Field of the invention

The present invention relates inter alia to methods of determining the margin of a tumour of squamous cell carcinoma (SCC). In certain embodiments, the invention relates to determining the expression of Ambra-1 and p62 in one or more sections of tissue peripheral to the tumour. The invention further relates to methods of excising tumours, and to related assays and kits.

Background to the invention

SCC (also known as epidermoid carcinoma) comprises a range of cancer types that result from squamous cells. These cells form the surface of skin, the lining of hollow organs in the body and the lining of the respiratory and digestive tracts.

SCC comprises one of the largest subsets of cancer. For example, cutaneous squamous cell carcinoma (cSCC) is the second most common form of skin cancer with an increasing worldwide incidence. Recent figures report over 2 million new cases of cSCC diagnosed annually across the world, 40,000 of these in the UK alone. The incidence of cSCC has increased by 50-200% in the last 30 years depending on country. It makes up about 20% of all skin cancer cases. cSCC arises from keratinocyte skin cells of the epidermis. cSCC is locally invasive and has the capacity to metastasise. In particular, cSCC can spread to draining lymph nodes or to distant sites of the body via entry into the bloodstream.

As with many cancers, prognosis and survival for cSCC is highly dependent on early diagnosis and treatment. Surgical excision with a predetermined clinical margin is the recommended treatment for the majority of cSCC. For clinically well-defined, low-risk tumours, a clinical margin of 4 mm will achieve histological clearance in over 95 per cent of cases. In invasive cSCC, however, the evidence on peripheral margins required is limited.

A major challenge with the management of SCC therefore relates to the accurate determination of the margin of tumours. Typically, clinicians focus on examination of the horizontal extensibility of the tumour to determine the safety margin for complete resection. However, it is often difficult to determine where the tumour ends and the normal tissue begins due to varying degrees of abnormal cells (dysplasia) surrounding tumours leading to incomplete resection of the tumour and facilitating recurrence or spread (metastasis). Thus, there remains a need to identify tools that allow accurate determination and excision of tumours of SCC.

It is an aim of certain embodiments of the present invention to at least party mitigate the above- mentioned problems associated with the prior art.

Summary of certain embodiments of the invention

Certain aspects of the present invention relate to the identification of biomarkers to accurately determine the margins of tumours. The combination of Ambra-1 and p62 markers is shown to accurately distinguish tumour positive and tumour negative tissue at the peripheral margin of a tumour. This allows the margin of a tumour to be determined in order to refine complete excision of the tumour.

Accordingly, the invention provides:

a method of determining the margin of a tumour in a tissue sample obtained from a subject with SCC, the method comprising:

(i) determining the expression of Ambra-1 and p62 in one or more sections of tissue peripheral to the tumour; and

(ii) comparing the expression obtained in (i) with reference tissue or levels obtained therefrom,

wherein a decrease or loss in expression of Ambra-1 and an increase in p62 expression compared to the reference tissue or levels is indicative of tumour positive tissue; and/or wherein no significant difference in expression of Ambra-1 and p62 expression compared to the reference tissue or levels is indicative of tumour negative tissue; a method of excising a tumour from a subject with SCC, the method comprising:

(i) excising one or more sections of tissue peripheral to the tumour to obtain a tissue sample from the subject; and

(ii) determining the margin of the tumour in the tissue sample according to any method described herein; an in vitro assay for determining the margin of a tumour in a tissue sample, the assay comprising:

(i) contacting one or more sections of tissue peripheral to the tumour with a first ligand specific for Ambra-1 , wherein the presence of Ambra-1 creates an Ambra-1 - ligand complex; (ii) contacting the one or more sections of tissue peripheral to the tumour with a second ligand specific for p62, wherein the presence of p62 creates a p62 - ligand complex; and

(iii) detecting and/or quantifying the Ambra-1 - ligand complex and p62-ligand complex; and a kit for determining the margin of a tumour in a tissue sample, the kit comprising: a first ligand specific for Ambra-1 ; and

a second ligand specific for p62.

Detailed description of certain embodiments

Embodiments of the present invention will now be described hereinafter, by way of example only, with reference to the accompanying drawings in which:

Figure 1 shows that AMBRA1 is a biomarker of keratinocyte differentiation. A: schematic and representative IHC expression of AMBRA1 in normal skin. Ambra-1 expression is low within the basal layer but increases throughout the stratum spinosum and stratum corneum. Scale bar: 100mm. B&C: Immunoblot of AMBRA 1, Loricrin, GAPDH or b Actin expression in CCD1 106 (B) or primary keratinocytes (C) in the presence or absence of culture in 1 .3mM calcium chloride for 5 days.

Figure 2 shows AMBRA1 is required for normal keratinocyte differentiation. A: immunoblot or B: relative AMBRA 1 or Loricrin protein or mRNA levels in primary keratinocytes following siRNA AMBRA1 . C: Mean proliferation of primary keratinocytes following siAMBRAI or transfection with non-targeting control siRNA (siCTRL).

Figure 3 shows representative immunochemistry images of stained epidermis, illustrating strongly stained normal epidermis (A), clusters of cells with decreased expression of Ambra- 1 representing carcinoma in-situ (B). Figure 3C and D both illustrate relatively high expression of Ambra-1 in well-differentiated SCC. Figure 3E and F show decreased expression in poorly differentiated (aggressive type) SCC.

Figure 4 shows progression of keratinocyte dysplasia from normal epidermis, to in-situ and invasive well- and poorly differentiated SCC is associated with changes in expression of AMBRA1 and p62. A, B: Ambra-1 expression in normal epidermis (adjacent to SCC) increases in line with keratinocyte differentiation from the basal layer to the stratum corneum whilst nuclear p62 expression decreases with differentiation. C, D: in-situ SCC (*) involving the epidermis only, is associated with loss of Ambra-1 expression, but an increase in p62 expression. E, F: Well differentiated invasive SCC is associated with a relative increase of Ambra-1 expression within the tumour (*) compared to normal epidermis, with increased nuclear p62 levels. Scale bars = 100mm.

Figure 5 shows nuclear p62 is a potential marker of epidermal dysplasia. A: p62 expression within the normal epidermis (n) contains little nuclear p62 expression. p62 nuclear expression increases in epidermis adjacent to SCCs (*; the invasive SCC is situated to the left of the image) and is associated with areas of solar elastosis (s) as a marker of UV dermal collagen damage. B: p62 nuclear and cytoplasmic expression increases in areas of actinic keratosis represented by dysplasia and hyperkeratosis (*). C: Areas of in-situ SCC (Bowen’s disease) are associated with full epidermal thickness dysplasia, hyperkeratosis and greatly increased cytoplasmic p62 expression (*). Scale bar = 100mm.

Sequence listing

SEQ ID NO: 1 shows the amino acid sequence of HCDR1 of the anti-Ambra-1 antibody AbD33473 (SYWIH) ;

SEQ ID NO: 2 shows the amino acid sequence of HCDR2 of the anti-Ambra-1 antibody AbD33473 (TIFPSRSYTTYSPSFQG) ;

SEQ ID NO: 3 shows the amino acid sequence of HCDR3 of the anti-Ambra-1 antibody AbD33473 (DTPSTALKSPFDY) ;

SEQ ID NO: 4 shows the amino acid sequence of LCDR1 of the anti-Ambra-1 antibody AbD33473 (SGSSSNIGYNYVY) ;

SEQ ID NO: 5 shows the amino acid sequence of LCDR2 of the anti-Ambra-1 antibody AbD33473 (ENNKRPS) ;

SEQ ID NO: 6 shows the amino acid sequence of LCDR3 of the anti-Ambra-1 antibody AbD33473 (SSWDSHSNSYV) ;

SEQ ID NO: 7 shows the amino acid sequence of HCFR1 of the anti-Ambra-1 antibody AbD33473 (EVQLVQSGAEVKKPGESLKISCKGSGYSFS ) ;

SEQ ID NO: 8 shows the amino acid sequence of HCFR2 of the anti-Ambra-1 antibody AbD33473 (WVRQMPGKGLEWMG) ;

SEQ ID NO: 9 shows the amino acid sequence of HCFR3 of the anti-Ambra-1 antibody AbD33473 (QVTISADKSISTAYLQWSSLKASDTAMYYCAR) ;

SEQ ID NO: 10 shows the amino acid sequence of HCFR4 of the anti-Ambra-1 antibody AbD33473 (WGQGTLVTVSS ) ; SEQ ID NO: 1 1 shows the amino acid sequence of LCFR1 of the anti-Ambra-1 antibody AbD33473 (DIVLTQPPSVSGAPGQRVTISC) ;

SEQ ID NO: 12 shows the amino acid sequence of LCFR2 of the anti-Ambra-1 antibody AbD33473 (WYQQLPGTAPKLLIY) ;

SEQ ID NO: 13 shows the amino acid sequence of LCFR3 of the anti-Ambra-1 antibody AbD33473 (GVPDRFSGSKSGTSASLAITGLQAEDEADYYC) ;

SEQ ID NO: 14 shows the amino acid sequence of LCFR4 of the anti-Ambra-1 antibody AbD33473 (FGGGTKLTVLGQ) ;

SEQ I D NO: 15 shows the amino acid sequence of the V _H domain of the anti-Ambra-1 antibody AbD33473;

EVQLVQSGAEVKKPGESLKISCKGSGYSFSSYWIHWVRQMPGKGLEWMGTIFPSRSYTTY SPSFQGQV

TISADKSISTAYLQWSSLKASDTAMYYCARDTPSTALKSPFDYWGQGTLVTVSS

SEQ ID NO: 16 shows the amino acid sequence of the VL domain of the anti-Ambra-1 antibody AbD33473;

DIVLTQPPSVSGAPGQRVTISCSGSSSNIGYNYVYWYQQLPGTAPKLLIYENNKRPSGVP DRFSGSKS

GTSASLAITGLQAEDEADYYCSSWDSHSNSYVFGGGTKLTVLGQ

SEQ ID NO: 17 shows the amino acid sequence of the Fd chain (V _H domain and constant domain) of the Fab region of the anti-Ambra-1 antibody AbD33473;

EVQLVQSGAEVKKPGESLKISCKGSGYSFSSYWIHWVRQMPGKGLEWMGTIFPSRSYTTY SPSFQGQVTISADKS ISTAYLQWSSLKASDTAMYYCARDTP STALKSPFDYWGQGTLVTVSSASTKGPSVFPLAP SSKSTSGGTAALGCL VKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHK PSNTKVDKKVEPKS

SEQ ID NO: 18 shows the amino acid sequence of the light chain (VL domain and constant domain) of the Fab region of the anti-Ambra-1 antibody AbD33473;

DIVLTQPP SVSGAPGQRVTI SCSGSSSNIGYNYVYWYQQLPGTAPKLLIYENNKRP SGVPDRFSGSKSGTSASL AITGLQAEDEADYYCSSWDSHSNSYVFGGGTKLTVLGQPKAAPSVTLFPP SSEELQANKATLVCLI SDFYPGAV TVAWKADSSPVKAGVETTTP SKQSNNKYAASSYLSLTPEQWKSHRSYSCQVTHEGSTVEKTVAPTEA

SEQ ID NO: 19 shows the nucleic acid sequence encoding the Fd chain of the Fab region and tags (alkaline phosphatase dimerization domain sequence (AP), FLAG tag (DYKDDDDK) and His6 tag of the anti-Ambra-1 antibody AbD33473;

GAAGTGCAATTGGTGCAGAGCGGTGCGGAAGTGAAAAAACCGGGCGAAAGCCTGAAAATT AGCTGCAAAGGCTC CGGATATAGCTTCTCTTCTTACTGGATCCATTGGGTGCGCCAGATGCCGGGCAAAGGTCT CGAGTGGATGGGCA CTATCTTCCCGTCTCGTAGCTACACCACTTATAGCCCGAGCTTTCAGGGCCAGGTGACCA TTAGCGCGGATAAA AGCATCAGCACCGCGTATCTGCAATGGAGCAGCCTGAAAGCGAGCGATACCGCGATGTAT TATTGCGCGCGTGA CACTCCGTCTACTGCTCTGAAATCTCCGTTCGATTACTGGGGCCAAGGCACCCTGGTGAC TGTTAGCTCAGCGT CGACCAAAGGCCCGAGCGTGTTTCCGCTGGCCCCGAGCAGCAAAAGCACCAGCGGCGGCA CCGCCGCACTGGGC TGCCTGGTGAAAGATTATTTCCCGGAACCAGTGACCGTGAGCTGGAACAGCGGTGCCCTG ACCAGCGGCGTGCA TACCTTTCCGGCGGTGCTGCAAAGCAGCGGCCTGTATAGCCTGAGCAGCGTTGTGACCGT GCCGAGCAGCAGCC TGGGCACCCAGACCTATATTTGCAACGTCAACCATAAACCGAGCAACACCAAAGTCGATA AAAAAGTCGAACCG AAAAGCGAATTCAAGGCTGAAATGCCTGTTCTGGAAAACCGGGCTGCTCAGGGCGATATT ACTACACCCGGCGG TGCTCGCCGTTTAACGGGTGATCAGACTGCCGCTCTGCGTGATTCTCTTAGCGATAAACC TGCAAAAAATATTA TTTTGCTGATTGGCGATGGGATGGGGGACTCGGAAATTACTGCCGCACGTAATTATGCCG AAGGTGCGGGCGGC _{TTTTTTAAAGGTATAGATGCCTTACCGCTTACCGGGCAATACACTCACTATGCGC TGAATAGAAAAACCGGCAA}

