36 TGCCTGCTCCTGTACTTGTCCTCAG
696 ASAHl 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC
697 MGLL 0.35 TGGACCCCACTGGCTGAGAATCTGG
698 SERPINB6 0.51 AAGCCTATACGTTTCTGTGGAGTAA
699 HSPA5 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
700 ZFP36L1 0.39 TCCTTGTGCCTGCTCCTGTACTTGT
701 COL4A1 0.3 ACTTGTCCTCAGCTTGGGCTTCTTC
702 NIPA2 0.36 ACTTGTCCTCAGCTTGGGCTTCTTC
703 FKBP9 0.48 AAATGTTTCCTTGTGCCTGCTCCTG
704 IL6ST 0.4 GCCCCACTGGACAACACTGATTCCT
705 DKFZP564G2022 0.39 TTGGACATCTCTAGTGTAGCTGCCA
706 PPAP2B 0.33 TGGACCCCACTGGCTGAGAATCTGG
707 MAPlB 0.3 CACCCAGCTGGTCCTGTGGATGGGA
708 MAPKl 0.3 TGGACCCCACTGGCTGAGAATCTGG
709 MYOlB 0.38 ACTTGTCCTCAGCTTGGGCTTCTTC
710 CAST 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
711 RRAS2 0.52 AAATGTTTCCTTGTGCCTGCTCCTG
712 QKI 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
713 LHFPL2 0.36 TCCTTGTGCCTGCTCCTGTACTTGT
714 SEPTlO 0.38 GCCCCACTGGACAACACTGATTCCT
715 ARHE 0.5 AAGCCTATACGTTTCTGTGGAGTAA
716 KIAA1078 0.34 AAGCCTATACGTTTCTGTGGAGTAA
717 FTL 0.38 TCCTGTACTTGTCCTCAGCTTGGGC
718 KIAA0877 0.41 AAATGTTTCCTTGTGCCTGCTCCTG
719 PLCBl 0.3 AAGCCTATACGTTTCTGTGGAGTAA
720 KIAA0802 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
721 RAB3GAP 0.43 TGCCTGCTCCTGTACTTGTCCTCAG
722 SERPINBl 0.46 TGCCTGCTCCTGTACTTGTCCTCAG
723 TIMM17A 0.38 AAATGTTTCCTTGTGCCTGCTCCTG
724 SOD2 0.35 TTGGACATCTCTAGTGTAGCTGCCA
725 HLA-A 0.33 TTGGACATCTCTAGTGTAGCTGCCA
726 NOMO2 0.43 CACCCAGCTGGTCCTGTGGATGGGA
727 LOC55831 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
728 PHLDAl 0.32 CACCCAGCTGGTCCTGTGGATGGGA
729 TMEM2 0.47 TGGACCCCACTGGCTGAGAATCTGG
730 MLPH 0.35 ACTTGTCCTCAGCTTGGGCTTCTTC
731 FAD104 0.34 ACTTGTCCTCAGCTTGGGCTTCTTC
732 LRRC5 0.42 CACCCAGCTGGTCCTGTGGATGGGA
733 RAB7L1 0.41 TTGGACATCTCTAGTGTAGCTGCCA
734 FLJ35036 0.36 TCCTGTACTTGTCCTCAGCTTGGGC
735 DOCKlO 0.41 TCCTCCATCACCTGAAACACTGGAC
736 LRP12 0.36 AAGCCTATACGTTTCTGTGGAGTAA
737 TXNDC5 0.4 ACTTGTCCTCAGCTTGGGCTTCTTC
738 CDC14B 0.39 TGCCTGCTCCTGTACTTGTCCTCAG
739 HRMTlLl 0.38 CACCCAGCTGGTCCTGTGGATGGGA
740 DNAJClO 0.31 TTGGACATCTCTAGTGTAGCTGCCA
741 TNPOl 0.33 GCCCCACTGGACAACACTGATTCCT
742 LONP 0.32 AAATGTTTCCTTGTGCCTGCTCCTG
743 AMIGO2 0.38 AAGCCTATACGTTTCTGTGGAGTAA
744 DNAPTP6 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
745 ADAMTSl 0.37 TTGGACATCTCTAGTGTAGCTGCCA
Table 43. Rituximab (e.g., Mabthera) biomarkers.
SEQIDNO Gene Correlation Medianprobe
746 PSMB2 0.89 TCCTCCATCACCTGAAACACTGGAC
747 BATl 0.88 AAGCCTATACGTTTCTGTGGAGTAA
748 ASCC3L1 0.89 TCCTTGTGCCTGCTCCTGTACTTGT
749 SET 0.94 AAATGTTTCCTTGTGCCTGCTCCTG
750 YWHAZ 0.83 TCCTTGTGCCTGCTCCTGTACTTGT
751 GLUL 0.8 TGGACCCCACTGGCTGAGAATCTGG
752 LDHA 0.8 TCCTTGTGCCTGCTCCTGTACTTGT
753 HMGBl 0.84 AAATGTTTCCTTGTGCCTGCTCCTG
754 SFRS2 0.87 AAATGTTTCCTTGTGCCTGCTCCTG
755 DPYSL2 0.82 TCCTGTACTTGTCCTCAGCTTGGGC
756 MGC8721 0.82 CACCCAGCTGGTCCTGTGGATGGGA
757 NOL5A 0.86 TGCCTGCTCCTGTACTTGTCCTCAG
758 SFRSlO 0.88 AAATGTTTCCTTGTGCCTGCTCCTG
759 SF3B1 0.82 TCCTGTACTTGTCCTCAGCTTGGGC
760 K-ALPHA-I 0.86 TGCCTGCTCCTGTACTTGTCCTCAG
761 TXNRDl 0.86 TGGACCCCACTGGCTGAGAATCTGG
762 ARHGDIB 0.83 CACCCAGCTGGTCCTGTGGATGGGA
763 ZFP36L2 0.92 TTGGACATCTCTAGTGTAGCTGCCA
764 DHXl5 0.81 TGGACCCCACTGGCTGAGAATCTGG
765 SOX4 0.85 CACCCAGCTGGTCCTGTGGATGGGA
766 GRSFl 0.81 TGGACCCCACTGGCTGAGAATCTGG
767 MCM3 0.85 GCCCCACTGGACAACACTGATTCCT
768 IFITMl 0.82 TCCTCCATCACCTGAAACACTGGAC
769 RPA2 0.86 TCCTCCATCACCTGAAACACTGGAC
770 LBR 0.87 ACTTGTCCTCAGCTTGGGCTTCTTC
771 CKSlB 0.85 AAGCCTATACGTTTCTGTGGAGTAA
772 NASP 0.82 TGGACCCCACTGGCTGAGAATCTGG
773 HNRPDL 0.81 TCCTCCATCACCTGAAACACTGGAC
774 CUGBP2 0.81 TGCCTGCTCCTGTACTTGTCCTCAG lib PTBPl 0.87 TCCTTGTGCCTGCTCCTGTACTTGT
116 ARL7 0.83 TTGGACATCTCTAGTGTAGCTGCCA
111 CTCF 0.83 ACTTGTCCTCAGCTTGGGCTTCTTC
778 HMGCR 0.86 TCCTTGTGCCTGCTCCTGTACTTGT
779 ITM2A 0.88 AAATGTTTCCTTGTGCCTGCTCCTG
780 SFRS3 0.93 TCCTTGTGCCTGCTCCTGTACTTGT
781 SRPK2 0.82 TCCTTGTGCCTGCTCCTGTACTTGT
782 JARID2 0.92 CACCCAGCTGGTCCTGTGGATGGGA
783 M96 0.84 TCCTGTACTTGTCCTCAGCTTGGGC
784 MAD2L1 0.87 TCCTCCATCACCTGAAACACTGGAC
785 SATBl 0.81 ACTTGTCCTCAGCTTGGGCTTCTTC
786 TMPO 0.9 ACTTGTCCTCAGCTTGGGCTTCTTC
787 SIVA 0.84 ACTTGTCCTCAGCTTGGGCTTCTTC
788 SEMA4D 0.9 TCCTCCATCACCTGAAACACTGGAC
789 TFDP2 0.87 TCCTTGTGCCTGCTCCTGTACTTGT
790 SKP2 0.86 AAGCCTATACGTTTCTGTGGAGTAA
791 SH3YL1 0.88 GCCCCACTGGACAACACTGATTCCT
792 RFC4 0.87 TCCTCCATCACCTGAAACACTGGAC
793 PCBP2 0.83 AAGCCTATACGTTTCTGTGGAGTAA
794 IL2RG 0.84 GCCCCACTGGACAACACTGATTCCT
795 CDC45L 0.89 TCCTGTACTTGTCCTCAGCTTGGGC
796 GTSEl 0.83 TTGGACATCTCTAGTGTAGCTGCCA
797 KIFIl 0.85 AAGCCTATACGTTTCTGTGGAGTAA
798 FENl 0.88 TTGGACATCTCTAGTGTAGCTGCCA
799 MYB 0.9 TGGACCCCACTGGCTGAGAATCTGG
800 LCK 0.87 TCCTCCATCACCTGAAACACTGGAC
801 CENPA 0.84 GCCCCACTGGACAACACTGATTCCT
802 CCNE2 0.84 GCCCCACTGGACAACACTGATTCCT
803 H2AFX 0.88 TTGGACATCTCTAGTGTAGCTGCCA
804 SNRPG 0.84 TCCTCCATCACCTGAAACACTGGAC
805 CD3G 0.94 TCCTTGTGCCTGCTCCTGTACTTGT
806 STK6 0.9 ACTTGTCCTCAGCTTGGGCTTCTTC
807 PTP4A2 0.81 TGCCTGCTCCTGTACTTGTCCTCAG
808 FDFTl 0.91 AAATGTTTCCTTGTGCCTGCTCCTG
809 HSPA8 0.84 AAATGTTTCCTTGTGCCTGCTCCTG
810 HNRPR 0.94 TCCTTGTGCCTGCTCCTGTACTTGT
811 MCM7 0.92 AAATGTTTCCTTGTGCCTGCTCCTG
812 SFRS6 0.85 TGGACCCCACTGGCTGAGAATCTGG
813 PAK2 0.8 CACCCAGCTGGTCCTGTGGATGGGA
814 LCPl 0.85 TCCTGTACTTGTCCTCAGCTTGGGC
815 STAT3 0.81 ACTTGTCCTCAGCTTGGGCTTCTTC
816 OK/SW-cl.56 0.8 TCCTTGTGCCTGCTCCTGTACTTGT
817 WHSCl 0.81 TGGACCCCACTGGCTGAGAATCTGG
818 DIAPHl 0.88 AAGCCTATACGTTTCTGTGGAGTAA
819 KIF2C 0.88 TCCTGTACTTGTCCTCAGCTTGGGC
820 HDGFRP3 0.89 CACCCAGCTGGTCCTGTGGATGGGA
821 PNMA2 0.93 TTGGACATCTCTAGTGTAGCTGCCA
822 GATA3 0.93 TCCTGTACTTGTCCTCAGCTTGGGC
823 BUBl 0.88 AAATGTTTCCTTGTGCCTGCTCCTG
824 TPX2 0.8 CACCCAGCTGGTCCTGTGGATGGGA
825 SH2D1A 0.86 TCCTTGTGCCTGCTCCTGTACTTGT
826 TNFAIP8 0.9 TCCTCCATCACCTGAAACACTGGAC
827 CSElL 0.83 AAATGTTTCCTTGTGCCTGCTCCTG
828 MCAM 0.8 TCCTGTACTTGTCCTCAGCTTGGGC
829 AFlQ 0.83 GCCCCACTGGACAACACTGATTCCT
830 CD47 0.86 CACCCAGCTGGTCCTGTGGATGGGA
831 SFRSl 0.85 AAGCCTATACGTTTCTGTGGAGTAA
832 FYB 0.92 TCCTGTACTTGTCCTCAGCTTGGGC
833 TRB@ 0.84 ACTTGTCCTCAGCTTGGGCTTCTTC
834 CXCR4 0.94 GCCCCACTGGACAACACTGATTCCT
835 H3F3B 0.84 TCCTCCATCACCTGAAACACTGGAC
836 MKI67 0.83 ACTTGTCCTCAGCTTGGGCTTCTTC
837 MAC30 0.82 TCCTTGTGCCTGCTCCTGTACTTGT
838 ARID5B 0.88 AAGCCTATACGTTTCTGTGGAGTAA
839 LOC339287 0.81 AAGCCTATACGTTTCTGTGGAGTAA
840 CD3D 0.82 TCCTTGTGCCTGCTCCTGTACTTGT
841 ZAP70 0.87 AAGCCTATACGTTTCTGTGGAGTAA
842 LAPTM4B 0.83 TCCTCCATCACCTGAAACACTGGAC
843 SFRS7 0.87 TCCTTGTGCCTGCTCCTGTACTTGT
844 HNRPAl 0.9 AAGCCTATACGTTTCTGTGGAGTAA
845 HSPCA 0.88 AAGCCTATACGTTTCTGTGGAGTAA
846 AIFl 0.82 TCCTTGTGCCTGCTCCTGTACTTGT
847 GTF3A 0.87 AAGCCTATACGTTTCTGTGGAGTAA
848 MCM5 0.91 TTGGACATCTCTAGTGTAGCTGCCA
849 GTL3 0.85 AAGCCTATACGTTTCTGTGGAGTAA
850 ZNF22 0.89 TGCCTGCTCCTGTACTTGTCCTCAG
851 FLJ22794 0.83 GCCCCACTGGACAACACTGATTCCT
852 LZTFLl 0.89 ACTTGTCCTCAGCTTGGGCTTCTTC
853 e(y)2 0.87 TCCTCCATCACCTGAAACACTGGAC
854 FLJ20152 0.92 TCCTCCATCACCTGAAACACTGGAC
855 C10orf3 0.86 ACTTGTCCTCAGCTTGGGCTTCTTC
856 NRNl 0.86 AAATGTTTCCTTGTGCCTGCTCCTG
857 FLJ10858 0.81 GCCCCACTGGACAACACTGATTCCT 858 BCLIlB 0.89 GCCCCACTGGACAACACTGATTCCT 859 ASPM 0.91 AAGCCTATACGTTTCTGTGGAGTAA 860 LEFl 0.9 TTGGACATCTCTAGTGTAGCTGCCA 861 LOC146909 0.83 ACTTGTCCTCAGCTTGGGCTTCTTC
Table 44 5-Aza-2 ' -deoxycytidine (decitabine) biomarkers . SEQIDNO Gene Correlation Medianprobe
862 CD99 0.31 T TTTGGGGAACCAATTCCTTCCTAGTGTAGCTGCCA
863 SNRPA 0.32 TTCCCCTTGGTTAACCTTTTGGTCCTCAGCTTGGGC
864 CUGBP2 0.32 TTCCCCTTGGTTAACCTTTTGGTCCTCAGCTTGGGC
865 STAT5A 0.32 GGCCCCCCCCAACCTTGGGGAACAACACTGATTCCT
866 SLA 0.38 TTTTGGGGAACCAATTCCTTCCTAGTGTAGCTGCCA
867 IL2RG 0.33 TTGGGGAACCCCCCCCAACCTTGGCTGAGAATCTGG
868 GTSEl 0.32 AACCTTTTGGTTCCCCTTCCAAGCTTGGGCTTCTTC
869 MYB 0.36 TTGGGGAACCCCCCCCAACCTTGGCTGAGAATCTGG
870 PTPN7 0.33 TTCCCCTTGGTTAACCTTTTGGTCCTCAGCTTGGGC
871 CXorf9 0.42 TTCCCCTTGGTTAACCTTTTGGTCCTCAGCTTGGGC
872 RHOH 0.38 AAAAAATTGGTTTTTTCCCCTTTGTGCCTGCTCCTG
873 ZNFNlAl 0.33 AAAAGGCCCCTTAATTAACCGGTTTCTGTGGAGTAA
874 CENTBl 0.35 CCAACCCCCCAAGGCCTTGGGGTCCTGTGGATGGGA
875 LCP2 0.3 AAAAAATTGGTTTTTTCCCCTTTGTGCCTGCTCCTG
876 HIST1H4C 0.33 TTGGGGAACCCCCCCCAACCTTGGCTGAGAATCTGG
877 CCR7 0.37 TTGGCCCCTTGGCCTTCCCCTTGTACTTGTCCTCAG
878 APOBEC3B 0.31 TTCCCCTTTTGGTTGGCCCCTTGCTCCTGTACTTGT
879 MCM7 0.31 TTGGGGAACCCCCCCCAACCTTGGCTGAGAATCTGG
880 LCPl 0.31 AAAAGGCCCCTTAATTAACCGGTTTCTGTGGAGTAA
881 SELPLG 0.4 TTGGGGAACCCCCCCCAACCTTGGCTGAGAATCTGG
882 CD3Z 0.35 TTCCCCTTGGTTAACCTTTTGGTCCTCAGCTTGGGC
883 PRKCQ 0.39 TTGGCCCCTTGGCCTTCCCCTTGTACTTGTCCTCAG
884 GZMB 0.32 GGCCCCCCCCAACCTTGGGGAACAACACTGATTCCT
885 SCN3A 0.4 AAAAGGCCCCTTAATTAACCGGTTTCTGTGGAGTAA
886 LAIRl 0.35 TTGGCCCCTTGGCCTTCCCCTTGTACTTGTCCTCAG
887 SH2D1A 0.35 GGCCCCCCCCAACCTTGGGGAACAACACTGATTCCT
SEPT6 0.35 AACCTTTTGGTTCCCCTTCCAAGCTTGGGCTTCTTC
889 CG018 0.32 AACCTTTTGGTTCCCCTTCCAAGCTTGGGCTTCTTC 890 CD3D 0.31 TTGGGGAACCCCCCCCAACCTTGGCTGAGAATCTGG 891 ClδorflO 0.33 TTCCCCTTTTGGTTGGCCCCTTGCTCCTGTACTTGT 892 PRFl 0.31 TTCCCCTTCCCCAATTCCAACCCTGAAACACTGGAC 893 AIFl 0.31 TTTTGGGGAACCAATTCCTTCCTAGTGTAGCTGCCA 894 MCM5 0.31 AACCTTTTGGTTCCCCTTCCAAGCTTGGGCTTCTTC 895 LPXN 0.35 TTCCCCTTCCCCAATTCCAACCCTGAAACACTGGAC 896 C22orfl8 0.33 AAAAAATTGGTTTTTTCCCCTTTGTGCCTGCTCCTG 897 ARHGAP15 0.31 AAAAAATTGGTTTTTTCCCCTTTGTGCCTGCTCCTG 898 LEFl 0.43 GGCCCCCCCCAACCTTGGGGAACAACACTGATTCCT
Table 45 . I Iddaarruubbicin biomarkers.
SEQIDNO Gene Correlation Medianprobe
899 SLC9A3P 0.31 TGGACCCCACTGGCTGAGAATCTGG
900 RPS19 0.32 TGGACCCCACTGGCTGAGAATCTGG
901 ITM2A 0.34 TCCTGTACTTGTCCTCAGCTTGGGC
902 SSBP2 0.31 AAGCCTATACGTTTCTGTGGAGTAA
903 CXorf9 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
904 RHOH 0.32 TCCTCCATCACCTGAAACACTGGAC
905 ZNFNlAl 0.36 AAATGTTTCCTTGTGCCTGCTCCTG
906 FXYD2 0.35 CACCCAGCTGGTCCTGTGGATGGGA
907 CCR9 0.39 TGGACCCCACTGGCTGAGAATCTGG 908 NAPlLl 0.3 TTGGACATCTCTAGTGTAGCTGCCA 909 CXCR4 0.31 AAATGTTTCCTTGTGCCTGCTCCTG 910 SH2D1A 0.3 TCCTGTACTTGTCCTCAGCTTGGGC 911 CDlA 0.3 AAGCCTATACGTTTCTGTGGAGTAA 912 TRB@ 0.32 AAATGTTTCCTTGTGCCTGCTCCTG 913 SEPT6 0.32 GCCCCACTGGACAACACTGATTCCT 914 RPS2 0.33 TGCCTGCTCCTGTACTTGTCCTCAG 915 DOCK2 0.32 TGCCTGCTCCTGTACTTGTCCTCAG 916 CD3D 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC 917 CD6 0.3 GCCCCACTGGACAACACTGATTCCT 918 ZAP70 0.34 ACTTGTCCTCAGCTTGGGCTTCTTC 919 AIFl 0.3 TGCCTGCTCCTGTACTTGTCCTCAG 920 CDlE 0.32 TGCCTGCTCCTGTACTTGTCCTCAG 921 CYFIP2 0.3 TTGGACATCTCTAGTGTAGCTGCCA 922 ADA 0.41 TCCTGTACTTGTCCTCAGCTTGGGC 923 TRIM 0.31 TCCTTGTGCCTGCTCCTGTACTTGT 924 GLTSCR2 0.32 TGCCTGCTCCTGTACTTGTCCTCAG 925 FLJ10858 0.35 GCCCCACTGGACAACACTGATTCCT 926 BCLIlB 0.34 TCCTGTACTTGTCCTCAGCTTGGGC 927 GIMAP6 0.36 TGCCTGCTCCTGTACTTGTCCTCAG 928 STAG3 0.34 TTGGACATCTCTAGTGTAGCTGCCA 929 UBASH3A 0.39 ACTTGTCCTCAGCTTGGGCTTCTTC
Table 46. Melphalan biomarkers . SEQIDNO Gene Correlation Medianprobe
930 CD99 0.31 TGGACCCCACTGGCTGAGAATCTGG
931 HLA-DPBl 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
932 ARHGDIB 0.35 TGCCTGCTCCTGTACTTGTCCTCAG
933 IFITMl 0.33 CACCCAGCTGGTCCTGTGGATGGGA
934 UBE2L6 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
935 ITM2A 0.37 TCCTTGTGCCTGCTCCTGTACTTGT
936 SERPINAl 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
937 STAT5A 0.38 AAATGTTTCCTTGTGCCTGCTCCTG
938 INPP5D 0.37 TCCTTGTGCCTGCTCCTGTACTTGT
939 DGKA 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
940 SATBl 0.34 TGCCTGCTCCTGTACTTGTCCTCAG
941 SEMA4D 0.37 AAATGTTTCCTTGTGCCTGCTCCTG
942 TFDP2 0.31 CACCCAGCTGGTCCTGTGGATGGGA
943 SLA 0.49 TCCTCCATCACCTGAAACACTGGAC
944 IL2RG 0.42 CACCCAGCTGGTCCTGTGGATGGGA
945 CD48 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
946 MFNG 0.48 ACTTGTCCTCAGCTTGGGCTTCTTC
947 ALOX5AP 0.3 CACCCAGCTGGTCCTGTGGATGGGA
948 GPSM3 0.31 AAGCCTATACGTTTCTGTGGAGTAA
949 PSMB9 0.34 GCCCCACTGGACAACACTGATTCCT
950 KIAA0711 0.37 TGGACCCCACTGGCTGAGAATCTGG
951 SELL 0.32 AAATGTTTCCTTGTGCCTGCTCCTG
952 ADA 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
953 EDGl 0.49 TTGGACATCTCTAGTGTAGCTGCCA
954 RIMS3 0.3 CACCCAGCTGGTCCTGTGGATGGGA
955 FMNLl 0.33 AAGCCTATACGTTTCTGTGGAGTAA
956 MYB 0.3 GCCCCACTGGACAACACTGATTCCT
957 PTPN7 0.34 AAATGTTTCCTTGTGCCTGCTCCTG
958 LCK 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
959 CXorf9 0.55 CACCCAGCTGGTCCTGTGGATGGGA
960 RHOH 0.35 TGGACCCCACTGGCTGAGAATCTGG
961 ZNFNlAl 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
962 CENTBl 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
963 LCP2 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
964 FXYD2 0.55 CACCCAGCTGGTCCTGTGGATGGGA
965 CDlD 0.44 AAGCCTATACGTTTCTGTGGAGTAA
966 BATF 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
967 STAT4 0.33 TCCTCCATCACCTGAAACACTGGAC
968 VAVl 0.31 TCCTCCATCACCTGAAACACTGGAC
969 MAP4K1 0.39 CACCCAGCTGGTCCTGTGGATGGGA
970 CCR7 0.44 TCCTGTACTTGTCCTCAGCTTGGGC
971 PDE4C 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
972 CD3G 0.32 AAGCCTATACGTTTCTGTGGAGTAA
973 CCR9 0.36 TTGGACATCTCTAGTGTAGCTGCCA
974 SPIlO 0.34 TCCTGTACTTGTCCTCAGCTTGGGC
975 LCPl 0.35 AAATGTTTCCTTGTGCCTGCTCCTG
976 IFI16 0.32 GCCCCACTGGACAACACTGATTCCT
977 CXCR4 0.36 ACTTGTCCTCAGCTTGGGCTTCTTC
978 ARHGEF6 0.47 AAGCCTATACGTTTCTGTGGAGTAA
979 GATA3 0.55 TTGGACATCTCTAGTGTAGCTGCCA
980 SELPLG 0.47 TTGGACATCTCTAGTGTAGCTGCCA
981 SEC31L2 0.36 TGGACCCCACTGGCTGAGAATCTGG
982 CD3Z 0.5 TTGGACATCTCTAGTGTAGCTGCCA
983 PRKCQ 0.56 GCCCCACTGGACAACACTGATTCCT
984 SH2D1A 0.33 TCCTCCATCACCTGAAACACTGGAC
985 GZMB 0.39 TGCCTGCTCCTGTACTTGTCCTCAG
986 CDlA 0.55 TGCCTGCTCCTGTACTTGTCCTCAG
987 SCN3A 0.64 CACCCAGCTGGTCCTGTGGATGGGA
988 LAIRl 0.32 CACCCAGCTGGTCCTGTGGATGGGA
989 FYB 0.49 TTGGACATCTCTAGTGTAGCTGCCA
990 TRB@ 0.37 TTGGACATCTCTAGTGTAGCTGCCA
991 SEPT6 0.32 GCCCCACTGGACAACACTGATTCCT
992 HA-I 0.48 GCCCCACTGGACAACACTGATTCCT
993 DOCK2 0.33 TTGGACATCTCTAGTGTAGCTGCCA
994 CG018 0.37 AAATGTTTCCTTGTGCCTGCTCCTG
995 CD3D 0.32 TCCTCCATCACCTGAAACACTGGAC
996 T3JAM 0.41 TGCCTGCTCCTGTACTTGTCCTCAG
997 FNBPl 0.36 TCCTGTACTTGTCCTCAGCTTGGGC
998 CD6 0.36 AAGCCTATACGTTTCTGTGGAGTAA
999 ZAP70 0.36 TGGACCCCACTGGCTGAGAATCTGG
1000 LSTl 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
1001 GPR65 0.42 TTGGACATCTCTAGTGTAGCTGCCA
1002 PRFl 0.41 GCCCCACTGGACAACACTGATTCCT
1003 AIFl 0.32 GCCCCACTGGACAACACTGATTCCT
1004 FLJ20331 0.42 TCCTCCATCACCTGAAACACTGGAC
1005 RAG2 0.31 CACCCAGCTGGTCCTGTGGATGGGA
1006 WDR45 0.37 TCCTGTACTTGTCCTCAGCTTGGGC
1007 CDlE 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
1008 CYFIP2 0.4 TCCTCCATCACCTGAAACACTGGAC
1009 TARP 0.36 CACCCAGCTGGTCCTGTGGATGGGA
1010 TRIM 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
1011 RPLlOL 0.3 TTGGACATCTCTAGTGTAGCTGCCA
1012 GLTSCR2 0.46 CACCCAGCTGGTCCTGTGGATGGGA
1013 GIMAP5 0.32 AAGCCTATACGTTTCTGTGGAGTAA
1014 ARHGAP15 0.36 TGCCTGCTCCTGTACTTGTCCTCAG
1015 NOTCHl 0.34 GCCCCACTGGACAACACTGATTCCT
1016 BIN2 0.36 TGGACCCCACTGGCTGAGAATCTGG 1017 C13orfl8 0.34 TCCTTGTGCCTGCTCCTGTACTTGT 1018 CECRl 0.32 TCCTGTACTTGTCCTCAGCTTGGGC 1019 BCLIlB 0.32 TCCTTGTGCCTGCTCCTGTACTTGT 1020 GIMAP6 0.3 TCCTTGTGCCTGCTCCTGTACTTGT 1021 STAG3 0.58 TTGGACATCTCTAGTGTAGCTGCCA 1022 TM6SF1 0.31 TCCTGTACTTGTCCTCAGCTTGGGC 1023 HSD17B7 0.32 GCCCCACTGGACAACACTGATTCCT 1024 UBASH3A 0.3 ACTTGTCCTCAGCTTGGGCTTCTTC 1025 MGC5566 0.45 TCCTCCATCACCTGAAACACTGGAC 1026 FLJ22457 0.39 AAGCCTATACGTTTCTGTGGAGTAA 1027 TPKl 0.33 TGCCTGCTCCTGTACTTGTCCTCAG 1028 PHFIl 0.3 AAATGTTTCCTTGTGCCTGCTCCTG 1029 DKFZP434B0335 0.4 TCCTTGTGCCTGCTCCTGTACTTGT
Table 47, IL4-PR38 fusion protein biomarkers
SEQIDNO Gene Correlation Medianprobe
1030 MCLl 0.3 TCCTCCATCACCTGAAACACTGGAC
1031 DDX23 0.35 CACCCAGCTGGTCCTGTGGATGGGA
1032 JUNB 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
1033 ZFP36 0.33 CACCCAGCTGGTCCTGTGGATGGGA
1034 IFITMl 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
1035 CKSlB 0.3 TGGACCCCACTGGCTGAGAATCTGG
1036 SERPINAl 0.31 GCCCCACTGGACAACACTGATTCCT
1037 IL4R 0.3 ACTTGTCCTCAGCTTGGGCTTCTTC
1038 CLDN3 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
1039 ARL4A 0.33 AAATGTTTCCTTGTGCCTGCTCCTG
1040 HMMR 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
1041 FLJ12671 0.42 TCCTTGTGCCTGCTCCTGTACTTGT
1042 ANKHDl 0.42 GCCCCACTGGACAACACTGATTCCT
1043 KIF2C 0.37 ACTTGTCCTCAGCTTGGGCTTCTTC
1044 RPA3 0.34 CACCCAGCTGGTCCTGTGGATGGGA
1045 MCCC2 0.34 TGCCTGCTCCTGTACTTGTCCTCAG
1046 CDH17 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
1047 LSM5 0.33 TTGGACATCTCTAGTGTAGCTGCCA
1048 PRFl 0.32 GCCCCACTGGACAACACTGATTCCT
1049 RODl 0.34 TCCTCCATCACCTGAAACACTGGAC
1050 FLJ12666 0.37 TCCTCCATCACCTGAAACACTGGAC
1051 SUV420H1 0.31 TTGGACATCTCTAGTGTAGCTGCCA
1052 MUC13 0.36 TCCTCCATCACCTGAAACACTGGAC
1053 C13orfl8 0.35 GCCCCACTGGACAACACTGATTCCT
1054 CDCA8 0.35 TGCCTGCTCCTGTACTTGTCCTCAG
Table 48 . Valproic acid (VPA) biomarkers.
SEQIDNO Gene Correlation Medianprobe
1055 STOM 0.32 AAATGTTTCCTTGTGCCTGCTCCTG
1056 TNFAIP3 0.32 TGGACCCCACTGGCTGAGAATCTGG
1057 ASNS 0.31 GCCCCACTGGACAACACTGATTCCT
1058 GARS 0.37 TGCCTGCTCCTGTACTTGTCCTCAG
1059 CXCR4 0.32 AAGCCTATACGTTTCTGTGGAGTAA
1060 EGLN3 0.31 TGGACCCCACTGGCTGAGAATCTGG
1061 LBH 0.35 TCCTGTACTTGTCCTCAGCTTGGGC
1062 GDFl5 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
Table 49. All-trans retinoic acid (ATRA) biomarkers. SEQIDNO Gene Correlation Medianprobe
1063 PPIB 0.31 AAGCCTATACGTTTCTGTGGAGTAA
1064 ZFP36L2 0.48 AAGCCTATACGTTTCTGTGGAGTAA
1065 IFI30 0.46 ACTTGTCCTCAGCTTGGGCTTCTTC
1066 USP7 0.35 TCCTCCATCACCTGAAACACTGGAC
1067 SRM 0.43 TCCTCCATCACCTGAAACACTGGAC
1068 SH3BP5 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
1069 ALDOC 0.41 TTGGACATCTCTAGTGTAGCTGCCA
1070 FADS2 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC
1071 GUSB 0.38 TTGGACATCTCTAGTGTAGCTGCCA
1072 PSCDl 0.48 TCCTGTACTTGTCCTCAGCTTGGGC
1073 IQGAP2 0.34 TCCTGTACTTGTCCTCAGCTTGGGC
1074 STS 0.34 GCCCCACTGGACAACACTGATTCCT
1075 MFNG 0.36 TGGACCCCACTGGCTGAGAATCTGG
1076 FLIl 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC
1077 PIM2 0.35 TGGACCCCACTGGCTGAGAATCTGG
1078 INPP4A 0.54 TCCTGTACTTGTCCTCAGCTTGGGC
1079 LRMP 0.51 GCCCCACTGGACAACACTGATTCCT
1080 ICAM2 0.3 AAATGTTTCCTTGTGCCTGCTCCTG
1081 EVI2A 0.33 CACCCAGCTGGTCCTGTGGATGGGA
1082 MAL 0.46 AAATGTTTCCTTGTGCCTGCTCCTG
1083 BTN3A3 0.43 TTGGACATCTCTAGTGTAGCTGCCA
1084 PTPN7 0.4 TTGGACATCTCTAGTGTAGCTGCCA
1085 ILlORA 0.42 TTGGACATCTCTAGTGTAGCTGCCA
1086 SPIl 0.41 AAGCCTATACGTTTCTGTGGAGTAA
1087 TRAFl 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
1088 ITGB7 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
1089 ARHGAP6 0.32 TGGACCCCACTGGCTGAGAATCTGG
1090 MAP4K1 0.52 GCCCCACTGGACAACACTGATTCCT
1091 CD28 0.34 AAGCCTATACGTTTCTGTGGAGTAA
1092 PTP4A3 0.3 TCCTCCATCACCTGAAACACTGGAC
1093 LTB 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
1094 Clorf38 0.4 TGCCTGCTCCTGTACTTGTCCTCAG
1095 WBSCR22 0.53 TCCTCCATCACCTGAAACACTGGAC
1096 CD8B1 0.35 TCCTCCATCACCTGAAACACTGGAC
1097 LCPl 0.35 ACTTGTCCTCAGCTTGGGCTTCTTC
1098 FLJ13052 0.31 TCCTCCATCACCTGAAACACTGGAC
1099 MEF2C 0.71 TTGGACATCTCTAGTGTAGCTGCCA
1100 PSCDBP 0.41 AAATGTTTCCTTGTGCCTGCTCCTG
1101 IL16 0.51 TGGACCCCACTGGCTGAGAATCTGG
1102 SELPLG 0.53 TGCCTGCTCCTGTACTTGTCCTCAG
1103 MAGEA9 0.6 AAATGTTTCCTTGTGCCTGCTCCTG
1104 LAIRl 0.43 TCCTCCATCACCTGAAACACTGGAC
1105 TNFRSF25 0.53 TCCTCCATCACCTGAAACACTGGAC
1106 EVI2B 0.42 ACTTGTCCTCAGCTTGGGCTTCTTC
1107 IGJ 0.37 TCCTTGTGCCTGCTCCTGTACTTGT
1108 PDCD4 0.47 AAATGTTTCCTTGTGCCTGCTCCTG
1109 RASA4 0.52 CACCCAGCTGGTCCTGTGGATGGGA
1110 HA-I 0.73 AAGCCTATACGTTTCTGTGGAGTAA
1111 PLCL2 0.47 TCCTGTACTTGTCCTCAGCTTGGGC
1112 RNASE6 0.31 AAGCCTATACGTTTCTGTGGAGTAA
1113 WBSCR20C 0.35 TTGGACATCTCTAGTGTAGCTGCCA
1114 NUP210 0.36 AAGCCTATACGTTTCTGTGGAGTAA
1115 RPLlOL 0.39 ACTTGTCCTCAGCTTGGGCTTCTTC
1116 Cllorf2 0.33 TGGACCCCACTGGCTGAGAATCTGG
1117 CABCl 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
1118 ARHGEF3 0.37 TCCTGTACTTGTCCTCAGCTTGGGC
1119 TAPBPL 0.42 TGCCTGCTCCTGTACTTGTCCTCAG
1120 CHST12 0.35 AAATGTTTCCTTGTGCCTGCTCCTG
1121 FKBPIl 0.54 TGCCTGCTCCTGTACTTGTCCTCAG
1122 FLJ35036 0.42 TTGGACATCTCTAGTGTAGCTGCCA
1123 MYLIP 0.38 CACCCAGCTGGTCCTGTGGATGGGA
1124 TXNDC5 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
1125 PACAP 0.3 TCCTCCATCACCTGAAACACTGGAC
1126 TOSO 0.34 TCCTGTACTTGTCCTCAGCTTGGGC
1127 PNAS-4 0.37 TGGACCCCACTGGCTGAGAATCTGG
1128 IL21R 0.57 AAGCCTATACGTTTCTGTGGAGTAA
1129 TCF4 0.64 TCCTTGTGCCTGCTCCTGTACTTGT
Table 50. Cytoxan biomarkers .
SEQIDNO Gene Correlation Medianprobe
1130 C6orf29 0.31 AAGCCTATACGTTTCTGTGGAGTAA
1131 TRIM31 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
1132 CD69 0.37 GCCCCACTGGACAACACTGATTCCT
1133 LRRN3 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
1134 GPR35 0.41 TCCTCCATCACCTGAAACACTGGAC
1135 CDW52 0.48 TTGGACATCTCTAGTGTAGCTGCCA
Table 51. Topotecan (Hycamtin) biomarkers. SEQIDNO Gene Correlation Medianprobe
1136 K-ALPHA-] L 0.32 AAGCCTATACGTTTCTGTGGAGTAA
1137 CSDA 0.32 AAGCCTATACGTTTCTGTGGAGTAA
1138 UCHLl 0.32 TTGGACATCTCTAGTGTAGCTGCCA
1139 NAPlLl 0.3 TCCTCCATCACCTGAAACACTGGAC
1140 ATP5G2 0.3 TCCTGTACTTGTCCTCAGCTTGGGC
1141 HDGFRP3 0.3 AAGCCTATACGTTTCTGTGGAGTAA
1142 IFI44 0.3 GCCCCACTGGACAACACTGATTCCT
Table 52 . Suberoyl Lanili
Zolinza) biomarkers .
SEQIDNO Gene C Coorrrreelation Medianprobe
1143 NOL5A 0.35 TCCTTGTGCCTGCTCCTGTACTTGT
1144 STOM 0.35 TGCCTGCTCCTGTACTTGTCCTCAG
1145 SIATl 0.36 AAATGTTTCCTTGTGCCTGCTCCTG
1146 CUGBP2 0.39 GCCCCACTGGACAACACTGATTCCT
1147 GUSB 0.33 TGGACCCCACTGGCTGAGAATCTGG
1148 ITM2A 0.34 TCCTTGTGCCTGCTCCTGTACTTGT
1149 JARID2 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
1150 RUNX3 0.32 CACCCAGCTGGTCCTGTGGATGGGA
1151 ICAM2 0.35 TGCCTGCTCCTGTACTTGTCCTCAG
1152 PTPN7 0.37 AAGCCTATACGTTTCTGTGGAGTAA
1153 VAVl 0.35 TTGGACATCTCTAGTGTAGCTGCCA
1154 PTP4A3 0.42 AAGCCTATACGTTTCTGTGGAGTAA
1155 MCAM 0.35 ACTTGTCCTCAGCTTGGGCTTCTTC
1156 MEF2C 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
1157 IDH3B 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
1158 RFP 0.31 TCCTCCATCACCTGAAACACTGGAC
1159 SEPT6 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
1160 SLC43A3 0.34 GCCCCACTGGACAACACTGATTCCT
1161 WBSCR20C 0.46 TGGACCCCACTGGCTGAGAATCTGG
1162 SHMT2 0.34 TCCTGTACTTGTCCTCAGCTTGGGC
1163 GLTSCR2 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
1164 CABCl 0.33 TCCTGTACTTGTCCTCAGCTTGGGC
12
1165 FLJ20859 0.42 ACTTGTCCTCAGCTTGGGCTTCTTC 1166 FLJ20010 0.51 TCCTGTACTTGTCCTCAGCTTGGGC 1167 MGC10993 0.33 TCCTTGTGCCTGCTCCTGTACTTGT 1168 FKBPIl 0.31 TCCTCCATCACCTGAAACACTGGAC
Table 53. Depsipeptide (FR901228) biomarkers.
SEQIDNO Gene Correlation Medianprobe
1169 ZFP36L2 0.32 AAATGTTTCCTTGTGCCTGCTCCTG
1170 TRIB2 0.35 TGCCTGCTCCTGTACTTGTCCTCAG
1171 LCP2 0.37 ACTTGTCCTCAGCTTGGGCTTCTTC
1172 C6orf32 0.35 TGCCTGCTCCTGTACTTGTCCTCAG
1173 ILl 6 0.34 CACCCAGCTGGTCCTGTGGATGGGA
1174 CACNAlG 0.31 AAGCCTATACGTTTCTGTGGAGTAA
1175 SPDEF 0.31 GCCCCACTGGACAACACTGATTCCT
1176 HABl 0.39 TCCTCCATCACCTGAAACACTGGAC
1177 TOSO 0.31 TGGACCCCACTGGCTGAGAATCTGG
1178 ARHGAP25 0.33 AAGCCTATACGTTTCTGTGGAGTAA
Table 54. Bortezomib biomarkers.
SEQIDNO Gene Correlation Medianprobe
1179 PLEKHB2 0.32 A AAAAATTGGTTTTTTCCCCTTTGTGCCTGCTCCTG
1180 ARPClB 0.32 TTGGGGAACCCCCCCCAACCTTGGCTGAGAATCTGG
1181 MXl 0.39 TTCCCCTTTTGGTTGGCCCCTTGCTCCTGTACTTGT
1182 CUGBP2 0.37 AAAAGGCCCCTTAATTAACCGGTTTCTGTGGAGTAA
1183 IFI16 0.33 AAAAGGCCCCTTAATTAACCGGTTTCTGTGGAGTAA
1184 TNFRSF14 0.3 AAAAAATTGGTTTTTTCCCCTTTGTGCCTGCTCCTG
1185 SPIlO 0.39 TTGGGGAACCCCCCCCAACCTTGGCTGAGAATCTGG
1186 ELFl 0.33 TTGGGGAACCCCCCCCAACCTTGGCTGAGAATCTGG
1187 LPXN 0.33 TTCCCCTTGGTTAACCTTTTGGTCCTCAGCTTGGGC
1188 IFRG28 0.31 TTCCCCTTGGTTAACCTTTTGGTCCTCAGCTTGGGC
1189 LEFl 0.33 GGCCCCCCCCAACCTTGGGGAACAACACTGATTCCT
1190 PYCARD 0.31 TTCCCCTTGGTTAACCTTTTGGTCCTCAGCTTGGGC
Table 55. Leukeran biomarkers .
SEQIDNO Gene Correlation M Meeddiiaannpprroobbe
' 1191 SSRPl 0.31 G GCCCCCCCCAACCTTGGGGACAACACTGATTCCT
1192 ALDOC 0.36 A AAAAATTGGTTTTTTCCCCTTGTGCCTGCTCCTG
1193 ClQRl 0.31 T TGGCCCCTTGGCCTTCCCCTGTACTTGTCCTCAG
1194 TTFl 0.31 T TCCCCTTGGTTAACCTTTTGTCCTCAGCTTGGGC
1195 PRIMl 0.31 G GCCCCCCCCAACCTTGGGGACAACACTGATTCCT
1196 USP34 0.38 T TCCCCTTCCCCAATTCC^ACCTGAAACACTGGAC
1197 TK2 0.33 T TCCCCTTGGTTAACCTTTTGTCCTCAGCTTGGGC
1198 GOLGIN-67 0.31 T TGGCCCCTTGGCCTTCCCCTGTACTTGTCCTCAG
1199 NPD014 0.35 A ACCTTTTGGTTCCCCTTCCAGCTTGGGCTTCTTC
1200 KIAA0220 0.31 T TCCCCTTCCCCAATTCC^ACCTGAAACACTGGAC
1201 SLC43A3 0.3 T TTTGGGGAACCAATTCCTTCTAGTGTAGCTGCCA
1202 WBSCR20C 0.3 C CAACCCCCCAAGGCCTTGGGTCCTGTGGATGGGA
1203 ICAM2 0.3 T TGGCCCCTTGGCCTTCCCCTGTACTTGTCCTCAG
1204 TEXlO 0.32 T TGGGGAACCCCCCCCAACCTGGCTGAGAATCTGG
1205 CHD7 0.3 A ACCTTTTGGTTCCCCTTCCAGCTTGGGCTTCTTC
1206 SAMSNl 0.34 T TTTGGGGAACCAATTCCTTCTAGTGTAGCTGCCA
1207 TPRT 0.35 A ACCTTTTGGTTCCCCTTCCAGCTTGGGCTTCTTC
Table 56. Fludarabine biomarkers.
SEQIDNO Gene Correlation Medianprobe
1208 HLA-E 0.3 ACTTGTCCTCAGCTTGGGCTTCTTC
1209 BAT3 0.34 TGCCTGCTCCTGTACTTGTCCTCAG
1210 ENO2 0.37 TGGACCCCACTGGCTGAGAATCTGG
1211 UBE2L6 0.3 TCCTGTACTTGTCCTCAGCTTGGGC
1212 CUGBP2 0.35 TGCCTGCTCCTGTACTTGTCCTCAG
1213 ITM2A 0.32 GCCCCACTGGACAACACTGATTCCT
1214 PALM2-AKAP2 0.41 GCCCCACTGGACAACACTGATTCCT
1215 JARID2 0.33 GCCCCACTGGACAACACTGATTCCT
1216 DGKA 0.33 TGGACCCCACTGGCTGAGAATCTGG
1217 SLC7A6 0.4 AAGCCTATACGTTTCTGTGGAGTAA
1218 TFDP2 0.35 AAATGTTTCCTTGTGCCTGCTCCTG
1219 ADA 0.41 TGCCTGCTCCTGTACTTGTCCTCAG
1220 EDGl 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
1221 ICAM2 0.46 AAGCCTATACGTTTCTGTGGAGTAA
1222 PTPN7 0.33 TCCTCCATCACCTGAAACACTGGAC
1223 CXorf9 0.35 AAGCCTATACGTTTCTGTGGAGTAA
1224 RHOH 0.31 CACCCAGCTGGTCCTGTGGATGGGA
1225 MX2 0.32 AAATGTTTCCTTGTGCCTGCTCCTG
1226 ZNFNlAl 0.31 TCCTCCATCACCTGAAACACTGGAC
1227 COCH 0.33 TGGACCCCACTGGCTGAGAATCTGG
1228 LCP2 0.34 TGGACCCCACTGGCTGAGAATCTGG
1229 CLGN 0.31 TCCTCCATCACCTGAAACACTGGAC
1230 BNCl 0.38 GCCCCACTGGACAACACTGATTCCT
1231 FLNC 0.3 TCCTGTACTTGTCCTCAGCTTGGGC
1232 HLA-DRB3 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
1233 UCP2 0.34 TGGACCCCACTGGCTGAGAATCTGG
1234 HLA-DRBl 0.3 GCCCCACTGGACAACACTGATTCCT
1235 GATA3 0.37 TCCTTGTGCCTGCTCCTGTACTTGT
1236 PRKCQ 0.39 AAATGTTTCCTTGTGCCTGCTCCTG
1237 SH2D1A 0.37 ACTTGTCCTCAGCTTGGGCTTCTTC
1238 NFATC3 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC
1239 TRB@ 0.35 AAATGTTTCCTTGTGCCTGCTCCTG
1240 FNBPl 0.34 TCCTCCATCACCTGAAACACTGGAC
1241 SEPT6 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC
1242 NME4 0.32 AAGCCTATACGTTTCTGTGGAGTAA
1243 DKFZP434C171 0.3 TCCTTGTGCCTGCTCCTGTACTTGT
1244 ZC3HAV1 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
1245 SLC43A3 0.37 AAATGTTTCCTTGTGCCTGCTCCTG
1246 CD3D 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
1247 AIFl 0.35 TCCTCCATCACCTGAAACACTGGAC
1248 SPTANl 0.34 TCCTCCATCACCTGAAACACTGGAC
1249 CDlE 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
1250 TRIM 0.31 AAGCCTATACGTTTCTGTGGAGTAA
1251 DATFl 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
1252 FHODl 0.37 TCCTGTACTTGTCCTCAGCTTGGGC
1253 ARHGAPl 5 0.3 CACCCAGCTGGTCCTGTGGATGGGA
1254 STAG3 0.34 AAGCCTATACGTTTCTGTGGAGTAA
1255 SAP130 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
1256 CYLD 0.3 ACTTGTCCTCAGCTTGGGCTTCTTC
Table 57. Vinblastine biomarkers . SEQIDNO Gene Correlation Medianprobe
1257 CD99 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC
Table 58. Busulfan biomarkers.
SEQIDNO Gene Correlation Medianprobe
1258 RPLP2 0.37 TCCTCCATCACCTGAAACACTGGAC
1259 BTGl 0.36 ACTTGTCCTCAGCTTGGGCTTCTTC 1260 CSDA 0.31 TGCCTGCTCCTGTACTTGTCCTCAG 1261 ARHGDIB 0.38 AAGCCTATACGTTTCTGTGGAGTAA 1262 INSIGl 0.41 TCCTCCATCACCTGAAACACTGGAC 1263 ALDOC 0.36 TTGGACATCTCTAGTGTAGCTGCCA 1264 WASPIP 0.31 TCCTCCATCACCTGAAACACTGGAC 1265 ClQRl 0.46 TCCTGTACTTGTCCTCAGCTTGGGC 1266 EDEMl 0.36 TGGACCCCACTGGCTGAGAATCTGG 1267 SLA 0.35 TCCTTGTGCCTGCTCCTGTACTTGT 1268 MFNG 0.4 TCCTTGTGCCTGCTCCTGTACTTGT 1269 GPSM3 0.75 GCCCCACTGGACAACACTGATTCCT 1270 ADA 0.53 ACTTGTCCTCAGCTTGGGCTTCTTC 1271 LRMP 0.31 TCCTGTACTTGTCCTCAGCTTGGGC 1272 EVI2A 0.52 TCCTCCATCACCTGAAACACTGGAC 1273 FMNLl 0.45 ACTTGTCCTCAGCTTGGGCTTCTTC 1274 PTPN7 0.3 ACTTGTCCTCAGCTTGGGCTTCTTC 1275 RHOH 0.39 ACTTGTCCTCAGCTTGGGCTTCTTC 1276 ZNFNlAl 0.36 AAGCCTATACGTTTCTGTGGAGTAA 1277 CENTBl 0.33 TTGGACATCTCTAGTGTAGCTGCCA 1278 MAP4K1 0.31 TGGACCCCACTGGCTGAGAATCTGG 1279 CD28 0.51 TCCTGTACTTGTCCTCAGCTTGGGC 1280 SPIlO 0.38 TCCTTGTGCCTGCTCCTGTACTTGT 1281 NAPlLl 0.31 TGCCTGCTCCTGTACTTGTCCTCAG 1282 IFI16 0.35 TCCTCCATCACCTGAAACACTGGAC 1283 ARHGEF6 0.42 AAATGTTTCCTTGTGCCTGCTCCTG 1284 SELPLG 0.45 TCCTGTACTTGTCCTCAGCTTGGGC 1285 CD3Z 0.35 CACCCAGCTGGTCCTGTGGATGGGA 1286 SH2D1A 0.38 CACCCAGCTGGTCCTGTGGATGGGA 1287 LAIRl 0.34 TGCCTGCTCCTGTACTTGTCCTCAG 1288 RAFTLIN 0.36 GCCCCACTGGACAACACTGATTCCT 1289 HA-I 0.61 ACTTGTCCTCAGCTTGGGCTTCTTC 1290 DOCK2 0.4 TGCCTGCTCCTGTACTTGTCCTCAG 1291 CD3D 0.31 GCCCCACTGGACAACACTGATTCCT 1292 T3JAM 0.35 ACTTGTCCTCAGCTTGGGCTTCTTC 1293 ZAP70 0.36 TGGACCCCACTGGCTGAGAATCTGG 1294 GPR65 0.32 TCCTCCATCACCTGAAACACTGGAC 1295 CYFIP2 0.58 CACCCAGCTGGTCCTGTGGATGGGA 1296 LPXN 0.34 TTGGACATCTCTAGTGTAGCTGCCA 1297 RPLlOL 0.41 TCCTGTACTTGTCCTCAGCTTGGGC 1298 GLTSCR2 0.33 AAATGTTTCCTTGTGCCTGCTCCTG 1299 ARHGAP15 0.47 CACCCAGCTGGTCCTGTGGATGGGA 1300 BCLIlB 0.31 TGCCTGCTCCTGTACTTGTCCTCAG 1301 TM6SF1 0.39 AAGCCTATACGTTTCTGTGGAGTAA 1302 PACAP 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC 1303 TCF4 0.32 TGGACCCCACTGGCTGAGAATCTGG
Table 59, Dacarbazine biomarkers.
SEQIDNO Gene Correlation Medianprobe
1304 ARHGDIB 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
1305 ITM2A 0.4 TCCTCCATCACCTGAAACACTGGAC
1306 SSBP2 0.33 CACCCAGCTGGTCCTGTGGATGGGA
1307 PIM2 0.39 GCCCCACTGGACAACACTGATTCCT
1308 SELL 0.31 GCCCCACTGGACAACACTGATTCCT
1309 ICAM2 0.43 TCCTGTACTTGTCCTCAGCTTGGGC
1310 EVI2A 0.32 AAGCCTATACGTTTCTGTGGAGTAA
1311 MAL 0.32 TTGGACATCTCTAGTGTAGCTGCCA
1312 PTPN7 0.34 ACTTGTCCTCAGCTTGGGCTTCTTC
1313 ZNFNlAl 0 .32 TCCTTGTGCCTGCTCCTGTACTTGT
1314 LCP2 0 .3 GCCCCACTGGACAACACTGATTCCT
1315 ARHGAP6 0 .33 TGGACCCCACTGGCTGAGAATCTGG
1316 CD28 0 .33 ACTTGTCCTCAGCTTGGGCTTCTTC
1317 CD8B1 0 .32 TCCTCCATCACCTGAAACACTGGAC
1318 LCPl 0 .34 TCCTTGTGCCTGCTCCTGTACTTGT
1319 NPD014 0 .31 TGCCTGCTCCTGTACTTGTCCTCAG
1320 CD69 0 .32 AAGCCTATACGTTTCTGTGGAGTAA
1321 NFATC3 0 .32 AAGCCTATACGTTTCTGTGGAGTAA
1322 TRB@ 0 .32 AAATGTTTCCTTGTGCCTGCTCCTG
1323 IGJ 0 .33 AAGCCTATACGTTTCTGTGGAGTAA
1324 SLC43A3 0 .3 TTGGACATCTCTAGTGTAGCTGCCA
1325 DOCK2 0 .36 TCCTCCATCACCTGAAACACTGGAC
1326 FHODl 0 .33 TGGACCCCACTGGCTGAGAATCTGG
1327 PACAP 0 .31 AAGCCTATACGTTTCTGTGGAGTAA
Table 60 . Oxaliplatin biomark
SEQIDNO Gene Correlation Medianprobe
1328 RPL18 0.38 TTGGACATCTCTAGTGTAGCTGCCA
1329 RPLlOA 0.32 AAATGTTTCCTTGTGCCTGCTCCTG
1330 RPS3A 0.34 TGGACCCCACTGGCTGAGAATCTGG
1331 EEF1B2 0.39 CACCCAGCTGGTCCTGTGGATGGGA
1332 GOT2 0.32 AAGCCTATACGTTTCTGTGGAGTAA
1333 RPL13A 0.33 AAATGTTTCCTTGTGCCTGCTCCTG
1334 RPS15 0.41 GCCCCACTGGACAACACTGATTCCT
1335 NOL5A 0.37 TGCCTGCTCCTGTACTTGTCCTCAG
1336 RPLP2 0.36 TGCCTGCTCCTGTACTTGTCCTCAG
1337 SLC9A3R1 0.43 TGGACCCCACTGGCTGAGAATCTGG
1338 EIF3S3 0.43 GCCCCACTGGACAACACTGATTCCT
1339 MTHFD2 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
1340 IMPDH2 0.34 ACTTGTCCTCAGCTTGGGCTTCTTC
1341 ALDOC 0.44 TGCCTGCTCCTGTACTTGTCCTCAG
1342 FABP5 0.33 CACCCAGCTGGTCCTGTGGATGGGA
1343 ITM2A 0.35 TCCTTGTGCCTGCTCCTGTACTTGT
1344 PCK2 0.36 ACTTGTCCTCAGCTTGGGCTTCTTC
1345 MFNG 0.33 GCCCCACTGGACAACACTGATTCCT
1346 GCHl 0.37 TGGACCCCACTGGCTGAGAATCTGG
1347 PIM2 0.39 CACCCAGCTGGTCCTGTGGATGGGA
1348 ADA 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
1349 ICAM2 0.31 TCCTCCATCACCTGAAACACTGGAC
1350 TTFl 0.47 TTGGACATCTCTAGTGTAGCTGCCA
1351 MYB 0.36 TGCCTGCTCCTGTACTTGTCCTCAG
1352 PTPN7 0.37 CACCCAGCTGGTCCTGTGGATGGGA
1353 RHOH 0.42 TCCTCCATCACCTGAAACACTGGAC
1354 ZNFNlAl 0.39 ACTTGTCCTCAGCTTGGGCTTCTTC
1355 PRIMl 0.36 TCCTTGTGCCTGCTCCTGTACTTGT
1356 FHIT 0.48 TCCTCCATCACCTGAAACACTGGAC
1357 ASS 0.45 TGGACCCCACTGGCTGAGAATCTGG
1358 SYK 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
1359 OXAlL 0.32 TTGGACATCTCTAGTGTAGCTGCCA
1360 LCPl 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
1361 DDX18 0.32 AAGCCTATACGTTTCTGTGGAGTAA
1362 NOLA2 0.35 AAATGTTTCCTTGTGCCTGCTCCTG
1363 KIAA0922 0.41 TCCTCCATCACCTGAAACACTGGAC
1364 PRKCQ 0.34 TCCTTGTGCCTGCTCCTGTACTTGT
1365 NFATC3 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
1366 ANAPC5 0.34 TCCTCCATCACCTGAAACACTGGAC
1367 TRB@ 0.4 TGGACCCCACTGGCTGAGAATCTGG
1368 CXCR4 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
1369 FNBP4 0.3 TCCTGTACTTGTCCTCAGCTTGGGC
1370 SEPT6 0.53 TTGGACATCTCTAGTGTAGCTGCCA
1371 RPS2 0.35 TCCTCCATCACCTGAAACACTGGAC
1372 MDNl 0.41 ACTTGTCCTCAGCTTGGGCTTCTTC
1373 PCCB 0.32 AAGCCTATACGTTTCTGTGGAGTAA
1374 RASA4 0.33 TGGACCCCACTGGCTGAGAATCTGG
1375 WBSCR20C 0.31 CACCCAGCTGGTCCTGTGGATGGGA
1376 SFRS7 0.32 TTGGACATCTCTAGTGTAGCTGCCA
1377 WBSCR20A 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
1378 NUP210 0.43 TGGACCCCACTGGCTGAGAATCTGG
1379 SHMT2 0.36 TCCTTGTGCCTGCTCCTGTACTTGT
1380 RPLPO 0.33 TTGGACATCTCTAGTGTAGCTGCCA
1381 MAP4K1 0.31 CACCCAGCTGGTCCTGTGGATGGGA
1382 HNRPAl 0.37 TCCTCCATCACCTGAAACACTGGAC
1383 CYFIP2 0.3 GCCCCACTGGACAACACTGATTCCT
1384 RPLlOL 0.32 TCCTCCATCACCTGAAACACTGGAC
1385 GLTSCR2 0.39 TGGACCCCACTGGCTGAGAATCTGG
1386 MRPL16 0.38 TCCTGTACTTGTCCTCAGCTTGGGC
1387 MRPS2 0.34 GCCCCACTGGACAACACTGATTCCT
1388 FLJ12270 0.31 AAGCCTATACGTTTCTGTGGAGTAA
1389 CDK5RAP3 0.32 TTGGACATCTCTAGTGTAGCTGCCA
1390 ARHGAPl5 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
1391 CUTC 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
1392 FKBPIl 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
1393 ADPGK 0.41 AAGCCTATACGTTTCTGTGGAGTAA
1394 FLJ22457 0.32 GCCCCACTGGACAACACTGATTCCT
1395 PUS3 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
1396 PACAP 0.36 TGCCTGCTCCTGTACTTGTCCTCAG
1397 CALML4 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
Table 61 . Hydroxyurea biomark
SEQIDNO Gene Correlation Medianprobe
1398 CSDA 0.31 TCCTCCATCACCTGAAACACTGGAC
1399 INSIGl 0.38 AAGCCTATACGTTTCTGTGGAGTAA
1400 UBE2L6 0.33 CACCCAGCTGGTCCTGTGGATGGGA
1401 PRGl 0.36 GCCCCACTGGACAACACTGATTCCT
1402 ITM2A 0.3 ACTTGTCCTCAGCTTGGGCTTCTTC
1403 DGKA 0.31 CACCCAGCTGGTCCTGTGGATGGGA
1404 SLA 0.47 CACCCAGCTGGTCCTGTGGATGGGA
1405 PCBP2 0.51 TGGACCCCACTGGCTGAGAATCTGG
1406 IL2RG 0.42 ACTTGTCCTCAGCTTGGGCTTCTTC
1407 ALOX5AP 0.31 AAGCCTATACGTTTCTGTGGAGTAA
1408 PSMB9 0.33 GCCCCACTGGACAACACTGATTCCT
1409 LRMP 0.36 TTGGACATCTCTAGTGTAGCTGCCA
1410 ICAM2 0.31 TGGACCCCACTGGCTGAGAATCTGG
1411 PTPN7 0.36 TCCTCCATCACCTGAAACACTGGAC
1412 CXorf9 0.38 TCCTTGTGCCTGCTCCTGTACTTGT
1413 RHOH 0.41 TGCCTGCTCCTGTACTTGTCCTCAG
1414 ZNFNlAl 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
1415 CENTBl 0.36 TTGGACATCTCTAGTGTAGCTGCCA
1416 LCP2 0.37 CACCCAGCTGGTCCTGTGGATGGGA
1417 STAT4 0.32 GCCCCACTGGACAACACTGATTCCT
1418 CCR7 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
1419 CD3G 0.33 AAATGTTTCCTTGTGCCTGCTCCTG
1420 SPIlO 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
1421 TNFAIP8 0.31 TCCTCCATCACCTGAAACACTGGAC
1422 IFI16 0.4 TGGACCCCACTGGCTGAGAATCTGG
1423 CXCR4 0.37 ACTTGTCCTCAGCTTGGGCTTCTTC
1424 ARHGEF6 0.37 TTGGACATCTCTAGTGTAGCTGCCA
1425 SELPLG 0.3 TCCTCCATCACCTGAAACACTGGAC
1426 CD3Z 0.38 TCCTCCATCACCTGAAACACTGGAC
1427 PRKCQ 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
1428 SH2D1A 0.3 TCCTTGTGCCTGCTCCTGTACTTGT
1429 CDlA 0.31 TTGGACATCTCTAGTGTAGCTGCCA
1430 NFATC3 0.33 TGGACCCCACTGGCTGAGAATCTGG
1431 LAIRl 0.34 TCCTCCATCACCTGAAACACTGGAC
1432 TRB@ 0.3 CACCCAGCTGGTCCTGTGGATGGGA
1433 SEPT6 0.34 CACCCAGCTGGTCCTGTGGATGGGA
1434 RAFTLIN 0.3 TCCTTGTGCCTGCTCCTGTACTTGT
1435 DOCK2 0.32 TGGACCCCACTGGCTGAGAATCTGG
1436 CD3D 0.37 TGCCTGCTCCTGTACTTGTCCTCAG
1437 CD6 0.42 AAGCCTATACGTTTCTGTGGAGTAA
1438 AIFl 0.4 TGCCTGCTCCTGTACTTGTCCTCAG
1439 CDlE 0.41 GCCCCACTGGACAACACTGATTCCT
1440 CYFIP2 0.35 TCCTGTACTTGTCCTCAGCTTGGGC
1441 TARP 0.38 AAATGTTTCCTTGTGCCTGCTCCTG
1442 ADA 0.33 AAGCCTATACGTTTCTGTGGAGTAA
1443 ARHGAP15 0.32 TGGACCCCACTGGCTGAGAATCTGG
1444 GIMAP6 0.34 GCCCCACTGGACAACACTGATTCCT
1445 STAG3 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
1446 FLJ22457 0.31 AAGCCTATACGTTTCTGTGGAGTAA
1447 PACAP 0.35 AAGCCTATACGTTTCTGTGGAGTAA
1448 TCF4 0.4 TCCTGTACTTGTCCTCAGCTTGGGC
Table 62 . Tegafur biomarkers .