ACCGGACTACGTCACCAGCTCGGCTGCATCAGCAACCGCCTGGTCAACCGGTGTCAA AACCTATAACGGCGCGC

TGGGCGTCGATATTCACGAAAAAGATCACCCAACGATTCTGGAAATGGCAAAAGCCG CAGGTCTGGCGACCGGT

AACGTTTCTACCGCAGAGTTGCAGGATGCCACGCCCGCTGCGCTGGTGGCACATGTG ACCTCGCGCAAATGCTA

CGGTCCGAGCGCGACCAGTGAAAAATGTCCGGGTAACGCTCTGGAAAAAGGCGGAAA AGGATCGATTACCGAAC

AGCTGCTTAACGCTCGTGCCGACGTTACGCTTGGCGGCGGCGCAAAAACCTTTGCTG AAACGGCAACCGCTGGT

GAATGGCAGGGAAAAACGCTGCGTGAACAGGCACAGGCGCGTGGTTATCAGTTGGTG AGCGATGCTGCCTCACT

GAACTCGGTGACGGAAGCGAATCAGCAAAAACCCCTGCTTGGCCTGTTTGCTGACGG CAATATGCCAGTGCGCT

GGCTAGGACCGAAAGCAACGTACCATGGCAATATCGATAAGCCCGCAGTCACCTGTA CGCCAAATCCGCAACGT

AATGACAGTGTACCAACCCTGGCGCAGATGACCGACAAAGCCATTGAATTGTTGAGT AAAAATGAGAAAGGCTT

TTTCCTGCAAGTTGAAGGTGCGTCAATCGATAAACAGGATCATGCTGCGAATCCTTG TGGGCAAATTGGCGAGA

CGGTCGATCTCGATGAAGCCGTACAACGGGCGCTGGAGTTCGCTAAAAAGGAGGGTA ACACGCTGGTCATAGTC

ACCGCTGATCACGCCCACGCCAGCCAGATTGTTGCGCCGGATACCAAAGCTCCGGGC CTCACCCAGGCGCTAAA

TACCAAAGATGGCGCAGTGATGGTGATGAGTTACGGGAACTCCGAAGAGGATTCACA AGAACATACCGGCAGTC

AGTTGCGTATTGCGGCGTATGGCCCGCATGCCGCCAATGTTGTTGGACTGACCGACC AGACCGATCTCTTCTAC

ACCATGAAAGCCGCTCTGGGGCTGAAAGGCGCGCCGGACTATAAAGATGACGATGAC AAAGGCGCGCCGCACCA

TCATCACCATCAC

SEQ ID NO: 20 shows the nucleic acid sequence encoding the light chain of the Fab region of the anti-Ambra-1 antibody AbD33473;

GATATCGTGCTGACCCAGCCGCCGAGCGTGAGCGGTGCACCGGGCCAGCGCGTGACCATT AGCTGTAGCGGCAG CAGCAGCAACATTGGTTACAACTACGTGTACTGGTACCAGCAGCTGCCGGGCACGGCGCC GAAACTGCTGATCT ACGAAAACAACAAACGCCCGAGCGGCGTGCCGGATCGCTTTAGCGGATCCAAAAGCGGCA CCAGCGCCAGCCTG GCGATTACCGGCCTGCAAGCAGAAGACGAAGCGGATTATTACTGCTCTTCTTGGGACTCT CATTCTAACTCTTA CGTGTTTGGCGGCGGCACGAAGTTAACCGTTCTTGGCCAGCCGAAAGCCGCCCCAAGCGT GACCCTGTTTCCGC CGAGCAGCGAAGAACTGCAAGCCAACAAAGCCACCCTGGTTTGCCTGATCAGCGATTTTT ATCCGGGTGCCGTG ACCGTGGCCTGGAAAGCCGATAGCAGCCCGGTGAAAGCCGGCGTGGAAACCACCACCCCG AGCAAACAGAGCAA CAACAAATATGCCGCCAGCAGCTATCTGAGCCTGACCCCGGAACAGTGGAAAAGCCATCG CAGCTATAGTTGTC AAGTGACCCATGAAGGCAGCACCGTGGAAAAAACCGTGGCCCCGACCGAGGCC

SEQ ID NO: 21 shows the amino acid sequence of human Ambra-1 ;

MKWPEKNAVRILWGRERGARAMGAQRLLQELVEDKTRWMKWEGKRVELPDSPRSTFLLAF SPDRTLLASTHVNH NIYITEVKTGKCVHSLIGHRRTPWCVTFHPTI SGLIASGCLDGEVRIWDLHGGSESWFTDSNNAIASLAFHPTAQ LLLIATANEIHFWDWSRREPFAWKTASEMERVRLVRFDPLGHYLLTAIVNP SNQQGDDEPEIP IDGTELSHYRQ RALLQSQPVRRTPLLHNFLHMLSSRSSGIQVGEQSTVQDSATPSPPPPPPQP STERPRTSAYIRLRQRVSYPTAE CCQHLGILCLCSRCSGTRVP SLLPHQDSVPPASARATTPSFSFVQTEPFHPPEQASSTQQDQGLLNRP SAFSTVQ SSTAGNTLRNLSLGPTRRSLGGPLSSHP SRYHREIAPGLTGSEWTRTVLSLNSRSEAESMPPPRTSASSVSLLSV LRQQEGGSQASVYTSATEGRGFPASGLATESDGGNGSSQNNSGSIRHELQCDLRRFFLEY DRLQELDQSLSGEAP QTQQAQEMLNNNIESERPGPSHQPTPHSSENNSNLSRGHLNRCRACHNLLTFNNDTLRWE RTTPNYSSGEASSSW QVPSSFESVPSSGSQLPPLERTEGQTPSSSRLELSSSASPQEERTVGVAFNQETGHWERI YTQSSRSGTVSQEAL HQDMPEESSEEDSLRRRLLESSLI SLSRYDGAGSREHP IYPDPARLSPAAYYAQRMIQYLSRRDSIRQRSMRYQQ NRLRSSTSSSSSDNQGPSVEGTDLEFEDFEDNGDRSRHRAPRNARMSAPSLGRFVPRRFL LPEYLPYAGIFHERG QPGLATHSSVNRVLAGAVIGDGQSAVASNIANTTYRLQWWDFTKFDLPEI SNASVNVLVQNCKIYNDASCDI SAD GQLLAAFIPSSQRGFPDEGILAVYSLAPHNLGEMLYTKRFGPNAISVSLSPMGRYVMVGL ASRRILLHPSTEHMV AQVFRLQQAHGGETSMRRVFNVLYPMPADQRRHVSINSARWLPEPGLGLAYGTNKGDLVI CRPEALNSGVEYYWD QLNETVFTVHSNSRSSERPGTSRATWRTDRDMGLMNAIGLQPRNPATSVTSQGTQTLALQ LQNAETQTEREVPEP GTAASGPGEGEGSEYGASGEDALSRIQRLMAEGGMTAVVQREQSTTMASMGGFGNNIIVS HRIHRSSQTGTEPGA AHTSSPQPSTSRGLLPEAGQLAERGLSPRTASWDQPGTPGREPTQPTLPSSSPVPIPVSL PSAEGPTLHCELTNN NHLLDGGSSRGDAAGPRGEPRNR

SEQ ID NO: 22 shows the amino acid sequence of the peptide to which anti-Ambra-1 antibodies were raised (CGGSSRGDAAGPRGEPRNR) ; SEQ ID NO: 23 shows the amino acid sequence of HCDR1 of anti-p62 antibody AbD34907

(TYYLH) ;

SEQ ID NO: 24 shows the amino acid sequence of HCDR2 of the anti-p62 antibody AbD34907; LINPNNGGTNYAQKFQG

SEQ ID NO: 25 shows the amino acid sequence of HCDR3 of the anti-p62 antibody AbD34907;

GPGRLRPFGLYFDV

SEQ ID NO: 26 shows the amino acid sequence of LCDR1 of the anti-p62 antibody AbD34907;

RASQGIYTFLN SEQ ID NO: 27 shows the amino acid sequence of LCDR2 of the anti-p62 antibody AbD34907;

AASTLQS

SEQ ID NO: 28 shows the amino acid sequence of LCDR3 of the anti-p62 antibody AbD34907;

FQYSSWPRT

SEQ ID NO: 29 shows the amino acid sequence of HCFR1 of the anti-p62 antibody AbD34907;; QVQLVQSGAEVKKPGASVKVSCKASGYTFN

SEQ ID NO: 30 shows the amino acid sequence of HCFR2 of the anti-p62 antibody AbD34907;

WVRQAPGQGLEWMG

SEQ ID NO: 31 shows the amino acid sequence of HCFR3 of the anti-p62 antibody AbD34907;

RVTMTRDTSI STAYMELSRLRSEDTAVYYCAR SEQ ID NO: 32 shows the amino acid sequence of HCFR4 of the anti-p62 antibody AbD34907;

WGQGTLVTVSS

SEQ ID NO: 33 shows the amino acid sequence of LCFR1 of the anti-p62 antibody AbD34907;

DIQMTQSP SSLSASVGDRVTITC

SEQ ID NO: 34 shows the amino acid sequence of LCFR2 of the anti-p62 antibody AbD34907; WYQQKPGKAPKLLIY

SEQ ID NO: 35 shows the amino acid sequence of LCFR3 of the anti-p62 antibody AbD34907;

GVPSRFSGSGSGTDFTLTISSLQPEDFATYYC SEQ ID NO: 36 shows the amino acid sequence of LCFR4 of the anti-p62 antibody AbD34907;

FGQGTKVEIK

SEQ ID NO: 37 shows the amino acid sequence of the V _H domain of the anti-p62 antibody AbD34907;

QVQLVQSGAEVKKPGASVKVSCKASGYTFNTYYLHWVRQAPGQGLEWMGLINPNNGGTNY AQKFQGRVTMTRDTS

ISTAYMELSRLRSEDTAVYYCARGPGRLRPFGLYFDVWGQGTLVTVSS

SEQ ID NO: 38 shows the amino acid sequence of the VL domain of the anti-p62 antibody AbD34907;

DIQMTQSP SSLSASVGDRVTITCRASQGIYTFLNWYQQKPGKAPKLLIYAASTLQSGVPSRFSGSGSG TDFTLTI SSLQPEDFATYYCFQYSSWPRTFGQGTKVEIK

SEQ ID NO: 39 shows the amino acid sequence of the Fd chain (V _H domain and constant domain) of the Fab region of the anti-p62 antibody AbD34907;

QVQLVQSGAEVKKPGASVKVSCKASGYTFNTYYLHWVRQAPGQGLEWMGLINPNNGGTNY AQKFQGRVTMTRDTS ISTAYMELSRLRSEDTAVYYCARGPGRLRPFGLYFDVWGQGTLVTVSSASTKGP SVFPLAPSSKSTSGGTAALGC LVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSWTVPSSSLGTQTYICNVNHK P SNTKVDKKVEPKS

SEQ ID NO: 40 shows the amino acid sequence of the light chain (VL domain and constant domain) of the Fab region of the anti-p62 antibody AbD34907;

DIQMTQSPSSLSASVGDRVTITCRASQGIYTFLNWYQQKPGKAPKLLIYAASTLQSGVPS RFSGSGSGTDFTLTI SSLQPEDFATYYCFQYSSWPRTFGQGTKVEIKRTVAAP SVFIFPPSDEQLKSGTASWCLLNNFYPREAKVQWKV DNALQSGNSQESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFN RGEA

SEQ ID NO: 41 shows the amino acid sequence of HCDR1 of anti-p62 antibody AbD34908;

NYWIG

SEQ ID NO: 42 shows the amino acid sequence of HCDR2 of the anti-p62 antibody AbD34908;

IIDPSGSFTRYSPSFQG

SEQ ID NO: 43 shows the amino acid sequence of HCDR3 of the anti-p62 antibody AbD34908;

KYVPPVYSYWSYGTLDV

SEQ ID NO: 44 shows the amino acid sequence of LCDR1 of the anti-p62 antibody AbD34908;

RASQSVSASRLA

SEQ ID NO: 45 shows the amino acid sequence of LCDR2 of the anti-p62 antibody AbD34908;

GSSTRAT

SEQ ID NO: 46 shows the amino acid sequence of LCDR3 of the anti-p62 antibody AbD34908;

QQYLHLYT SEQ ID NO: 47 shows the amino acid sequence of HCFR1 of the anti-p62 antibody AbD34908;