SEQIDNO Gene Correlation Medianprobe
1449 RPLIl 0.31 GCCCCACTGGACAACACTGATTCCT
1450 RPL17 0.38 TGCCTGCTCCTGTACTTGTCCTCAG
1451 ANAPC5 0.34 CACCCAGCTGGTCCTGTGGATGGGA
1452 RPL13A 0.34 TCCTGTACTTGTCCTCAGCTTGGGC
1453 STOM 0.37 TCCTCCATCACCTGAAACACTGGAC
1454 TUFM 0.38 GCCCCACTGGACAACACTGATTCCT
1455 SCARBl 0.35 TCCTGTACTTGTCCTCAGCTTGGGC
1456 FABP5 0.33 CACCCAGCTGGTCCTGTGGATGGGA
1457 KIAA0711 0.35 TCCTTGTGCCTGCTCCTGTACTTGT
1458 IL6R 0.33 TCCTCCATCACCTGAAACACTGGAC
1459 WBSCR22 0.3 AAATGTTTCCTTGTGCCTGCTCCTG
1460 UCK2 0.4 TGCCTGCTCCTGTACTTGTCCTCAG
1461 GZMB 0.3 AAGCCTATACGTTTCTGTGGAGTAA
1462 Clorf38 0.32 CACCCAGCTGGTCCTGTGGATGGGA
1463 PCBP2 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
1464 GPR65 0.44 TGCCTGCTCCTGTACTTGTCCTCAG
1465 GLTSCR2 0.38 TCCTTGTGCCTGCTCCTGTACTTGT
1466 FKBPIl 0.38 TGGACCCCACTGGCTGAGAATCTGG
Table 63. Daunorubicin biomarkers.
SEQIDNO Gene Correlation Medianprobe
1467 ALDOC 0.41 TGCCTGCTCCTGTACTTGTCCTCAG
1468 ITM2A 0.32 GCCCCACTGGACAACACTGATTCCT
1469 SLA 0.41 TCCTTGTGCCTGCTCCTGTACTTGT
1470 SSBP2 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
1471 IL2RG 0.31 TGGACCCCACTGGCTGAGAATCTGG
1472 MFNG 0.47 TTGGACATCTCTAGTGTAGCTGCCA
1473 SELL 0.33 TCCTCCATCACCTGAAACACTGGAC
1474 STCl 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
1475 LRMP 0.33 AAGCCTATACGTTTCTGTGGAGTAA
1476 MYB 0.41 GCCCCACTGGACAACACTGATTCCT
1477 PTPN7 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
1478 CXorf9 0.38 TGGACCCCACTGGCTGAGAATCTGG
1479 RHOH 0.32 AAATGTTTCCTTGTGCCTGCTCCTG
1480 ZNFNlAl 0.36 CACCCAGCTGGTCCTGTGGATGGGA
1481 CENTBl 0.37 TGGACCCCACTGGCTGAGAATCTGG
1482 MAP4K1 0.32 TGGACCCCACTGGCTGAGAATCTGG
1483 CCR7 0.3 TCCTGTACTTGTCCTCAGCTTGGGC
1484 CD3G 0.33 AAATGTTTCCTTGTGCCTGCTCCTG
1485 CCR9 0.33 TGGACCCCACTGGCTGAGAATCTGG
1486 CBFA2T3 0.31 CACCCAGCTGGTCCTGTGGATGGGA
1487 CXCR4 0.41 AAATGTTTCCTTGTGCCTGCTCCTG
1488 ARHGEF6 0.4 TCCTGTACTTGTCCTCAGCTTGGGC
1489 SELPLG 0.45 TCCTTGTGCCTGCTCCTGTACTTGT
1490 SEC31L2 0.38 TCCTGTACTTGTCCTCAGCTTGGGC
1491 CD3Z 0.33 CACCCAGCTGGTCCTGTGGATGGGA
1492 SH2D1A 0.33 TCCTGTACTTGTCCTCAGCTTGGGC
1493 CDlA 0.35 TGGACCCCACTGGCTGAGAATCTGG
1494 SCN3A 0.33 CACCCAGCTGGTCCTGTGGATGGGA
1495 LAIRl 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
1496 TRBg 0.3 AAATGTTTCCTTGTGCCTGCTCCTG
1497 DOCK2 0.35 AAGCCTATACGTTTCTGTGGAGTAA
1498 WBSCR20C 0.38 CACCCAGCTGGTCCTGTGGATGGGA
1499 CD3D 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
1500 T3JAM 0.34 CACCCAGCTGGTCCTGTGGATGGGA
1501 CD6 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC
1502 ZAP70 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
1503 GPR65 0.33 TCCTGTACTTGTCCTCAGCTTGGGC
1504 AIFl 0.3 GCCCCACTGGACAACACTGATTCCT
1505 WDR45 0.3 TCCTCCATCACCTGAAACACTGGAC
1506 CDlE 0.3 TCCTTGTGCCTGCTCCTGTACTTGT
1507 CYFIP2 0.39 AAGCCTATACGTTTCTGTGGAGTAA
1508 TARP 0.38 TTGGACATCTCTAGTGTAGCTGCCA
1509 TRIM 0.34 TCCTGTACTTGTCCTCAGCTTGGGC
1510 ARHGAP15 0.37 ACTTGTCCTCAGCTTGGGCTTCTTC
1511 NOTCHl 0.39 AAGCCTATACGTTTCTGTGGAGTAA
1512 STAG3 0.35 AAGCCTATACGTTTCTGTGGAGTAA
1513 UBASH3A 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
1514 MGC5566 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
1515 PACAP 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
Table 64. Bleomycin biomarkers.
SEQIDNO Gene Correlation Medianprobe
1516 PFNl 0.32 CACCCAGCTGGTCCTGTGGATGGGA
1517 CALU 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
1518 ZYX 0.34 CACCCAGCTGGTCCTGTGGATGGGA
1519 PSMD2 0.36 GCCCCACTGGACAACACTGATTCCT
1520 RAPlB 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
1521 EPASl 0.35 TCCTGTACTTGTCCTCAGCTTGGGC
1522 PGAMl 0.36 GCCCCACTGGACAACACTGATTCCT
1523 STATl 0.38 TGCCTGCTCCTGTACTTGTCCTCAG
1524 CKAP4 0.38 GCCCCACTGGACAACACTGATTCCT
1525 DUSPl 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
1526 RCNl 0.32 TCCTCCATCACCTGAAACACTGGAC
1527 UCHLl 0.44 TGGACCCCACTGGCTGAGAATCTGG
1528 ITGA5 0.33 AAATGTTTCCTTGTGCCTGCTCCTG
1529 NFKBIA 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
1530 LAMBl 0.4 GCCCCACTGGACAACACTGATTCCT
1531 TGFBI 0.37 TTGGACATCTCTAGTGTAGCTGCCA
1532 FHLl 0.31 GCCCCACTGGACAACACTGATTCCT
1533 GJAl 0.32 TCCTCCATCACCTGAAACACTGGAC
1534 PRGl 0.33 CACCCAGCTGGTCCTGTGGATGGGA
1535 EXTl 0.35 CACCCAGCTGGTCCTGTGGATGGGA
1536 MVP 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
1537 NNMT 0.38 TGGACCCCACTGGCTGAGAATCTGG
1538 TAPl 0.37 TCCTCCATCACCTGAAACACTGGAC
1539 CRIMl 0.41 TGGACCCCACTGGCTGAGAATCTGG
1540 PLOD2 0.36 GCCCCACTGGACAACACTGATTCCT
1541 RPS19 0.34 TCCTGTACTTGTCCTCAGCTTGGGC
1542 AXL 0.43 GCCCCACTGGACAACACTGATTCCT
1543 PALM2-AKAP2 0.42 TCCTCCATCACCTGAAACACTGGAC
1544 IL8 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
1545 LOXL2 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
1546 PAPSS2 0.31 CACCCAGCTGGTCCTGTGGATGGGA
1547 CAVl 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
1548 F2R 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
1549 PSMB9 0.38 CACCCAGCTGGTCCTGTGGATGGGA
1550 LOX 0.36 TGGACCCCACTGGCTGAGAATCTGG
1551 Clorf29 0.36 TCCTGTACTTGTCCTCAGCTTGGGC
1552 STCl 0.32 TTGGACATCTCTAGTGTAGCTGCCA
1553 LIF 0.34 TCCTTGTGCCTGCTCCTGTACTTGT
1554 KCNJ8 0.46 GCCCCACTGGACAACACTGATTCCT
1555 SMAD3 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
1556 HPCALl 0.45 AAATGTTTCCTTGTGCCTGCTCCTG
1557 WNT5A 0.34 TCCTTGTGCCTGCTCCTGTACTTGT
1558 BDNF 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
1559 TNFRSFlA 0.38 TCCTGTACTTGTCCTCAGCTTGGGC
1560 NCOR2 0.45 CACCCAGCTGGTCCTGTGGATGGGA
1561 FLNC 0.44 TTGGACATCTCTAGTGTAGCTGCCA
1562 HMGA2 0.41 AAATGTTTCCTTGTGCCTGCTCCTG
1563 HLA-B 0.42 AAGCCTATACGTTTCTGTGGAGTAA
1564 FLOTl 0.3 AAATGTTTCCTTGTGCCTGCTCCTG
1565 PTRF 0.36 CACCCAGCTGGTCCTGTGGATGGGA
1566 IFI16 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
1567 MGC4083 0.34 TCCTCCATCACCTGAAACACTGGAC
1568 TNFRSFlOB 0.4 ACTTGTCCTCAGCTTGGGCTTCTTC
1569 PNMA2 0.38 TCCTGTACTTGTCCTCAGCTTGGGC
1570 TFPI 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
1571 CLECSF2 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
1572 SPIlO 0.34 GCCCCACTGGACAACACTGATTCCT
1573 PLAUR 0.35 ACTTGTCCTCAGCTTGGGCTTCTTC
1574 ASPH 0.42 TCCTTGTGCCTGCTCCTGTACTTGT
1575 FSCNl 0.38 TGCCTGCTCCTGTACTTGTCCTCAG
1576 HIC 0.46 TCCTCCATCACCTGAAACACTGGAC
1577 HLA-C 0.34 TGGACCCCACTGGCTGAGAATCTGG
1578 COL6A1 0.34 TCCTCCATCACCTGAAACACTGGAC
1579 IL6ST 0.45 AAATGTTTCCTTGTGCCTGCTCCTG
1580 IFITM3 0.36 GCCCCACTGGACAACACTGATTCCT
1581 MAPlB 0.31 TCCTCCATCACCTGAAACACTGGAC
1582 FLJ46603 0.3 ACTTGTCCTCAGCTTGGGCTTCTTC
1583 RAFTLIN 0.32 GCCCCACTGGACAACACTGATTCCT
1584 FTL 0.37 CACCCAGCTGGTCCTGTGGATGGGA
1585 KIAA0877 0.43 TCCTCCATCACCTGAAACACTGGAC
1586 MTlE 0.41 TGGACCCCACTGGCTGAGAATCTGG
1587 CDClO 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
1588 ZNF258 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
1589 BCATl 0.39 TTGGACATCTCTAGTGTAGCTGCCA
1590 IFI44 0.36 AAATGTTTCCTTGTGCCTGCTCCTG
1591 SOD2 0.36 GCCCCACTGGACAACACTGATTCCT
1592 TMSBlO 0.33 TCCTCCATCACCTGAAACACTGGAC
1593 FLJ10350 0.3 TTGGACATCTCTAGTGTAGCTGCCA
1594 Clorf24 0.34 CACCCAGCTGGTCCTGTGGATGGGA
1595 EFHD2 0.36 AAATGTTTCCTTGTGCCTGCTCCTG
1596 RPS27L 0.33 AAGCCTATACGTTTCTGTGGAGTAA
1597 TNFRSF12A 0.43 CACCCAGCTGGTCCTGTGGATGGGA
1598 FAD104 0.38 TTGGACATCTCTAGTGTAGCTGCCA
1599 RAB7L1 0.58 ACTTGTCCTCAGCTTGGGCTTCTTC
1600 NME7 0.36 TTGGACATCTCTAGTGTAGCTGCCA
1601 TMEM22 0.34 TTGGACATCTCTAGTGTAGCTGCCA
1602 TPKl 0.31 GCCCCACTGGACAACACTGATTCCT
1603 ELK3 0.36 TGGACCCCACTGGCTGAGAATCTGG
1604 CYLD 0.3 AAGCCTATACGTTTCTGTGGAGTAA
1605 AMIGO2 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
1606 ADAMTSl 0.43 ACTTGTCCTCAGCTTGGGCTTCTTC
1607 ACTB 0.36 ACTTGTCCTCAGCTTGGGCTTCTTC
Table 65. Estramustine biomarkers. SEQIDNO Gene Correlation Medianprobe
1608 HSPCB 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
1609 LDHA 0.42 TGCCTGCTCCTGTACTTGTCCTCAG
1610 TM4SF7 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
Table 66 . Chlorambucil
SEQIDNO Gene C Coorrrrelation Medianprobe
1611 CSDA 0.33 TGGACCCCACTGGCTGAGAATCTGG
1612 INSIGl 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
1613 UBE2L6 0.39 TGGACCCCACTGGCTGAGAATCTGG
1614 PRGl 0.37 TCCTTGTGCCTGCTCCTGTACTTGT
1615 ITM2A 0.3 GCCCCACTGGACAACACTGATTCCT
1616 DGKA 0.38 TCCTTGTGCCTGCTCCTGTACTTGT
1617 TFDP2 0.32 AAATGTTTCCTTGTGCCTGCTCCTG
1618 SLA 0.32 TCCTCCATCACCTGAAACACTGGAC
1619 IL2RG 0.44 AAGCCTATACGTTTCTGTGGAGTAA
1620 ALOX5AP 0.45 GCCCCACTGGACAACACTGATTCCT
1621 GPSM3 0.34 TTGGACATCTCTAGTGTAGCTGCCA
1622 PSMB9 0.36 ACTTGTCCTCAGCTTGGGCTTCTTC
1623 SELL 0.42 TGCCTGCTCCTGTACTTGTCCTCAG
1624 ADA 0.35 ACTTGTCCTCAGCTTGGGCTTCTTC
1625 EDGl 0.33 AAATGTTTCCTTGTGCCTGCTCCTG
1626 FMNLl 0.3 TCCTCCATCACCTGAAACACTGGAC
1627 PTPN7 0.5 TCCTTGTGCCTGCTCCTGTACTTGT
1628 CXorf9 0.41 TGGACCCCACTGGCTGAGAATCTGG
1629 RHOH 0.35 TTGGACATCTCTAGTGTAGCTGCCA
1630 ZNFNlAl 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
1631 CENTBl 0.47 TCCTGTACTTGTCCTCAGCTTGGGC
1632 LCP2 0.37 TCCTCCATCACCTGAAACACTGGAC
1633 CDlD 0.36 AAGCCTATACGTTTCTGTGGAGTAA
1634 STAT4 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
1635 VAVl 0.35 AAATGTTTCCTTGTGCCTGCTCCTG
1636 MAP4K1 0.36 TTGGACATCTCTAGTGTAGCTGCCA
1637 CCR7 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
1638 PDE4C 0.42 GCCCCACTGGACAACACTGATTCCT
1639 CD3G 0.41 AAGCCTATACGTTTCTGTGGAGTAA
1640 CCR9 0.43 AAGCCTATACGTTTCTGTGGAGTAA
1641 SPIlO 0.43 TTGGACATCTCTAGTGTAGCTGCCA
1642 TNFAIP8 0.48 TTGGACATCTCTAGTGTAGCTGCCA
1643 LCPl 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
1644 IFI16 0.5 TCCTCCATCACCTGAAACACTGGAC
1645 CXCR4 0.37 ACTTGTCCTCAGCTTGGGCTTCTTC
1646 ARHGEF6 0.37 ACTTGTCCTCAGCTTGGGCTTCTTC
1647 SELPLG 0.43 TTGGACATCTCTAGTGTAGCTGCCA
1648 SEC31L2 0.32 TGGACCCCACTGGCTGAGAATCTGG
1649 CD3Z 0.3 AAGCCTATACGTTTCTGTGGAGTAA
1650 PRKCQ 0.31 GCCCCACTGGACAACACTGATTCCT
1651 SH2D1A 0.47 ACTTGTCCTCAGCTTGGGCTTCTTC
1652 GZMB 0.48 TGGACCCCACTGGCTGAGAATCTGG
1653 CDlA 0.3 AAGCCTATACGTTTCTGTGGAGTAA
1654 LAIRl 0.32 TTGGACATCTCTAGTGTAGCTGCCA
1655 AFlQ 0.41 TTGGACATCTCTAGTGTAGCTGCCA
1656 TRB@ 0.35 TCCTCCATCACCTGAAACACTGGAC
1657 SEPT6 0.35 TGGACCCCACTGGCTGAGAATCTGG
1658 DOCK2 0.39 AAGCCTATACGTTTCTGTGGAGTAA
1659 RPS19 0.41 TTGGACATCTCTAGTGTAGCTGCCA
1660 CD3D 0.4 TTGGACATCTCTAGTGTAGCTGCCA
1661 T3JAM 0.32 TGGACCCCACTGGCTGAGAATCTGG
1662 FNBPl 0.31 GCCCCACTGGACAACACTGATTCCT
1663 CD6 0.33 TGGACCCCACTGGCTGAGAATCTGG
1664 ZAP70 0.52 CACCCAGCTGGTCCTGTGGATGGGA
1665 LSTl 0.34 AAATGTTTCCTTGTGCCTGCTCCTG
1666 BCATl 0.35 AAGCCTATACGTTTCTGTGGAGTAA
1667 PRFl 0.4 AAGCCTATACGTTTCTGTGGAGTAA
1668 AIFl 0.3 TTGGACATCTCTAGTGTAGCTGCCA
1669 RAG2 0.38 TGGACCCCACTGGCTGAGAATCTGG
1670 CDlE 0.35 ACTTGTCCTCAGCTTGGGCTTCTTC
1671 CYFIP2 0.38 TTGGACATCTCTAGTGTAGCTGCCA
1672 TARP 0.3 TGGACCCCACTGGCTGAGAATCTGG
1673 TRIM 0.36 CACCCAGCTGGTCCTGTGGATGGGA
1674 GLTSCR2 0.37 TCCTCCATCACCTGAAACACTGGAC
1675 GIMAP5 0.3 ACTTGTCCTCAGCTTGGGCTTCTTC
1676 ARHGAP15 0.32 AAGCCTATACGTTTCTGTGGAGTAA
1677 NOTCHl 0.31 CACCCAGCTGGTCCTGTGGATGGGA
1678 BCLIlB 0.3 TCCTTGTGCCTGCTCCTGTACTTGT
1679 GIMAP6 0.34 TTGGACATCTCTAGTGTAGCTGCCA
1680 STAG3 0.4 TCCTGTACTTGTCCTCAGCTTGGGC
1681 TM6SF1 0.39 TTGGACATCTCTAGTGTAGCTGCCA
1682 UBASH3A 0.37 TCCTGTACTTGTCCTCAGCTTGGGC
1683 MGC5566 0.36 CACCCAGCTGGTCCTGTGGATGGGA
1684 FLJ22457 0.31 TCCTCCATCACCTGAAACACTGGAC
1685 TPKl 0.33 AAATGTTTCCTTGTGCCTGCTCCTG
Table 67 . Mechlore :tham
SEQIDNO Gene C Coorrrrelation Medianprobe
1686 PRGl 0.37 GCCCCACTGGACAACACTGATTCCT
1687 SLC2A3 0.35 ACTTGTCCTCAGCTTGGGCTTCTTC
1688 RPS19 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
1689 PSMBlO 0.34 TGCCTGCTCCTGTACTTGTCCTCAG
1690 ITM2A 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
1691 DGKA 0.37 TGCCTGCTCCTGTACTTGTCCTCAG
1692 SEMA4D 0.34 TCCTCCATCACCTGAAACACTGGAC
1693 SLA 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
1694 IL2RG 0.3 TGGACCCCACTGGCTGAGAATCTGG
1695 MFNG 0.42 AAGCCTATACGTTTCTGTGGAGTAA
1696 ALOX5AP 0.31 AAGCCTATACGTTTCTGTGGAGTAA
1697 GPSM3 0.34 AAGCCTATACGTTTCTGTGGAGTAA
1698 PSMB9 0.36 ACTTGTCCTCAGCTTGGGCTTCTTC
1699 SELL 0.34 CACCCAGCTGGTCCTGTGGATGGGA
1700 ADA 0.35 AAATGTTTCCTTGTGCCTGCTCCTG
1701 FMNLl 0.4 CACCCAGCTGGTCCTGTGGATGGGA
1702 MYB 0.34 TGGACCCCACTGGCTGAGAATCTGG
1703 PTPN7 0.43 AAGCCTATACGTTTCTGTGGAGTAA
1704 CXorf9 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
1705 RHOH 0.33 TTGGACATCTCTAGTGTAGCTGCCA
1706 ZNFNlAl 0.31 TCCTCCATCACCTGAAACACTGGAC
1707 CENTBl 0.43 TCCTCCATCACCTGAAACACTGGAC
1708 FXYD2 0.35 TTGGACATCTCTAGTGTAGCTGCCA
1709 CDlD 0.4 TTGGACATCTCTAGTGTAGCTGCCA
1710 STAT4 0.44 TTGGACATCTCTAGTGTAGCTGCCA
1711 MAP4K1 0.34 GCCCCACTGGACAACACTGATTCCT
1712 CCR7 0.39 TGGACCCCACTGGCTGAGAATCTGG
1713 PDE4C 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
1714 CD3G 0.4 GCCCCACTGGACAACACTGATTCCT
1715 CCR9 0.34 TGGACCCCACTGGCTGAGAATCTGG
1716 SPIlO 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
1717 TK2 0.33 TCCTGTACTTGTCCTCAGCTTGGGC
1718 TNFAIP8 0.34 GCCCCACTGGACAACACTGATTCCT
1719 NAPlLl 0.35 TCCTGTACTTGTCCTCAGCTTGGGC
1720 SELPLG 0.35 TCCTGTACTTGTCCTCAGCTTGGGC
1721 SEC31L2 0.38 TGCCTGCTCCTGTACTTGTCCTCAG
1722 CD3Z 0.44 TTGGACATCTCTAGTGTAGCTGCCA
1723 PRKCQ 0.37 TCCTGTACTTGTCCTCAGCTTGGGC
1724 SH2D1A 0.41 GCCCCACTGGACAACACTGATTCCT
1725 GZMB 0.43 TGGACCCCACTGGCTGAGAATCTGG
1726 CDlA 0.39 TGGACCCCACTGGCTGAGAATCTGG
1727 LAIRl 0.35 TGGACCCCACTGGCTGAGAATCTGG
1728 TRB@ 0.33 TTGGACATCTCTAGTGTAGCTGCCA
1729 SEPT6 0.3 CACCCAGCTGGTCCTGTGGATGGGA
1730 DOCK2 0.34 TGGACCCCACTGGCTGAGAATCTGG
1731 CG018 0.33 TGGACCCCACTGGCTGAGAATCTGG
1732 WBSCR20C 0.34 TCCTGTACTTGTCCTCAGCTTGGGC
1733 CD3D 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC
1734 CD6 0.32 AAGCCTATACGTTTCTGTGGAGTAA
1735 LSTl 0.33 TTGGACATCTCTAGTGTAGCTGCCA
1736 GPR65 0.42 AAGCCTATACGTTTCTGTGGAGTAA 1737 PRFl 0.34 CACCCAGCTGGTCCTGTGGATGGGA 1738 ALMSl 0.41 TCCTGTACTTGTCCTCAGCTTGGGC 1739 AIFl 0.31 GCCCCACTGGACAACACTGATTCCT 1740 CDlE 0.31 CACCCAGCTGGTCCTGTGGATGGGA 1741 CYFIP2 0.33 GCCCCACTGGACAACACTGATTCCT 1742 TARP 0.31 AAATGTTTCCTTGTGCCTGCTCCTG 1743 GLTSCR2 0.31 AAGCCTATACGTTTCTGTGGAGTAA 1744 FLJ12270 0.34 TGGACCCCACTGGCTGAGAATCTGG 1745 ARHGAP15 0.33 GCCCCACTGGACAACACTGATTCCT 1746 NAP1L2 0.32 GCCCCACTGGACAACACTGATTCCT 1747 CECRl 0.34 TCCTTGTGCCTGCTCCTGTACTTGT 1748 GIMAP6 0.35 TCCTGTACTTGTCCTCAGCTTGGGC 1749 STAG3 0.33 CACCCAGCTGGTCCTGTGGATGGGA 1750 TM6SF1 0.3 CACCCAGCTGGTCCTGTGGATGGGA 1751 C15orf25 0.36 TTGGACATCTCTAGTGTAGCTGCCA 1752 MGC5566 0.32 TCCTGTACTTGTCCTCAGCTTGGGC 1753 FLJ22457 0.34 AAATGTTTCCTTGTGCCTGCTCCTG 1754 ET 0.32 CACCCAGCTGGTCCTGTGGATGGGA 1755 TPKl 0.34 CACCCAGCTGGTCCTGTGGATGGGA 1756 PHFIl 0.36 TTGGACATCTCTAGTGTAGCTGCCA
Table 68. Streptozocin biomarkers .
SEQIDNO Gene Correlation Medianprobe
1757 PGKl 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
1758 SCD 0.31 TGGACCCCACTGGCTGAGAATCTGG
1759 INSIGl 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
1760 IGBPl 0.39 TCCTCCATCACCTGAAACACTGGAC
1761 TNFAIP3 0.31 TCCTCCATCACCTGAAACACTGGAC
1762 TNFSFlO 0.31 CACCCAGCTGGTCCTGTGGATGGGA
1763 ABCAl 0.34 TGCCTGCTCCTGTACTTGTCCTCAG
1764 AGA 0.31 TGGACCCCACTGGCTGAGAATCTGG
1765 ABCA8 0.31 CACCCAGCTGGTCCTGTGGATGGGA
1766 DBCl 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
1767 PTGER2 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
1768 UGT1A3 0.32 TCCTCCATCACCTGAAACACTGGAC
1769 ClOorflO 0.3 CACCCAGCTGGTCCTGTGGATGGGA
1770 TM4SF13 0.34 TGGACCCCACTGGCTGAGAATCTGG
1771 CGI-90 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
1772 LXN 0.31 AAGCCTATACGTTTCTGTGGAGTAA
1773 DNAJC12 0.35 TTGGACATCTCTAGTGTAGCTGCCA
1774 HIPK2 0.31 CACCCAGCTGGTCCTGTGGATGGGA
1775 C9orf95 0.36 ACTTGTCCTCAGCTTGGGCTTCTTC
Table 69. Carmustine biomarkers .