EVQLVQSGAEVKKPGESLKI SCKGSGYSFT

SEQ ID NO: 48 shows the amino acid sequence of HCFR2 of the anti-p62 antibody AbD34908;

WVRQMPGKGLEWMG

SEQ ID NO: 49 shows the amino acid sequence of HCFR3 of the anti-p62 antibody AbD34908;

QVTI SADKSI STAYLQWSSLKASDTAMYYCAR

SEQ ID NO: 50 shows the amino acid sequence of HCFR4 of the anti-p62 antibody AbD34908;

WGQGTLVTVSS

SEQ ID NO: 51 shows the amino acid sequence of LCFR1 of the anti-p62 antibody AbD34908;

DIVLTQSPATLSLSPGERATLSC

SEQ ID NO: 52 shows the amino acid sequence of LCFR2 of the anti-p62 antibody AbD34908;

WYQQKPGQAPRLLIY

SEQ ID NO: 53 shows the amino acid sequence of LCFR3 of the anti-p62 antibody AbD34908;

GIPARFSGSGSGTDFTLTISSLEPEDFAVYYC

SEQ ID NO: 54 shows the amino acid sequence of LCFR4 of the anti-p62 antibody AbD34908;

FGQGTKVEIK

SEQ ID NO: 55 shows the amino acid sequence of the V _H domain of the anti-p62 antibody AbD34908;

EVQLVQSGAEVKKPGESLKI SCKGSGYSFTNYWIGWVRQMPGKGLEWMGI IDPSGSFTRYSP SFQGQVTI SADKS ISTAYLQWSSLKASDTAMYYCARKYVPPVYSYWSYGTLDVWGQGTLVTVSS

SEQ ID NO: 56 shows the amino acid sequence of the Vi _. domain of the anti-p62 antibody AbD34908;

DIVLTQSPATLSLSPGERATLSCRASQSVSASRLAWYQQKPGQAPRLLIYGSSTRATGIP ARFSGSGSGTDFTLT

ISSLEPEDFAVYYCQQYLHLYTFGQGTKVEIK

SEQ ID NO: 57 shows the amino acid sequence of the Fd chain (VH domain and constant domain) of the Fab region of the anti-p62 antibody AbD34908;

EVQLVQSGAEVKKPGESLKI SCKGSGYSFTNYWIGWVRQMPGKGLEWMGI IDPSGSFTRYSP SFQGQVTI SADKS ISTAYLQWSSLKASDTAMYYCARKYVPPVYSYWSYGTLDVWGQGTLVTVSSASTKGPSVF PLAP SSKSTSGGTAA LGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICN VNHKPSNTKVDKKVE PKS SEQ ID NO: 58 shows the amino acid sequence of the light chain (VL domain and constant domain) of the Fab region of the anti-p62 antibody AbD34908;

DIVLTQSPATLSLSPGERATLSCRASQSVSASRLAWYQQKPGQAPRLLIYGSSTRATGIP ARFSGSGSGTDFTLT ISSLEPEDFAVYYCQQYLHLYTFGQGTKVEIKRTVAAP SVFIFPPSDEQLKSGTASWCLLNNFYPREAKVQWKV DNALQSGNSQESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFN RGEA

SEQ ID NO: 59 shows full amino acid sequence of the anti-p62 antibody AbD34907 including alkaline phosphatase dimerization domain sequence (AP), FLAG and His6 tag;

DIQMTQSP SSLSASVGDRVTITCRASQGIYTFLNWYQQKPGKAPKLLIYAASTLQSGVPSRFSGSGSG TDFTLTI SSLQPEDFATYYCFQYSSWPRTFGQGTKVEIKRTVAAP SVFIFPPSDEQLKSGTASWCLLNNFYPREAKVQWKV DNALQSGNSQESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFN RGEA*QVQLVQSGAE VKKPGASVKVSCKASGYTFNTYYLHWVRQAPGQGLEWMGLINPNNGGTNYAQKFQGRVTM TRDTSI STAYMELSR LRSEDTAVYYCARGPGRLRPFGLYFDVWGQGTLVTVSSASTKGP SVFPLAPSSKSTSGGTAALGCLVKDYFPEPV TVSWNSGALTSGVHTFPAVLQSSGLYSLSSWTVPSSSLGTQTYICNVNHKP SNTKVDKKVEPKSEFKAEMPVLE NRAAQGDITTPGGARRLTGDQTAALRDSLSDKPAKNIILLIGDGMGDSEITAARNYAEGA GGFFKGIDALPLTGQ YTHYALNRKTGKPDYVTSSAASATAWSTGVKTYNGALGVDIHEKDHPTILEMAKAAGLAT GNVSTAELQDATPAA LVAHVTSRKCYGPSATSEKCPGNALEKGGKGSITEQLLNARADVTLGGGAKTFAETATAG EWQGKTLREQAQARG YQLVSDAASLNSVTEANQQKPLLGLFADGNMPVRWLGPKATYHGNIDKPAVTCTPNPQRN DSVPTLAQMTDKAIE LLSKNEKGFFLQVEGASIDKQDHAANPCGQIGETVDLDEAVQRALEFAKKEGNTLVIVTA DHAHASQIVAPDTKA PGLTQALNTKDGAVMVMSYGNSEEDSQEHTGSQLRIAAYGPHAANVVGLTDQTDLFYTMK AALGLKGAPDYKDDD DKGAPHHHHHH

SEQ ID NO: 60 shows full amino acid sequence of the anti-p62 antibody AbD34908 including alkaline phosphatase dimerization domain sequence (AP), FLAG and His6 tag;

DIVLTQSPATLSLSPGERATLSCRASQSVSASRLAWYQQKPGQAPRLLIYGSSTRAT GIPARFSGSGSGTDFTLT ISSLEPEDFAVYYCQQYLHLYTFGQGTKVEIKRTVAAP SVFIFPPSDEQLKSGTASWCLLNNFYPREAKVQWKV DNALQSGNSQESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFN RGEA*EVQLVQSGAE VKKPGE SLKI SCKGSGYSFTNYWIGWVRQMPGKGLEWMGI IDP SGSFTRYSP SFQGQVTI SADKSI STAYLQWS S LKASDTAMYYCARKYVPPVYSYWSYGTLDVWGQGTLVTVS SASTKGP SVFPLAP SSKSTSGGTAALGCLVKDYFP EPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKV DKKVEPKSEFKAEMP VLENRAAQGDITTPGGARRLTGDQTAALRDSLSDKPAKNIILLIGDGMGDSEITAARNYA EGAGGFFKGIDALPL TGQYTHYALNRKTGKPDYVTSSAASATAWSTGVKTYNGALGVDIHEKDHPTILEMAKAAG LATGNVSTAELQDAT PAALVAHVTSRKCYGP SATSEKCPGNALEKGGKGSITEQLLNARADVTLGGGAKTFAETATAGEWQGKTLREQAQ ARGYQLVSDAASLNSVTEANQQKPLLGLFADGNMPVRWLGPKATYHGNIDKPAVTCTPNP QRNDSVPTLAQMTDK AIELLSKNEKGFFLQVEGASIDKQDHAANPCGQIGETVDLDEAVQRALEFAKKEGNTLVI VTADHAHASQIVAPD TKAPGLTQALNTKDGAVMVMSYGNSEEDSQEHTGSQLRIAAYGPHAANWGLTDQTDLFYT MKAALGLKGAPDYK DDDDKGAPHHHHHH

SEQ ID NO: 61 shows the amino acid sequence of human p62;

MASLTVKAYLLGKEDAAREIRRFSFCCSPEPEAEAEAAAGPGPCERLLSRVAALFPA LRPGGFQAHYRDEDGDLV AFSSDEELTMAMSYVKDDIFRIYIKEKKECRRDHRPPCAQEAPRNMVHPNVICDGCNGPV VGTRYKCSVCPDYDL CSVCEGKGLHRGHTKLAFPSPFGHLSEGFSHSRWLRKVKHGHFGWPGWEMGPPGNWSPRP PRAGEARPGPTAESA SGPSEDPSVNFLKNVGESVAAALSPLGIEVDIDVEHGGKRSRLTPVSPESSSTEEKSSSQ PSSCCSDPSKPGGNV EGATQSLAEQMRKIALESEGRPEEQMESDNCSGGDDDWTHLSSKEVDP STGELQSLQMPESEGP SSLDPSQEGPT GLKEAALYPHLPPEADPRLIESLSQMLSMGFSDEGGWLTRLLQTKNYDIGAALDTIQYSK HPPPL SEQ ID NO: 62 shows the p62 protein fragment used to generate anti-p62 antibodies;

MAMSYVKDDIFRIYIKEKKECRRDHRPPCAQEAPRNMVHPNVICDGCNGPWGTRYKC SVCPDYDLCSVC EGKGLHRGHTKLAFPSPFGHLSEGFSHSRWLRKVKHGHFGWPGWEMGPPGNWSPRPPRAG EARPGPTAES ASGPSEDPSVNFLKNVGESVAAALSPLGIEVDIDVEHGGKRSRLTPVSPESSSTEERSSS QPSSCCSDPS KPGGNVEGATQSLAEQMRKIALESEGRPEEQMESDNCSGGDDDWTHLSSKEVDP STGELQSLQMPESEGP SSLDPSQEGPTGLKEAALYPHLPPEADPRLIESLSQMLSMGFSDEGGWLTRLLQTKNYDI GAALDTIQYS KHPPPLLEHHHHHH

SEQ ID NO: 63 shows the Ambra-1 C-terminal sequence used for replacement analysis in epitope mapping

(VSLPSAEGPTLHCELTNNNHLLDGGSSRGDAAGPRGEPRNR)

SEQ ID NO: 64 shows the REPNET epitope of the Anti-Ambra-1 antibodies

(DGGSSRGDAAGPRGEPRNR)

SEQ ID NO: 65 shows the LIN epitope of the Anti-Ambra-1 antibodies (HLLDGGSSR)

SEQ ID NO: 66 shows the LOOP epitope of the Anti-Ambra-1 antibodies (NHLLDGGSSR)

SEQ ID NO: 67 shows a core epitope of the Anti-Ambra-1 antibodies (EPRN)

SEQ ID NO: 68 shows a core epitope of the Anti-Ambra-1 antibodies (EPR)

The practice of embodiments of the present invention employs, unless otherwise indicated, conventional techniques of chemistry, molecular biology, pharmaceutical formulation, pharmacology and medicine, which are within the skill of those working in the art. Most general chemistry techniques can be found in Comprehensive Heterocyclic Chemistry IF (Katritzky et al., 1996, published by Pergamon Press); Comprehensive Organic Functional Group Transformations (Katritzky et al., 1995, published by Pergamon Press); Comprehensive Organic Synthesis (Trost et al,. 1991 , published by Pergamon); Heterocyclic Chemistry (Joule et al. published by Chapman & Hall); Protective Groups in Organic Synthesis (Greene et al., 1999, published by Wiley-lnterscience); and Protecting Groups (Kocienski et al., 1994). Most general molecular biology techniques can be found in Sambrook et al, Molecular Cloning, A Laboratory Manual (2001 ) Cold Harbor-Laboratory Press, Cold Spring Harbor, N.Y. or Ausubel et al., Current Protocols in Molecular Biology (1990) published by John Wiley and Sons, N.Y.

Most general pharmaceutical formulation techniques can be found in Pharmaceutical Preformulation and Formulation (2 ^nd Edition edited by Mark Gibson) and Pharmaceutical Excipients: Properties, Functionality and Applications in Research and Industry (edited by Otilia M Y Koo, published by Wiley). Most general pharmacological techniques can be found in A Textbook of Clinical Pharmacology and Therapeutics (5 ^th Edition published by Arnold Hodder).

Most general techniques on the prescribing, dispensing and administering of medicines can be found in the British National Formulary 72 (published jointly by BMJ Publishing Group Ltd and Royal Pharmaceutical Society).

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs. For example, the Concise Dictionary of Biomedicine and Molecular Biology, Juo, Pei-Show, 2 ^nd ed., 2002, CRC Press; The Dictionary of Cell and Molecular Biology, 3 ^rd ed., Academic Press; and the Oxford University Press, provide a person skilled in the art with a general dictionary of many of the terms used in this disclosure. For chemical terms, the skilled person may refer to the International Union of Pure and Applied Chemistry (lUPAC).

Units, prefixes and symbols are denoted in their Systeme International d’Unites (SI) accepted form. Numeric ranges are inclusive of the numbers defining the range.

Margins of tumours in SCC

In certain embodiments, the invention provides a method of determining the margin(s) of a tumour (i.e., SCC) in a tissue sample obtained from a subject with SCC. Typically, the method is ex vivo. Typically, the SCC is cSCC.

As used herein, the“margin of a tumour” refers to tissue peripheral (e.g. surrounding and/or adjacent) the tumour. The margin of a tumour may be the outermost layer of tumour-positive tissue originating from a primary tumour. Determining the margin of the tumour may allow visualisation of the boundary between tumour positive and tumour negative tissue.