SEQIDNO Gene Correlation Medianprobe
1776 RPLP2 0.34 TGCCTGCTCCTGTACTTGTCCTCAG
1777 CD99 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
1778 IFITMl 0.36 TCCTCCATCACCTGAAACACTGGAC
1779 INSIGl 0.31 TCCTCCATCACCTGAAACACTGGAC
1780 ALDOC 0.4 TGCCTGCTCCTGTACTTGTCCTCAG
1781 ITM2A 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
1782 SERPINAl 0.39 TTGGACATCTCTAGTGTAGCTGCCA
1783 ClQRl 0.35 AAGCCTATACGTTTCTGTGGAGTAA
1784 STAT5A 0.39 TTGGACATCTCTAGTGTAGCTGCCA
1785 INPP5D 0.44 TCCTTGTGCCTGCTCCTGTACTTGT
1786 SATBl 0.36 AAATGTTTCCTTGTGCCTGCTCCTG
1787 VPS16 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
1788 SLA 0.37 TCCTGTACTTGTCCTCAGCTTGGGC
1789 IL2RG 0.45 TCCTCCATCACCTGAAACACTGGAC
1790 MFNG 0.33 TCCTCCATCACCTGAAACACTGGAC
1791 SELL 0.38 AAGCCTATACGTTTCTGTGGAGTAA
1792 LRMP 0.41 GCCCCACTGGACAACACTGATTCCT
1793 ICAM2 0.54 TCCTCCATCACCTGAAACACTGGAC
1794 MYB 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
1795 PTPN7 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
1796 ARHGAP25 0.42 TTGGACATCTCTAGTGTAGCTGCCA
1797 LCK 0.41 TGGACCCCACTGGCTGAGAATCTGG
1798 CXorf9 0.35 TGGACCCCACTGGCTGAGAATCTGG
1799 RHOH 0.41 AAATGTTTCCTTGTGCCTGCTCCTG
1800 ZNFNlAl 0.37 TGCCTGCTCCTGTACTTGTCCTCAG
1801 CENTBl 0.59 ACTTGTCCTCAGCTTGGGCTTCTTC
1802 ADD2 0.34 TCCTTGTGCCTGCTCCTGTACTTGT
1803 LCP2 0.33 TTGGACATCTCTAGTGTAGCTGCCA
1804 SPIl 0.39 TGCCTGCTCCTGTACTTGTCCTCAG
1805 DBT 0.42 ACTTGTCCTCAGCTTGGGCTTCTTC
1806 GZMA 0.34 CACCCAGCTGGTCCTGTGGATGGGA
1807 CD2 0.36 TGGACCCCACTGGCTGAGAATCTGG
1808 BATF 0.38 ACTTGTCCTCAGCTTGGGCTTCTTC
1809 HIST1H4C 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
1810 ARHGAP6 0.4 TCCTCCATCACCTGAAACACTGGAC
1811 VAVl 0.42 TGGACCCCACTGGCTGAGAATCTGG
1812 MAP4K1 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
1813 CCR7 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
1814 PDE4C 0.57 TCCTCCATCACCTGAAACACTGGAC
1815 CD3G 0.44 AAGCCTATACGTTTCTGTGGAGTAA
1816 CCR9 0.37 AAATGTTTCCTTGTGCCTGCTCCTG
1817 SP140 0.48 TCCTGTACTTGTCCTCAGCTTGGGC
1818 TK2 0.31 TGGACCCCACTGGCTGAGAATCTGG
1819 LCPl 0.38 TCCTCCATCACCTGAAACACTGGAC
1820 IFI16 0.34 GCCCCACTGGACAACACTGATTCCT
1821 CXCR4 0.42 GCCCCACTGGACAACACTGATTCCT
1822 ARHGEF6 0.45 AAATGTTTCCTTGTGCCTGCTCCTG
1823 PSCDBP 0.42 TCCTGTACTTGTCCTCAGCTTGGGC
1824 SELPLG 0.52 TGGACCCCACTGGCTGAGAATCTGG
1825 SEC31L2 0.42 TCCTGTACTTGTCCTCAGCTTGGGC
1826 CD3Z 0.34 TCCTCCATCACCTGAAACACTGGAC
1827 PRKCQ 0.46 TCCTTGTGCCTGCTCCTGTACTTGT
1828 SH2D1A 0.46 TGCCTGCTCCTGTACTTGTCCTCAG
1829 GZMB 0.55 TTGGACATCTCTAGTGTAGCTGCCA
1830 CDlA 0.34 TCCTTGTGCCTGCTCCTGTACTTGT
1831 GATA2 0.41 TTGGACATCTCTAGTGTAGCTGCCA
1832 LY9 0.54 TCCTCCATCACCTGAAACACTGGAC
1833 LAIRl 0.3 TTGGACATCTCTAGTGTAGCTGCCA
1834 TRB@ 0.33 TCCTCCATCACCTGAAACACTGGAC
1835 SEPT6 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
1836 HA-I 0.32 TCCTCCATCACCTGAAACACTGGAC
1837 SLC43A3 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
1838 DOCK2 0.31 TCCTCCATCACCTGAAACACTGGAC
1839 CG018 0.42 ACTTGTCCTCAGCTTGGGCTTCTTC
1840 MLCl 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
1841 CD3D 0.35 TCCTGTACTTGTCCTCAGCTTGGGC
1842 T3JAM 0.34 CACCCAGCTGGTCCTGTGGATGGGA
1843 CD6 0.43 TCCTGTACTTGTCCTCAGCTTGGGC
1844 ZAP70 0.43 GCCCCACTGGACAACACTGATTCCT
1845 DOK2 0.3 TCCTGTACTTGTCCTCAGCTTGGGC
1846 LSTl 0.36 TCCTGTACTTGTCCTCAGCTTGGGC
1847 GPR65 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
1848 PRFl 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
1849 ALMSl 0.38 TTGGACATCTCTAGTGTAGCTGCCA
1850 AIFl 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
1851 PRDX2 0.48 GCCCCACTGGACAACACTGATTCCT
1852 FLJ12151 0.36 AAATGTTTCCTTGTGCCTGCTCCTG
1853 FBXW12 0.37 TGCCTGCTCCTGTACTTGTCCTCAG
1854 CDlE 0.34 AAGCCTATACGTTTCTGTGGAGTAA
1855 CYFIP2 0.3 TCCTTGTGCCTGCTCCTGTACTTGT
1856 TARP 0.33 TCCTGTACTTGTCCTCAGCTTGGGC
1857 TRIM 0.38 CACCCAGCTGGTCCTGTGGATGGGA
1858 RPLlOL 0.43 AAATGTTTCCTTGTGCCTGCTCCTG
1859 GLTSCR2 0.43 CACCCAGCTGGTCCTGTGGATGGGA
1860 CKIP-I 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
1861 NRNl 0.3 TCCTTGTGCCTGCTCCTGTACTTGT
1862 ARHGAP15 0.4 TCCTCCATCACCTGAAACACTGGAC
1863 NOTCHl 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
1864 PSCD4 0.4 CACCCAGCTGGTCCTGTGGATGGGA
1865 C13orfl8 0.31 AAGCCTATACGTTTCTGTGGAGTAA
1866 BCLIlB 0.35 ACTTGTCCTCAGCTTGGGCTTCTTC
1867 GIMAP6 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC
1868 STAG3 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
1869 NARF 0.34 TCCTGTACTTGTCCTCAGCTTGGGC
1870 TM6SF1 0.48 TCCTCCATCACCTGAAACACTGGAC
1871 C15orf25 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
1872 FLJ11795 0.35 GCCCCACTGGACAACACTGATTCCT
1873 SAMSNl 0.37 GCCCCACTGGACAACACTGATTCCT
1874 UBASH3A 0.4 TCCTGTACTTGTCCTCAGCTTGGGC
1875 PACAP 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
1876 LEFl 0.3 CACCCAGCTGGTCCTGTGGATGGGA
1877 IL21R 0.34 AAGCCTATACGTTTCTGTGGAGTAA
1878 TCF4 0.41 GCCCCACTGGACAACACTGATTCCT
1879 DKFZP434B0335 0.33 TCCTGTACTTGTCCTCAGCTTGGGC
Table 70 . Lomustine bic ^marker
SEQIDNO Gene Correlation Medianprobe
1880 RPS15 0. 43 TCCTGTACTTGTCCTCAGCTTGGGC
1881 INSIGl 0. 31 TGGACCCCACTGGCTGAGAATCTGG
1882 ALDOC 0. 39 TGCCTGCTCCTGTACTTGTCCTCAG
1883 ITM2A 0. 32 TCCTCCATCACCTGAAACACTGGAC
1884 ClQRl 0. 33 TGCCTGCTCCTGTACTTGTCCTCAG
1885 STAT5A 0. 37 TGCCTGCTCCTGTACTTGTCCTCAG
1886 INPP5D 0. 32 TCCTGTACTTGTCCTCAGCTTGGGC
1887 VPS16 0. 32 TGCCTGCTCCTGTACTTGTCCTCAG
1888 SLA 0. 32 TGCCTGCTCCTGTACTTGTCCTCAG
1889 USP20 0. 41 ACTTGTCCTCAGCTTGGGCTTCTTC
1890 IL2RG 0. 31 TCCTGTACTTGTCCTCAGCTTGGGC
1891 MFNG 0. 4 ACTTGTCCTCAGCTTGGGCTTCTTC
1892 LRMP 0. 43 GCCCCACTGGACAACACTGATTCCT
1893 EVI2A 0. 35 ACTTGTCCTCAGCTTGGGCTTCTTC
1894 PTPN7 0. 35 TCCTTGTGCCTGCTCCTGTACTTGT
1895 ARHGAP25 0.39 TCCTGTACTTGTCCTCAGCTTGGGC
1896 RHOH 0.31 AAGCCTATACGTTTCTGTGGAGTAA
1897 ZNFNlAl 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
1898 CENTBl 0.35 TCCTGTACTTGTCCTCAGCTTGGGC
1899 LCP2 0.41 TGGACCCCACTGGCTGAGAATCTGG
1900 SPIl 0.35 TGCCTGCTCCTGTACTTGTCCTCAG
1901 ARHGAP6 0.33 TTGGACATCTCTAGTGTAGCTGCCA
1902 MAP4K1 0.34 CACCCAGCTGGTCCTGTGGATGGGA
1903 CCR7 0.35 TCCTCCATCACCTGAAACACTGGAC
1904 LY96 0.35 GCCCCACTGGACAACACTGATTCCT
1905 C6orf32 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
1906 MAGEAl 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
1907 SP140 0.35 TTGGACATCTCTAGTGTAGCTGCCA
1908 LCPl 0.36 TCCTCCATCACCTGAAACACTGGAC
1909 IFI16 0.39 TGCCTGCTCCTGTACTTGTCCTCAG
1910 ARHGEF6 0.33 TCCTCCATCACCTGAAACACTGGAC
1911 PSCDBP 0.43 AAGCCTATACGTTTCTGTGGAGTAA
1912 SELPLG 0.3 ACTTGTCCTCAGCTTGGGCTTCTTC
1913 CD3Z 0.35 AAGCCTATACGTTTCTGTGGAGTAA
1914 PRKCQ 0.4 TCCTTGTGCCTGCTCCTGTACTTGT
1915 GZMB 0.31 AAGCCTATACGTTTCTGTGGAGTAA
1916 LAIRl 0.38 TGGACCCCACTGGCTGAGAATCTGG
1917 SH2D1A 0.36 TCCTGTACTTGTCCTCAGCTTGGGC
1918 TRB@ 0.39 TTGGACATCTCTAGTGTAGCTGCCA
1919 RFP 0.35 TGCCTGCTCCTGTACTTGTCCTCAG
1920 SEPT6 0.41 TCCTCCATCACCTGAAACACTGGAC
1921 HA-I 0.43 TCCTGTACTTGTCCTCAGCTTGGGC
1922 SLC43A3 0.4 ACTTGTCCTCAGCTTGGGCTTCTTC
1923 CD3D 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
1924 T3JAM 0.3 TGGACCCCACTGGCTGAGAATCTGG
1925 GPR65 0.34 GCCCCACTGGACAACACTGATTCCT
1926 PRFl 0.36 TGCCTGCTCCTGTACTTGTCCTCAG
1927 AIFl 0.33 TGGACCCCACTGGCTGAGAATCTGG
1928 LPXN 0.38 AAATGTTTCCTTGTGCCTGCTCCTG
1929 RPLlOL 0.3 TGGACCCCACTGGCTGAGAATCTGG
1930 SITPEC 0.36 CACCCAGCTGGTCCTGTGGATGGGA
1931 ARHGAP15 0.33 TGGACCCCACTGGCTGAGAATCTGG
1932 C13orfl8 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
1933 NARF 0.35 TGGACCCCACTGGCTGAGAATCTGG
1934 TM6SF1 0.34 TCCTTGTGCCTGCTCCTGTACTTGT
1935 PACAP 0.31 AAGCCTATACGTTTCTGTGGAGTAA
1936 TCF4 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
Table 71 . Mercaptopurin
SEQIDNO Gene C Coorrrrelation Medianprobe
1937 SSRPl 0.31 GCCCCACTGGACAACACTGATTCCT
1938 ALDOC 0.36 AAATGTTTCCTTGTGCCTGCTCCTG
1939 ClQRl 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
1940 TTFl 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
1941 PRIMl 0.31 GCCCCACTGGACAACACTGATTCCT
1942 USP34 0.38 TCCTCCATCACCTGAAACACTGGAC
1943 TK2 0.33 TCCTGTACTTGTCCTCAGCTTGGGC
1944 GOLGIN-67 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
1945 NPD014 0.35 ACTTGTCCTCAGCTTGGGCTTCTTC
1946 KIAA0220 0.31 TCCTCCATCACCTGAAACACTGGAC
1947 SLC43A3 0.3 TTGGACATCTCTAGTGTAGCTGCCA
1948 WBSCR20C 0.3 CACCCAGCTGGTCCTGTGGATGGGA
1949 ICAM2 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
1950 TEXlO 0.32 TGGACCCCACTGGCTGAGAATCTGG
1951 CHD7 0.3 ACTTGTCCTCAGCTTGGGCTTCTTC
1952 SAMSNl 0.34 TTGGACATCTCTAGTGTAGCTGCCA
1953 TPRT 0.35 ACTTGTCCTCAGCTTGGGCTTCTTC
Table 72 . Teniposide biomarke
SEQIDNO Gene Correlation Medianprobe
1954 CD99 0.35 TGCCTGCTCCTGTACTTGTCCTCAG
1955 INSIGl 0.35 AAGCCTATACGTTTCTGTGGAGTAA
1956 PRGl 0.36 TGCCTGCTCCTGTACTTGTCCTCAG
1957 ALDOC 0.3 ACTTGTCCTCAGCTTGGGCTTCTTC
1958 ITM2A 0.33 AAGCCTATACGTTTCTGTGGAGTAA
1959 SLA 0.43 GCCCCACTGGACAACACTGATTCCT
1960 SSBP2 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
1961 IL2RG 0.37 AAATGTTTCCTTGTGCCTGCTCCTG
1962 MFNG 0.32 TTGGACATCTCTAGTGTAGCTGCCA
1963 ALOX5AP 0.32 TCCTCCATCACCTGAAACACTGGAC
1964 Clorf29 0.3 TCCTCCATCACCTGAAACACTGGAC
1965 SELL 0.33 CACCCAGCTGGTCCTGTGGATGGGA
1966 STCl 0.47 TGGACCCCACTGGCTGAGAATCTGG
1967 LRMP 0.33 TCCTCCATCACCTGAAACACTGGAC
1968 MYB 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
1969 PTPN7 0.34 AAGCCTATACGTTTCTGTGGAGTAA
1970 CXorf9 0.42 TTGGACATCTCTAGTGTAGCTGCCA
1971 RHOH 0.31 AAGCCTATACGTTTCTGTGGAGTAA
1972 ZNFNlAl 0.34 CACCCAGCTGGTCCTGTGGATGGGA
1973 CENTBl 0.37 TGGACCCCACTGGCTGAGAATCTGG
1974 ADD2 0.31 TGCCTGCTCCTGTACTTGTCCTCAG
1975 CDlD 0.37 ACTTGTCCTCAGCTTGGGCTTCTTC
1976 BATF 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
1977 MAP4K1 0.3 GCCCCACTGGACAACACTGATTCCT
1978 CCR7 0.48 TCCTGTACTTGTCCTCAGCTTGGGC
1979 PDE4C 0.33 TGGACCCCACTGGCTGAGAATCTGG
1980 CD3G 0.33 TTGGACATCTCTAGTGTAGCTGCCA
1981 CCR9 0.36 ACTTGTCCTCAGCTTGGGCTTCTTC
1982 SPIlO 0.34 AAATGTTTCCTTGTGCCTGCTCCTG
1983 TNFAIP8 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
1984 NAPlLl 0.32 AAGCCTATACGTTTCTGTGGAGTAA
1985 CXCR4 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
1986 ARHGEF6 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
1987 GATA3 0.36 TCCTGTACTTGTCCTCAGCTTGGGC
1988 SELPLG 0.38 AAGCCTATACGTTTCTGTGGAGTAA
1989 SEC31L2 0.46 TGGACCCCACTGGCTGAGAATCTGG
1990 CD3Z 0.35 GCCCCACTGGACAACACTGATTCCT
1991 SH2D1A 0.45 AAATGTTTCCTTGTGCCTGCTCCTG
1992 GZMB 0.35 TCCTTGTGCCTGCTCCTGTACTTGT
1993 CDlA 0.45 GCCCCACTGGACAACACTGATTCCT
1994 SCN3A 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
1995 LAIRl 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
1996 AFlQ 0.3 TCCTCCATCACCTGAAACACTGGAC
1997 TRB@ 0.32 AAGCCTATACGTTTCTGTGGAGTAA
1998 DOCK2 0.33 TCCTGTACTTGTCCTCAGCTTGGGC
1999 MLCl 0.31 TCCTCCATCACCTGAAACACTGGAC
2000 CD3D 0.31 TGGACCCCACTGGCTGAGAATCTGG
2001 T3JAM 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC 2002 CD6 0.38 TGCCTGCTCCTGTACTTGTCCTCAG 2003 ZAP70 0.34 TCCTCCATCACCTGAAACACTGGAC 2004 IFI44 0.37 TCCTTGTGCCTGCTCCTGTACTTGT 2005 GPR65 0.34 TCCTGTACTTGTCCTCAGCTTGGGC 2006 PRFl 0.34 TCCTCCATCACCTGAAACACTGGAC 2007 AIFl 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC 2008 WDR45 0.41 GCCCCACTGGACAACACTGATTCCT 2009 CDlE 0.31 AAGCCTATACGTTTCTGTGGAGTAA 2010 CYFIP2 0.32 TGGACCCCACTGGCTGAGAATCTGG 2011 TARP 0.42 CACCCAGCTGGTCCTGTGGATGGGA 2012 TRIM 0.33 TGGACCCCACTGGCTGAGAATCTGG 2013 ARHGAP15 0.38 AAGCCTATACGTTTCTGTGGAGTAA 2014 NOTCHl 0.32 TGCCTGCTCCTGTACTTGTCCTCAG 2015 STAG3 0.32 GCCCCACTGGACAACACTGATTCCT 2016 NARF 0.31 AAGCCTATACGTTTCTGTGGAGTAA 2017 TM6SF1 0.33 GCCCCACTGGACAACACTGATTCCT 2018 UBASH3A 0.33 TCCTGTACTTGTCCTCAGCTTGGGC 2019 MGC5566 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
Table 73. . Dactinomycin biomarkers.
SEQIDNO Gene Correlation Medianprobe
2020 ALDOC 0.37 GCCCCACTGGACAACACTGATTCCT
2021 ClQRl 0.36 TGGACCCCACTGGCTGAGAATCTGG
2022 SLA 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
2023 WBSCR20A 0.31 AAGCCTATACGTTTCTGTGGAGTAA
2024 MFNG 0. ,33 ACTTGTCCTCAGCTTGGGCTTCTTC
2025 SELL 0.,33 GCCCCACTGGACAACACTGATTCCT
2026 MYB 0.,3366 TTGGACATCTCTAGTGTAGCTGCCA
2027 RHOH 0 0..3322 TCCTTGTGCCTGCTCCTGTACTTGT
2028 ZNFNlAl 0.3 AAATGTTTCCTTGTGCCTGCTCCTG
2029 LCP2 0.3 CACCCAGCTGGTCCTGTGGATGGGA
2030 MAP4K1 0 0..3344 AAGCCTATACGTTTCTGTGGAGTAA
2031 CBFA2T3 00..3355 TCCTTGTGCCTGCTCCTGTACTTGT
2032 LCPl 00..3322 GCCCCACTGGACAACACTGATTCCT
2033 SELPLG 00..3333 ACTTGTCCTCAGCTTGGGCTTCTTC
2034 CD3Z 00..3355 GCCCCACTGGACAACACTGATTCCT
2035 LAIRl 00..3333 TGGACCCCACTGGCTGAGAATCTGG
2036 WBSCR20C 0.3 AAGCCTATACGTTTCTGTGGAGTAA
2037 CD3D 0.35 CACCCAGCTGGTCCTGTGGATGGGA
2038 GPR65 0.32 AAATGTTTCCTTGTGCCTGCTCCTG
2039 ARHGAP15 0.32 TCCTCCATCACCTGAAACACTGGAC
2040 FLJ10178 0.36 TCCTTGTGCCTGCTCCTGTACTTGT
2041 NARF 0.35 TCCTCCATCACCTGAAACACTGGAC
2042 PUS3 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
Table 74 Tretinoin biomarkers.
SEQIDNO Gene Correlation Medianprobe
2043 PPIB 0.31 AAGCCTATACGTTTCTGTGGAGTAA
2044 ZFP36L2 0.48 AAGCCTATACGTTTCTGTGGAGTAA
2045 IFI 30 0.46 ACTTGTCCTCAGCTTGGGCTTCTTC
2046 USP7 0.35 TCCTCCATCACCTGAAACACTGGAC
2047 SRM 0.43 TCCTCCATCACCTGAAACACTGGAC
2048 SH3BP5 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
2049 ALDOC 0.41 TTGGACATCTCTAGTGTAGCTGCCA
2050 FADS2 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC
2051 GUSB 0.38 TTGGACATCTCTAGTGTAGCTGCCA
2052 PSCDl 0.48 TCCTGTACTTGTCCTCAGCTTGGGC
2053 IQGAP2 0.34 TCCTGTACTTGTCCTCAGCTTGGGC
2054 STS 0.34 GCCCCACTGGACAACACTGATTCCT
2055 MFNG 0.36 TGGACCCCACTGGCTGAGAATCTGG
2056 FLIl 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC
2057 PIM2 0.35 TGGACCCCACTGGCTGAGAATCTGG
2058 INPP4A 0.54 TCCTGTACTTGTCCTCAGCTTGGGC
2059 LRMP 0.51 GCCCCACTGGACAACACTGATTCCT
2060 ICAM2 0.3 AAATGTTTCCTTGTGCCTGCTCCTG
2061 EVI2A 0.33 CACCCAGCTGGTCCTGTGGATGGGA
2062 MAL 0.46 AAATGTTTCCTTGTGCCTGCTCCTG
2063 BTN3A3 0.43 TTGGACATCTCTAGTGTAGCTGCCA
2064 PTPN7 0.4 TTGGACATCTCTAGTGTAGCTGCCA
2065 ILlORA 0.42 TTGGACATCTCTAGTGTAGCTGCCA
2066 SPIl 0.41 AAGCCTATACGTTTCTGTGGAGTAA
2067 TRAFl 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
2068 ITGB7 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
2069 ARHGAP6 0.32 TGGACCCCACTGGCTGAGAATCTGG
2070 MAP4K1 0.52 GCCCCACTGGACAACACTGATTCCT
2071 CD28 0.34 AAGCCTATACGTTTCTGTGGAGTAA
2072 PTP4A3 0.3 TCCTCCATCACCTGAAACACTGGAC
2073 LTB 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
2074 Clorf38 0.4 TGCCTGCTCCTGTACTTGTCCTCAG
2075 WBSCR22 0.53 TCCTCCATCACCTGAAACACTGGAC
2076 CD8B1 0.35 TCCTCCATCACCTGAAACACTGGAC
2077 LCPl 0.35 ACTTGTCCTCAGCTTGGGCTTCTTC
2078 FLJ13052 0.31 TCCTCCATCACCTGAAACACTGGAC
2079 MEF2C 0.71 TTGGACATCTCTAGTGTAGCTGCCA
2080 PSCDBP 0.41 AAATGTTTCCTTGTGCCTGCTCCTG
2081 IL16 0.51 TGGACCCCACTGGCTGAGAATCTGG
2082 SELPLG 0.53 TGCCTGCTCCTGTACTTGTCCTCAG
2083 MAGEA9 0.6 AAATGTTTCCTTGTGCCTGCTCCTG
2084 LAIRl 0.43 TCCTCCATCACCTGAAACACTGGAC
2085 TNFRSF25 0.53 TCCTCCATCACCTGAAACACTGGAC
2086 EVI2B 0.42 ACTTGTCCTCAGCTTGGGCTTCTTC
2087 IGJ 0.37 TCCTTGTGCCTGCTCCTGTACTTGT
2088 PDCD4 0.47 AAATGTTTCCTTGTGCCTGCTCCTG
2089 RASA4 0.52 CACCCAGCTGGTCCTGTGGATGGGA
2090 HA-I 0.73 AAGCCTATACGTTTCTGTGGAGTAA
2091 PLCL2 0.47 TCCTGTACTTGTCCTCAGCTTGGGC
2092 RNASE6 0.31 AAGCCTATACGTTTCTGTGGAGTAA
2093 WBSCR20C 0.35 TTGGACATCTCTAGTGTAGCTGCCA
2094 NUP210 0.36 AAGCCTATACGTTTCTGTGGAGTAA
2095 RPLlOL 0.39 ACTTGTCCTCAGCTTGGGCTTCTTC
2096 Cllorf2 0.33 TGGACCCCACTGGCTGAGAATCTGG
2097 CABCl 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
2098 ARHGEF3 0.37 TCCTGTACTTGTCCTCAGCTTGGGC
2099 TAPBPL 0.42 TGCCTGCTCCTGTACTTGTCCTCAG
2100 CHST12 0.35 AAATGTTTCCTTGTGCCTGCTCCTG
2101 FKBPIl 0.54 TGCCTGCTCCTGTACTTGTCCTCAG
2102 FLJ35036 0.42 TTGGACATCTCTAGTGTAGCTGCCA
2103 MYLIP 0.38 CACCCAGCTGGTCCTGTGGATGGGA
2104 TXNDC5 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
2105 PACAP 0.3 TCCTCCATCACCTGAAACACTGGAC
2106 TOSO 0.34 TCCTGTACTTGTCCTCAGCTTGGGC
2107 PNAS-4 0.37 TGGACCCCACTGGCTGAGAATCTGG
2108 IL21R 0.57 AAGCCTATACGTTTCTGTGGAGTAA
2109 TCF4 0.64 TCCTTGTGCCTGCTCCTGTACTTGT
Table 75 . Ifosfamide b
SEQIDNO Gene C Coorrrrelation Medianprobe
2110 ARHGDIB 0.36 TGGACCCCACTGGCTGAGAATCTGG
2111 ZFP36L2 0.45 TGGACCCCACTGGCTGAGAATCTGG
2112 ITM2A 0.39 AAGCCTATACGTTTCTGTGGAGTAA
2113 LGALS9 0.54 AAATGTTTCCTTGTGCCTGCTCCTG
2114 INPP5D 0.53 TCCTGTACTTGTCCTCAGCTTGGGC
2115 SATBl 0.35 TTGGACATCTCTAGTGTAGCTGCCA
2116 TFDP2 0.32 AAGCCTATACGTTTCTGTGGAGTAA
2117 IL2RG 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
2118 CD48 0.5 ACTTGTCCTCAGCTTGGGCTTCTTC
2119 SELL 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
2120 ADA 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
2121 LRMP 0.34 GCCCCACTGGACAACACTGATTCCT
2122 RIMS3 0.37 AAGCCTATACGTTTCTGTGGAGTAA
2123 LCK 0.37 TCCTGTACTTGTCCTCAGCTTGGGC
2124 CXorf9 0.4 CACCCAGCTGGTCCTGTGGATGGGA
2125 RHOH 0.3 GCCCCACTGGACAACACTGATTCCT
2126 ZNFNlAl 0.31 TTGGACATCTCTAGTGTAGCTGCCA
2127 LCP2 0.37 TCCTGTACTTGTCCTCAGCTTGGGC
2128 CDlD 0.49 TCCTCCATCACCTGAAACACTGGAC
2129 CD2 0.42 CACCCAGCTGGTCCTGTGGATGGGA
2130 ZNF91 0.45 AAATGTTTCCTTGTGCCTGCTCCTG
2131 MAP4K1 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
2132 CCR7 0.44 TTGGACATCTCTAGTGTAGCTGCCA
2133 IGLLl 0.43 TGCCTGCTCCTGTACTTGTCCTCAG
2134 CD3G 0.3 TCCTCCATCACCTGAAACACTGGAC
2135 ZNF430 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
2136 CCR9 0.31 TTGGACATCTCTAGTGTAGCTGCCA
2137 CXCR4 0.37 ACTTGTCCTCAGCTTGGGCTTCTTC
2138 KIAA0922 0.31 AAGCCTATACGTTTCTGTGGAGTAA
2139 TARP 0.31 GCCCCACTGGACAACACTGATTCCT
2140 FYN 0.35 TCCTGTACTTGTCCTCAGCTTGGGC
2141 SH2D1A 0.34 TTGGACATCTCTAGTGTAGCTGCCA
2142 CDlA 0.31 AAGCCTATACGTTTCTGTGGAGTAA
2143 LSTl 0.33 TTGGACATCTCTAGTGTAGCTGCCA
2144 LAIRl 0.36 ACTTGTCCTCAGCTTGGGCTTCTTC
2145 TRB@ 0.34 TGGACCCCACTGGCTGAGAATCTGG
2146 SEPT6 0.39 TTGGACATCTCTAGTGTAGCTGCCA
2147 CD3D 0.37 TCCTCCATCACCTGAAACACTGGAC
2148 CD6 0.32 AAATGTTTCCTTGTGCCTGCTCCTG
2149 AIFl 0.34 TGCCTGCTCCTGTACTTGTCCTCAG
2150 CDlE 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
2151 TRIM 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
2152 GLTSCR2 0.34 TCCTGTACTTGTCCTCAGCTTGGGC
2153 ARHGAP15 0.33 TCCTGTACTTGTCCTCAGCTTGGGC
2154 BIN2 0.33 TGCCTGCTCCTGTACTTGTCCTCAG
2155 SH3TC1 0.32 TGGACCCCACTGGCTGAGAATCTGG
2156 CECRl 0.36 TCCTCCATCACCTGAAACACTGGAC
2157 BCLIlB 0.38 TCCTCCATCACCTGAAACACTGGAC
2158 GIMAP6 0.32 GCCCCACTGGACAACACTGATTCCT
2159 STAG3 0.46 TTGGACATCTCTAGTGTAGCTGCCA
2160 GALNT6 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
2161 MGC5566 0.49 TCCTTGTGCCTGCTCCTGTACTTGT
2162 PACAP 0.48 TCCTGTACTTGTCCTCAGCTTGGGC
2163 LEFl 0.4 TGCCTGCTCCTGTACTTGTCCTCAG
Table 76 . Tamoxifen biomarkers
SEQIDNO Gene Correlation Medianprobe
2164 MLP 0.33 TCCTGTACTTGTCCTCAGCTTGGGC
2165 GLUL 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
2166 SLC9A3R1 0.37 CACCCAGCTGGTCCTGTGGATGGGA
2167 ZFP36L2 0.33 TTGGACATCTCTAGTGTAGCTGCCA
2168 INSIGl 0.31 TCCTCCATCACCTGAAACACTGGAC
2169 TBLlX 0.36 TCCTGTACTTGTCCTCAGCTTGGGC
2170 NDUFABl 0.43 AAATGTTTCCTTGTGCCTGCTCCTG
2171 EBP 0.31 TGGACCCCACTGGCTGAGAATCTGG
2172 TRIM14 0.43 TTGGACATCTCTAGTGTAGCTGCCA
2173 SRPK2 0.41 GCCCCACTGGACAACACTGATTCCT
2174 PMM2 0.4 AAATGTTTCCTTGTGCCTGCTCCTG
2175 CLDN3 0.41 AAGCCTATACGTTTCTGTGGAGTAA
2176 GCHl 0.34 TTGGACATCTCTAGTGTAGCTGCCA
2177 IDIl 0.34 AAATGTTTCCTTGTGCCTGCTCCTG
2178 TTFl 0.46 TCCTTGTGCCTGCTCCTGTACTTGT
2179 MYB 0.39 CACCCAGCTGGTCCTGTGGATGGGA
2180 RASGRPl 0.32 CACCCAGCTGGTCCTGTGGATGGGA
2181 HIST1H3H 0.38 TGGACCCCACTGGCTGAGAATCTGG
2182 CBFA2T3 0.34 AAATGTTTCCTTGTGCCTGCTCCTG
2183 SRRM2 0.43 GCCCCACTGGACAACACTGATTCCT
2184 ANAPC5 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
2185 MBD4 0.5 TCCTGTACTTGTCCTCAGCTTGGGC
2186 GATA3 0.32 TCCTCCATCACCTGAAACACTGGAC
2187 HIST1H2BG 0.32 AAGCCTATACGTTTCTGTGGAGTAA
2188 RAB14 0.31 TGGACCCCACTGGCTGAGAATCTGG
2189 PIK3R1 0.36 AAGCCTATACGTTTCTGTGGAGTAA
2190 MGC50853 0.37 CACCCAGCTGGTCCTGTGGATGGGA
2191 ELFl 0.35 GCCCCACTGGACAACACTGATTCCT
2192 ZRFl 0.32 TCCTTGTGCCTGCTCCTGTACTTGT
2193 ZNF394 0.31 AAATGTTTCCTTGTGCCTGCTCCTG
2194 S100A14 0.39 AAATGTTTCCTTGTGCCTGCTCCTG
2195 SLC6A14 0.31 CACCCAGCTGGTCCTGTGGATGGGA
2196 GALNT6 0.37 TCCTCCATCACCTGAAACACTGGAC
2197 SPDEF 0.44 AAATGTTTCCTTGTGCCTGCTCCTG
2198 TPRT 0.5 AAGCCTATACGTTTCTGTGGAGTAA
2199 CALML4 0.31 TTGGACATCTCTAGTGTAGCTGCCA
Table 77 . Floxuridine biomarke
SEQIDNO Gene Correlation
2200 CSDA 0.33 ACTTGTCCTCAGCTTGGGCTTCTTC
2201 F8A1 0.31 TGGACCCCACTGGCTGAGAATCTGG
2202 KYNU 0.32 TGGACCCCACTGGCTGAGAATCTGG
2203 PHF14 0.31 AAGCCTATACGTTTCTGTGGAGTAA
2204 SERPINB2 0.34 TCCTCCATCACCTGAAACACTGGAC
2205 OPHNl 0.31 GCCCCACTGGACAACACTGATTCCT
2206 HRMT1L2 0.31 AAGCCTATACGTTTCTGTGGAGTAA
2207 TNFRSFlA 0.3 GCCCCACTGGACAACACTGATTCCT
2208 PPP4C 0.31 AAGCCTATACGTTTCTGTGGAGTAA
2209 CESl 0.3 TCCTCCATCACCTGAAACACTGGAC
2210 TP53AP1 0.3 GCCCCACTGGACAACACTGATTCCT
2211 TM4SF4 0.32 GCCCCACTGGACAACACTGATTCCT
2212 RPL5 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
2213 BC008967 0.32 TGGACCCCACTGGCTGAGAATCTGG
2214 TLK2 0.35 TTGGACATCTCTAGTGTAGCTGCCA
2215 COL4A6 0.31 TCCTTGTGCCTGCTCCTGTACTTGT
2216 PAK3 0.32 CACCCAGCTGGTCCTGTGGATGGGA
2217 RECK 0.34 TCCTTGTGCCTGCTCCTGTACTTGT
2218 LOC51321 0.32 AAGCCTATACGTTTCTGTGGAGTAA
2219 MST4 0.36 TCCTCCATCACCTGAAACACTGGAC
2220 DERP6 0.32 TGGACCCCACTGGCTGAGAATCTGG
2221 SCD4 0.33 TCCTTGTGCCTGCTCCTGTACTTGT
2222 FLJ22800 0.31 TGGACCCCACTGGCTGAGAATCTGG
Table 78 . Irinotecan biomarke
SEQIDNO Gene Correlation Medianprobe
2223 CSDA 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
2224 UBE2L6 0.32 GCCCCACTGGACAACACTGATTCCT
2225 TAPl 0.44 TGGACCCCACTGGCTGAGAATCTGG
2226 RPS19 0.32 TGCCTGCTCCTGTACTTGTCCTCAG
2227 SERPINAl 0.32 ACTTGTCCTCAGCTTGGGCTTCTTC
2228 ClQRl 0.31 TTGGACATCTCTAGTGTAGCTGCCA
2229 SLA 0.33 CACCCAGCTGGTCCTGTGGATGGGA
2230 GPSM3 0.46 TGCCTGCTCCTGTACTTGTCCTCAG
2231 PSMB9 0.3 TGCCTGCTCCTGTACTTGTCCTCAG
2232 EDGl 0.34 TGCCTGCTCCTGTACTTGTCCTCAG
2233 FMNLl 0.4 GCCCCACTGGACAACACTGATTCCT
2234 PTPN7 0.39 TTGGACATCTCTAGTGTAGCTGCCA
2235 ZNFNlAl 0.32 AAGCCTATACGTTTCTGTGGAGTAA
2236 CENTBl 0.33 TTGGACATCTCTAGTGTAGCTGCCA
2237 BATF 0.41 ACTTGTCCTCAGCTTGGGCTTCTTC
2238 MAP4K1 0.39 AAATGTTTCCTTGTGCCTGCTCCTG
2239 PDE4C 0.31 AAGCCTATACGTTTCTGTGGAGTAA
2240 SPIlO 0.35 TCCTTGTGCCTGCTCCTGTACTTGT
2241 HLA-DRA 0.31 TGGACCCCACTGGCTGAGAATCTGG
2242 IFI 16 0.36 TTGGACATCTCTAGTGTAGCTGCCA
2243 HLA-DRBl 0.32 AAGCCTATACGTTTCTGTGGAGTAA
2244 ARHGEF6 0.43 ACTTGTCCTCAGCTTGGGCTTCTTC
2245 SELPLG 0.35 TCCTTGTGCCTGCTCCTGTACTTGT
2246 SEC31L2 0.35 CACCCAGCTGGTCCTGTGGATGGGA
2247 CD3Z 0.51 TCCTCCATCACCTGAAACACTGGAC
2248 PRKCQ 0.39 TTGGACATCTCTAGTGTAGCTGCCA
2249 SH2D1A 0.43 AAGCCTATACGTTTCTGTGGAGTAA
2250 GZMB 0.49 TCCTCCATCACCTGAAACACTGGAC
2251 TRB@ 0.43 ACTTGTCCTCAGCTTGGGCTTCTTC
2252 HLA-DPAl 0.47 ACTTGTCCTCAGCTTGGGCTTCTTC
2253 AIMl 0.36 TCCTTGTGCCTGCTCCTGTACTTGT
2254 DOCK2 0.39 TGGACCCCACTGGCTGAGAATCTGG
2255 CD3D 0.31 TCCTGTACTTGTCCTCAGCTTGGGC
2256 IFITMl 0.31 TTGGACATCTCTAGTGTAGCTGCCA
2257 ZAP70 0.31 GCCCCACTGGACAACACTGATTCCT
2258 PRFl 0.47 CACCCAGCTGGTCCTGTGGATGGGA
2259 Clorf24 0.39 GCCCCACTGGACAACACTGATTCCT
2260 ARHGAP15 0.48 TCCTCCATCACCTGAAACACTGGAC
2261 C13orfl8 0.33 CACCCAGCTGGTCCTGTGGATGGGA
2262 TM6SF1 0.37 TCCTTGTGCCTGCTCCTGTACTTGT
Table 79. Satraplatin biomarkers .