In SCC, it may be difficult to determine whether tissue peripheral to the tumour is tumour positive or tumour negative. For example, tissue peripheral to the tumour may appear histologically normal by gross or microscopic inspection, but in fact comprise pre-cancerous (e.g. abnormal) cells leading to metastasis or recurrence of the tumour. In such embodiments, the tissue peripheral to the tumour may be tumour positive.

In certain embodiments, the method of determining the margin of a tumour comprises determining whether one or more sections of tissue peripheral to the tumour are tumour positive or tumour negative. Thus, the invention provides a method of determining where tumour tissue ends and normal tissue begins.

In certain embodiments, tissue“peripheral” to the tumour refers to tissue originally located about 8mm, about 7mm, about 6mm, about 5mm, about 4mm, about 3mm, about 2mm, about 1 mm, about 0.5mm or less from the tumour.

As used herein, the term“tumour positive” is understood to include tumour tissue or cells and/or pre-cancerous (e.g. abnormal) tissue or cells that risk recurrence or metastasis of the tumour. For example, tumour positive tissue may include cells that are poorly or undifferentiated. Tumour positive tissue may include precursor lesions. Tumour positive tissue may include dysplastic cells. Tumour positive tissue may include actinic keratosis, Bowenoid actinic keratosis and/or Bowen’s disease. Tumour positive tissue may include tumour tissue that may be determined as tumour positive by gross-examination (e.g. R2 tissue). T umour positive tissue may include tumour cells, pre-cancerous cells and/or abnormal cells that may be determined as tumour positive by microscopic inspection (e.g. R1 tissue). Tumour positive tissue may not substantially include normal cells.

As used herein, the term“tumour negative” is understood to include normal tissue or cells that do not risk recurrence or metastasis of the tumour. For example, tumour negative tissue may include cells that are well differentiated. Tumour negative tissue may include epidermal cells peripheral to the tumour. Tumour negative tissue may include tissue where pre-cancerous cells and/or abnormal cells are not capable of being determined microscopically (e.g. R0 tissue). Tumour negative tissue may not substantially include tumour cells and/or pre- cancerous (e.g. abnormal) cells.

Typically, the tumour is a primary tumour (e.g. of a primary SCC). As used herein, the term "primary tumour" refers to a malignant tumour on the skin at the site of origin, regardless of thickness, in patients without clinical or histologic evidence of regional or distant metastatic disease.

In certain embodiments, the tissue sample has previously been obtained from the subject such that the sampling itself does not form a part of the methods of the invention. The sample may have been obtained immediately prior to the method, or hours, days or weeks prior to the method. In certain embodiments, the method may additionally comprise the step of obtaining the tissue sample from the subject. For example, the tissue sample may be obtained from the subject during or after surgery to excise the tumour.

Typically, the tissue sample may be a biopsy, or a section thereof, obtained from the subject. A tissue sample, such as a biopsy, can be obtained through a variety of sampling methods known to those skilled in the art, including a punch biopsy, shave biopsy, wide local excision and other means. Aptly, the tissue sample is taken from a surgical site from which the tumour has or is being excised from the subject.

Typically, the tissue sample may be frozen, fresh, fixed (e.g. formalin fixed), centrifuged, and/or embedded (e.g. paraffin embedded), etc. The tissue sample may be or have been subjected to a variety of well-known post-collection preparative and storage techniques (e.g., nucleic acid and/or protein extraction, fixation, storage, freezing, ultrafiltration, concentration, evaporation, centrifugation, etc.) prior to assessing the amount of Ambra-1 and/or p62 in the sample. Likewise, biopsies may also be subjected to post-collection preparative and storage techniques, e.g., fixation. A tissue sample, or a section thereof, may be mounted on a solid support, such as a slide.

In certain embodiments, the tissue sample comprises one or more sections of tissue. Typically, the tissue sample comprises more than one section (e.g. serial sections). Typically, the tissue sample comprises one or more sections of tissue peripheral to the tumour. As such, determining the margin of the tumour may comprise classifying whether or not this tissue is tumour positive or tumour negative.

In certain embodiments, the one or more sections are topographically marked. For example, the one or more sections may be marked (e.g. notched) to maintain orientation. The one or more sections may be marked to allow them to be located to the wound during or after surgery. More than one section may be marked to allow different sections to be distinguished from each other. The one or more sections may be used to map the margin of the tumour.

In certain embodiments, the tissue sample comprises a surgical (e.g. resection) margin. For example, the one or more sections of tissue peripheral to the tumour may comprise a surgical margin. As used herein, the“surgical margin” refers to tissue comprising the outermost layer of tissue (e.g. border) of tissue excised (or being excised) from a subject during surgery to remove the tumour.

In certain embodiments, the tissue sample comprises one or more horizontal sections of the tumour. In certain embodiments, the tissue sample comprises horizontal sections of tissue peripheral to the tumour. Typically, the one or more sections of tissue are thin (e.g. about 2mm, 1 .5mm, 1 mm or less). Typically, the one or more sections of tissue are examined intraoperatively using frozen sections (e.g. Mohs surgery) or on paraffin sections (e.g.“slow Mohs surgery).

In certain embodiments, the tissue sample comprises (or may be deemed to be at risk of comprising) tumour positive tissue. For example, the one or more sections of tissue peripheral to the tumour may comprise (or be suspected of comprising) the margin (e.g. outermost layer) of the tumour. For example, the tissue may comprise the outermost boundary of tumour positive tissue. The tissue may further comprise tumour negative tissue adjacent to the tumour boundary.

In certain embodiments, the method is performed on a tissue sample obtained from a subject with SCC. In certain embodiments, the tissue sample is obtained from a subject with SCC that has already undergone surgery to remove the tumour. In such embodiments, the tissue sample may comprise the surgical margin. In such embodiments, the method may comprise determining whether or not the surgical margin is tumour positive or tumour negative. As explained in more detail below, subsequent treatment of the subject may be tailored according to whether or not the tumour was completely removed.

In alternative embodiments, the tissue sample is obtained from a subject with SCC who is undergoing surgery to remove the tumour (e.g. intraoperatively). In such embodiments, the tissue sample may comprise the surgical margin. In such embodiments, the method may comprise determining whether or not the surgical margin is tumour positive or tumour negative. As explained in more detail below, subsequent surgery (and/or treatment) may be tailored accordingly to whether or not it was possible to completely remove the tumour.

The subject may be any animal such as a horse, cat or dog. Typically, the subject is a human. Typically, the subject has already been determined as having SCC. Typically, the subject has been determined as having high-risk SCC. Typically, the tumour is of an invasive SCC.

As used herein, the term“SCC” (i.e., epidermoid carcinoma) refers to a form of cancer arising from squamous cells. Squamous cells may be found in the tissue that forms the surface of the skin, the lining of hollow organs in the body and the lining of the respiratory and digestive tracts.

In preferred embodiments, the SCC is cutaneous SCC. As used herein, the term“cutaneous squamous cell carcinoma (cSCC)” refers to a form of skin cancer arising from malignant proliferation of the keratinocyte cells of the epidermis, which may mediate cellular invasion. Disease-related cell invasion and/or proliferation may be any abnormal, undesirable or pathological cell invasion and/or proliferation, for example tumour-related cell invasion and/or proliferation.

As used herein, the term “invasive SCC” is understood to include SCC that has been determined to have high-risk features of metastasis (e.g. high risk SCC). For example, such high-risk features include size of the tumour (e.g. more than 2cm in diameter), failure of any previous treatment, immunosuppression, depth or invasion of tumour (e.g. more than 2mm thickness), Clark level (greater than 4), peri-neural invasion, primary site ear or lip and/or poorly differentiated or undifferentiated cells. See, for example, Tumour-Node-Metastasis (TNM) Classification of Malignant Tumours, 7 ^th edition, incorporated by reference herein. As used herein, the term "metastasis" refers to the recurrence or disease progression that may occur locally (such as local recurrence and in transit disease), regionally (such as nodal micro-metastasis or macro-metastasis), or distally (such as brain, lung and other tissues). In some embodiments, the term“metastasis” is used to refer to metastatic disease following a primary tumour. Typically, metastasis originating from a primary tumour may spread to the lungs and/or brain of the subject as well as other locations.

As used herein, the term "primary tumour" refers to a malignant tumour on the skin at the site of origin, regardless of thickness, in patients without clinical or histologic evidence of regional or distant metastatic disease.

The stage of SCC is a description of how widespread it is. This includes its thickness (e.g. in the skin or other organ), whether it has spread to nearby lymph nodes or any other organs, and certain other factors. The stage is based on the results of the physical exam, biopsies, and any imaging tests (CT or MRI scan, etc.) or other tests that have been done. Such tests will be known to those skilled in the art. For example, the system used to stage cSCC is the American Joint Commission on Cancer (AJCC) TNM system. Table 1 below describes the features identifying each stage.

Table 1. AJCC 7 ^th edition cSCC tumor staging system ¹ .

¹ ln the absence of nodal or distant metastasis, T is = Stage 0, T1 = Stage I, and T2 = Stage II.

² High-risk features include depth >2mm or Clark level ³ 4, perineural invasion, location on the ear or lip, and poor differentiation.

In some embodiments, the subject is suffering from TX, T0, Tis, T 1 (i.e. Stage I) or T2 (i.e. Stage II) SCC. In some embodiments, the methods further comprise staging a primary carcinoma present in the tissue sample obtained from the subject in accordance with AJCC staging.

In certain embodiments, the methods of the invention further comprise determining whether the subject has an increased risk of metastasis by determining the expression of Ambra-1 and p62 in tumour tissue obtained from the subject.

As used herein, the term“increased risk of metastasis” refers to an increased chance of a tumor spreading from the primary site. Invasive, poorly differentiated tumours (e.g. high-risk SCC) may be determined as having loss or decrease of Ambra-1 expression and increased p62 expression (e.g. increased cytoplasmic p62 expression) compared to reference tissue or levels (e.g. normal tissue).

Conversely, non-invasive, well differentiated tumours (e.g. low risk SCC) may be determined as having increased (or no significant difference) in the expression of Ambra-1 and no significant difference in the expression of p62 (or increased nuclear p62 expression only) compared to reference tissue or levels (e.g. normal tissue).

A subject determined as having high-risk SCC may be particular suitable for the methods of determining the margins of tumours described herein.

In certain embodiments, determining the margin of a tumour ex vivo subsequently allows the complete excision of tumour positive tissue during surgery whilst minimising (or avoiding) excision of tumour negative tissue. This may be particularly advantageous, for example, during surgery where the tumour is being removed from the face or neck of a subject.

In certain embodiments, the tissue sample is obtained from a subject undergoing Mohs micrographic surgery as explained further below.

Ambra-1 and p62 biomarkers

In certain embodiments, the method of determining the margin of the tumour comprises determining the expression of Ambra-1 and/or p62 in one or more sections of tissue peripheral to the tumour. For example, determining the expression of Ambra-1 and/or p62 may comprise determine the level and/or pattern of expression of Ambra-1 and/or p62 protein. Surprisingly, the combination of Ambra-1 and p62 markers is shown to accurately determine the margin of a tumour of SCC. In other words, the combination of Ambra-1 and p62 markers allows the classification of tissue peripheral to the tumour as tumour positive or tumour negative.

Ambra-1 (activating molecule in Beclin-1 regulated autophagy protein 1 ) is a WD40-containing protein. Studies have implicated Ambra-1 in the control of autophagy and cellular differentiation. The full length human amino acid sequence of Ambra-1 is set forth in SEQ ID NO: 21 .

p62 (also known as sequestosome-1/SQSTM1 ) is a multidomain adaptor protein transporting ubiquitinated proteins during autophagy. The full length human amino acid sequence of p62 is set forth in SEQ ID NO: 61 .

In particular, it is considered that a decrease or loss of expression of Ambra-1 and increase in expression of p62 as compared to reference tissue or levels (e.g. normal tissue) is indicative of tumour positive tissue.

Conversely, it is considered that no significant difference in expression of Ambra-1 and p62 compared to the reference tissue or levels (e.g. normal tissue) is indicative of tumour negative tissue.

As used herein, the term“indicative of” may refer to an increased likelihood of one or more sections of tissue peripheral to the tumour being tumour positive or tumour negative. An “increased likelihood”, for example, may refer to a 70%, 80%, 90%, 95%, 97%, 99% or more likelihood that the one or more sections of tissue peripheral to the tumour are tumour positive or tumour negative. As discussed further below, the expression of Ambra-1 and/or p62 may be scored to determine whether the tissue is tumour positive or tumour negative.

In certain embodiments, a step-wise progression from normal to cancerous squamous cells (e.g. cSCC) is associated with increased nuclear p62 expression. For example, an increase in nuclear p62 expression compared to the reference levels or tissue (e.g. normal tissue) may be indicative of tumour positive tissue adjacent (e.g. immediately or directly adjacent) to normal tissue. Conversely, no significant difference in nuclear p62 expression compared to the reference levels or tissue (e.g. normal tissue) may be indicative of tumour negative tissue adjacent (e.g. immediately or directly adjacent) to the tumour (e.g. the outermost boundary of the tumour). Thus, determining the expression of p62 in the nucleus of cells within the one more sections of tissue may allow the margin of the tumour to be accurately determined.

In certain embodiments, determining the expression of Ambra-1 and p62 in the tissue sample comprises measuring the levels of each of the proteins present in the tissue sample. This may be achieved by methods known to those skilled in the art. Such methods include immunoassays, for example immunohistochemistry (IHC), immunofluorescence (IF), immunoblotting, flow cytometry (e.g., FACS™) or enzyme-linked immunosorbent assay (ELISA), and the like.

In certain embodiments, determining the expression of Ambra-1 and p62 in the tissue sample comprises:

contacting the tissue with a first ligand specific for Ambra-1 , wherein the presence of Ambra-1 creates an Ambra-1 -ligand complex;

contacting the tissue with a second ligand specific for p62, wherein the presence of p62 creates a p62-ligand complex; and

detecting and/or quantifying the Ambra-1 -ligand complex and the p62-ligand complex.

In some embodiments, the first ligand comprises an anti-Ambra-1 antibody or aptamer. In some embodiments, the anti-Ambra-1 antibody or aptamer binds specifically to a protein (or region thereof) having the sequence shown in SEQ ID NO: 21 , 22, 63, 64, 65, 66, 67 and/or 68

As used herein, the term“aptamer” refers to a non-naturally occurring oligonucleotide that can form a three-dimensional structure that binds to another molecule with high affinity and specificity. As used herein, the terms "nucleic acid ligand" and "aptamer” may be used interchangeably. Aptamer specificity may be comparable or even higher than that of an antibody.

Aptamers have the ability to fold into a variety of complex, sequence-specific tertiary conformations, meaning that they can bind a wide range of targets and rival antibodies in their potential diversity. It is recognized that affinity interactions are a matter of degree; however, in this context, the "specific binding affinity" of an aptamer for its target means that the aptamer binds to its target, i.e. a target molecule, generally with a much higher degree of affinity than it binds to other, non-target, components in a mixture or sample.

An "aptamer" or "nucleic acid ligand" is a set of copies of one type or species of nucleic acid molecule that has a particular nucleotide sequence. An aptamer can include any suitable number of nucleotides. "Aptamers" refers to more than one such set of molecules. Different aptamers can have either the same or different numbers of nucleotides. Aptamers may be DNA or RNA and may be single stranded, double stranded, or contain double stranded regions. In one embodiment, the aptamer comprises single-stranded DNA (ss-DNA) or single stranded RNA (ss-RNA). In some embodiments, the second ligand comprises an anti-p62 antibody or aptamer. In some embodiments, the anti-p62 antibody or aptamer binds specifically to a protein having the sequence shown in SEQ ID NO: 61 or 62.

In certain embodiments, the anti-Ambra-1 and/or anti-p62 antibody is an antibody as further described herein.

The amino acid sequences of human Ambra-1 and p62 are provided herein as examples. However, it will be appreciated that variants of these sequences may be known or identified. In some embodiments, the subject is a non-human mammal. It should therefore also be appreciated that references herein to Ambra-1 and p62 include the sequences of non-human homologues thereof.

In some embodiments, the first ligand comprises a first detection moiety and the second ligand comprises a second detection moiety. The first detection moiety may be the same as the second detection moiety, or it may be different.

In some embodiments, the method comprises contacting a first portion of the tissue with the first ligand and contacting a second portion or section of the tissue with the second ligand. This is particularly suitable for embodiments wherein the first detection moiety is the same as the second detection moiety. In some alternative embodiments, the method comprises contacting the portion of tissue with the first ligand and contacting the same portion of tissue with the second ligand. It may be possible to detect and/or quantify both the Ambra-1 -ligand complex and the p62-ligand complex in the same portion of tissue, particularly if the first and second detection moieties are different.

Aptly, the first and/or second ligands may be used in combination with one or more capture agents. Thus, in some embodiments, the step of detecting and/or quantifying the Ambra-1 - ligand complex and the p62-ligand complex comprises contacting the tissue with at least one capture agent. Aptly, a first capture agent which binds specifically to the first ligand may be used to detect and/or quantify the Ambra-1 -ligand complex, while a second capture agent which binds specifically to the second ligand may be used to the detect and/or quantify the p62-ligand complex. Alternatively, a single capture agent may be used which is capable of binding specifically to both the first and second ligands.

In some embodiments, the capture agent comprises a binding moiety and a detection moiety.

In some embodiments, the binding moiety is a secondary antibody which binds specifically to the first and/or second ligands. For example, the binding moiety may be a universal anti-lgG antibody that is capable of binding to primary antibodies used as the first and second ligands. In some embodiments, the method further comprises one or more wash steps to remove unbound first and second ligands and, optionally, unbound capture agents.

In certain embodiments, the expression of Ambra-1 and/or p62 is determined using an antibody against Ambra-1 and/or an antibody against p62 as further described below. Typically, the expression of Ambra-1 and/or p62 is determined by contacting the SCC tissue with the antibodies and detecting the presence of the bound antibodies. For example, presence of the bound antibodies may be detected by visualising the antibodies in the SCC tissue sample with reagent(s) that generate detectable signal(s) (e.g. detection moieties as described herein).

In some embodiments, the method comprises contacting the SCC tissue with the antibody under conditions permissive for binding of the anti-Ambra-1 antibody and/or anti-p62 antibody to Ambra-1 and/or p62 and detecting whether a complex is formed between the anti-Ambra-1 antibody and/or anti-p62 antibody and Ambra-1 and/or p62 respectively.

In some embodiments, the first and/or second ligand comprises a detection moiety (e.g. a fluorescent label). A detection moiety enables the direct or indirect detection and/or quantification of the complexes formed.

Reference tissue or levels

In certain embodiments, methods for determining the margins of a tumour in a tissue sample further comprise comparing the expression of Ambra-1 and/or p62 with a reference tissue or levels obtained therefrom.

In some embodiments, the reference comprises levels of Ambra-1 and/or p62 expression that are characteristic of normal tissue. Typically, reference levels of Ambra-1 and/or p62 are obtained by determining the expression of Ambra-1 and/or p62 in a reference tissue.

In some embodiments, the expression levels of Ambra-1 and/or p62 in a reference tissue are determined by visual or automated assessment. In some embodiments, reference levels of Ambra-1 and/or p62 expression that are characteristic of normal tissue are obtained by determining expression levels in tissue samples obtained from one or more (e.g. a cohort) of healthy subjects.

In some embodiments, the reference tissue comprises normal tissue. In some embodiments, the normal tissue comprises tissue which does not include a primary tumour. Typically, the reference tissue comprises tumour negative tissue as described herein.

In some embodiments, the reference tissue (or levels obtained therefrom) is an internal reference (i.e. obtained from the subject). In some embodiments, the reference tissue is tissue obtained from the tumour itself (e.g. primary tumour). In other embodiments, the reference tissue is obtained from a site of the subject which is remote from the tumour (e.g. comprising normal cells).

Thus, in some embodiments, the reference level is the level of expression of Ambra-1 and/or p62 in normal tissue. The reference tissue may be taken from normal epidermis and the reference level is a level of expression in the keratinocytes of the normal epidermis. The expression of Ambra-1 and/or p62 in the reference tissue, for example, to generate reference levels, can be determined using the methods described herein.

Ambra-1 expression

In the method of determining the margin of the tumour, a decrease or loss in the expression of Ambra-1 in the tissue sample compared to the reference tissue or levels (e.g. normal tissue) is indicative of tumour positive tissue.

For example, a decrease or loss in the expression of Ambra-1 may be a level of expression of Ambra-1 less than about 75%, less than about 50%, less than about 25%, less than about 10%, less than about 5% or less of the reference level. Typically, a decrease in expression of Ambra-1 is a level of expression of Ambra-1 from about 25% to about 75% compared to the reference level. Typically, a loss of expression of Ambra-1 is a level of expression of Ambra- 1 less than about 25% compared to the reference level.

In certain embodiments, the expression level of Ambra-1 in the SCC tissue sample is from about 25% to about 75% of the reference level. In some embodiments, the expression level of Ambra-1 is no greater than 75%, no greater than 70%, no greater than 60%, no greater than 50%, no greater than 40% or no greater than 30% of the reference level. In some embodiments, there is substantially no expression of Ambra-1 in the SCC tissue sample. In certain embodiments, the expression of Ambra-1 is less than 25%.

In certain embodiments, the expression of Ambra-1 is determined in the nucleus and/or cytoplasm of cells within the SCC tissue. For example, the % of Ambra-1 positive cells may be scored and compared to the reference tissue or levels.

Conversely, no significant difference in the expression of Ambra-1 in the SCC tissue sample compared to the reference tissue or levels (e.g. normal tissue) is indicative of tumour negative tissue.

For example, no significant difference in the expression of Ambra-1 in the SCC tissue sample compared to the reference level (e.g.“normal expression”) may be a level of Ambra-1 greater than about 75% of the reference level. In particular, the expression level of Ambra-1 in the SCC tissue sample may be from about 75% to 125% as compared to the reference level. In certain embodiments, the reference level is a level of Ambra-1 expression in the stratum corneum of epidermal tissue. In normal epidermal tissue, Ambra-1 has increasing expression from the basal layer to the stratum corneum in line with increasing keratinocyte differentiation. p62 expression

In the method of determining the margin of the tumour, an increase in the expression of p62 in the tissue sample compared to the reference tissue or levels (e.g. normal tissue) is indicative of tumour positive tissue.

For example, an increase in the expression of p62 may be a level of expression of p62 more than about 125% of the respective reference level. Typically, an increase in expression of p62 is a level of expression of p62 from about 125%, about 150%, about 175%, about 200%, about 300%, about 400%, about 500% or more of the reference level.

In certain embodiments, the expression p62 is determined in the nucleus and/or cytoplasm of cells within the SCC tissue. For example, the % of p62 positive cells may be scored and compared to the reference tissue or levels.

In certain embodiments, an increase in the expression of nuclear p62 in the SCC tissue sample compared to the reference tissue or levels is indicative of tumour positive tissue adjacent (e.g. immediately or directly adjacent) to normal tissue.

For example, an increase in the nuclear expression of p62 may be a level of expression of p62 more than about 125% of a reference level in the nucleus. Typically, an increase in expression of p62 is a level of expression of p62 from about 125%, 150%, 175%, 200%, 300%, 400%, 500% or more of a reference level in the nucleus.

Conversely, no significant difference in the expression of p62 in the SCC tissue sample compared to the reference tissue or levels (e.g. normal tissue) is indicative of tumour negative tissue.

For example, no significant difference in the expression of p62 in the SCC tissue sample compared to the reference level (e.g.“normal expression”) may be a level of p62 greater than about 75% of the reference level. In particular, the expression level of p62 in the SCC tissue sample may be from about 75% to 125% as compared to the reference level.

In certain embodiments, the reference level is a level of p62 expression in the stratum basale of epidermal tissue. In normal epidermal tissue, p62 has decreasing expression from the basal layer to the stratum corneum in line with increasing keratinocyte differentiation. Normal epidermal tissue contains low nuclear p62 expression.

The term“comparing” and“compare” may refer to a comparison of corresponding parameters or levels, e.g., an absolute amount is compared to an absolute reference amount while a concentration is compared to a reference concentration or a signal intensity signal obtained from the tissue sample is compared to the same type of signal intensity obtained from the reference. The comparison may be carried out manually, for example by visual assessment, or it may be automated (e.g. using an automated scanner or computer-assisted). Thus, the comparison may be carried out by a computing device.

In certain embodiments, the expression of Ambra-1 and/or p62 is scored on the basis of the intensity and/or proportion of positive cells in the SCC tissue sample. Scoring methods have been described and are well known to one of ordinary skill in the art.

In one embodiment, an intensity score may be defined as follows: 0=no appreciable staining in the cells, 1 =faint/barely perceptible partial staining in the cytoplasm and/or nucleus of the cells, 2=weak to moderate staining of the cytoplasm and/or nucleus of the cells, and 3=strong staining of the cytoplasm and/or nucleus of the cells. A proportion score may be defined as follows: 0=less than 5%, 1 =from 5% to 25%, 2=from 26% to 50%, 3=from 51 % to 75%, and 4=more than 75%. A total score may be calculated by multiplying the intensity score and the proportion score, producing a total range of 0 to 12. In certain embodiments, scores of 0 to 3 may be indicative of decrease or loss of expression. In certain embodiments, scores of 4 to 12 may be indicative of an increase in expression.

In another embodiment, a H-score may be calculated (McCarty et aL, Cancer Res 1986 46(8 Sup!);4244s-424Ss). An intensity score may be defined as follows:

The H score combines components of staining intensity with the percentage of positive ceils it has a value between 0 and 300 and is defined as:

1 ^* (percentage of ceils staining at 1 + intensity);

+ 2 ^* (percentage of ceils staining at 2+ intensity);

+ 3 ^* (percentage of ceils staining at 3+ intensity);

= H score.