SEQIDNO Gene Correlation Medianprobe
2263 STATl 0.32 TCCTGTACTTGTCCTCAGCTTGGGC
2264 HSBPl 0.33 AAATGTTTCCTTGTGCCTGCTCCTG
2265 IFI30 0.35 AAGCCTATACGTTTCTGTGGAGTAA
2266 RIOK3 0.36 TCCTCCATCACCTGAAACACTGGAC
2267 TNFSFlO 0.31 ACTTGTCCTCAGCTTGGGCTTCTTC
2268 ALOX5AP 0.3 TCCTTGTGCCTGCTCCTGTACTTGT
2269 ADFP 0.33 TGGACCCCACTGGCTGAGAATCTGG
2270 IRS2 0.37 TCCTGTACTTGTCCTCAGCTTGGGC
2271 EFEMP2 0.31 TTGGACATCTCTAGTGTAGCTGCCA
2272 RIPK2 0.35 TGGACCCCACTGGCTGAGAATCTGG
2273 DKFZp564I1922 0.33 TCCTCCATCACCTGAAACACTGGAC
2274 MTlK 0.34 TCCTCCATCACCTGAAACACTGGAC
2275 RNASET2 0.38 ACTTGTCCTCAGCTTGGGCTTCTTC
2276 EFHD2 0.31 CACCCAGCTGGTCCTGTGGATGGGA
2277 TRIB3 0.33 GCCCCACTGGACAACACTGATTCCT
2278 ACSL5 0.42 AAATGTTTCCTTGTGCCTGCTCCTG
2279 IFIHl 0.37 ACTTGTCCTCAGCTTGGGCTTCTTC
2280 DNAPTP6 0.42 TGCCTGCTCCTGTACTTGTCCTCAG
Table 80. Vincristine microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2281 Hcd892 left 0.3 GAGGGCTGGAGAGGTTGGGTGCGCTTGTGCGTTTCACTTT
2282 Hcd678 right 0.27 GCCCTGAAGCTCCGGACTACAGCTCCCAGGCCTCTCCAAG
2283 mir-00: 7-1-prec 0.28 TGTTGGCCTAGTTCTGTGTGGAAGACTAGTGATTTTGTTG
2284 MPR243 left 0.25 GTATTTACCTAGTTGTAATGTGGGTTGCCATGGTGTTTTG
2285 Hcd654 left 0.25 AACGAGTAAAAGGCGTACATGGGAGCGCGGGGCGGCAGAG
2286 mir-487Nol 0.26 TTATGACGAATCATACAGGGACATCCAGTTTTTCAGTATC
2287 Hcd794 right 0.35 GGCCACCACAGACACCAACAAGTTCAGTCCGTTTCTGCAG
2288 Hcd739 right 0.32 TATTAGCTGAGGGAGGGCTGGAGGCGGCTGCATTCCGACT
2289 Hcd562 right 0.28 CGCATGTCCTGGCCCTCGTCCTTCCATGGCACTGGCACCG
Table 81. Cisplatm microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2290 HUMTRF 0.34 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
2291 HPR187 right 0.25 TATTTATTACAAGGTCCTTCTTCCCCGTAAAACTTTGTCC
2292 mir-450-1 0.26 AACGATACTAAACTGTTTTTGCGATGTGTTCCTAATATGC
2293 mir-155-prec 0.31 TTAATGCTAATCGTGATAGGGGTTTTTGCCTCCAACTGAC
2294 mir-515-15p 0.25 GATCTCATGCAGTCATTCTCCAAAAGAAAGCACTTTCTGT
2295 mir-181b-precNo2 0.25 ACCATCGACCGTTGATTGTACCCTATGGCTAACCATCATC
2296 mir-124a-l-precl 0.26 ATACAATTAAGGCACGCGGTGAATGCCAAGAATGGGGCTG
2297 mir-450-2Nol 0.3 GAAAGATGCTAAACTATTTTTGCGATGTGTTCCTAATATG
2298 Hcd923 right 0.31 CTGGAGATAATGATTCTGCATTTCTAATTAACTCCCAGGT
2299 mir-342Nol 0.31 GTCTCACACAGAAATCGCACCCGTCACCTTGGCCTACTTA
2300 mir-142-prec 0.27 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2301 mir-223-prec 0.26 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT
2302 Hcd754 left 0.38 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC
2303 Hcd213 HPR182 left 0.3 CTGTTTCATACTTGAGGAGAAATTATCCTTGGTGTGTTCG
Table 82 Azaguamne microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2304 MPR121 left 0.3 CACCTGGCTCTGAGAACTGAATTCCATAGGCTGTGAGCTC
2305 HUMTRS 0.26 TCTAGCGACAGAGTGGTTCAATTCCACCTTTCGGGCGCCA
2306 mir-213-precNol 0.26 AACATTCATTGCTGTCGGTGGGTTGAACTGTGTGGACAAG
2307 mir-155-prec 0.4 TTAATGCTAATCGTGATAGGGGTTTTTGCCTCCAACTGAC
2308 mir-147-prec 0.47 GACTATGGAAGCCAGTGTGTGGAAATGCTTCTGCTAGATT
2309 mir-lOONol 0.26 CCTGTTGCCACAAACCCGTAGATCCGAACTTGTGGTATTA
2310 mir-138-l-prec 0.29 AGCTGGTGTTGTGAATCAGGCCGTTGCCAATCAGAGAACG
2311 mir-140No2 0.38 TTCTACCACAGGGTAGAACCACGGACAGGATACCGGGGCA
2312 mir-146-prec 0.51 TGAGAACTGAATTCCATGGGTTGTGTCAGTGTCAGACCTC
2313 mir-509Nol 0.25 ATTAAAAATGATTGGTACGTCTGTGGGTAGAGTACTGCAT
2314 mir-146bNol 0.33 CACCTGGCACTGAGAACTGAATTCCATAGGCTGTGAGCTC
2315 Hcd514 right 0.26 ATTAGAGACTCGTTAAGAGAAGGTGAGAAGGGCTCAGTAA 2316 Hcd397 left 0.34 GTGTGTATACTTATGTGTGTGTATGTGTGAGTGTGAATAT 2317 Hcd731 left 0.27 AATTGTGACAACTGAGTGGGAGGTTTGTGTGATGATTATC 2318 mir-034-precNo2 0.32 AGTAAGGAAGCAATCAGCAAGTATACTGCCCTAGAAGTGC 2319 mir-100-l/2-prec 0.3 TGAGGCCTGTTGCCACAAACCCGTAGATCCGAACTTGTGG
Table 83. Etoposide microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2320 Hcd415 right 0.28 GATGTTTGGGAAACAATGGGAGTGAGAGAATGGGAGAGCT
2321 Hcd768 right 0.37 GCCCTGGCGGAACGCTGAGAAGACAGTCGAACTTGACTAT
2322 HUMTRF 0.38 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
2323 Hcd866 right 0.26 GTCATGCTGCCACCAGCAGGCAGAGAAGAAGCAGAAGAAC
2324 Hcdl45 left 0.33 AAAAATCCCAGCGGCCACCTTTCCTCCCTGCCCCATTGGG
2325 HUMTRAB 0.29 ATGGTAGAGCGCTCGCTTTGCTTGCGAGAGGTAGCGGGAT
2326 Hcd913 right 0.36 CAAACATCATGTGACGTCTGTGGAGCGGCGGCGGCGGCGG
2327 HPR163 left 0.29 GCTGCCCCCTCCCTTAGCAACGTGGCCCCGGCGTTCCAAA
2328 Hcd697 right 0.27 GGCCTCATGCTGCCAAGGGCTGGCAAGAAGTCCCTGCTTG
2329 Hcd755 left 0.26 GGAAGTGGAGCAAATGGATGGAAAGCAATTTTTGGAAGAT
2330 Hcd716 right 0.25 CAATAAATGTGCCTATAAAGGCGCCGGCTCCGGGGCGCGG
2331 MPR207 right 0.33 AACAACTTTGTGCTGGTGCCGGGGAAGTTTGTGTCTCCTA
2332 HSTRNL 0.26 TCCGGATGGAGCGTGGGTTCGAATCCCACTTCTGACACCA
2333 HPR206 left 0.29 CTATATTGGACCGCAGCGCTGAGAGCTTTTGTGTTTAATG
2334 MPR243 left 0.27 GTATTTACCTAGTTGTAATGTGGGTTGCCATGGTGTTTTG
2335 Hcd654 left 0.4 AACGAGTAAAAGGCGTACATGGGAGCGCGGGGCGGCAGAG
2336 MPR130 left 0.28 AGGCCAAGGTGACGGGTGCGATTTCTGTGTGAGACAATTC
2337 Hcd782 left 0.26 GGAGCCCTGTCTGCAAAGAGTGGTGCGTGTGCGTGTGTGA
2338 Hcd794 right 0.26 GGCCACCACAGACACCAACAAGTTCAGTCCGTTTCTGCAG
2339 Hcd739 right 0.3 TATTAGCTGAGGGAGGGCTGGAGGCGGCTGCATTCCGACT
2340 mir-142-prec 0.29 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2341 HSHELAOl 0.29 GGCCGCAGCAACCTCGGTTCGTATCCGAGTCACGGCACCA
2342 HUMTRVlA 0.29 ACGCGAAAGGTCCCCGGTTCGAAACCGGGCGGAAACACCA
2343 Hcd754 left 0.34 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC
Table 84. Carboplatin microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2344 Hcd829 right 0.27 AAAATGGCGGCGGGAAAAGCGAGCGGCGAGAGCGAGGAGG
2345 HUMTRF 0.26 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
2346 HPR187 left 0.29 TGTGTGTTGCGGGGGTGGGGGCCGGTGAAAGTGATTTGAT
2347 Hcd210_HPR205 right 0.32 CGAAACATTCGCGGTGCACTTCTTTTTCAGTATCCTATTC
2348 mir-379Nol 0.26 TTCCGTGGTTCCTGAAGAGATGGTAGACTATGGAACGTAG
2349 mir-213-precNol 0.26 AACATTCATTGCTGTCGGTGGGTTGAACTGTGTGGACAAG
2350 mir-4325p 0.29 CCAGGTCTTGGAGTAGGTCATTGGGTGGATCCTCTATTTC
2351 mir-450-1 0.3 AACGATACTAAACTGTTTTTGCGATGTGTTCCTAATATGC
2352 mir-155-prec 0.25 TTAATGCTAATCGTGATAGGGGTTTTTGCCTCCAACTGAC
2353 Hcd28_HPR39right 0.26 AAGCTCCCAAATTAGCTTTTTAAATAGAAGCTGAGAGTTA
2354 MPR244 right 0.27 TAAACATAGAGGAAATTTCACGTTTTCAGTGTCAAATGCT
2355 mir-409-3p 0.3 GACGAATGTTGCTCGGTGAACCCCTTTTCGGTATCAAATT
2356 mir-124a-l-precl 0.28 ATACAATTAAGGCACGCGGTGAATGCCAAGAATGGGGCTG
2357 mir-154-preclNol 0.26 GTGGTACTTGAAGATAGGTTATCCGTGTTGCCTTCGCTTT
2358 mir-495Nol 0.32 GTGACGAAACAAACATGGTGCACTTCTTTTTCGGTATCAA
2359 mir-515-23p 0.25 CAGAGTGCCTTCTTTTGGAGCGTTACTGTTTGAGAAAAAC
2360 Hcd43 8right 0.27 GTGTTTATTTGAATCTCACATCGCTCATAAGAATACACGC
2361 Hcd770 left 0.3 CCAGTATACAATCCGTTTTTCAGTTTAGCTTGAGATCAGA
2362 mir-382 0.32 GGTACTTGAAGAGAAGTTGTTCGTGGTGGATTCGCTTTAC
2363 mir-223-prec 0.3 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT
2364 Hcd754 left 0.48 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC
2365 Hcd213_HPR182 left 0.31 CTGTTTCATACTTGAGGAGAAATTATCCTTGGTGTGTTCG
Table 85, Adriamycin microRNA biomarkers .
SEQIDNO Medianprobe Corr Sequence
2366 Hcd768 right 0.25 GCCCTGGCGGAACGCTGAGAAGACAGTCGAACTTGACTAT
2367 mir-483Nol 0.28 ATCACGCCTCCTCACTCCTCTCCTCCCGTCTTCTCCTCTC
2368 Hcdl45 left 0.28 AAAAATCCCAGCGGCCACCTTTCCTCCCTGCCCCATTGGG
2369 mir-197-prec 0.25 TAAGAGCTCTTCACCCTTCACCACCTTCTCCACCCAGCAT
2370 mir-212-precNol 0.27 CCTCAGTAACAGTCTCCAGTCACGGCCACCGACGCCTGGC
2371 HPR163 left 0.3 GCTGCCCCCTCCCTTAGCAACGTGGCCCCGGCGTTCCAAA
2372 Hcd654 left 0.26 AACGAGTAAAAGGCGTACATGGGAGCGCGGGGCGGCAGAG
2373 mir-342Nol 0.32 GTCTCACACAGAAATCGCACCCGTCACCTTGGCCTACTTA
2374 Hcd794 right 0.32 GGCCACCACAGACACCAACAAGTTCAGTCCGTTTCTGCAG
2375 mir-142-prec 0.38 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG 2376 Hcd754 left 0.28 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC
Table 86. Aclarubicm microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2377 mir-092-prec-X=092-2 0.32 GTTCTATATAAAGTATTGCACTTGTCCCGGCCTGTGGAAG
2378 mir-096-prec-7No2 0.29 TGGCCGATTTTGGCACTAGCACATTTTTGCTTGTGTCTCT
2379 Hcd605 left 0.26 ATTACTAGCAGTTAATGATTGGTTTGTTAGTTAATGGCCC
2380 mir-007-2-precNo2 0.34 GGACCGGCTGGCCCCATCTGGAAGACTAGTGATTTTGTTG
2381 mir-019b-2-prec 0.28 GTGGCTGTGCAAATCCATGCAAAACTGATTGTGATAATGT
2382 MPR216 left 0.26 GATCCTAGTAGTGCCAAAGTGCTCATAGTGCAGGTAGTTT
2383 mir-019b-l-prec 0.25 TTCTGCTGTGCAAATCCATGCAAAACTGACTGTGGTAGTG
2384 mir-135-2-prec 0.26 CACTCTAGTGCTTTATGGCTTTTTATTCCTATGTGATAGT
2385 HSTRNL 0.26 TCCGGATGGAGCGTGGGTTCGAATCCCACTTCTGACACCA
2386 mir-025-prec 0.31 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG
2387 mir-007-l-prec 0.4 TGTTGGCCTAGTTCTGTGTGGAAGACTAGTGATTTTGTTG
2388 mir-019a-prec 0.26 TGTAGTTGTGCAAATCTATGCAAAACTGATGGTGGCCTGC
2389 mir-380-5p 0.31 AGGTACCTGAAAAGATGGTTGACCATAGAACATGCGCTAT
2390 irur-093-prec-7.1=093- 1 0.37 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT
2391 mir-106-prec-X 0.37 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
2392 mir-142-prec 0.32 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2393 mir-018-prec 0.31 TAAGGTGCATCTAGTGCAGATAGTGAAGTAGATTAGCATC
2394 mir-020-prec 0.36 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
Table 87 Mitoxantrone microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2395 Hcd768 left 0.26 GATGGTTTAGTGAGGCCCTCGGATCAGCCCGCTGGGTCAG
2396 HUMTRF 0.31 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
2397 mir-213-precNol 0.28 AACATTCATTGCTGTCGGTGGGTTGAACTGTGTGGACAAG
2398 mir-181b-precNol 0.26 TGAGGTTGCTTCAGTGAACATTCAACGCTGTCGGTGAGTT
2399 MPR244 right 0.27 TAAACATAGAGGAAATTTCACGTTTTCAGTGTCAAATGCT
2400 mir-409-3p 0.29 GACGAATGTTGCTCGGTGAACCCCTTTTCGGTATCAAATT
2401 HSTRNL 0.33 TCCGGATGGAGCGTGGGTTCGAATCCCACTTCTGACACCA
2402 mir-382 0.34 GGTACTTGAAGAGAAGTTGTTCGTGGTGGATTCGCTTTAC
2403 mir-342Nol 0.3 GTCTCACACAGAAATCGCACCCGTCACCTTGGCCTACTTA
2404 mir-142-prec 0.27 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2405 Hcd200 right 0.29 CAATTAGCCAATTGTGGGTATAATTAGCTGCATGTAGAAT
Table 88. Mitomycin microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2406 HUMTRF 0.26 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
2407 Hcdl48_HPR2251eft 0.27 AATTAATGACCAAAATGTCAGATGTGTCCACAGCTAATTA 2408 Hcd938 right 0.26 ATTCCCTGCATCACTCTCATGAAATGGCTGAGAAAGTGAG 2409 MPR174 left 0.32 GAGCCGGTCTCTTTACATCTCAAATACCAGGTATTTAGGT 2410 mir-4323p 0.29 CCTTACGTGGGCCACTGGATGGCTCCTCCATGTCTTGGAG
Table 89, Paclitaxel (Taxol) microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2411 mir-092-prec-X=092-2 0.29 GTTCTATATAAAGTATTGCACTTGTCCCGGCCTGTGGAAG
2412 mir-096-prec-7Nol 0.36 CTCCGCTCTGAGCAATCATGTGCAGTGCCAATATGGGAAA
2413 mir-lOl-prec-9 0.38 GCTGTATATCTGAAAGGTACAGTACTGTGATAACTGAAGA
2414 mir-20bNol 0.28 AGTACCAAAGTGCTCATAGTGCAGGTAGTTTTGGCATGAC
2415 mir-019b-2-prec 0.28 GTGGCTGTGCAAATCCATGCAAAACTGATTGTGATAATGT
2416 mir-032-precNo2 0.29 GGAGATATTGCACATTACTAAGTTGCATGTTGTCACGGCC
2417 MPR156 left 0.25 TCCCTCACTTGAACTGACTGCCAGAGTTCACAGACAGCTG
2418 mir-019b-l-prec 0.28 TTCTGCTGTGCAAATCCATGCAAAACTGACTGTGGTAGTG
2419 mir-135-2-prec 0.36 CACTCTAGTGCTTTATGGCTTTTTATTCCTATGTGATAGT
2420 mir-025-prec 0.36 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG
2421 mir-007-l-prec 0.27 TGTTGGCCTAGTTCTGTGTGGAAGACTAGTGATTTTGTTG
2422 mir-361Nol 0.29 GGATTTGGGAGCTTATCAGAATCTCCAGGGGTACTTTATA
2423 mir-093-prec-7.1=093-1 0.37 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT
2424 mir-106-prec-X 0.38 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
2425 mir-098-prec-X 0.29 TGAGGTAGTAAGTTGTATTGTTGTGGGGTAGGGATATTAG
2426 mir-142-prec 0.27 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2427 HPR169 right 0.26 GTTTCTTTCTCACGGTAACTGGCAGCCTCGTTGTGGGCTG
2428 mir-018-prec 0.4 TAAGGTGCATCTAGTGCAGATAGTGAAGTAGATTAGCATC
2429 mir-020-prec 0.36 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
Table 90. Gemcitabine (Gemzar) microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2430 mir-123-precNo2 0.27 TGTGACACTTCAAACTCGTACCGTGAGTAATAATGCGCCG
2431 Hcd257 right 0.29 CTTGGTTTTTGCAATAATGCTAGCAGAGTACACACAAGAA
2432 mir-155-prec 0.35 TTAATGCTAATCGTGATAGGGGTTTTTGCCTCCAACTGAC
2433 ath-MIR180aNo2 0.26 TGAGAATCTTGATGATGCTGCATCGGCAATCAACGACTAT
2434 Hcd448 left 0.33 TGTAATTCCATTGAGGGTTTCTGGTGACTCCAGCTTCGTA
2435 HSTRNL 0.31 TCCGGATGGAGCGTGGGTTCGAATCCCACTTCTGACACCA
2436 MPR174 right 0.29 CATTAGGGACACGTGTGAGTGTGCCAGGCTCATTCCTGAG
2437 Hcd200 right 0.29 CAATTAGCCAATTGTGGGTATAATTAGCTGCATGTAGAAT
2438 mir-4323p 0.26 CCTTACGTGGGCCACTGGATGGCTCCTCCATGTCTTGGAG
2439 HPR244 right 0.3 TAGTTCATGGCGTCCAGCAGCAGCTTCTGGCAGACCGGGT
Table 91. Taxotere (docetaxel) microRNA biomarkers. SEQIDNO Medianprobe Corr Sequence
2440 mir-096-prec-7Nol 0.28 CTCCGCTCTGAGCAATCATGTGCAGTGCCAATATGGGAAA
2441 mir-095-prec-4 0.27 CGTTACATTCAACGGGTATTTATTGAGCACCCACTCTGTG 2442 HSTRNL 0.26 TCCGGATGGAGCGTGGGTTCGAATCCCACTTCTGACACCA 2443 mir-007-l-prec 0.37 TGTTGGCCTAGTTCTGTGTGGAAGACTAGTGATTTTGTTG
Table 392 Dexamethasone microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2444 MPR141 left 0.42 CTCAGTCGTGCCCTAGCAGCGGGAACAGTACTGCAGTGAG
2445 mir-424No2 0.35 GTTCAAAACGTGAGGCGCTGCTATACCCCCTCGTGGGGAA
2446 Hcd690 right 0.26 GGACAAGGGAGGAGACACGCAGAGGTGACAGAAAGGTTAG
2447 Hcd783 left 0.26 CAGGCTCACACCTCCCTCCCCCAACTCTCTGGAATGTATA
2448 mir-150-prec 0.38 CTCCCCATGGCCCTGTCTCCCAACCCTTGTACCAGTGCTG
2449 Hcd266 left 0.37 AAGGTCTTTGGTCTTGGAGGAAGGTGTGCTACTGGAAGAG
2450 mir-503Nol 0.34 CTCAGCCGTGCCCTAGCAGCGGGAACAGTTCTGCAGTGAG
2451 mir-128b-precNol 0.29 TCACAGTGAACCGGTCTCTTTCCCTACTGTGTCACACTCC
2452 Hcd397 left 0.26 GTGTGTATACTTATGTGTGTGTATGTGTGAGTGTGAATAT
2453 mir-484 0.38 GTCAGGCTCAGTCCCCTCCCGATAAACCCCTAAATAGGGA
Table 93 Ara-C (Cytarabme hydrochloride) microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2454 HUMTRF 0.33 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
2455 mir-155-prec 0.28 TTAATGCTAATCGTGATAGGGGTTTTTGCCTCCAACTGAC
2456 mir-515-15p 0.27 GATCTCATGCAGTCATTCTCCAAAAGAAAGCACTTTCTGT
2457 Hcd938 right 0.26 ATTCCCTGCATCACTCTCATGAAATGGCTGAGAAAGTGAG
2458 Hcd642 right 0.25 TCAGGGTTTATGAAGTTATCAAAGCCCCTTGATGGAATTA
2459 Hcdl20 left 0.26 CTTGGTGTGTTCTCGGTAGCTATGGAAATCCCAGGGTTTC
2460 mir-380-5p 0.25 AGGTACCTGAAAAGATGGTTGACCATAGAACATGCGCTAT
2461 mir-342Nol 0.25 GTCTCACACAGAAATCGCACCCGTCACCTTGGCCTACTTA
2462 mir-142-prec 0.27 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2463 mir-223-prec 0.31 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT
2464 mir-4323p 0.28 CCTTACGTGGGCCACTGGATGGCTCCTCCATGTCTTGGAG
Table 94 Methylprednisolone microRNA biomarkers .
SEQIDNO Medianprobe Corr Sequence
2465 Hcd544 left 0.26 TTCCAGGTGTCCACCAAGGACGTGCCGCTGGCGCTGATGG
2466 mir-181c-precNol 0.28 TGCCAAGGGTTTGGGGGAACATTCAACCTGTCGGTGAGTT
2467 Hcd517 left 0.25 TTAAAGCAGGAGAGGTGAGAGGAAGAATTAATGTGTGCTC
2468 MPR151 left 0.27 GGGATTAATGACCAGCTGGGGGAGTTGATAGCCCTCAGTG
2469 mir-213-precNol 0.34 AACATTCATTGCTGTCGGTGGGTTGAACTGTGTGGACAAG
2470 mir-181b-precNo2 0.36 ACCATCGACCGTTGATTGTACCCTATGGCTAACCATCATC
2471 mir-150-prec 0.27 CTCCCCATGGCCCTGTCTCCCAACCCTTGTACCAGTGCTG
2472 mir-153-l-precl 0.28 CAGTTGCATAGTCACAAAAGTGATCATTGGCAGGTGTGGC
2473 mir-128b-precNol 0.48 TCACAGTGAACCGGTCTCTTTCCCTACTGTGTCACACTCC
2474 Hcd812 left 0.25 CTGTGGGATCTGGTTCTGTAGCTGAGAGCACATCGCTAAA
2475 mir-195-prec 0.3 TCTAGCAGCACAGAAATATTGGCACAGGGAAGCGAGTCTG
2476 mir-342Nol 0.38 GTCTCACACAGAAATCGCACCCGTCACCTTGGCCTACTTA
2477 mir-370Nol 0.28 TTACACAGCTCACGAGTGCCTGCTGGGGTGGAACCTGGTC
2478 mir-142-prec 0.32 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2479 mir-223-prec 0.36 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT
2480 mir-484 0.36 GTCAGGCTCAGTCCCCTCCCGATAAACCCCTAAATAGGGA
Table 95. Methotrexate microRNA biomarkers. SEQIDNO Medianprobe Corr Sequence
2481 mir-092-prec-X=092-2 0.37 GTTCTATATAAAGTATTGCACTTGTCCCGGCCTGTGGAAG
2482 mir-096-prec-7Nol 0.33 CTCCGCTCTGAGCAATCATGTGCAGTGCCAATATGGGAAA
2483 mir-123-precNol 0 , 25 GACGGGACATTATTACTTTTGGTACGCGCTGTGACACTTC
2484 Hcd250 left 0.26 GTTCTGTTGCTAAGACAACAGGATGCTAGCAGGCATATGC
2485 mir-518e/526c 0 , 3 TCTCAGGCTGTGACCCTCTAGAGGGAAGCGCTTTCTGTTG
2486 HPR232 right 0 , 3 TGAATTATTGCACAATAAATTCATGCCCTGTTGTGTCTTA
2487 Hcd263 left 0 ,29 GAGCATTAAGATTTCCTATTCTTTGAGGCAAATATTGACC
2488 mir-516-33p 0 , 35 GTGAAAGAAAGTGCTTCCTTTCAGAGGGTTACTCTTTGAG
2489 Hcd605 left 0 , 27 ATTACTAGCAGTTAATGATTGGTTTGTTAGTTAATGGCCC
2490 Hcd373 right 0.25 CCTGAAAGGTCTGGTGTTAAGCAAATACTCGGTGACCAGA
2491 MPR254 right 0.28 GTTCACAGTGGGAGAAATATGCTTCGTATTACTCTTTCTC
2492 MPR215 left 0.3 CAGCTATGTGGACTCTAGCTGCCAAAGGCGCTTCTCCTTC
2493 HUMTRF 0.28 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
2494 mir-106aNol 0.27 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
2495 mir-20bNol 0.37 AGTACCAAAGTGCTCATAGTGCAGGTAGTTTTGGCATGAC
2496 Hcd361 right 0.28 AACTTGGCTACAAGGCTCTTTCCCTCTCTATGAAGGACAG
2497 Hcd412 left 0.25 AGTTGGGGAGAACTTTATGATTATTCTCATGCATCATCTT
2498 Hcd781 left 0.26 GAGTGTGGATCTAATCTTCAGCTGATTAAATGTCCCTCAT
2499 mir-019b-2-prec 0.33 GTGGCTGTGCAAATCCATGCAAAACTGATTGTGATAATGT
2500 HPR214 right 0.29 AGCAAAAGCTATTATTTGCCCTTGATGAGCCAATCAGATG
2501 Hcd807 right 0.26 GCGCTGACAAATCTTGCCTGATTCTGTATGATCCATGAGA
2502 Hcd817 left 0.37 TAATGAGAATTATGTTTGCACATTGAGGCAGGATAAATCC
2503 Hcd788 left 0 ,25 GACAAACATGCAGGAAAAATTATCCCCTGGGGATTCTACA
2504 Hcd970 left 0 , 31 TTGTGGGTCAGCTGCCCAGCTATCGGCTGGATTAGTGAAT
2505 Hcdl48 HPR2251eft 0.26 AATTAATGACCAAAATGTCAGATGTGTCCACAGCTAATTA
2506 Hcdl02 left 0.27 ACTGGAATTATGTTTTATCTTAAGTCCACACTGGATCCTC
2507 Hcd246 right 0.29 TAAAGTGAGTTATGGAGGTTACTCTCCTGTGAGAGGAAAT
2508 HPR199 right 0.28 TACACCTAAGGCATGTACTGTATTAATGAACCAATAAAAC
2509 HPR233 right 0.27 CATGATGGGGTGGGGTGAGATGGGGAGCGAAGACTATTAC
2510 Hcd383 left 0.28 GCCCGGGCATGCATTTTATCTAGCACCATGTGTTTCAGCT
2511 MPR224 right 0.29 TGAATTATTGCACAATAAATTCATGCCCTGTTGTGTCTTA
2512 HPR172 right 0.26 GTTTAAACAGCCAGTGCAAACATTTAGATCTGAGTCAAAA
2513 MPR216 left 0.34 GATCCTAGTAGTGCCAAAGTGCTCATAGTGCAGGTAGTTT
2514 mir-321No2 0.25 CAGGGATTGTGGGTTCGAGTCCCACCCGGGGTAAAGAAAG
2515 Hcd586 right 0.28 GAACTGTTTGCTTTGGATGGGCTTGGTCCTCATTGGCTGA
2516 Hcd587 right 0.3 AAATAATGACTGGCCATAAGATCAAGACAAGTGTCCAAAG
2517 Hcd249 right 0.39 CAGGTACATGTTGATCAGCAGGGGCTGGGAGGCGCCGCTC
2518 Hcd279 right 0.27 CTCACGGCGTTGCCATGGAGACAACTCCGGGGCTGGGGCTC
2519 HPR159 left 0.3 TCCGTCACTTGAACTGGCTGCCAGCGTTCACAGACAGCTG
2520 Hcd689 right 0.28 GTACATCTGGATGTAGTTGTGCTGCAGCTGCTTCTGGTAG
2521 Hcd691 right 0.32 CGGCAAAAACCTCTGTCAGAACAAAATTAGGTGATCTATC
2522 mir-019b-l-prec 0.32 TTCTGCTGTGCAAATCCATGCAAAACTGACTGTGGTAGTG
2523 Hcd413 right 0.26 CACAAAAAGGCATAAGCAGACATCTTGCCCTTTGGTTTCT
2524 Hcd581 right 0.26 AGGAGATATGCCAAGATATATTCACAGCTTTATATACACA
2525 Hcd536 HPR104 right 0.28 GCTGCTCTGCTGAGGGGCTGGACTCTGTCCAGAAGCACCA
2526 Hcd230 left 0.28 CATTCTCTACAAGCATATGGCCTTGGGACATTAAGATGGC
2527 HPR154 left 0.28 AACATCAAGATCTATTGACCTGAGAGGTAAATATTGACCG
2528 Hcd270 right 0.31 AAATGTTGTTATAGTATCCCACCTACCCTGATGTATCTTT
2529 Hcd649 right 0.26 GAACAGGCTTCAAGGTTCTTGGCAGGAATATTCCGTGTAG
2530 Hcd889 right 0.27 ATGCCTTGTGCTCTGTGCTAATTCAGAAGAATAAGCCTGT
2531 Hcd938 left 0.36 CTTGTCGACTAGCCAGTTATGAACAGAGGAGGATGTTCTC
2532 HPR266 right 0.32 GGAGATCCCTTCAAGGTACTTAGTTTTAAATGAGTGCTCT
2533 mir-025-prec 0.39 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG
2534 Hcd355 HPR190 left 0.25 TTGTGCACTGCACAACCCTAGTGGCGCCATTCAATTATAG
2535 MPR162 left 0.26 CTCTCTTTTTCCTGCTTGATTTGCCTAATGGAAGCTGACA
2536 Hcd923 right 0.34 CTGGAGATAATGATTCTGCATTTCTAATTAACTCCCAGGT
2537 MPR237 left 0.32 AGCACATCCCATGATCACAGTAATGTTCTTTGGAGATGTA
2538 MPR174 left 0.32 GAGCCGGTCTCTTTACATCTCAAATACCAGGTATTTAGGT
2539 mir-019a-prec 0.31 TGTAGTTGTGCAAATCTATGCAAAACTGATGGTGGCCTGC
2540 hsa mir 490 Hcd20 right 0.25 ACCAACCTGGAGGACTCCATGCTGTTGAGCTGTTCACAAG
2541 mir-380-5p 0.36 AGGTACCTGAAAAGATGGTTGACCATAGAACATGCGCTAT
2542 mir-093-prec-7.1=093-1 0.38 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT
2543 mir-106-prec-X 0.45 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
2544 Hcd627 left 0.3 GCATTAGGGAGAATAGTTGATGGATTACAAATCTCTGCAT
2545 mir-142-prec 0.27 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2546 HPR169 right 0.29 GTTTCTTTCTCACGGTAACTGGCAGCCTCGTTGTGGGCTG
2547 mir-OOlb-2-prec 0.28 TAAGCTATGGAATGTAAAGAAGTATGTATCTCAGGCCGGG
2548 mir-018-prec 0.4 TAAGGTGCATCTAGTGCAGATAGTGAAGTAGATTAGCATC
2549 mir-020-prec 0.48 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
2550 Hcd404 left 0.29 TGCTGCTGTTAATGCCATTAGGATGACTATTTATATCACC
2551 mir-384 0.25 CATAAGTCATTCCTAGAAATTGTTCATAATGCCTGTAACA 2552 mir-4323p 0.4 CCTTACGTGGGCCACTGGATGGCTCCTCCATGTCTTGGAG
Table 96. Bleomycin microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2553 mir-376aNol 0.27 AATCATAGAGGAAAATCCACGTTTTCAGTATCAAATGCTG
2554 mir-155-prec 0.35 TTAATGCTAATCGTGATAGGGGTTTTTGCCTCCAACTGAC
2555 mir-409-3p 0.28 GACGAATGTTGCTCGGTGAACCCCTTTTCGGTATCAAATT
2556 mir-495Nol 0.29 GTGACGAAACAAACATGGTGCACTTCTTTTTCGGTATCAA
2557 Hcd498 right 0.28 CACGAAGAAGTTCAGCAACCAGGAGACCAGGTGGGGGCCG
2558 mir-199a-2-prec 0.41 TCGCCCCAGTGTTCAGACTACCTGTTCAGGACAATGCCGT
2559 mir-382 0.3 GGTACTTGAAGAGAAGTTGTTCGTGGTGGATTCGCTTTAC
2560 HPR271 right 0.27 AATTGAGCAAACAGTGCAATTTTCTGTAATTATGCCAGTG
2561 mir-145-prec 0.31 CCTCACGGTCCAGTTTTCCCAGGAATCCCTTAGATGCTAA
2562 mir-199a-l-prec 0.35 GCCAACCCAGTGTTCAGACTACCTGTTCAGGAGGCTCTCA
Table 97. Methyl-GAG (methyl glyoxal bis amidinohydrazone dihydrochloride) microRNA biomarkers .