A H-score of about 100, 1 10, 120, 130, 140, 150 or above may indicate increased expression of Ambra-1 or p62. Conversely, a H-score of less than about 150,140, 130, 120, 1 10 or 100 may indicate decreased expression of Ambra-1 or p62.

In certain embodiments,“weak”,“moderate” or“strong” staining of the cells is relative to levels of Ambra-1 or p62 characteristic of the reference or normal tissue.

In certain embodiments, the method of comparing the expression of Ambra-1 and/or p62 comprises outputting, optionally on a computer, (i) an indication of the expression pattern and/or levels of Ambra-1 and/or p62 and (ii) this indicates whether the tissue is tumour positive or negative.

Antibodies against Ambra-1 or p62

In certain embodiments of the invention, antibodies against Ambra-1 are used to determine the expression of Ambra-1 in a SCC tissue sample obtained from the subject. Similarly, antibodies against p62 may be used to determine the expression of p62 in the SCC tissue obtained from the subject.

Antibodies against Ambra-1 or p62 include any polyclonal antibodies, any monoclonal antibodies, including chimeric antibodies, humanized antibodies, bi-specific antibodies and domains and fragments of monoclonal antibodies including Fab, Fab', F(ab')2, scFv, dsFv, ds- scFv, dimers, minibodies, diabodies, and multimers thereof. Monoclonal antibodies can be fragmented using conventional techniques. Monoclonal antibodies may be from any animal origin, including birds and mammals (e.g., human, murine, donkey, sheep, rabbit, goat, guinea pig, camel, horse, or chicken), transgenic animals, or from recombinant sources. Typically, the monoclonal antibodies against Ambra-1 or p62 are fully human. Monoclonal antibodies may be prepared using any methods known to those skilled in the art, including by recombination.

Typically, the antibody against Ambra-1 or p62 is isolated. An "isolated" antibody is an antibody that has been identified and separated and/or recovered from a component of its natural environment. Contaminant components of its natural environment are materials that would interfere with diagnostic or therapeutic uses for the antibody, and may include enzymes, hormones, and other proteinaceous or non-proteinaceous solutes. In certain embodiments, the antibody will be purified (1 ) to greater than 95% by weight of antibody as determined by the Lowry method, and most preferably more than 99% by weight, (2) to a degree sufficient to obtain at least 15 residues of N-terminal or internal amino acid sequence by use of a spinning cup sequenator, or (3) to homogeneity by SDS-PAGE under reducing or nonreducing conditions using Coomassie blue or, silver stain. In certain embodiments, the antibody against Ambra-1 is a fragment that specifically binds Ambra-1.

In certain embodiments, the antibody against p62 is a fragment that specifically binds p62.

An "antibody fragment" is a portion of an intact antibody that includes an antigen binding site of the intact antibody and thus retaining the ability to bind Ambra-1 or p62 respectively. Antibody fragments include:

(i) Fab fragments, having V _L , CL, V _H and CH1 domains;

(ii) Fab' fragments, which is a Fab fragment having one or more cysteine residues at the C -terminus of the CH1 domain;

(iii) Fd fragments having V _H and CH1 domains;

(iv) Fd' fragments having V _H and CH1 domains and one or more cysteine residues at the C-terminus of the CH1 domain;

(v) Fv fragments having the V _L and V _H domains of a single arm of an antibody;

(vi) dAb fragments (Ward et al., Nature 341 , 544-546 (1989)) which consist of a VH domain;

(vii) isolated CDR regions, including any one or more of SEQ ID Nos 1 to 6;

(viii) F(ab') ₂ fragments, a bivalent fragment including two Fab' fragments linked by a disulphide bridge at the hinge region;

(ix) single chain antibody molecules (e.g. single chain Fv; scFv) (Bird et al, Science 242:423-426 (1988); and Huston et al., PNAS (USA) 85:5879-5883 (1988));

(x) "diabodies" with two antigen binding sites, comprising a heavy chain variable domain (VH) connected to a light chain variable domain (VL) in the same polypeptide chain (see, e.g., EP 404,097 and WO 93/1 1 161 ;

(xi) "linear antibodies" comprising a pair of tandem Fd segments (VH-CH1 -VH- CH1 ) which, together with complementary light chain polypeptides, form a pair of antigen binding regions (Zapata et al. Protein Eng. 8 (10): 1057-1062 (1995); and US Patent No. 5,641 ,870).

Typically, the antibody against Ambra-1 or p62 is a recombinant monoclonal antibody. A “recombinant monoclonal antibody” is an antibody or antibody fragment produced using recombinant antibody coding genes. In certain embodiments, the antibodies of the invention are generated from a human combinatorial antibody library (e.g. HuCAL, BioRad).

Typically, the antibody against Ambra-1 or p62 is a monovalent Fab or bivalent Fab fragment. A“bivalent Fab fragment” may be considered as equivalent to a F(ab’)2 fragment and formed via dimerization. For example, a bivalent Fab fragment is formed via dimerization of a synthetic double helix loop helix motif (dHLX) or a bacterial alkaline phosphatase (AP) domain. In certain embodiments, the antibody against Ambra-1 and/or the antibody against p62 comprises a dimerization domain sequence and one or more linker sequences.

In certain embodiments, the antibody against Ambra-1 or p62 is a recombinant monoclonal antibody fragment converted into an immunoglobulin (Ig) format. For example, when an Fc region is required, the variable heavy and light chain genes may be cloned into vectors with the desired constant regions and co-transfected for expression in mammalian cells using methods known to those skilled in the art. In certain embodiments, antibody fragments are converted to human IgA, IgE, lgG1 , lgG2, lgG3, lgG3 or IgM.

In certain embodiments, the antibody against Ambra-1 or p62 is labelled with at least one epitope tag. Typical epitope tags include His6, Flag (e.g. DYKDDDDK), V5 (e.g. GKPIPNPLLGLDST), Strep (e.g. WSHPQFEK) and/or any combination thereof. Typically, the antibody against Ambra-1 and/or the antibody against p62 is a monovalent Fab or bivalent Fab fragment with one or more (e.g. two) epitopes. In certain embodiments, the antibody against Ambra-1 or p62 is conjugated to an enzyme and/or fluorescent label.

In certain embodiments, the antibody specifically binds to Ambra-1 . In other words, the antibody against Ambra-1 may bind Ambra-1 with a binding dissociation equilibrium constant (K _D ) of less than about 30nM, less than about 20nM, less than about 10nm, less than about 1 nm or less than about 200mm.

In certain embodiments, the antibody specifically binds to p62. In other words, the antibody against p62 may bind p62 with a binding dissociation equilibrium constant (KD) of less than about 30nM, less than about 20nM, less than about 10nm, less than about 1 nm or less than about 200mm.

The skilled person would understand techniques for measuring binding strengths (e.g. koff- rate determination;‘secondary screening’) include, for example, Bio-Layer Interferometry (e.g. using the Pall ForteBio Octet ^® System).

In certain embodiments, the antibody against Ambra-1 is available from a commercial supplier. For example, the antibody against Ambra-1 may be AbCAM Ab69501 as described herein. Alternatively, the antibody against Ambra-1 may be BioRad AbD33473 as described herein.

In certain embodiments, the antibody against Ambra-1 comprises the following heavy chain variable domain complementarity determining regions (CDRs):

(a) HCDR1 comprising the amino acid sequence of SEQ ID NO: 1 ; (b) HCDR2 comprising the amino acid sequence of SEQ ID NO: 2; and/or

(c) HCDR3 comprising the amino acid sequence of SEQ ID NO: 3.

In certain embodiments, the antibody against Ambra-1 further comprises the following light chain variable domain CDRs:

(d) LCDR1 comprising the amino acid sequence of SEQ ID NO: 4

(e) LCDR2 comprising the amino acid sequence of SEQ ID NO: 5; and/or

(f) LCDR3 comprising the amino acid sequence of SEQ ID NO: 6.

As used herein, the term "Complementarity Determining Regions" (CDRs) refers to the amino acid residues of an antibody variable domain the presence of which are necessary for antigen binding. Each variable domain typically has three CDR regions identified as CDR1 , CDR2 and CDR3. Each complementarity determining region may comprise amino acid residues from a "complementarity determining region" as defined by Kabat (i.e. about residues 24-34 (L1 ), 50- 56 (L2) and 89-97 (L3) in the light chain variable domain and 31 -35 (H1 ), 50-65 (H2) and 95- 102 (H3) in the heavy chain variable domain; Kabat et al., Sequences of Proteins of Immunological Interest, 5th Ed. Public Health Service, National Institutes of Health, Bethesda, MD. (1991 )) and/or those residues from a "hypervariable loop" (i.e. about residues 26-32 (L1 ), 50-52 (L2) and 91 -96 (L3) in the light chain variable domain and 26-32 (H1 ), 53-55 (H2) and 96-101 (H3) in the heavy chain variable domain; Chothia and Lesk J. Mol. Biol. 196:901 -917 (1987)). In some instances, a CDR region can include amino acids from both a CDR region defined according to Kabat and a hypervariable loop.

Unless otherwise specified herein, numbering of amino acid residues in the Fc region or constant region is according to the EU numbering system, also called the EU index, as described in Kabat et al.

In certain embodiments, the antibody against Ambra-1 further comprises the following heavy chain variable domain framework regions (FRs):

(a) HCFR1 comprising the amino acid sequence of SEQ ID NO:7;

(b) HCFR2 comprising the amino acid sequence of SEQ ID NO:8;

(c) HCFR3 comprising the amino acid sequence of SEQ ID NO: 9; and/or

(d) HCFR4 comprising the amino acid sequence of SEQ ID NO: 10.

In certain embodiments, the antibody against Ambra-1 further comprises the following light chain variable domain FRs: (e) LCFR1 comprising the amino acid sequence of SEQ ID NO:1 1 ;

(f) LCFR2 comprising the amino acid sequence of SEQ ID NO:12;

(g) LCFR3 comprising the amino acid sequence of SEQ ID NO: 13; and/or

(h) LCFR4 comprising the amino acid sequence of SEQ ID NO: 14.

As used herein, "Framework regions (FRs)" are those variable domain residues other than the CDR residues. Each variable domain typically has four FRs identified as FR1 , FR2, FR3 and FR4. If the CDRs are defined according to Kabat, the light chain FR residues are positioned at about residues 1 -23 (LCFR1 ), 35-49 (LCFR2), 57-88 (LCFR3), and 98-107 (LCFR4) and the heavy chain FR residues are positioned about at residues 1 -30 (HCFR1 ), 36-49 (HCFR2), 66-94 (HCFR3), and 103-1 13 (HCFR4) in the heavy chain residues.

If the CDRs comprise amino acid residues from hypervariable loops, the light chain FR residues are positioned about at residues 1 -25 (LCFR1 ), 33-49 (LCFR2), 53-90 (LCFR3), and 97-107 (LCFR4) in the light chain and the heavy chain FR residues are positioned about at residues 1 -25 (HCFR1 ), 33-52 (HCFR2), 56-95 (HCFR3), and 102-1 13 (HCFR4) in the heavy chain residues. In some instances, when the CDR comprises amino acids from both a CDR as defined by Kabat and those of a hypervariable loop, the FR residues will be adjusted accordingly. For example, when CDRH1 includes amino acids H26-H35, the heavy chain FR1 residues are at positions 1 -25 and the FR2 residues are at positions 36-49.

In certain embodiments, the antibody against Ambra-1 further comprises an antibody variable domain comprising:

(a) a V _H sequence having at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or more sequence identity to the amino acid sequence of SEQ ID NO: 15;

(b) a VL sequence having at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or more sequence identity to the amino acid sequence of SEQ ID NO 16; or

(c) a VH sequence as in (a) and a VL sequence as in (b).

In certain embodiments, the antibody against Ambra-1 comprises:

(d) a V _H sequence comprising SEQ ID NO:15;

(e) a V _L sequence comprising SEQ ID NO: 16; or

(f) a V _H sequence as in (d) and a V _L sequence as in (e). As used herein, "antibody variable domain" refers to the portions of the light and heavy chains of antibody molecules that include amino acid sequences of the CDRs (i.e., CDR1 , CDR2, and CDR3) and the FRs (i.e., FR1 , FR2, FR3 and FR4). VH refers to the variable domain of the heavy chain. V _L refers to the variable domain of the light chain.

As used herein,“sequence identity” refers to a sequence having the specified percentage of amino acid residues that are the same, when compared and aligned (introducing gaps, if necessary) for maximum correspondence, not considering any conservative amino acid substitutions as part of the sequence identity. The percent identity can be measured using sequence comparison software or algorithms or by visual inspection. Various algorithms and software are known in the art that can be used to obtain alignments of amino acid sequences. Suitable programs to determine percent sequence identity include for example the BLAST suite of programs available from the U.S. Government’s National Center for Biotechnology Information BLAST web site. Comparisons between two sequences can be carried using either the BLASTN or BLASTP algorithm. BLASTN is used to compare nucleic acid sequences, while BLASTP is used to compare amino acid sequences. ALIGN, ALIGN-2 (Genentech, South San Francisco, California) or MegAlign, available from DNASTAR, are additional publicly available software programs that can be used to align sequences. One skilled in the art can determine appropriate parameters for maximal alignment by alignment software. In certain embodiments, the default parameters of the alignment software are used.

In certain embodiments, the antibody against Ambra-1 comprises a Fab fragment comprising the Fd chain of SEQ ID NO: 17; and/or the light chain of SEQ ID NO: 18. Typically, such antibodies further comprise one or more dimerization domain sequences, one or more linker sequences and/or one or more epitope tags as described herein.

In certain embodiments, the antibody against p62 is available from a commercial supplier. For example, the antibody against p62 may be AbCAM Ab96134 as described herein. Alternatively, the antibody against Ambra-1 may be BioRad AbD34907 or AbD34908 as described herein.

In certain embodiments, the antibody against p62 comprises the following heavy chain variable domain complementarity determining regions (CDRs):

(a) HCDR1 comprising the amino acid sequence of SEQ ID NO: 23 or 41 ;

(b) HCDR2 comprising the amino acid sequence of SEQ ID NO: 24 or 42; and/or

(c) HCDR3 comprising the amino acid sequence of SEQ ID NO: 25 or 43.

In certain embodiments, the antibody against p62 further comprises the following light chain variable domain CDRs: (d) LCDR1 comprising the amino acid sequence of SEQ ID NO: 26 or 44;

(e) LCDR2 comprising the amino acid sequence of SEQ ID NO: 27 or 45; and/or

(f) LCDR3 comprising the amino acid sequence of SEQ ID NO: 28 or 46.

In certain embodiments, the antibody against p62 further comprises the following heavy chain variable domain framework regions (FRs):

(a) HCFR1 comprising the amino acid sequence of SEQ ID NO: 29 or 47;

(b) HCFR2 comprising the amino acid sequence of SEQ ID NO: 30 or 48;

(c) HCFR3 comprising the amino acid sequence of SEQ ID NO: 31 or 49; and/or

(d) HCFR4 comprising the amino acid sequence of SEQ ID NO: 32 or 50.

In certain embodiments, the antibody against p62 further comprises the following light chain variable domain FRs:

(e) LCFR1 comprising the amino acid sequence of SEQ ID NO: 33 or 51 ;

(f) LCFR2 comprising the amino acid sequence of SEQ ID NO: 34 or 52;

(g) LCFR3 comprising the amino acid sequence of SEQ ID NO: 35 or 53; and /or

(h) LCFR4 comprising the amino acid sequence of SEQ ID NO: 36 or 54.

In certain embodiments, the antibody against p62 further comprises an antibody variable domain comprising:

(a) a V _H sequence having at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or more sequence identity to the amino acid sequence of SEQ ID NO: 37 or 55;

(b) a V _L sequence having at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99% or more sequence identity to the amino acid sequence of SEQ ID NO 38 or 56; or

(c) a V _H sequence as in (a) and a V _L sequence as in (b).

In certain embodiments, the antibody against p62 comprises:

(d) a V _H sequence comprising SEQ ID NO: 37 or 55;

(e) a VL sequence comprising SEQ ID NO: 38 or 56; or

(f) a VH sequence as in (d) and a VL sequence as in (e).

In certain embodiments, the antibody against p62 comprises a Fab fragment comprising the Fd chain of SEQ ID NO:39 and/or the light chain of SEQ ID NO:40. Alternatively, the antibody against p62 may comprise a Fab fragment comprising the Fd chain of SEQ ID NO: 57 and/or the light chain of SEQ ID NO: 58. Typically, such antibodies further comprise one or more dimerization domain sequences, one or more linker sequences and/or one or more epitope tags as described herein.

The invention provides use of antibodies (or aptamers) against Ambra-1 or p62 as described herein. Typically, the antibodies (or aptamers) against Ambra-1 or p62 are used in methods of determining the margin of a tumour in a tissue sample obtained from a subject with SCC as described herein.

The invention also provides antibodies (or aptamers) that compete for binding to Ambra-1 or p62 with antibodies (or aptamers) as described herein. Typically, competition assays are used to identify an antibody (or aptamer) that competes for binding to Ambra-1 or p62. In an exemplary competition assay, immobilized Ambra-1 or p62 is incubated in a solution comprising a first labelled antibody (or aptamer) that binds to Ambra-1 or p62 and a second unlabelled antibody (or aptamer) that is being tested for its ability to compete with the first antibody (or aptamer) for binding to Ambra-1 or p62. The second antibody (or aptamer) may be present in a hybridoma supernatant. As a control, immobilized Ambra-1 or p62 may be incubated in a solution comprising the first labelled antibody (or aptamer) but not the second unlabelled antibody (or aptamer). After incubation under conditions permissive for binding of the first antibody (or aptamer) to Ambra-1 or p62 excess unbound antibody (or aptamer) may be removed, and the amount of label associated with immobilized Ambra-1 or p62 measured. If the amount of label associated with immobilized Ambra-1 or p62 is substantially reduced in the test sample relative to the control sample, then that indicates that the second antibody (or aptamer) is competing with the first antibody (or aptamer) for binding to Ambra-1 or p62 respectively. See, e.g., Harlow et al. Antibodies: A Laboratory Manual. Ch.14 (Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, 1988).

In certain embodiments, antibodies (or aptamers) that compete for binding to Ambra-1 or p62 bind to the same epitope (e.g., a linear or a conformational epitope) as the antibodies (or aptamers) described herein. Detailed exemplary methods for mapping an epitope to which an antibody binds are provided in Morris "Epitope Mapping Protocols, " in Methods in Molecular Biology Vol. 66 (Humana Press, Totowa, NJ, 1996).

Certain aspects of the present invention further provide isolated nucleic acids that encode any of the antibodies (or aptamers) described herein. Also provided is a vector (e.g., an expression vector) comprising the nucleic acid for expressing any of the antibodies (or aptamers) described herein. Also provided are host cells comprising the preceding nucleic acids and/or vectors.

Certain aspects of the present invention further provide immunoconjugates comprising any of the antibodies (or aptamers) described herein conjugated to one or more capture agents. As described herein, a capture agent typically comprises a binding and/or detection moiety (e.g. an enzyme and/or fluorescent label).

Certain aspects of the present invention further provide antibodies (or aptamers) that bind to the same epitope as the anti-Ambra-1 or p62 antibodies(or aptamers) as described herein.

In certain embodiments, the invention provides antibodies (or aptamers) that bind specifically to peptides near the carboxyl-terminus of human Ambra-1.

In certain embodiments, the invention provides antibodies (or aptamers) that bind specifically to peptides near the carboxyl-terminus of human Ambra-1.

In certain embodiments, the invention provides antibodies (or aptamers) that bind to p62, wherein said antibodies (or aptamers) specifically bind near the carboxyl-terminus of human p62. In certain embodiments, the invention provides antibodies (or aptamers) that bind to p62, wherein said antibodies (or aptamers) specifically bind to a region comprising 8, 9, 10, 1 1 , 12, 13, 14, 15, 16, 17, 18, 19, 20 or more of the amino acids shown in SEQ ID NO: 62.

As used herein, the term“epitope” means a protein determinant capable of specific binding to an antibody. Typically, an epitope comprises chemically active surface groupings of molecules such as amino acids or sugar side chains usually having specific three-dimensional structural and charge characteristics. The epitope may comprise amino acid residues directly involved in the binding and optionally additional amino acid residues that are not directly involved in the binding.

As used herein, an antibody (or aptamer) that“specifically” binds to an epitope refers to an antibody (or aptamer) that recognizes the epitope while only having little or no detectable reactivity with other portions of Ambra-1 . Such relative specificity can be determined e.g. by competition assays, foot-printing techniques or mass spectrometry techniques as known in the art. In certain embodiments, the epitope comprises peptide antigenic determinants within single peptide chains of Ambra-1 . In certain embodiments, the epitope comprises conformational antigenic determinants comprising one or more contiguous amino acids on a particular chain and/or on spatially contiguous but separate peptide chains. In certain embodiments, the epitope comprises post-translational antigenic determinants comprising molecular structures (e.g. carbohydrate groups) covalently attached to Ambra-1 .

The epitope may comprise any suitable number and/or type of amino acids, in any suitable position as defined herein. For example, the epitope may comprise about 3 to about 10 amino acids, typically about 3 to about 8 amino acids, in or more contiguous or non-contiguous locations with respect to the amino acid sequence of Ambra-1 as set forth in SEQ ID NO: 21 , 22 and/or 63.

In certain embodiments, the invention provides antibodies (or aptamers) that bind to Ambra- 1 , wherein said antibodies (or aptamers) specifically bind to a region comprising 8, 9, 10, 1 1 , 12, 13, 14, 15, 16, 17, 18, 19, 20 or more of the amino acids 1270 to 1298 of human Ambra- 1 sequence shown in SEQ ID NO: 21 . Typically, such antibodies (or aptamers) specifically bind to a region comprising amino acids 1280 to 1281 of SEQ ID NO: 21 , amino acids 1294 to 1296 of SEQ ID NO: 21 and/or amino acids 1294 to 1297 of SEQ ID NO: 21 .

In certain embodiments, the invention provides antibodies (or aptamers) that bind to Ambra- 1 , wherein said antibodies (or aptamers) specifically bind to a region comprising 8, 9, 10, 1 1 , 12, 13, 14, 15 or more of CGGSSRGDAAGPRGEPRNR (SEQ ID NO: 22). Typically, such antibodies (or aptamers) specifically bind to a region comprising at least EPRN (SEQ ID NO: 67) or EPR (SEQ ID NO: 68) of Ambra-1.

In certain embodiments, the invention provides antibodies (or aptamers) that bind to Ambra- 1 , wherein said antibodies (or aptamers) specifically bind to a region comprising 8, 9, 10, 1 1 , 12, 13, 14, 15 or more of DGGSSRGDAAGPRGEPRNR (SEQ ID NO: 64). Typically, such antibodies (or aptamers) specifically bind to a region comprising at least DG, EPRN (SEQ ID NO: 67) and/or EPR (SEQ ID NO: 68) of Ambra-1 .

In certain embodiments, the invention provides antibodies (or aptamers) that bind to Ambra- 1 , wherein said antibodies (or aptamers) specifically bind to a region comprising HLLDGGSSR (SEQ ID NO: 65) and/or EPR (SEQ ID NO: 68) of Ambra-1 .

In certain embodiments, the invention provides antibodies (or aptamers) that bind to Ambra- 1 , wherein said antibodies (or aptamers) specifically bind to a region comprising NHLLDGGSSR (SEQ ID NO: 66) and/or EPR (SEQ ID NO: 68) of Ambra-1 . Visualisation of antibodies

In certain embodiments, the invention provides a method of labelling Ambra-1 and/or p62 in a SCC tissue sample, the method comprising:

(a) contacting the SCC tissue with an antibody (or aptamer) against Ambra-1 and/or an antibody (or aptamer) against p62 as described herein; and

(b) visualising the antibody (or aptamer) against Ambra-1 and/or antibody (or aptamer) against p62 in the SCC tissue with a reagent that generates a detectable signal.

The SCC tissue sample may further comprise at least a portion of a peri-tumoral epidermis overlying the primary tumour. In certain embodiments, the SCC tissue sample further comprises normal tissue adjacent the primary tumour. Typically, the SCC tissue sample is a biopsy, or a section thereof, obtained from a subject suffering from SCC.

In certain embodiments, a decrease or loss in the expression of Ambra-1 compared to reference tissue or levels (e.g. normal tissue) may be determined (e.g. visualised) within the SCC tissue. Such an expression pattern may be indicative of tumour positive tissue (e.g. immediately or directly adjacent to normal tissue).

Alternatively, no significant difference in the expression of Ambra-1 compared to reference tissue or levels (e.g. normal tissue) may be determined (e.g. visualised) within the SCC tissue. Such an expression pattern may be indicative of tumour negative tissue (e.g. immediately or directly adjacent to the tumour).

In certain embodiments, an increase in the expression of p62 (e.g. nuclear p62) compared to reference tissue or levels (e.g. normal tissue) may be determined (e.g. visualised) within the SCC tissue. Such an expression pattern may be indicative of tumour positive tissue (e.g. immediately or directly adjacent to normal tissue).

Alternatively, no significant difference in p62 expression (e.g. nuclear p62) compared to reference tissue or levels (e.g. normal tissue) may be determined (e.g. visualised) within the SCC tissue. Such an expression pattern may be indicative of tumour negative tissue (e.g. immediately or directly adjacent to the tumour).

Aptly, immunohistochemistry (e.g. semi-quantitative automated IHC) is used to determine and/or quantify the expression pattern of Ambra-1 and/or p62 in the SCC tissue sample.

Methods of excising tumours In certain embodiments, the invention provides a method of excising a tumour from a subject with SCC as described herein (e.g. cSCC). Typically, the tumour is a primary tumour. Typically, the SCC is invasive and/or AJCC Stage I or II.