SEQIDNO Medianprobe Corr Sequence
2563 mir-092-prec-X=092-2 0.32 GTTCTATATAAAGTATTGCACTTGTCCCGGCCTGTGGAAG
2564 mir-lOl-prec-9 0.3 GCTGTATATCTGAAAGGTACAGTACTGTGATAACTGAAGA
2565 mir-144-precNo2 0.29 CCCTGGCTGGGATATCATCATATACTGTAAGTTTGCGATG
2566 mir-519a-l/526c 0.29 TCAGGCTGTGACACTCTAGAGGGAAGCGCTTTCTGTTGTC
2567 mir-519b 0.33 GAAAAGAAAGTGCATCCTTTTAGAGGTTTACTGTTTGAGG
2568 mir-015b-precNo2 0.26 TGCTACAGTCAAGATGCGAATCATTATTTGCTGCTCTAGA
2569 itur-106aNol 0.27 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
2570 mir-16-lNol 0.26 GTCAGCAGTGCCTTAGCAGCACGTAAATATTGGCGTTAAG
2571 mir-181dNol 0.27 GAGGTCACAATCAACATTCATTGTTGTCGGTGGGTTGTGA
2572 mir-017-precNo2 0.31 GTCAGAATAATGTCAAAGTGCTTACAGTGCAGGTAGTGAT
2573 mir-019b-2-prec 0.32 GTGGCTGTGCAAATCCATGCAAAACTGATTGTGATAATGT
2574 mir-192No2 0.26 TGCCAATTCCATAGGTCACAGGTATGTTCGCCTCAATGCC
2575 mir-213-precNol 0.25 AACATTCATTGCTGTCGGTGGGTTGAACTGTGTGGACAAG
2576 mir-215-precNo2 0.3 CATTTCTTTAGGCCAATATTCTGTATGACTGTGCTACTTC
2577 mir-107Nol 0.28 GGCATGGAGTTCAAGCAGCATTGTACAGGGCTATCAAAGC
2578 mir-200bNol 0.28 GTCTCTAATACTGCCTGGTAATGATGACGGCGGAGCCCTG
2579 mir-103-prec-5=103-l 0.3 TATGGATCAAGCAGCATTGTACAGGGCTATGAAGGCATTG
2580 mir-519a-l/526c 0.37 TCAGGCTGTGACACTCTAGAGGGAAGCGCTTTCTGTTGTC
2581 MPR216 left 0.28 GATCCTAGTAGTGCCAAAGTGCTCATAGTGCAGGTAGTTT
2582 mir-019b-l-prec 0.31 TTCTGCTGTGCAAATCCATGCAAAACTGACTGTGGTAGTG
2583 mir-107-prec-lO 0.29 GGCATGGAGTTCAAGCAGCATTGTACAGGGCTATCAAAGC
2584 mir-135-2-prec 0.39 CACTCTAGTGCTTTATGGCTTTTTATTCCTATGTGATAGT
2585 mir-103-2-prec 0.29 GTAGCATTCAGGTCAAGCAACATTGTACAGGGCTATGAAA
2586 mir-519a-2No2 0.29 TCTCAGGCTGTGTCCCTCTACAGGGAAGCGCTTTCTGTTG
2587 mir-025-prec 0.33 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG
2588 mir-16-2Nol 0.33 GTTCCACTCTAGCAGCACGTAAATATTGGCGTAGTGAAAT
2589 MPR95 left 0.28 TTGTTGGACACTCTTTCCCTGTTGCACTACTGTGGGCCTC
2590 mir-016b-chr3 0.29 GTTCCACTCTAGCAGCACGTAAATATTGGCGTAGTGAAAT
2591 Hcd948 right 0.27 TGATATAAATAGTCATCCTAATGGCATTAACAGCAGCACT
2592 mir-195-prec 0.35 TCTAGCAGCACAGAAATATTGGCACAGGGAAGCGAGTCTG
2593 mir-093-prec-7.1=093-1 0.38 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT
2594 mir-106-prec-X 0.42 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
2595 mir-142-prec 0.37 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2596 mir-519c/526c 0.27 TCTCAGCCTGTGACCCTCTAGAGGGAAGCGCTTTCTGTTG
2597 mir-200a-prec 0.29 GTCTCTAATACTGCCTGGTAATGATGACGGCGGAGCCCTG
2598 mir-016a-chrl3 0.29 CAATGTCAGCAGTGCCTTAGCAGCACGTAAATATTGGCGT
2599 mir-018-prec 0.41 TAAGGTGCATCTAGTGCAGATAGTGAAGTAGATTAGCATC
2600 mir-020-prec 0.39 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
Table 98 . pXDIOl HDAC inhibitors microRNA biomarkers. SEQIDNO Medianprobe Corr Sequence
2601 mir-092-prec-X=092-2 0.42 GTTCTATATAAAGTATTGCACTTGTCCCGGCCTGTGGAAG
2602 mir-123-precNo2 0.31 TGTGACACTTCAAACTCGTACCGTGAGTAATAATGCGCCG
2603 mir-106aNol 0.36 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
2604 mir-20bNol 0.36 AGTACCAAAGTGCTCATAGTGCAGGTAGTTTTGGCATGAC
2605 mir-017-precNo2 0.32 GTCAGAATAATGTCAAAGTGCTTACAGTGCAGGTAGTGAT
2606 mir-019b-2-prec 0.42 GTGGCTGTGCAAATCCATGCAAAACTGATTGTGATAATGT
2607 mir-033-prec 0.3 GTGGTGCATTGTAGTTGCATTGCATGTTCTGGTGGTACCC
2608 mir-092-prec-13=092-lNo2 0.31 TCTGTATGGTATTGCACTTGTCCCGGCCTGTTGAGTTTGG
2609 mir-122a-prec 0.29 CCTTAGCAGAGCTGTGGAGTGTGACAATGGTGTTTGTGTC
2610 Hcd783 left 0.27 CAGGCTCACACCTCCCTCCCCCAACTCTCTGGAATGTATA
2611 MPR216 left 0.29 GATCCTAGTAGTGCCAAAGTGCTCATAGTGCAGGTAGTTT
2612 mir-019b-l-prec 0.41 TTCTGCTGTGCAAATCCATGCAAAACTGACTGTGGTAGTG
2613 mir-135-2-prec 0.46 CACTCTAGTGCTTTATGGCTTTTTATTCCTATGTGATAGT
2614 mir-128b-precNol 0.39 TCACAGTGAACCGGTCTCTTTCCCTACTGTGTCACACTCC
2615 mir-025-prec 0.45 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG
2616 Hcdδll right 0.26 TACCTCAGAAGCCTCACTCAACCCTCTCCCGCTGAGTCTC
2617 mir-093-prec-7.1=093-1 0.45 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT
2618 mir-106-prec-X 0.5 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
2619 mir-142-prec 0.5 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2620 HPR169 right 0.26 GTTTCTTTCTCACGGTAACTGGCAGCCTCGTTGTGGGCTG
2621 mir-223-prec 0.26 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT
2622 mir-018-prec 0.48 TAAGGTGCATCTAGTGCAGATAGTGAAGTAGATTAGCATC
2623 mir-020-prec 0.52 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
Table 99 . 55--FFlluuoorroouurraacciill mmiiccrrooRRNI JAA bbiiomarkers.
SEQIDNO Medianprobe Corr Sequence
2624 mir-096-prec-7No2 0.27 TGGCCGATTTTGGCACTAGCACATTTTTGCTTGTGTCTCT
2625 mir-429Nol 0.25 CTAATACTGTCTGGTAAAACCGTCCATCCGCTGCCTGATC
2626 Hcd693 right 0.25 AGGCTTTGTGCGCGCATTAAAGCTCGCCGGACCCCCGACC
2627 HPR214 right 0.27 AGCAAAAGCTATTATTTGCCCTTGATGAGCCAATCAGATG
2628 Hcd586 left 0.26 GTCCTGTCTAAAGGAAGAAGTTTGTTCTACTGTAAACAGT
2629 Hcd249 right 0.26 CAGGTACATGTTGATCAGCAGGGGCTGGGAGGCGCCGCTC
2630 Hcd689 right 0.27 GTACATCTGGATGTAGTTGTGCTGCAGCTGCTTCTGGTAG
2631 mir-194-2Nol 0.25 TGGTTCCCGCCCCCTGTAACAGCAACTCCATGTGGAAGTG
2632 Hcd581 right 0.26 AGGAGATATGCCAAGATATATTCACAGCTTTATATACACA
2633 Hcd270 right 0.3 AAATGTTGTTATAGTATCCCACCTACCCTGATGTATCTTT
2634 mir-025-prec 0.27 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG
2635 Hcd340 left 0.27 GGACAATTCAACAGTGGTGAGTCACTTCGCCACTTTTCAG
2636 mir-007-l-prec 0.27 TGTTGGCCTAGTTCTGTGTGGAAGACTAGTGATTTTGTTG
2637 mir-093-prec-7.1=093-1 0.25 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT
2638 mir-106-prec-X 0.26 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
2639 Hcd794 right 0.27 GGCCACCACAGACACCAACAAGTTCAGTCCGTTTCTGCAG
2640 mir-020-prec 0.26 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
2641 mir-4323p 0.26 CCTTACGTGGGCCACTGGATGGCTCCTCCATGTCTTGGAG
Table 100. Radiation microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2642 mir-136-precNo2 0.3 TGAGCCCTCGGAGGACTCCATTTGTTTTGATGATGGATTC
2643 Hcd570 right 0.26 GCCCAACAGAACAACTTGTTTCTCCAGAGCCTGAGGTTTA
2644 Hcd873 left 0.26 TCTTCTGACAATGAAGGTAGGCGGACAACGAGGAGATTGC
2645 Hcd282PO right 0.26 GAAGACGGACTTGGTTCCGTTTGACCAGCCAGAGCAGGGG
2646 Hcd799 left 0.25 GTCCGGCGCGAGTGGAGCTGTTGTAAAATGGCGGCCGAAG
2647 Hcd829 right 0.39 AAAATGGCGGCGGGAAAAGCGAGCGGCGAGAGCGAGGAGG
2648 Hcd210_HPR205 right 0.32 CGAAACATTCGCGGTGCACTTCTTTTTCAGTATCCTATTC
2649 mir-219-prec 0.26 ATTGTCCAAACGCAATTCTCGAGTCTATGGCTCCGGCCGA
2650 mir-202* 0.31 CCGCCCGCCGTTCCTTTTTCCTATGCATATACTTCTTTGA
2651 mir-429No2 0.42 CACCGCCGGCCGATGGGCGTCTTACCAGACATGGTTAGAC
2652 Hcd693 right 0.32 AGGCTTTGTGCGCGCATTAAAGCTCGCCGGACCCCCGACC
2653 mir-022-prec 0.34 TGTCCTGACCCAGCTAAAGCTGCCAGTTGAAGAACTGTTG
2654 MPR88 right 0.32 CTTACCCTGGTGCGTGGGGCCGCAGGGCTAACACCAAAAA
2655 mir-198-prec 0.39 TCATTGGTCCAGAGGGGAGATAGGTTCCTGTGATTTTTCC
2656 mir-199b-precNol 0.29 GTCTGCACATTGGTTAGGCTGGGCTGGGTTAGACCCTCGG
2657 Hcdl45 left 0.26 AAAAATCCCAGCGGCCACCTTTCCTCCCTGCCCCATTGGG
2658 mir-124a-2-prec 0.34 TTAAGGCACGCGGTGAATGCCAAGAGCGGAGCCTACGGCT
2659 mir-138-2-prec 0.39 AGCTGGTGTTGTGAATCAGGCCGACGAGCAGCGCATCCTC
2660 Hcd960 left 0.29 CTCAGTCTGCGGGCCCCGAGGAGGGTTGTGGGCCCTTTTT
2661 Hcd869 left 0.31 CGAGAGGCACTTTGTACTTCTGCCAGGAGACCATATGATA
2662 Hcd384 left 0.41 TTACCCAGCCGGGCCGCCAACACCAGATCCTTCTCCTTCT
2663 mir-027b-prec 0.31 CCGCTTTGTTCACAGTGGCTAAGTTCTGCACCTGAAGAGA
2664 Hcd444 right 0.31 GTATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
2665 mir-194-2Nol 0.3 TGGTTCCCGCCCCCTGTAACAGCAACTCCATGTGGAAGTG
2666 mir-197-prec 0.44 TAAGAGCTCTTCACCCTTCACCACCTTCTCCACCCAGCAT
2667 Hcd913 right 0.39 CAAACATCATGTGACGTCTGTGGAGCGGCGGCGGCGGCGG
2668 HPR163 left 0.39 GCTGCCCCCTCCCTTAGCAACGTGGCCCCGGCGTTCCAAA
2669 mir-138-l-prec 0.25 AGCTGGTGTTGTGAATCAGGCCGTTGCCAATCAGAGAACG
2670 mir-OlOa-precNol 0.25 GTCTGTCTTCTGTATATACCCTGTAGATCCGAATTTGTGT
2671 mir-023b-prec 0.34 AATCACATTGCCAGGGATTACCACGCAACCACGACCTTGG
2672 mir-193bNo2 0.35 CTGTGGTCTCAGAATCGGGGTTTTGAGGGCGAGATGAGTT
2673 Hcd654 left 0.43 AACGAGTAAAAGGCGTACATGGGAGCGCGGGGCGGCAGAG
2674 Hcd542 left 0.26 ATCTCAGTAGCCAATATTTTTCTCTGCTGGTATCAAATGA
2675 mir-199a-2-prec 0.28 TCGCCCCAGTGTTCAGACTACCTGTTCAGGACAATGCCGT
2676 mir-214-prec 0.43 TGTACAGCAGGCACAGACAGGCAGTCACATGACAACCCAG
2677 Hcd608 right 0.31 CTTGTGTTTTCACAGCAGCCACAGGCCCTACATCCTTCCT
2678 Hcd684 right 0.28 AGAAGGCGCTCCCTGCTAGCCCGGCTCTGTTCTAATTATA
2679 mir-145-prec 0.4 CCTCACGGTCCAGTTTTCCCAGGAATCCCTTAGATGCTAA
2680 mir-023a-prec 0.37 TCCTGTCACAAATCACATTGCCAGGGATTTCCAACCGACC
2681 mir-024-2-prec 0.32 AGTTGGTTTGTGTACACTGGCTCAGTTCAGCAGGAACAGG
2682 mir-199a-l-prec 0.29 GCCAACCCAGTGTTCAGACTACCTGTTCAGGAGGCTCTCA
Table 101 5-Aza-2 ' -deoxycytidme (decitabme) microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2683 mir-096-prec-7Nol 0.36 CTCCGCTCTGAGCAATCATGTGCAGTGCCAATATGGGAAA
2684 Hcd605 right 0.25 GGTTAAGACTCTAACAAACGAGTTGTGAATTGTAGCAATG
2685 mir-20bNol 0.3 AGTACCAAAGTGCTCATAGTGCAGGTAGTTTTGGCATGAC
2686 miR-373*Nol 0.26 GGGATACTCAAAATGGGGGCGCTTTCCTTTTTGTCTGTAC
2687 HUMTRAB 0.3 ATGGTAGAGCGCTCGCTTTGCTTGCGAGAGGTAGCGGGAT
2688 mir-019b-l-prec 0.25 TTCTGCTGTGCAAATCCATGCAAAACTGACTGTGGTAGTG
2689 HPR163 left 0.31 GCTGCCCCCTCCCTTAGCAACGTGGCCCCGGCGTTCCAAA
2690 mir-371Nol 0.25 ACTTTCTGCTCTCTGGTGAAAGTGCCGCCATCTTTTGAGT
2691 mir-025-prec 0.29 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG
2692 mir-18bNo2 0.27 AGCAGCTTAGAATCTACTGCCCTAAATGCCCCTTCTGGCA
2693 mir-093-prec-7.1=093-1 0.28 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT
2694 mir-106-prec-X 0.29 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
2695 mir-142-prec 0.29 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2696 mir-020-prec 0.29 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
Table 102 Idarubicin microRNA biomarkers .
SEQIDNO Medianprobe Corr Sequence
2697 HUMTRF 0.33 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
2698 mir-483Nol 0.3 ATCACGCCTCCTCACTCCTCTCCTCCCGTCTTCTCCTCTC
2699 MPR74 left 0.27 CAAAGGTCACAATTAACATTCATTGTTGTCGGTGGGTTGT
2700 mir-122a-prec 0.27 CCTTAGCAGAGCTGTGGAGTGTGACAATGGTGTTTGTGTC
2701 ath-MIR180aNo2 0.29 TGAGAATCTTGATGATGCTGCATCGGCAATCAACGACTAT
2702 mir-128b-precNol 0.26 TCACAGTGAACCGGTCTCTTTCCCTACTGTGTCACACTCC
2703 Hcd923 left 0.25 TGGGAACCTTGTTAAAATGCAGATTCTGATTCTCAGGTCT
2704 mir-106-prec-X 0.25 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
2705 mir-342Nol 0.36 GTCTCACACAGAAATCGCACCCGTCACCTTGGCCTACTTA
2706 mir-142-prec 0.34 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2707 HPR169 right 0.25 GTTTCTTTCTCACGGTAACTGGCAGCCTCGTTGTGGGCTG
2708 mir-223-prec 0.36 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT
2709 Hcd754 left 0.26 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC
2710 mir-020-prec 0.29 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
Table 103. Melphalan microRNA biomarkers . SEQIDNO Medianprobe Corr Sequence
2711 mir-124a-3-prec 0.32 TTAAGGCACGCGGTGAATGCCAAGAGAGGCGCCTCCGCCG
2712 mir-lδla-precNol 0.28 TCAGAGGACTCCAAGGAACATTCAACGCTGTCGGTGAGTT
2713 Hcd773 left 0.26 CTTCCTCCCTGGGCATCTCTAGCACAGGGGATCCCCAAAC
2714 Hcd683 left 0.25 CTATGACAGAAGGTACTCTGTGGGAGGGAGGAGATAATAG
2715 Hcd796 left 0.29 GGTGGGATTACCCGGCTGCCGCTGTCGCCTGGATGGTCTC
2716 HUMTRF 0.44 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
2717 HUMTRS 0.27 TCTAGCGACAGAGTGGTTCAATTCCACCTTTCGGGCGCCA
2718 mir-181b-2Nol 0.25 CTGATGGCTGCACTCAACATTCATTGCTGTCGGTGGGTTT
2719 Hcd294 left 0.26 TTATCATAAAATAATCACAGCCCTCAGGTGCTGTGAGGCA
2720 mir-20bNol 0.27 AGTACCAAAGTGCTCATAGTGCAGGTAGTTTTGGCATGAC
2721 mir-181dNol 0.27 GAGGTCACAATCAACATTCATTGTTGTCGGTGGGTTGTGA
2722 mir-213-precNol 0.4 AACATTCATTGCTGTCGGTGGGTTGAACTGTGTGGACAAG
2723 Hcdl48_HPR2251eft 0.29 AATTAATGACCAAAATGTCAGATGTGTCCACAGCTAATTA
2724 rair-515-15p 0.34 GATCTCATGCAGTCATTCTCCAAAAGAAAGCACTTTCTGT
2725 mir-181b-precNol 0.43 TGAGGTTGCTTCAGTGAACATTCAACGCTGTCGGTGAGTT
2726 Hcd783 left 0.26 CAGGCTCACACCTCCCTCCCCCAACTCTCTGGAATGTATA 2727 HUMTRAB 0.29 ATGGTAGAGCGCTCGCTTTGCTTGCGAGAGGTAGCGGGAT
2728 HUMTRN 0.27 CAATCGGTTAGCGCGTTCGGCTGTTAACCGAAAGGTTGGT
2729 mir- 181b- lNol 0.31 TTTAAAAGGTCACAATCAACATTCATTGCTGTCGGTGGGT
2730 mir- 124 a- l-precl 0.31 ATACAATTAAGGCACGCGGTGAATGCCAAGAATGGGGCTG
2731 mir-367Nol 0.26 TCTGTTGAATATAAATTGGAATTGCACTTTAGCAATGGTG
2732 mir- 128b-precNol 0.38 TCACAGTGAACCGGTCTCTTTCCCTACTGTGTCACACTCC
2733 Hcd43 8 πght 0.25 GTGTTTATTTGAATCTCACATCGCTCATAAGAATACACGC
2734 mir- 025-prec 0.3 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG
2735 mir-216-precNol 0.35 CTGGGATTATGCTAAACAGAGCAATTTCCTAGCCCTCACG
2736 Hcd731 left 0.26 AATTGTGACAACTGAGTGGGAGGTTTGTGTGATGATTATC
2737 mir- 093-prec-7 . 1=093-1 0.25 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT
2738 mir- 106-prec-X 0.27 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
2739 mir- 342Nol 0.36 GTCTCACACAGAAATCGCACCCGTCACCTTGGCCTACTTA
2740 mir- 142-prec 0.53 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2741 HSHELAOl 0.32 GGCCGCAGCAACCTCGGTTCGTATCCGAGTCACGGCACCA 2742 HUMTRVlA 0.25 ACGCGAAAGGTCCCCGGTTCGAAACCGGGCGGAAACACCA
2743 mi r-223-prec 0.46 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT
2744 Hcd754 left 0.45 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC
2745 mi r-020-prec 0.3 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
Table 104. IL4-PR38 fusion protein microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2746 Hcd829 right 0.28 AAAATGGCGGCGGGAAAAGCGAGCGGCGAGAGCGAGGAGG
2747 mir-197-prec 0.28 TAAGAGCTCTTCACCCTTCACCACCTTCTCCACCCAGCAT
2748 HPR163 left 0.28 GCTGCCCCCTCCCTTAGCAACGTGGCCCCGGCGTTCCAAA
2749 mir-150-prec 0.47 CTCCCCATGGCCCTGTCTCCCAACCCTTGTACCAGTGCTG
Table 105 . Valproic acid (VPA) microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2750 mir-034precNol 0.26 GAGTGTTTCTTTGGCAGTGTCTTAGCTGGTTGTTGTGAGC
2751 Hcd255 left 0.28 CTAGCTCCGTTCGTGATCCGGGAGCCTGGTGCCAGCGAGA
2752 Hcd712 right 0.27 GAAGATCGGTTGTCATCTGGTCTGGTCAGCCCGGCCCCGA
2753 Hcd965 left 0.26 TGTTAAGTGGAAAAGCCTCCAGGAACGTGGCAGAAAAAGG
2754 Hcd891 right 0.29 GCAACGGCCTGATTCACAACACCAGCTGCCCCACCACACC
2755 Hcd210 HPR205 πght 0.31 CGAAACATTCGCGGTGCACTTCTTTTTCAGTATCCTATTC
2756 mir-429No2 0.33 CACCGCCGGCCGATGGGCGTCTTACCAGACATGGTTAGAC
2757 Hcd753 left 0.27 GACCTGATTCCCATCTTTGTATTTGGCGACCACCCGACTG
2758 Hcd693 right 0.38 AGGCTTTGTGCGCGCATTAAAGCTCGCCGGACCCCCGACC
2759 MPR203 left 0.25 CTATATTGGACCGCAGCGCTGAGAGCTTTTGTGTTTAATG
2760 Hcd704 left 0.4 TCTGTATTTAATTTGGCTCAGCCGGGAAGATTTTTGGCTC
2761 Hcd863PO right 0.3 TTGCAGAGCCTAAGACACAGGCCCAGAGAGGCAGTGATCG
2762 mir-122a-prec 0.29 CCTTAGCAGAGCTGTGGAGTGTGACAATGGTGTTTGTGTC
2763 Hcd760 left 0.35 TGTGGTCACGTTTCTCCCTCTCTGCTGGCCCCCATCTGTC
2764 Hcd338 left 0.35 CTTCTCCTCCTGTTCGCCGCAGGCGCCCGTCCCAGTAGTC
2765 HPR213 right 0.33 AACAACTTTGTGCTGGTGCCGGGGAAGTTTGTGTCTCCAA
2766 Hcd852 right 0.26 AAAAGTAAACAACAATTTGCCGCTGCCAGCCTCCCATTAG
2767 Hcd366 left 0.28 ATACTAGATTAAATTTCAGCCCCGGGCCAATCTGTCAAAG
2768 MPR103 right 0.27 GAGGTGTTTGTGCTCCACTCGGCTCCCTTGGTTACATAAC
2769 Hcd669 right 0.27 ATGTTTAACAGTCCAGGTTTTGTAGAATATGTGGTGGACC
2770 mir-188-prec 0.27 TCACATCCCTTGCATGGTGGAGGGTGAGCTTTCTGAAAAC
Table 106 All-trans retinoic acid (ATRA) microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2771 Hcd257 left 0.42 CTTCTTGTATAAGCACTGTGCTAAAATTGCAGACACTAGG
2772 mir-148-prec 0.45 TGAGTATGATAGAAGTCAGTGCACTACAGAACTTTGTCTC
2773 Hcd512 left 0.28 CTGCGCTCTCGGAAATGACTCGCTCCAATCCCGCTTCGCG
2774 HPR227 right 0.25 CAGTGCAATGATATTGTCAAAGCATCTGGGACCAGCCTTG
2775 Hcd421 right 0.37 AGTAAACAATGTCGGCTTTCCGCCTCCTCCCCTGCCATCC
2776 MPR203 left 0.39 CTATATTGGACCGCAGCGCTGAGAGCTTTTGTGTTTAATG
2777 mir-017-precNol 0.26 GCATCTACTGCAGTGAAGGCACTTGTAGCATTATGGTGAC
2778 mir-219-2Nol 0.26 CTCAGGGGCTTCGCCACTGATTGTCCAAACGCAATTCTTG
2779 mir-328Nol 0.3 GAAAGTGCATACAGCCCCTGGCCCTCTCTGCCCTTCCGTC
2780 Hcd783 left 0.31 CAGGCTCACACCTCCCTCCCCCAACTCTCTGGAATGTATA
2781 Hcdl81 left 0.32 TTGGCGTCCTTGTCTCTCTCTCCCCTGCCCAGTGGCCTCC
2782 HPR213 right 0.3 AACAACTTTGTGCTGGTGCCGGGGAAGTTTGTGTCTCCAA
2783 mir-191-prec 0.31 CAACGGAATCCCAAAAGCAGCTGTTGTCTCCAGAGCATTC
2784 mir-375 0.31 TTTTGTTCGTTCGGCTCGCGTGAGGCAGGGGCGGCCTCTC
2785 mir-212-precNo2 0.26 CGGACAGCGCGCCGGCACCTTGGCTCTAGACTGCTTACTG
2786 Hcd913 right 0.34 CAAACATCATGTGACGTCTGTGGAGCGGCGGCGGCGGCGG
2787 Hcd716 right 0.48 CAATAAATGTGCCTATAAAGGCGCCGGCTCCGGGGCGCGG
2788 MPR207 right 0.3 AACAACTTTGTGCTGGTGCCGGGGAAGTTTGTGTCTCCTA
2789 HPR206 left 0.26 CTATATTGGACCGCAGCGCTGAGAGCTTTTGTGTTTAATG
2790 mir-016b-chr3 0.29 GTTCCACTCTAGCAGCACGTAAATATTGGCGTAGTGAAAT
2791 Hcd654 left 0.34 AACGAGTAAAAGGCGTACATGGGAGCGCGGGGCGGCAGAG
2792 mir-195-prec 0.3 TCTAGCAGCACAGAAATATTGGCACAGGGAAGCGAGTCTG
2793 Hcd425 left 0.25 GGTTCTACTCTCTTACCCCTCCCCCACGTGGTTGTTGCTG
2794 mir-148aNol 0.35 TGAGTATGATAGAAGTCAGTGCACTACAGAACTTTGTCTC
2795 mir-142-prec 0.36 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2796 mir-016a-chrl3 0.25 CAATGTCAGCAGTGCCTTAGCAGCACGTAAATATTGGCGT
Table 107. Cytoxan microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2797 Hcd99 right 0.25 CAATCCTGGCTGCAGGCATATTTGCATATTGGATGCTGTG
2798 mir-520c/526a 0.32 TCTCAGGCTGTCGTCCTCTAGAGGGAAGCACTTTCTGTTG
2799 mir-191-prec 0.32 CAACGGAATCCCAAAAGCAGCTGTTGTCTCCAGAGCATTC
2800 mir-205-prec 0.35 TCCTTCATTCCACCGGAGTCTGTCTCATACCCAACCAGAT
2801 mir-375 0.33 TTTTGTTCGTTCGGCTCGCGTGAGGCAGGGGCGGCCTCTC
2802 mir-423Nol 0.29 CAAAAGCTCGGTCTGAGGCCCCTCAGTCTTGCTTCCTAAC
2803 mir-449Nol 0.39 TGTGATGAGCTGGCAGTGTATTGTTAGCTGGTTGAATATG
2804 mir-196-2-precNo2 0.26 GCTGATCTGTGGCTTAGGTAGTTTCATGTTGTTGGGATTG
Table 108. Topotecan (Hycamtin) microRNA biomarkers. SEQIDNO Medianprobe Corr Sequence
2805 HUMTRF 0.26 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA 2806 MPR74 lleefftt 0.29 CAAAGGTCACAATTAACATTCATTGTTGTCGGTGGGTTGT 2807 mir-213-precNol 0.28 AACATTCATTGCTGTCGGTGGGTTGAACTGTGTGGACAAG 2808 mir-155-prec 0.31 TTAATGCTAATCGTGATAGGGGTTTTTGCCTCCAACTGAC 2809 mir-181b-precNol 0.31 TGAGGTTGCTTCAGTGAACATTCAACGCTGTCGGTGAGTT 2810 mir-342Nol 0.33 GTCTCACACAGAAATCGCACCCGTCACCTTGGCCTACTTA 2811 mir-4323p 0.28 CCTTACGTGGGCCACTGGATGGCTCCTCCATGTCTTGGAG
Table 109. Suberoylanilide hydroxamic acid (SAHA, vorinostat, Zolinza) microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2812 mir-092-prec-X=092-2 0.38 GTTCTATATAAAGTATTGCACTTGTCCCGGCCTGTGGAAG
2813 mir-123-precNol 0.31 GACGGGACATTATTACTTTTGGTACGCGCTGTGACACTTC
2814 mir-514-lNo2 0.29 TGTCTGTGGTACCCTACTCTGGAGAGTGACAATCATGTAT
2815 mir-lOl-prec-9 0.25 GCTGTATATCTGAAAGGTACAGTACTGTGATAACTGAAGA
2816 mir-148-prec 0.36 TGAGTATGATAGAAGTCAGTGCACTACAGAACTTTGTCTC
2817 mir-106aNol 0.34 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
2818 mir-20bNol 0.41 AGTACCAAAGTGCTCATAGTGCAGGTAGTTTTGGCATGAC
2819 Hcd781 right 0.32 AGTTTCTTTAATTAATGAAGTTTTTGGGTCTGCTCCACTT
2820 mir-017-precNo2 0.29 GTCAGAATAATGTCAAAGTGCTTACAGTGCAGGTAGTGAT
2821 mir-019b-2-prec 0.42 GTGGCTGTGCAAATCCATGCAAAACTGATTGTGATAATGT
2822 mir-033-prec 0.27 GTGGTGCATTGTAGTTGCATTGCATGTTCTGGTGGTACCC
2823 mir-092-prec-13=092-1NO2 0.28 TCTGTATGGTATTGCACTTGTCCCGGCCTGTTGAGTTTGG
2824 mir-107Nol 0.29 GGCATGGAGTTCAAGCAGCATTGTACAGGGCTATCAAAGC
2825 mir-103-prec-5=103-l 0.32 TATGGATCAAGCAGCATTGTACAGGGCTATGAAGGCATTG 2826 MPR216 left 0.29 GATCCTAGTAGTGCCAAAGTGCTCATAGTGCAGGTAGTTT 2827 mir-29b-2=102prec7.1=7 .2 0.27 AGTGATTGTCTAGCACCATTTGAAATCAGTGTTCTTGGGG 2828 mir-019b-l-prec 0.4 TTCTGCTGTGCAAATCCATGCAAAACTGACTGTGGTAGTG 2829 mir-107-prec-10 0.3 GGCATGGAGTTCAAGCAGCATTGTACAGGGCTATCAAAGC 2830 mir-135-2-prec 0.37 CACTCTAGTGCTTTATGGCTTTTTATTCCTATGTGATAGT 2831 Hcd581 right 0.28 AGGAGATATGCCAAGATATATTCACAGCTTTATATACACA 2832 mir-103-2-prec 0.29 GTAGCATTCAGGTCAAGCAACATTGTACAGGGCTATGAAA 2833 Hcd230 left 0.27 CATTCTCTACAAGCATATGGCCTTGGGACATTAAGATGGC 2834 inir-025-prec 0.4 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG 2835 mir-208-prec 0.31 ACCTGATGCTCACGTATAAGACGAGCAAAAAGCTTGTTGG 2836 mir-18bNo2 0.31 AGCAGCTTAGAATCTACTGCCCTAAATGCCCCTTCTGGCA 2837 mir-093-prec-7.1=093-1 0.39 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT 2838 mir-106-prec-X 0.48 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT 2839 mir-142-prec 0.37 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG 2840 HPR169 right 0.28 GTTTCTTTCTCACGGTAACTGGCAGCCTCGTTGTGGGCTG 2841 mir-018-prec 0.44 TAAGGTGCATCTAGTGCAGATAGTGAAGTAGATTAGCATC 2842 mir-020-prec 0.48 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
Table 110. Depsipeptide (FR901228) microRNA biomarkers. SEQIDNO Medianprobe Corr Sequence
2843 Hcd415 right 0.27 GATGTTTGGGAAACAATGGGAGTGAGAGAATGGGAGAGCT 2844 mir-147-prec 0.27 GACTATGGAAGCCAGTGTGTGGAAATGCTTCTGCTAGATT 2845 mir-033b-prec 0.34 GTGCATTGCTGTTGCATTGCACGTGTGTGAGGCGGGTGCA 2846 Hcd778 right 0.34 CAGAGGGGAGGCCCAGAGGAGAGGGAAGCTTGGGCAAAGG 2847 mir-127-prec 0.25 TCGGATCCGTCTGAGCTTGGCTGGTCGGAAGTCTCATCAT 2848 mir-324Nol 0.28 TGGAGACCCACTGCCCCAGGTGCTGCTGGGGGTTGTAGTC 2849 Hcd794 right 0.35 GGCCACCACAGACACCAACAAGTTCAGTCCGTTTCTGCAG 2850 Hcd634 left 0.27 CTGCTCCGCTCAGAGCCTTTTCCTCTCCACTTCCTGTTCA
Table 111 . Bortezomib microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2851 MPR121 left 0.31 CACCTGGCTCTGAGAACTGAATTCCATAGGCTGTGAGCTC
2852 Hcdll5 left 0.27 CTCTGTGGCCATTTCGGTTTTTCCAGTCCGATGCCCCTGA
2853 Hcd693 right 0.28 AGGCTTTGTGCGCGCATTAAAGCTCGCCGGACCCCCGACC
2854 Hcd704 left 0.25 TCTGTATTTAATTTGGCTCAGCCGGGAAGATTTTTGGCTC
2855 HPRlOO right 0.28 GGTGTTTGTGCTCCACTCAGCTCCCTTGGTTACATAACAG
2856 Hcd760 left 0.26 TGTGGTCACGTTTCTCCCTCTCTGCTGGCCCCCATCTGTC
2857 mir-147-prec 0.3 GACTATGGAAGCCAGTGTGTGGAAATGCTTCTGCTAGATT
2858 mir-033b-prec 0.29 GTGCATTGCTGTTGCATTGCACGTGTGTGAGGCGGGTGCA
2859 mir-146-prec 0.33 TGAGAACTGAATTCCATGGGTTGTGTCAGTGTCAGACCTC
2860 Hcdl42 right 0.3 TAAATGTGTAATTTCTCCCTTGACGGCCCCCGGCCGCTGG
2861 mir-501No2 0.33 ATGCAATGCACCCGGGCAAGGATTCTGAGAGGGTGAGCCC
2862 Hcd716 right 0.26 CAATAAATGTGCCTATAAAGGCGCCGGCTCCGGGGCGCGG
2863 MPR207 right 0.27 AACAACTTTGTGCTGGTGCCGGGGAAGTTTGTGTCTCCTA
2864 Hcd777 left 0.26 CAGGTGGGTGCTGAGGCCGCGTTGTTGCTTGAAGCTAGCC
2865 mir-204-precNo2 0.27 AGGCTGGGAAGGCAAAGGGACGTTCAATTGTCATCACTGG
2866 mir-146bNol 0.26 CACCTGGCACTGAGAACTGAATTCCATAGGCTGTGAGCTC
2867 Hcd511 right 0.29 TACCTCAGAAGCCTCACTCAACCCTCTCCCGCTGAGTCTC
2868 Hcd397 left 0.28 GTGTGTATACTTATGTGTGTGTATGTGTGAGTGTGAATAT
2869 MPR130 right 0.33 CAATCACAGATAGCACCCCTCACCTTGAGCCCATTTTCAC
2870 Hcd782 left 0.28 GGAGCCCTGTCTGCAAAGAGTGGTGCGTGTGCGTGTGTGA
2871 mir-324No2 0.28 CTGACTATGCCTCCCCGCATCCCCTAGGGCATTGGTGTAA
2872 Hcd794 right 0.34 GGCCACCACAGACACCAACAAGTTCAGTCCGTTTCTGCAG
2873 Hcd739 right 0.29 TATTAGCTGAGGGAGGGCTGGAGGCGGCTGCATTCCGACT
Table 112 Leukeran microRNA biomarkers .
SEQIDNO Medianprobe Corr Sequence
2874 mir-092-prec-X=092-2 0.39 GTTCTATATAAAGTATTGCACTTGTCCCGGCCTGTGGAAG
2875 mir-096-prec-7Nol 0.26 CTCCGCTCTGAGCAATCATGTGCAGTGCCAATATGGGAAA
2876 mir-123-precNo2 0.32 TGTGACACTTCAAACTCGTACCGTGAGTAATAATGCGCCG
2877 MPR249 left 0.26 TCGGTTTGGTTCAGCTGGTATGCTTTCCAGTATCTCATTC
2878 HPR232 right 0.28 TGAATTATTGCACAATAAATTCATGCCCTGTTGTGTCTTA
2879 mir-lOl-prec-9 0.4 GCTGTATATCTGAAAGGTACAGTACTGTGATAACTGAAGA
2880 mir-106aNol 0.31 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
2881 mir-20bNol 0.38 AGTACCAAAGTGCTCATAGTGCAGGTAGTTTTGGCATGAC
2882 Hcd861 right 0.25 AAGGTCTGGATTGATCGTACTGCTTTCTGAAAGGTAAAAA
2883 mir-017-precNo2 0.26 GTCAGAATAATGTCAAAGTGCTTACAGTGCAGGTAGTGAT
2884 mir-019b-2-prec 0.33 GTGGCTGTGCAAATCCATGCAAAACTGATTGTGATAATGT
2885 mir-033-prec 0.3 GTGGTGCATTGTAGTTGCATTGCATGTTCTGGTGGTACCC
2886 HcdlO2 left 0.26 ACTGGAATTATGTTTTATCTTAAGTCCACACTGGATCCTC
2887 MPR216 left 0.32 GATCCTAGTAGTGCCAAAGTGCTCATAGTGCAGGTAGTTT
2888 Hcd975 left 0.25 GGTTTTGTGTTTTTGTAAACAGCAGAAGGTATTAGTCCAT
2889 mir-019b-l-prec 0.3 TTCTGCTGTGCAAATCCATGCAAAACTGACTGTGGTAGTG
2890 mir-135-2-prec 0.38 CACTCTAGTGCTTTATGGCTTTTTATTCCTATGTGATAGT
2891 Hcd581 right 0.26 AGGAGATATGCCAAGATATATTCACAGCTTTATATACACA
2892 Hcd536_HPR104 right 0.25 GCTGCTCTGCTGAGGGGCTGGACTCTGTCCAGAAGCACCA
2893 mir-128b-precNo2 0.25 GGGGGCCGATACACTGTACGAGAGTGAGTAGCAGGTCTCA
2894 HSTRNL 0.37 TCCGGATGGAGCGTGGGTTCGAATCCCACTTCTGACACCA
2895 mir-025-prec 0.47 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG
2896 mir-18bNo2 0.27 AGCAGCTTAGAATCTACTGCCCTAAATGCCCCTTCTGGCA
2897 HPR262 left 0.26 TCAGTTTGGTTCAGCTGGTATGCTTTCCAGTATCTCATTC
2898 Hcd923 right 0.33 CTGGAGATAATGATTCTGCATTTCTAATTAACTCCCAGGT
2899 Hcd434 right 0.3 CACTTTTTCCTTTGTGGAAATCCTGGGTGACATCACCTCC
2900 Hcd658 right 0.28 GACTGCAGAGCAAAAGACACGATGGGTGTCTATTGTTTTC
2901 HPR129 left 0.29 TTTTCCTGCTTGATTTGCTTAATGGAAGCTGACAGTGAAG
2902 mir-380-5p 0.32 AGGTACCTGAAAAGATGGTTGACCATAGAACATGCGCTAT
2903 mir-093-prec-7.1=093-1 0.45 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT
2904 mir-106-prec-X 0.5 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
2905 Hcd627 left 0.31 GCATTAGGGAGAATAGTTGATGGATTACAAATCTCTGCAT
2906 mir-142-prec 0.33 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2907 mir-018-prec 0.46 TAAGGTGCATCTAGTGCAGATAGTGAAGTAGATTAGCATC
2908 mir-020-prec 0.5 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
Table 113. Fludarabine microRNA biomarkers . SEQIDNO Medianprobe Corr Sequence
2909 Hcd773 left 0.26 CTTCCTCCCTGGGCATCTCTAGCACAGGGGATCCCCAAAC
2910 Hcd248 right 0.33 CATTATGCAAATGGTATGAGAGGAAAATTAGGCAATAAGG
2911 mir-181dNol 0.34 GAGGTCACAATCAACATTCATTGTTGTCGGTGGGTTGTGA
2912 MPR74 left 0.3 CAAAGGTCACAATTAACATTCATTGTTGTCGGTGGGTTGT
2913 mir-213-precNol 0.37 AACATTCATTGCTGTCGGTGGGTTGAACTGTGTGGACAAG
2914 mir-155-prec 0.32 TTAATGCTAATCGTGATAGGGGTTTTTGCCTCCAACTGAC
2915 MPR197 right 0.29 TATTTATTACAAGGTCCTTCTTCCCCGTAAAACTTTGTCC
2916 mir-181b-precNol 0.26 TGAGGTTGCTTCAGTGAACATTCAACGCTGTCGGTGAGTT
2917 mir-29b-2=102prec7.1=7.2 0.32 AGTGATTGTCTAGCACCATTTGAAATCAGTGTTCTTGGGG
2918 mir-029c-prec 0.33 TTTTGTCTAGCACCATTTGAAATCGGTTATGATGTAGGGG
2919 Hcd318 right 0.32 CAAGTGGTTAATTGAGCCCACAAGTGACCTACTCAATCAG
2920 mir-128b-precNol 0.25 TCACAGTGAACCGGTCTCTTTCCCTACTGTGTCACACTCC
2921 mir-130a-precNo2 0.27 TGTCTGCACCTGTCACTAGCAGTGCAATGTTAAAAGGGCA
2922 mir-140No2 0.26 TTCTACCACAGGGTAGAACCACGGACAGGATACCGGGGCA
2923 mir-16-2Nol 0.31 GTTCCACTCTAGCAGCACGTAAATATTGGCGTAGTGAAAT
2924 mir-526a-2Nol 0.26 GATCTCGTGCTGTGACCCTCTAGAGGGAAGCACTTTCTGT
2925 mir-016b-chr3 0.3 GTTCCACTCTAGCAGCACGTAAATATTGGCGTAGTGAAAT
2926 mir-195-prec 0.34 TCTAGCAGCACAGAAATATTGGCACAGGGAAGCGAGTCTG
2927 mir-216-precNol 0.25 CTGGGATTATGCTAAACAGAGCAATTTCCTAGCCCTCACG
2928 mir-342Nol 0.26 GTCTCACACAGAAATCGCACCCGTCACCTTGGCCTACTTA
2929 mir-29b-lNol 0.34 AGTGATTGTCTAGCACCATTTGAAATCAGTGTTCTTGGGG
2930 Hcd627 left 0.33 GCATTAGGGAGAATAGTTGATGGATTACAAATCTCTGCAT
2931 mir-102-prec-l 0.33 TCTTTGTATCTAGCACCATTTGAAATCAGTGTTTTAGGAG
2932 mir-142-prec 0.32 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2933 mir-223-prec 0.34 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT
2934 let-7f-2-prec2 0.26 TGAGGTAGTAGATTGTATAGTTTTAGGGTCATACCCCATC
2935 mir-016a-chrl3 0.36 CAATGTCAGCAGTGCCTTAGCAGCACGTAAATATTGGCGT
Table 114. Vinblastine microRNA biomarkers. SEQIDNO Medianprobe Corr Sequence
2936 Hcd794 right 0.33 GGCCACCACAGACACCAACAAGTTCAGTCCGTTTCTGCAG
2937 Hcd754 left 0.25 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC
Table 115. Busulfan microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
2938 mir-096-prec-7No2 0.27 TGGCCGATTTTGGCACTAGCACATTTTTGCTTGTGTCTCT
2939 mir-124a-3-prec 0.25 TTAAGGCACGCGGTGAATGCCAAGAGAGGCGCCTCCGCCG
2940 mir-101-prec-9 0.25 GCTGTATATCTGAAAGGTACAGTACTGTGATAACTGAAGA
2941 Hcd712 right 0.27 GAAGATCGGTTGTCATCTGGTCTGGTCAGCCCGGCCCCGA
2942 Hcd693 right 0.26 AGGCTTTGTGCGCGCATTAAAGCTCGCCGGACCCCCGACC
2943 mir-219-2Nol 0.25 CTCAGGGGCTTCGCCACTGATTGTCCAAACGCAATTCTTG
2944 Hcdl45 left 0.29 AAAAATCCCAGCGGCCACCTTTCCTCCCTGCCCCATTGGG
2945 mir-155-prec 0.29 TTAATGCTAATCGTGATAGGGGTTTTTGCCTCCAACTGAC
2946 HPR213 right 0.3 AACAACTTTGTGCTGGTGCCGGGGAAGTTTGTGTCTCCAA
2947 mir-212-precNo2 0.34 CGGACAGCGCGCCGGCACCTTGGCTCTAGACTGCTTACTG
2948 Hcd913 right 0.33 CAAACATCATGTGACGTCTGTGGAGCGGCGGCGGCGGCGG
2949 Hcd716 right 0.51 CAATAAATGTGCCTATAAAGGCGCCGGCTCCGGGGCGCGG
2950 MPR207 right 0.26 AACAACTTTGTGCTGGTGCCGGGGAAGTTTGTGTCTCCTA
2951 Hcd559 right 0.33 TTCTTTGTCTATACATTTCCTAGATTTCTATGCAGTTGGG
2952 Hcd654 left 0.28 AACGAGTAAAAGGCGTACATGGGAGCGCGGGGCGGCAGAG
2953 Hcd739 right 0.27 TATTAGCTGAGGGAGGGCTGGAGGCGGCTGCATTCCGACT
2954 mir-142-prec 0.4 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
Table 116. Dacarbazme microRNA biomarkers. SEQIDNO Medianprobe Corr Sequence
2955 mir-092-prec-X=092-2 0. 25 GTTCTATATAAAGTATTGCACTTGTCCCGGCCTGTGGAAG 2956 mir-123-precNo2 0.28 TGTGACACTTCAAACTCGTACCGTGAGTAATAATGCGCCG 2957 mir-lOl-prec-9 0. 29 GCTGTATATCTGAAAGGTACAGTACTGTGATAACTGAAGA 2958 Hcd517 right 0. 3 GAGGGATTACAGATTAACTCCCACTTCTCCAGACTCAGAA 2959 Hcd796 left 0.37 GGTGGGATTACCCGGCTGCCGCTGTCGCCTGGATGGTCTC 2960 Hcd749 right 0.28 CGAGGAGGAGGTGACTGCTGTGGATGGTTATGAGACAGAC 2961 Hcd674 left 0.25 CTCCAGTGTGGTGTGCCTGCCCCCTTCCGTCATTGCTGTG 2962 mir-019b-2-prec 0. 27 GTGGCTGTGCAAATCCATGCAAAACTGATTGTGATAATGT 2963 mir-033-prec 0.29 GTGGTGCATTGTAGTTGCATTGCATGTTCTGGTGGTACCC 2964 mir-092-prec-13=092-lNo2 0.33 TCTGTATGGTATTGCACTTGTCCCGGCCTGTTGAGTTTGG 2965 mir-124a-2-prec 0. 29 TTAAGGCACGCGGTGAATGCCAAGAGCGGAGCCTACGGCT 2966 mir-143-prec 0. 36 CTGGTCAGTTGGGAGTCTGAGATGAAGCACTGTAGCTCAG 2967 mir-516-43p 0. 28 AAAGAAAAGAAAGTGCTTCCTTTCAGAGGGTTACTCTTTG 2968 mir-216-precNol 0. 31 CTGGGATTATGCTAAACAGAGCAATTTCCTAGCCCTCACG 2969 Hcd731 left 0.26 AATTGTGACAACTGAGTGGGAGGTTTGTGTGATGATTATC 2970 mir-106-prec-X 0.26 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT 2971 mir-142-prec 0. 48 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG 2972 mir-223-prec 0.48 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT 2973 Hcd754 left 0. 32 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC 2974 mir-018-prec 0.27 TAAGGTGCATCTAGTGCAGATAGTGAAGTAGATTAGCATC
Table 117 Oxaliplatin microRNA biomarkers .
SEQIDNO Medianprobe Corr Sequence
2975 mir-092-prec-X=092-2 0.36 GTTCTATATAAAGTATTGCACTTGTCCCGGCCTGTGGAAG
2976 mir-148-prec 0.27 TGAGTATGATAGAAGTCAGTGCACTACAGAACTTTGTCTC
2977 mir-20bNol 0.27 AGTACCAAAGTGCTCATAGTGCAGGTAGTTTTGGCATGAC
2978 mir-007-2-precNo2 0.28 GGACCGGCTGGCCCCATCTGGAAGACTAGTGATTTTGTTG
2979 mir-017-precNo2 0.28 GTCAGAATAATGTCAAAGTGCTTACAGTGCAGGTAGTGAT
2980 mir-019b-2-prec 0.32 GTGGCTGTGCAAATCCATGCAAAACTGATTGTGATAATGT
2981 Hcd760 left 0.27 TGTGGTCACGTTTCTCCCTCTCTGCTGGCCCCCATCTGTC
2982 Hcd783 left 0.36 CAGGCTCACACCTCCCTCCCCCAACTCTCTGGAATGTATA
2983 MPR216 left 0.26 GATCCTAGTAGTGCCAAAGTGCTCATAGTGCAGGTAGTTT
2984 mir-375 0.33 TTTTGTTCGTTCGGCTCGCGTGAGGCAGGGGCGGCCTCTC
2985 mir-019b-l-prec 0.36 TTCTGCTGTGCAAATCCATGCAAAACTGACTGTGGTAGTG
2986 mir-135-2-prec 0.32 CACTCTAGTGCTTTATGGCTTTTTATTCCTATGTGATAGT
2987 mir-150-prec 0.25 CTCCCCATGGCCCTGTCTCCCAACCCTTGTACCAGTGCTG
2988 mir-128b-precNol 0.33 TCACAGTGAACCGGTCTCTTTCCCTACTGTGTCACACTCC
2989 mir-499No2 0.26 GTGAACATCACAGCAAGTCTGTGCTGCTTCCCGTCCCTAC
2990 mir-025-prec 0.38 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG
2991 mir-007-l-prec 0.32 TGTTGGCCTAGTTCTGTGTGGAAGACTAGTGATTTTGTTG
2992 mir-019a-prec 0.33 TGTAGTTGTGCAAATCTATGCAAAACTGATGGTGGCCTGC
2993 mir-093-prec-7.1=093-1 0.46 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT
2994 mir-106-prec-X 0.45 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
2995 mir-142-prec 0.41 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
2996 HPR169 right 0.34 GTTTCTTTCTCACGGTAACTGGCAGCCTCGTTGTGGGCTG
2997 mir-018-prec 0.4 TAAGGTGCATCTAGTGCAGATAGTGAAGTAGATTAGCATC
2998 mir-020-prec 0.44 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
2999 mir-484 0.33 GTCAGGCTCAGTCCCCTCCCGATAAACCCCTAAATAGGGA
Table 118. Hydroxyurea microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
3000 Hcd257 left 0.34 CTTCTTGTATAAGCACTGTGCTAAAATTGCAGACACTAGG
3001 Hcd768 right 0.26 GCCCTGGCGGAACGCTGAGAAGACAGTCGAACTTGACTAT
3002 Hcd796 left 0.25 GGTGGGATTACCCGGCTGCCGCTGTCGCCTGGATGGTCTC
3003 HUMTRF 0.48 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
3004 HUMTRS 0.3 TCTAGCGACAGAGTGGTTCAATTCCACCTTTCGGGCGCCA
3005 MPR74 left 0.28 CAAAGGTCACAATTAACATTCATTGTTGTCGGTGGGTTGT
3006 mir-213-precNol 0.29 AACATTCATTGCTGTCGGTGGGTTGAACTGTGTGGACAAG
3007 mir-155-prec 0.35 TTAATGCTAATCGTGATAGGGGTTTTTGCCTCCAACTGAC
3008 Hcd763 right 0.25 GGTGCACTCTAAATTCCTGTCCCTGCGGAAGGCTGACTAA
3009 mir-181b-precNol 0.28 TGAGGTTGCTTCAGTGAACATTCAACGCTGTCGGTGAGTT
3010 ath-MIR180aNo2 0.26 TGAGAATCTTGATGATGCTGCATCGGCAATCAACGACTAT
3011 mir-216-precNol 0.37 CTGGGATTATGCTAAACAGAGCAATTTCCTAGCCCTCACG
3012 mir-342Nol 0.31 GTCTCACACAGAAATCGCACCCGTCACCTTGGCCTACTTA
3013 mir-142-prec 0.49 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
3014 HSHELAOl 0.31 GGCCGCAGCAACCTCGGTTCGTATCCGAGTCACGGCACCA
3015 HUMTRVlA 0.26 ACGCGAAAGGTCCCCGGTTCGAAACCGGGCGGAAACACCA
3016 mir-223-prec 0.59 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT
3017 Hcd754 left 0.46 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC
3018 mir-020-prec 0.26 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
Table 119. Tegafur microRNA bio
SEQIDNO Medianprobe Corr Sequence
3019 Hcd257 right 0.26 CTTGGTTTTTGCAATAATGCTAGCAGAGTACACACAAGAA
3020 Hcd946 left 0 26 CACAGGATTTCAGGGGAGAAACGGTGGATTTTCACAAGAG
3021 Hcd503 left 0 .3 GAGATGAGGTAGCTGCCAGGTGCCATGGGGGTATAGGTGA
3022 mir-429Nol 0.25 CTAATACTGTCTGGTAAAACCGTCCATCCGCTGCCTGATC
3023 Hcd693 right 0 32 AGGCTTTGTGCGCGCATTAAAGCTCGCCGGACCCCCGACC
3024 miR-373*Nol 0 33 GGGATACTCAAAATGGGGGCGCTTTCCTTTTTGTCTGTAC
3025 Hcd738 left 0.28 GAAAAACTTAAGATTCCCTCTCGGCCCTCATTTTTAGCTG
3026 mir-328Nol 0.3333 GAAAGTGCATACAGCCCCTGGCCCTCTCTGCCCTTCCGTC
3027 Hcd783 left 0.36 CAGGCTCACACCTCCCTCCCCCAACTCTCTGGAATGTATA
3028 Hcdl81 right 0.34 GCTCACTGGGCAGGAGCCCTAATCGGATTCGACAGCTGAG
3029 Hcd631 left 0.38 CAGATATTTTCTCAGGCAATCCTCAGCCACAGCCTTCTTG
3030 Hcd279 left 0.25 CGGACTAACACTCCGCGGGTGTTTCCATGGAGACCGAGGC
3031 mir-194-2Nol 0.3 TGGTTCCCGCCCCCTGTAACAGCAACTCCATGTGGAAGTG
3032 mir-197-prec 0.38 TAAGAGCTCTTCACCCTTCACCACCTTCTCCACCCAGCAT
3033 HPR163 left 0.39 GCTGCCCCCTCCCTTAGCAACGTGGCCCCGGCGTTCCAAA
3034 mir-150-prec 0.32 CTCCCCATGGCCCTGTCTCCCAACCCTTGTACCAGTGCTG
3035 Hcd323 left 0.26 GTTGTAGCATGTGGTTGTATTAATGAACGTTACAGGAGAG
3036 mir-103-2-prec 0.28 GTAGCATTCAGGTCAAGCAACATTGTACAGGGCTATGAAA
3037 Hcd243 right 0.27 TATTATACATCATTTCCCATCAATCGACGAACTAAAGCCT
3038 Hcd938 right 0.27 ATTCCCTGCATCACTCTCATGAAATGGCTGAGAAAGTGAG
3039 mir-025-prec 0.29 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG
3040 mir-007-l-prec 0.36 TGTTGGCCTAGTTCTGTGTGGAAGACTAGTGATTTTGTTG
3041 MPR243 left 0.26 GTATTTACCTAGTTGTAATGTGGGTTGCCATGGTGTTTTG
3042 Hcd511 right 0.27 TACCTCAGAAGCCTCACTCAACCCTCTCCCGCTGAGTCTC
3043 Hcd654 left 0.26 AACGAGTAAAAGGCGTACATGGGAGCGCGGGGCGGCAGAG
3044 mir-199a-2-prec 0.3 TCGCCCCAGTGTTCAGACTACCTGTTCAGGACAATGCCGT
3045 mir-214-prec 0.27 TGTACAGCAGGCACAGACAGGCAGTCACATGACAACCCAG
3046 mir-093-prec-7. 1=093-1 0.33 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT
3047 mir-106-prec-X 0.27 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
3048 Hcd794 right 0.41 GGCCACCACAGACACCAACAAGTTCAGTCCGTTTCTGCAG
3049 Hcd530 right 0.26 AAGGAAAATCAAACCCACAATGCTGAACACAACAATGACC
3050 HSHELAOl 0.34 GGCCGCAGCAACCTCGGTTCGTATCCGAGTCACGGCACCA
3051 Hcd754 left 0.29 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC
3052 mir-020-prec 0.29 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
Table 120. Daunorubicm microRN
SEQIDNO Medianprobe Corr Sequence
3053 Hcd768 right 0.25 GCCCTGGCGGAACGCTGAGAAGACAGTCGAACTTGACTAT
3054 HUMTRF 0.34 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
3055 Hcdl45 left 0.28 AAAAATCCCAGCGGCCACCTTTCCTCCCTGCCCCATTGGG
3056 Hcd923 right 0.27 CTGGAGATAATGATTCTGCATTTCTAATTAACTCCCAGGT
3057 mir-216-precNol 0.27 CTGGGATTATGCTAAACAGAGCAATTTCCTAGCCCTCACG
3058 mir-093-prec-7. 1=093-1 0.25 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT
3059 mir-342Nol 0.33 GTCTCACACAGAAATCGCACCCGTCACCTTGGCCTACTTA
3060 Hcd794 right 0.28 GGCCACCACAGACACCAACAAGTTCAGTCCGTTTCTGCAG
3061 mir-142-prec 0.48 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
3062 HSHELAOl 0.3 GGCCGCAGCAACCTCGGTTCGTATCCGAGTCACGGCACCA
3063 mir-223-prec 0.33 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT
3064 Hcd754 left 0.32 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC
Table 121.. BBlleeoommyycciinn mmiiccrrooRRNt^AA bbiiomarkers .
SEQIDNO Medianprobe Corr Sequence
3065 mir-125b-2-precNo2 0.29 ACCAGACTTTTCCTAGTCCCTGAGACCCTAACTTGTGAGG
3066 mir-022-prec 0.26 TGTCCTGACCCAGCTAAAGCTGCCAGTTGAAGAACTGTTG
3067 mir-125b-1 0.29 TCCCTGAGACCCTAACTTGTGATGTTTACCGTTTAAATCC
3068 mir-155-prec 0.38 TTAATGCTAATCGTGATAGGGGTTTTTGCCTCCAACTGAC
3069 mir-lOONol 0.25 CCTGTTGCCACAAACCCGTAGATCCGAACTTGTGGTATTA
3070 mir-409-3p 0.27 GACGAATGTTGCTCGGTGAACCCCTTTTCGGTATCAAATT
3071 mir-495Nol 0.31 GTGACGAAACAAACATGGTGCACTTCTTTTTCGGTATCAA
3072 mir-199a-2-prec 0.29 TCGCCCCAGTGTTCAGACTACCTGTTCAGGACAATGCCGT
3073 mir-382 0.28 GGTACTTGAAGAGAAGTTGTTCGTGGTGGATTCGCTTTAC
3074 mir-lOO-l/2-prec 0.26 TGAGGCCTGTTGCCACAAACCCGTAGATCCGAACTTGTGG
Table 122. Estramustine microRNA biomarkers. SEQIDNO Medianprobe Corr Sequence
3075 Hcd338 left 0.32 CTTCTCCTCCTGTTCGCCGCAGGCGCCCGTCCCAGTAGTC
3076 mir-099b-prec-19Nol 0.25 GCCTTCGCCGCACACAAGCTCGTGTCTGTGGGTCCGTGTC
3077 mir-149-prec 0.34 CGAGCTCTGGCTCCGTGTCTTCACTCCCGTGCTTGTCCGA
Table 123. Chlorambucil microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
3078 mir-181a-precNol 0.26 TCAGAGGACTCCAAGGAACATTCAACGCTGTCGGTGAGTT
3079 mir-181c-precNol 0.25 TGCCAAGGGTTTGGGGGAACATTCAACCTGTCGGTGAGTT
3080 HUMTRF 0.35 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
3081 mir-181dNol 0.26 GAGGTCACAATCAACATTCATTGTTGTCGGTGGGTTGTGA
3082 MPR74 left 0.28 CAAAGGTCACAATTAACATTCATTGTTGTCGGTGGGTTGT
3083 Hcd817 left 0.28 TAATGAGAATTATGTTTGCACATTGAGGCAGGATAAATCC
3084 mir-213-precNol 0.42 AACATTCATTGCTGTCGGTGGGTTGAACTGTGTGGACAAG
3085 mir-155-prec 0.33 TTAATGCTAATCGTGATAGGGGTTTTTGCCTCCAACTGAC
3086 Hcdl48_HPR2251eft 0.29 AATTAATGACCAAAATGTCAGATGTGTCCACAGCTAATTA
3087 mir-515-15p 0.27 GATCTCATGCAGTCATTCTCCAAAAGAAAGCACTTTCTGT
3088 mir-181b-precNol 0.41 TGAGGTTGCTTCAGTGAACATTCAACGCTGTCGGTGAGTT
3089 HUMTRN 0.27 CAATCGGTTAGCGCGTTCGGCTGTTAACCGAAAGGTTGGT
3090 mir-128b-precNol 0.37 TCACAGTGAACCGGTCTCTTTCCCTACTGTGTCACACTCC
3091 mir-450-2Nol 0.29 GAAAGATGCTAAACTATTTTTGCGATGTGTTCCTAATATG
3092 mir-216-precNol 0.29 CTGGGATTATGCTAAACAGAGCAATTTCCTAGCCCTCACG
3093 mir-342Nol 0.35 GTCTCACACAGAAATCGCACCCGTCACCTTGGCCTACTTA
3094 mir-142-prec 0.45 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
3095 mir-223-prec 0.39 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT
3096 Hcd754 left 0.37 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC
3097 mir-020-prec 0.28 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
Table 124 Mechlorethamme microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
3098 mir-124a-3-prec 0.33 TTAAGGCACGCGGTGAATGCCAAGAGAGGCGCCTCCGCCG
3099 Hcd946 left 0.3 CACAGGATTTCAGGGGAGAAACGGTGGATTTTCACAAGAG
3100 Hcd683 left 0.29 CTATGACAGAAGGTACTCTGTGGGAGGGAGGAGATAATAG
3101 HPR264 right 0.25 CAAATGGCGCATCAATGACTATCGCTCTTACAAAGCTCTT
3102 MPR185 right 0.3 CAGAACATGCAATGCAACTACAATGCACCACAGCTGCCCG
3103 HUMTRF 0.37 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
3104 Hcd294 left 0.25 TTATCATAAAATAATCACAGCCCTCAGGTGCTGTGAGGCA
3105 Hcd503 left 0.27 GAGATGAGGTAGCTGCCAGGTGCCATGGGGGTATAGGTGA
3106 mir-20bNol 0.27 AGTACCAAAGTGCTCATAGTGCAGGTAGTTTTGGCATGAC
3107 MPR74 left 0.25 CAAAGGTCACAATTAACATTCATTGTTGTCGGTGGGTTGT
3108 MPR234 right 0.28 GCTGACGTCACGGGCAGAATTGTCCCATTTAGGGATCCCG
3109 Hcd447 right 0.26 CTCAGGCCATTAACCTCAGTTGGTCACTAATCCCTAGGAA
3110 Hcd817 right 0.3 GAATCTTGCCCTTGGATGCATACTGTAATTTCCATTAAAG
3111 Hcdl48_HPR2251eft 0.32 AATTAATGACCAAAATGTCAGATGTGTCCACAGCTAATTA
3112 mir-515-15p 0.29 GATCTCATGCAGTCATTCTCCAAAAGAAAGCACTTTCTGT
3113 Hcd383 right 0.25 CTGATAGTACACGGGGCCAAAATAGATGTATGCTTCTAAG
3114 mir-181b-precNo2 0.31 ACCATCGACCGTTGATTGTACCCTATGGCTAACCATCATC
3115 Hcd783 left 0.33 CAGGCTCACACCTCCCTCCCCCAACTCTCTGGAATGTATA
3116 MPR224 left 0.34 TGAGGCCCTCTAGGCCGTGAATTAATGTGTCATAACTCAC
3117 HPR172 right 0.28 GTTTAAACAGCCAGTGCAAACATTTAGATCTGAGTCAAAA
3118 MPR216 left 0.32 GATCCTAGTAGTGCCAAAGTGCTCATAGTGCAGGTAGTTT
3119 HUMTRN 0.28 CAATCGGTTAGCGCGTTCGGCTGTTAACCGAAAGGTTGGT
3120 mir-321Nol 0.3 TTGGCCTCCTAAGCCAGGGATTGTGGGTTCGAGTCCCACC
3121 HPR159 left 0.25 TCCGTCACTTGAACTGGCTGCCAGCGTTCACAGACAGCTG
3122 MPR228 left 0.29 TTTTTGCTCCCAGTCAGTAGGAAGATTGTTTCAAATCTGT
3123 ath-MIR180aNo2 0.31 TGAGAATCTTGATGATGCTGCATCGGCAATCAACGACTAT
3124 mir-197-prec 0.28 TAAGAGCTCTTCACCCTTCACCACCTTCTCCACCCAGCAT
3125 mir-124a-l-precl 0.26 ATACAATTAAGGCACGCGGTGAATGCCAAGAATGGGGCTG
3126 mir-128b-precNol 0.31 TCACAGTGAACCGGTCTCTTTCCCTACTGTGTCACACTCC
3127 Hcd28 HPR391eft 0.28 CTGACTTTCAGTTCCTATTTAAAATGTCTGAATTGGGAGC
3128 Hcd889 right 0.25 ATGCCTTGTGCTCTGTGCTAATTCAGAAGAATAAGCCTGT
3129 Hcd350 right 0.26 TAGCACTTAGCAGGTTGTATTATCATTGTCCGTGTCTATG
3130 mir-025-prec 0.31 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG
3131 mir-208-prec 0.27 ACCTGATGCTCACGTATAAGACGAGCAAAAAGCTTGTTGG
3132 mir-450-2Nol 0.25 GAAAGATGCTAAACTATTTTTGCGATGTGTTCCTAATATG
3133 Hcd923 right 0.29 CTGGAGATAATGATTCTGCATTTCTAATTAACTCCCAGGT
3134 Hcd434 right 0.28 CACTTTTTCCTTTGTGGAAATCCTGGGTGACATCACCTCC
3135 HPR129 left 0.27 TTTTCCTGCTTGATTTGCTTAATGGAAGCTGACAGTGAAG
3136 HPR220 left 0.27 GGAGACACTGTAACAACATTTTACTCCTGACTGATTACAT
3137 mir-380-5p 0.3 AGGTACCTGAAAAGATGGTTGACCATAGAACATGCGCTAT
3138 mir-093-prec-7.1=093-1 0.29 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT
3139 mir-106-prec-X 0.3 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
3140 mir-342Nol 0.28 GTCTCACACAGAAATCGCACCCGTCACCTTGGCCTACTTA
3141 mir-142-prec 0.45 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
3142 HSHELAOl 0.29 GGCCGCAGCAACCTCGGTTCGTATCCGAGTCACGGCACCA
3143 mir-223-prec 0.32 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT
3144 Hcd754 left 0.32 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC
3145 mir-020-prec 0.37 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
3146 mir-4323p 0.26 CCTTACGTGGGCCACTGGATGGCTCCTCCATGTCTTGGAG
Table 125. Streptozocin microRNA biomarkers . SEQIDNO Medianprobe Corr Sequence
3147 mir-483Nol 0.2 ATCACGCCTCCTCACTCCTCTCCTCCCGTCTTCTCCTCTC
3148 Hcd631 right 0.21 AAAACCAAATGGCTGGCTACTCATGTACTGTTGAATGTCT
3149 mir-212-precNol 0.24 CCTCAGTAACAGTCTCCAGTCACGGCCACCGACGCCTGGC
3150 Hcd938 right 0.21 ATTCCCTGCATCACTCTCATGAAATGGCTGAGAAAGTGAG
3151 MPR133 right 0.2 CTGTAGATACTTTCTCCCTGAGCCCCTCCTGCCCCCCTGC
3152 Hcd794 right 0.21 GGCCACCACAGACACCAACAAGTTCAGTCCGTTTCTGCAG
3153 Hcd438 left 0.24 GTTTATTTGAATGTGTGATGGGGAGGTCATCAAAATGAAC
3154 Hcd886 right 0.23 CTCCAGTTGGGGGTGGGGAGTTGGGAACAGTGTGAATGGG
Table 126. Carmustme microRNA biomarkers. SEQIDNO Medianprobe Corr Sequence
3155 mir-092-prec-X=092-2 0.33 GTTCTATATAAAGTATTGCACTTGTCCCGGCCTGTGGAAG
3156 Hcd517 right 0.33 GAGGGATTACAGATTAACTCCCACTTCTCCAGACTCAGAA
3157 Hcd796 left 0.28 GGTGGGATTACCCGGCTGCCGCTGTCGCCTGGATGGTCTC
3158 HUMTRF 0.33 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
3159 mir-20bNol 0.29 AGTACCAAAGTGCTCATAGTGCAGGTAGTTTTGGCATGAC
3160 mir-019b-2-prec 0.25 GTGGCTGTGCAAATCCATGCAAAACTGATTGTGATAATGT
3161 mir-033-prec 0.27 GTGGTGCATTGTAGTTGCATTGCATGTTCTGGTGGTACCC
3162 mir-092-prec-13=092-lNo2 0.33 TCTGTATGGTATTGCACTTGTCCCGGCCTGTTGAGTTTGG
3163 Hcdl48_HPR2251eft 0.27 AATTAATGACCAAAATGTCAGATGTGTCCACAGCTAATTA
3164 HUMTRAB 0.3 ATGGTAGAGCGCTCGCTTTGCTTGCGAGAGGTAGCGGGAT
3165 Hcd975 left 0.26 GGTTTTGTGTTTTTGTAAACAGCAGAAGGTATTAGTCCAT
3166 mir-135-2-prec 0.28 CACTCTAGTGCTTTATGGCTTTTTATTCCTATGTGATAGT
3167 mir-128b-precNol 0.27 TCACAGTGAACCGGTCTCTTTCCCTACTGTGTCACACTCC
3168 mir-143-prec 0.32 CTGGTCAGTTGGGAGTCTGAGATGAAGCACTGTAGCTCAG
3169 mir-025-prec 0.33 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG
3170 mir-216-precNol 0.34 CTGGGATTATGCTAAACAGAGCAATTTCCTAGCCCTCACG
3171 mir-093-prec-7.1=093-1 0.3 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT
3172 mir-106-prec-X 0.33 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
3173 mir-142-prec 0.61 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
3174 HSHELAOl 0.26 GGCCGCAGCAACCTCGGTTCGTATCCGAGTCACGGCACCA
3175 HUMTRVlA 0.26 ACGCGAAAGGTCCCCGGTTCGAAACCGGGCGGAAACACCA
3176 mir-223-prec 0.52 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT
3177 Hcd754 left 0.46 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC
3178 mir-018-prec 0.34 TAAGGTGCATCTAGTGCAGATAGTGAAGTAGATTAGCATC
3179 mir-020-prec 0.35 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
Table 127. Lomustine microRNA biomarkers. SEQIDNO Medianprobe Corr Sequence
3180 mir-lOl-prec-9 0.27 GCTGTATATCTGAAAGGTACAGTACTGTGATAACTGAAGA
3181 Hcd796 left 0.26 GGTGGGATTACCCGGCTGCCGCTGTCGCCTGGATGGTCTC
3182 mir-20bNol 0.28 AGTACCAAAGTGCTCATAGTGCAGGTAGTTTTGGCATGAC 3183 HUMTRAB 0.35 ATGGTAGAGCGCTCGCTTTGCTTGCGAGAGGTAGCGGGAT 3184 mir-135-2-prec 0.27 CACTCTAGTGCTTTATGGCTTTTTATTCCTATGTGATAGT 3185 mir-153-l-precl 0.32 CAGTTGCATAGTCACAAAAGTGATCATTGGCAGGTGTGGC 3186 mir-025-prec 0.29 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG 3187 mir-093-prec-7.1=093-1 0.26 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT 3188 mir-106-prec-X 0.31 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT 3189 mir-142-prec 0.41 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG 3190 HUMTRVlA 0.28 ACGCGAAAGGTCCCCGGTTCGAAACCGGGCGGAAACACCA 3191 Hcd754 left 0.35 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC 3192 mir-018-prec 0.27 TAAGGTGCATCTAGTGCAGATAGTGAAGTAGATTAGCATC 3193 mir-020-prec 0.28 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
Table 128 Mercaptopurme microRNA biomarkers .
SEQIDNO Medianprobe Corr Sequence
3194 mir-092-prec-X=092-2 0.39 GTTCTATATAAAGTATTGCACTTGTCCCGGCCTGTGGAAG
3195 mir-096-prec-7Nol 0.26 CTCCGCTCTGAGCAATCATGTGCAGTGCCAATATGGGAAA
3196 mir-123-precNo2 0.32 TGTGACACTTCAAACTCGTACCGTGAGTAATAATGCGCCG
3197 MPR249 left 0.26 TCGGTTTGGTTCAGCTGGTATGCTTTCCAGTATCTCATTC
3198 HPR232 right 0.28 TGAATTATTGCACAATAAATTCATGCCCTGTTGTGTCTTA
3199 mir-lOl-prec-9 0.4 GCTGTATATCTGAAAGGTACAGTACTGTGATAACTGAAGA
3200 mir-106aNol 0.31 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
3201 mir-20bNol 0.38 AGTACCAAAGTGCTCATAGTGCAGGTAGTTTTGGCATGAC
3202 Hcd861 right 0.25 AAGGTCTGGATTGATCGTACTGCTTTCTGAAAGGTAAAAA
3203 mir-017-precNo2 0.26 GTCAGAATAATGTCAAAGTGCTTACAGTGCAGGTAGTGAT
3204 mir-019b-2-prec 0.33 GTGGCTGTGCAAATCCATGCAAAACTGATTGTGATAATGT
3205 mir-033-prec 0.3 GTGGTGCATTGTAGTTGCATTGCATGTTCTGGTGGTACCC
3206 HcdlO2 left 0.26 ACTGGAATTATGTTTTATCTTAAGTCCACACTGGATCCTC
3207 MPR216 left 0.32 GATCCTAGTAGTGCCAAAGTGCTCATAGTGCAGGTAGTTT
3208 Hcd975 left 0.25 GGTTTTGTGTTTTTGTAAACAGCAGAAGGTATTAGTCCAT
3209 mir-019b-l-prec 0.3 TTCTGCTGTGCAAATCCATGCAAAACTGACTGTGGTAGTG
3210 mir-135-2-prec 0.38 CACTCTAGTGCTTTATGGCTTTTTATTCCTATGTGATAGT
3211 Hcd581 right 0.26 AGGAGATATGCCAAGATATATTCACAGCTTTATATACACA
3212 Hcd536_HPR104 right 0.25 GCTGCTCTGCTGAGGGGCTGGACTCTGTCCAGAAGCACCA
3213 mir-128b-precNo2 0.25 GGGGGCCGATACACTGTACGAGAGTGAGTAGCAGGTCTCA
3214 HSTRNL 0.37 TCCGGATGGAGCGTGGGTTCGAATCCCACTTCTGACACCA
3215 mir-025-prec 0.47 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG
3216 mir-18bNo2 0.27 AGCAGCTTAGAATCTACTGCCCTAAATGCCCCTTCTGGCA
3217 HPR262 left 0.26 TCAGTTTGGTTCAGCTGGTATGCTTTCCAGTATCTCATTC
3218 Hcd923 right 0.33 CTGGAGATAATGATTCTGCATTTCTAATTAACTCCCAGGT
3219 Hcd434 right 0.3 CACTTTTTCCTTTGTGGAAATCCTGGGTGACATCACCTCC
3220 Hcd658 right 0.28 GACTGCAGAGCAAAAGACACGATGGGTGTCTATTGTTTTC
3221 HPR129 left 0.29 TTTTCCTGCTTGATTTGCTTAATGGAAGCTGACAGTGAAG
3222 mir-380-5p 0.32 AGGTACCTGAAAAGATGGTTGACCATAGAACATGCGCTAT
3223 mir-093-prec-7.1=093- 1 0.45 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT
3224 mir-106-prec-X 0.5 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
3225 Hcd627 left 0.31 GCATTAGGGAGAATAGTTGATGGATTACAAATCTCTGCAT
3226 mir-142-prec 0.33 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
3227 mir-018-prec 0.46 TAAGGTGCATCTAGTGCAGATAGTGAAGTAGATTAGCATC
3228 mir-020-prec 0.5 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
Table 129. Teniposide microRNA biomarkers . SEQIDNO Medianprobe Corr Sequence
3229 mir-124a-3-prec 0.25 TTAAGGCACGCGGTGAATGCCAAGAGAGGCGCCTCCGCCG
3230 Hcd768 right 0.28 GCCCTGGCGGAACGCTGAGAAGACAGTCGAACTTGACTAT
3231 HUMTRF 0.28 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
3232 mir-213-precNol 0.25 AACATTCATTGCTGTCGGTGGGTTGAACTGTGTGGACAAG
3233 mir-181b-precNo2 0.28 ACCATCGACCGTTGATTGTACCCTATGGCTAACCATCATC
3234 Hcd783 left 0.28 CAGGCTCACACCTCCCTCCCCCAACTCTCTGGAATGTATA
3235 mir-212-precNo2 0.32 CGGACAGCGCGCCGGCACCTTGGCTCTAGACTGCTTACTG
3236 mir-124a-l-precl 0.25 ATACAATTAAGGCACGCGGTGAATGCCAAGAATGGGGCTG
3237 mir-342Nol 0.29 GTCTCACACAGAAATCGCACCCGTCACCTTGGCCTACTTA
3238 mir-142-prec 0.49 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
3239 HSHELAOl 0.3 GGCCGCAGCAACCTCGGTTCGTATCCGAGTCACGGCACCA
3240 mir-223-prec 0.27 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT
3241 Hcd754 left 0.29 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC
Table 130. Dactinomycm microRNA biomarkers. SEQIDNO Medianprobe Corr Sequence
3242 mir-025-prec 0.27 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG 3243 mir-007-l-prec 0.28 TGTTGGCCTAGTTCTGTGTGGAAGACTAGTGATTTTGTTG 3244 mir-093-prec-7.1=093- 1 0.3 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT 3245 Hcd794 right 0.33 GGCCACCACAGACACCAACAAGTTCAGTCCGTTTCTGCAG 3246 mir-142-prec 0.34 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
Table 131 Tretinoin microRNA biomarkers .
SEQIDNO Medianprobe Corr Sequence
3247 Hcd257 left 0.42 CTTCTTGTATAAGCACTGTGCTAAAATTGCAGACACTAGG
3248 mir-148-prec 0.45 TGAGTATGATAGAAGTCAGTGCACTACAGAACTTTGTCTC
3249 Hcd512 left 0.28 CTGCGCTCTCGGAAATGACTCGCTCCAATCCCGCTTCGCG
3250 HPR227 right 0.25 CAGTGCAATGATATTGTCAAAGCATCTGGGACCAGCCTTG
3251 Hcd421 right 0.37 AGTAAACAATGTCGGCTTTCCGCCTCCTCCCCTGCCATCC
3252 MPR203 left 0.39 CTATATTGGACCGCAGCGCTGAGAGCTTTTGTGTTTAATG
3253 mir-017-precNol 0.26 GCATCTACTGCAGTGAAGGCACTTGTAGCATTATGGTGAC
3254 mir-219-2Nol 0.26 CTCAGGGGCTTCGCCACTGATTGTCCAAACGCAATTCTTG
3255 mir-328Nol 0.3 GAAAGTGCATACAGCCCCTGGCCCTCTCTGCCCTTCCGTC
3256 Hcd783 left 0.31 CAGGCTCACACCTCCCTCCCCCAACTCTCTGGAATGTATA
3257 Hcdl81 left 0.32 TTGGCGTCCTTGTCTCTCTCTCCCCTGCCCAGTGGCCTCC
3258 HPR213 right 0.3 AACAACTTTGTGCTGGTGCCGGGGAAGTTTGTGTCTCCAA
3259 mir-191-prec 0.31 CAACGGAATCCCAAAAGCAGCTGTTGTCTCCAGAGCATTC
3260 mir-375 0.31 TTTTGTTCGTTCGGCTCGCGTGAGGCAGGGGCGGCCTCTC
3261 mir-212-precNo2 0.26 CGGACAGCGCGCCGGCACCTTGGCTCTAGACTGCTTACTG
3262 Hcd913 right 0.34 CAAACATCATGTGACGTCTGTGGAGCGGCGGCGGCGGCGG
3263 Hcd716 right 0.48 CAATAAATGTGCCTATAAAGGCGCCGGCTCCGGGGCGCGG
3264 MPR207 right 0.3 AACAACTTTGTGCTGGTGCCGGGGAAGTTTGTGTCTCCTA
3265 HPR206 left 0.26 CTATATTGGACCGCAGCGCTGAGAGCTTTTGTGTTTAATG
3266 mir-016b-chr3 0.29 GTTCCACTCTAGCAGCACGTAAATATTGGCGTAGTGAAAT
3267 Hcd654 left 0.34 AACGAGTAAAAGGCGTACATGGGAGCGCGGGGCGGCAGAG
3268 mir-195-prec 0.3 TCTAGCAGCACAGAAATATTGGCACAGGGAAGCGAGTCTG
3269 Hcd425 left 0.25 GGTTCTACTCTCTTACCCCTCCCCCACGTGGTTGTTGCTG
3270 mir-148aNol 0.35 TGAGTATGATAGAAGTCAGTGCACTACAGAACTTTGTCTC
3271 mir-142-prec 0.36 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
3272 mir-016a-chrl3 0.25 CAATGTCAGCAGTGCCTTAGCAGCACGTAAATATTGGCGT
Table 132 . Ifosfamide microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
3273 mir-092-prec-X=092-2 0.28 GTTCTATATAAAGTATTGCACTTGTCCCGGCCTGTGGAAG
3274 mir-181b-2Nol 0.28 CTGATGGCTGCACTCAACATTCATTGCTGTCGGTGGGTTT
3275 Hcd417 right 0.28 GGATTTAATGAGAAATATTGAGCCCTTTGGTTCAGGAACT
3276 Hcd440 HPR257 right 0.28 GCTCTGTTGTGATAAATTGGCTGTGTGCTTCATTTGGACT
3277 mir-019b-2-prec 0.25 GTGGCTGTGCAAATCCATGCAAAACTGATTGTGATAATGT
3278 mir-213-precNol 0.39 AACATTCATTGCTGTCGGTGGGTTGAACTGTGTGGACAAG
3279 mir-033-prec 0.29 GTGGTGCATTGTAGTTGCATTGCATGTTCTGGTGGTACCC
3280 mir-092-prec-13=092-lNo2 0.3 TCTGTATGGTATTGCACTTGTCCCGGCCTGTTGAGTTTGG
3281 mir-181b-precNol 0.36 TGAGGTTGCTTCAGTGAACATTCAACGCTGTCGGTGAGTT
3282 mir-128b-precNol 0.46 TCACAGTGAACCGGTCTCTTTCCCTACTGTGTCACACTCC
3283 mir-526a-2No2 0.29 GAAAAGAACATGCATCCTTTCAGAGGGTTACTCTTTGAGA
3284 MPR95 left 0.25 TTGTTGGACACTCTTTCCCTGTTGCACTACTGTGGGCCTC
3285 HPR220 right 0.27 GAGCATCAGTATGTAGTGCAATCAGTCAGGAGAAAATGAG
3286 mir-133a-l 0.35 CCTCTTCAATGGATTTGGTCCCCTTCAACCAGCTGTAGCT
3287 mir-148aNol 0.3 TGAGTATGATAGAAGTCAGTGCACTACAGAACTTTGTCTC
3288 mir-142-prec 0.4 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
3289 HPR169 right 0.26 GTTTCTTTCTCACGGTAACTGGCAGCCTCGTTGTGGGCTG
3290 mir-223-prec 0.38 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT
3291 mir-018-prec 0.27 TAAGGTGCATCTAGTGCAGATAGTGAAGTAGATTAGCATC
3292 mir-020-prec 0.25 TAAAGTGCTTATAGTGCAGGTAGTGTTTAGTTATCTACTG
3293 mir-484 0.27 GTCAGGCTCAGTCCCCTCCCGATAAACCCCTAAATAGGGA
Table 133 Tamoxifen microRNA biomarkers .
SEQIDNO Medianprobe Corr Sequence
3294 mir-092-prec-X=092-2 0.31 GTTCTATATAAAGTATTGCACTTGTCCCGGCCTGTGGAAG
3295 Hcd547 left 0.27 AAAATCAGCTTTAATTAATTTGAGTGCCAGCTCTGTGTAT
3296 Hcd257 left 0.27 CTTCTTGTATAAGCACTGTGCTAAAATTGCAGACACTAGG
3297 mir-148-prec 0.27 TGAGTATGATAGAAGTCAGTGCACTACAGAACTTTGTCTC
3298 HUMTRS 0.25 TCTAGCGACAGAGTGGTTCAATTCCACCTTTCGGGCGCCA
3299 mir-033-prec 0.27 GTGGTGCATTGTAGTTGCATTGCATGTTCTGGTGGTACCC
3300 mir-092-prec-13=092-1NO2 0.25 TCTGTATGGTATTGCACTTGTCCCGGCCTGTTGAGTTTGG
3301 mir-375 0.46 TTTTGTTCGTTCGGCTCGCGTGAGGCAGGGGCGGCCTCTC
3302 mir -095-prec-4 0.28 CGTTACATTCAACGGGTATTTATTGAGCACCCACTCTGTG
3303 mir -025-prec 0.35 ACGCTGCCCTGGGCATTGCACTTGTCTCGGTCTGACAGTG
3304 mir -202-prec 0.34 GATCTGGCCTAAAGAGGTATAGGGCATGGGAAGATGGAGC
3305 mir -007-1-prec 0.26 TGTTGGCCTAGTTCTGTGTGGAAGACTAGTGATTTTGTTG
3306 mir -093-prec-7.1=093-1 0.44 CCAAAGTGCTGTTCGTGCAGGTAGTGTGATTACCCAACCT
3307 mir -106-prec-X 0.31 CCTTGGCCATGTAAAAGTGCTTACAGTGCAGGTAGCTTTT
3308 mir -142-prec 0.25 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG
3309 mir -223-prec 0.25 GAGTGTCAGTTTGTCAAATACCCCAAGTGCGGCACATGCT
3310 mir -018-prec 0.26 TAAGGTGCATCTAGTGCAGATAGTGAAGTAGATTAGCATC
Table 134 . . FFllooxxuurriiddiinnee mmiiccrrrooRRNNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
3311 HUMTRF 0.27 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
3312 HUMTRN 0.27 CAATCGGTTAGCGCGTTCGGCTGTTAACCGAAAGGTTGGT
3313 mir-124a-l-precl 0.31 ATACAATTAAGGCACGCGGTGAATGCCAAGAATGGGGCTG
3314 mir-150-prec 0.33 CTCCCCATGGCCCTGTCTCCCAACCCTTGTACCAGTGCTG
3315 Hcd923 left 0.26 TGGGAACCTTGTTAAAATGCAGATTCTGATTCTCAGGTCT
3316 HPR181 left 0.28 GAAGAAACATCTCAAATCATGCTGACAGCATTTTCACTAT
3317 Hcd569 right 0.26 TTATTGCTTGAATGAGTTTCAGGGTATTGGCCTTCATAAA
3318 mir-199a-2-prec 0.25 TCGCCCCAGTGTTCAGACTACCTGTTCAGGACAATGCCGT
3319 Hcd754 left 0.28 TCCTCCTCCTCCTTTTCGTTCCGGCTCCCTGGCTGGCTCC
3320 mir-4323p 0.3 CCTTACGTGGGCCACTGGATGGCTCCTCCATGTCTTGGAG
Table 135. Irinotecan microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
3321 HUMTRF 0.27 GATCTAAAGGTCCCTGGTTCGATCCCGGGTTTCGGCACCA
3322 mir-380-5p 0.27 AGGTACCTGAAAAGATGGTTGACCATAGAACATGCGCTAT 3323 mir-342Nol 0.25 GTCTCACACAGAAATCGCACCCGTCACCTTGGCCTACTTA 3324 mir-142-prec 0.35 CCCATAAAGTAGAAAGCACTACTAACAGCACTGGAGGGTG 3325 Hcd200 right 0.25 CAATTAGCCAATTGTGGGTATAATTAGCTGCATGTAGAAT
Table 136. Satraplatm microRNA biomarkers.
SEQIDNO Medianprobe Corr Sequence
3326 Hcd289 left 0.31 TTCCTCTCAGAGCATGTTGTCATAGAAGTAAATGAAAAGG
3327 Hcd939 right 0.25 CTCTCCTGCACATAATGAGGTCTGATTTACTGTGATCATT
3328 Hcd330 right 0.28 ATTAATGGTAATTATGTGCGTAAATCCCCATGCTCTCAAT
3329 HPR76 right 0.25 GAGCCGTTTAAATTTAGCGCTTTGGGCTGCCTGGAGCGAG
3330 Hcdlll left 0.29 GCAGGGGATTTGAGGGGTGGTTGTGTGATTTGTACAGCTG
3331 Hcd976 right 0.36 CTTCTCAGAGTTGGAGATGAAAGAAAGAGAAGGTGGCCAC
3332 mir-15aNol 0.29 CCTTGGAGTAAAGTAGCAGCACATAATGGTTTGTGGATTT
3333 mir-OOlb-1-precl 0.26 AATGCTATGGAATGTAAAGAAGTATGTATTTTTGGTAGGC
3334 mir-450-1 0.36 AACGATACTAAACTGTTTTTGCGATGTGTTCCTAATATGC
3335 mir-200bNo2 0.3 CCAGCTCGGGCAGCCGTGGCCATCTTACTGGGCAGCATTG
3336 Hcd578 right 0.3 AATGATTGTAGAGGGGCGGGGCATGAAGAGTGCCGTTCTG
3337 mir-200a-prec 0.28 GTCTCTAATACTGCCTGGTAATGATGACGGCGGAGCCCTG
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