In certain embodiments, the method of excising a tumour comprises excising one or more section(s) of tissue peripheral to the tumour to obtain a tissue sample from the subject.

The tissue sample may be any tissue sample as described herein. Typically, the tissue sample comprises one or more sections of tissue that are topographically marked. Typically, the tissue sample comprises one or more horizontal sections of the tumour. Typically, the tissue sample comprise one or more sections of tissue that are about 2mm or less. Typically, the tissue sample comprises a surgical margin.

In certain embodiments, the method of excising a tumour comprises determining the margin of the tumour in the tissue sample. The margin of the tumour may be determined by any method described herein. Typically, the one or more sections of tissue peripheral to the tumour are determined (e.g. classified) as tumour positive and/or tumour negative. In certain embodiments, one or more sections of tissue are used to map the margin of the tumour.

In certain embodiments, determining the margin of the tumour allows excision (e.g. removal) of the tumour by complete excision of tumour positive tissue whilst avoiding (or minimising) excision of tumour negative tissue. This may allow the complete excision of the tumour whilst sparing the removal of healthy tissue to minimise disfigurement or scarring after surgery.

In one embodiment, one or more sections of tissue peripheral to the tumour (e.g. the surgical margins) are assessed after the tumour has been removed (e.g. post-operatively). If such tissue is tumour negative, a normal recognised care pathway may be followed. If such tissue is tumour positive, further surgery may be performed to completely excise the tumour. In addition or alternatively, the subject may be treated with a systemic anti-carcinoma treatment regime.

In an alternative embodiment, one or more sections of tissue peripheral to the tumour (e.g. the surgical margins) are assessed during removal of the tumour (e.g. intra-operatively). If such tissue is tumour negative, no further corresponding section(s) of tissue peripheral to the tumour may need to be excised. If such tissue is tumour positive, then one or more further corresponding section(s) of tissue peripheral to the tumour may be excised until the tissue is tumour negative (or until no further tumour positive tissue is capable of being excised).

As used herein, a“corresponding section” of tissue refers to a section of tissue in the subject adjacent to the excised section of tissue. As such, the method of excising a tumour described herein allows the excision of tumour negative tissue to be minimised during surgery based on the determined margin of the tumour.

In certain embodiments, the subject is undergoing Mohs micrographic surgery. For example, the tumour may be removed a thin layer at a time (e.g. 2mm, 1 mm, 0.5mm or less). In such embodiments, the tissue sample obtained from the subject may comprise a thin section (e.g. 2mm, 1 mm, 0.5mm or less) of tissue.

In Mohs surgery, typically each layer of tissue is examined in horizontal sections. If the tissue sample is tumour positive, a further layer of tissue may be taken from any areas in which the tumour remains until all of the tumour positive tissue has been removed. Advantageously, this keeps the wound as small as possible. Furthermore, it may be certain that tumour positive tissue is completely removed during the procedure.

In certain embodiments of Mohs surgery, the SCC is first outlined (e.g. using a marker pen). The tumour may then be removed with a surgical margin of tissue (e.g. apparently non- cancerous tissue) peripheral to the tumour. Typically, a map of the surgical site and one or more sections of the tissue sample may be determined. If one or more further corresponding section(s) of tissue peripheral to the tumour need to be excised, this allows the correct position for any further localised surgery to be identified.

In certain embodiments, the sample may be obtained within about 24 hours, 12 hours, 6 hours or less prior to the method of determining the margins of the tumour. If one or more sections of tissue peripheral to the tumour are tumour positive, a further layer of tissue may be removed from the corresponding area on the wound. This process may be repeated as many times as necessary until one or more sections of tissue peripheral to the tumour are tumour negative.

The methods of the invention allow the tumour to be completely removed. For example, sometimes the tumour can be much larger than is visible at first on the surface of the skin. SCC most frequently arise in the head and neck region, where minimising surgical wounds is particularly important in order to ensure a good cosmetic outcome.

Methods of treatment

In certain embodiments, if the one or more sections of tissue peripheral to the tumour are tumour negative (e.g. if the tumour has been or is completely excised), a normal recognised care pathway may be followed.

In certain embodiments, a“normal recognized care pathway” may comprise regular (e.g. every 3-12 months) clinical assessment of the subject for up to 5 years. For example, the normal recognized care pathway may comprise a follow up plan comprising a risk assessment of locoregional recurrences, metastatic spread or development of new lesions. The normal recognized care pathway may further comprise carrying out a staging CT scan on the subject, from the head to the pelvis, at the time of diagnosis. For example, in some embodiments, the normal recognized care pathway may further comprise carrying out a sentinel lymph node biopsy.

In certain embodiments, a normal recognized care pathway may comprise topical chemotherapy, e.g. administration of fluorouracil (5-FU) or imiquimod to the skin and/or photodynamic therapy.

In certain embodiments, if the one or more sections of tissue peripheral to the tumour are tumour positive (e.g. if the tumour has not or cannot be completely excised), a systemic anticarcinoma treatment regime may be followed.

In certain embodiments, a“systemic anti-carcinoma treatment regime” is for preventing, inhibiting or delaying metastasis or decreasing the risk of metastasis in the subject. For example, the systemic anti-carcinoma treatment regime may comprise a regional lymph node dissection. In certain embodiments, the systemic anti-carcinoma treatment regime comprises administering a therapeutic agent to the subject.

In some embodiments, the therapeutic agent is a chemotherapeutic agent. Any suitable chemotherapeutic agent may be administered to the subject. As used herein, a “chemotherapeutic agent” means any therapeutic agent useful for the treatment of SCC (e.g. invasive SCC) including small molecules.

In some embodiments, the chemotherapeutic agent is a platinum-based chemotherapy. In some embodiments, the chemotherapeutic agent is selected from isotretinoin, interferon, retinoid, capecitabine, cisplatin and/or fluorouracil (5-FU). For example, the chemotherapeutic agent may be cisplatin and 5FU. In some embodiments, the chemotherapeutic agent is dacarbazine (DTIC) and/or temozolomide.

In some embodiments, the chemotherapeutic agent is a biological agent.

In certain embodiments, the biological agent may be an anti-EGFR therapy e.g. cetuximab or a tyrosine kinase inhibitor e.g. gefetinib and/or imatinib. In certain embodiments, the biological agent is nilotinib or palbociclib.

In certain embodiments, the biological agent is an inhibitor of the 26S proteasome such as bortezomib.

In certain embodiments, the biological agent is an inhibitor of Human Papilloma Virus (HPV). In certain embodiments, the biological agent is dabrafenib, trametinib, vemurafenib and/or cobimetinib.

In certain embodiments, the biological agent is a checkpoint inhibitor. For example, the biological agent may be an anti-CTLA-4 therapy (e.g. ipilimumab). The biological agent may be an anti- PD-1 therapy (e.g. nivolumab, pembrolizumab or spartazumab). The biological agent may be an anti-PD-L1 therapy (e.g. atezolizumab).

In certain embodiments, the biological agent may be an anti- LAG3, anti-TIM-3, anti-TIGIT, anti-VISTA, anti-B7-H3, anti-KIR, anti-TGF-b, anti-OX40, anti-ICOS, anti-GITR, anti-4-1 BB, anti-CD40, anti-IFO or anti-TLR therapy.

In certain embodiments, the biological agent is a CAR-T cell therapy.

In certain embodiments, the biological agent is a T-VEC vaccine (Imylgic), BCG vaccine, interferon, or IL-2.

In certain embodiments, the biological agent is a BRAF inhibitor and/or a MEK inhibitor.

In certain embodiments, the chemotherapeutic and/or biologic agent is used in combination with radiation.

In certain embodiments, the invention provides a method of treating a subject suffering from SCC (e.g. invasive SCC) comprising administering a therapeutic agent to a subject determined as having tumour positive tissue following the methods described herein.

Ideally, a subject determined as having tumour positive tissue as described herein is treated as soon as possible to minimize the chances of metastasis or recurrence of the tumour. Thus, in some embodiments the method or treatment regime is for preventing, inhibiting or delaying metastasis or decreasing the risk of metastasis of tumour positive tissue that remains in the subject after the surgery.

In some embodiments, the subject is treated immediately or shortly after being identified as having tumour positive tissue as described herein. For example, treatment with the therapeutic agent may be carried out after surgery to excise the primary tumour.

In some embodiments, a method of treatment or a treatment regime may further include one or more of: intensified imaging (e.g. CT scan, PET, MRI, X-ray) of the subject; discussion and/or offering of, or carrying out, a sentinel lymph node biopsy; partial or complete lymphadenectomy; inclusion of the subject in clinical trials; and radiation therapy.

In some embodiments, a therapeutic agent is administered to the subject no more than 12 weeks, no more than 10 weeks, no more than 6 weeks, no more than 4 weeks, no more than 2 weeks or no more than 1 week after the subject is identified as having tumour positive tissue according to the methods described herein.

Non-limiting routes of administration of the therapeutic agent include by oral, intravenous, intraperitoneal, subcutaneous, intramuscular, topical, intradermal, intranasal or intrabronchial administration (for example as effected by inhalation). In some embodiments, the therapeutic agent is administered parenterally, e.g., intravenously. Common modes of administration by which the therapeutic agent may be administered include, for example, administration as a bolus dose or as an infusion over a set period.

A therapeutic agent may be administered in an amount effective to prevent, inhibit or delay the development of metastasis. Suitable doses and dosage regimes for a given subject and therapeutic agent can be determined using a variety of different methods, such as body- surface area or body-weight, or in accordance with specialist literature and/or individual hospital protocols. Doses may be further adjusted following consideration of a subject's neutrophil count, renal and hepatic function, and history of any previous adverse effects to the therapeutic agent. Doses may also differ depending on whether a therapeutic agent is used alone or in combination.

The skilled person will recognize that further modes of administration, dosages of therapeutic agents and treatment regimens can be determined by the treating physician according to methods known in the art.

Assays

Certain aspects of the present invention provide in vitro assays for determining the margin of a tumour in a tissue sample.

Aptly, the assay comprises contacting one or more sections of tissue peripheral to the tumour as described herein with a ligand against Ambra-1 and/or p62 as described herein. In the assay, the presence of Ambra-1 creates an Ambra-1 -ligand complex. Conversely, the presence of p62 creates an p62-ligand complex. The assay may further comprise detecting and/or quantifying the Ambra-1 -ligand and the p62-ligand complex.

In some embodiments, the first and/or second ligand comprises a detection moiety (e.g. a fluorescent label). A detection moiety enables the direct or indirect detection and/or quantification of the complexes formed.

In some embodiments, the first ligand comprises a first detection moiety and the second ligand comprises a second detection moiety. The first detection moiety may be the same as the second detection moiety, or it may be different. In some embodiments, the method comprises contacting a first portion of the tissue with the first ligand, and contacting a second portion of the tissue with the second ligand. This is particularly suitable for embodiments wherein the first detection moiety is the same as the second detection moiety. In some alternative embodiments, the method comprises contacting the tissue with the first ligand and contacting the same portion of tissue with the second ligand. It may be possible to detect and/or quantify both the Ambra-1 -ligand complex and the p62- ligand complex in the same sample, or portion or section thereof, particularly if the first and second detection moieties are different.

Aptly, the first and/or second ligands may be used in combination with one or more capture agents. Thus, in some embodiments, the step of detecting and/or quantifying the Ambra-1 - ligand complex and the p62-ligand complex comprises contacting the tissue sample(s) (or the section(s) or portion(s) thereof) with at least one capture agent. Aptly, a first capture agent which binds specifically to the first ligand may be used to detect and/or quantify the Ambra-1 - ligand complex, while a second capture agent which binds specifically to the second ligand may be used to the detect and/or quantify the p62-ligand complex. Alternatively, a single capture agent may be used which is capable of binding specifically to both the first and second ligands.

In some embodiments, the capture agent comprises a binding moiety and a detection moiety.

In some embodiments, the binding moiety is a secondary antibody which binds specifically to the first and/or second ligands. For example, the binding moiety may be a universal anti-lgG antibody that is capable of binding to primary antibodies used as the first and second ligands.

In some embodiments, the method further comprises one or more wash steps to remove unbound first and second ligands and, optionally, unbound capture agents.

In some particular embodiments, there is provided an in vitro assay for determining the margin of a tumour in a tissue sample, the assay comprising:

- contacting one or more sections of tissue peripheral to the tumour with a first ligand specific for Ambra-1 , wherein the presence of Ambra-1 creates an Ambra-1 -ligand complex;

- contacting the one or more sections of tissue peripheral to the tumour for p62, wherein the presence of p62 creates a p62-ligand complex;

- washing the tissue to remove unbound ligands;

- contacting the tissue with one or more capture agents, wherein the capture agents comprise a detection moiety and a binding moiety specific for the first and/or second ligands; - washing the first and second portions of the tissue to remove unbound capture agent; and

- detecting and/or quantifying the one or more capture agents present in the tissue.

Aptly, a suitable detection moiety is selected from a fluorescent moiety, a luminescent moiety, a bioluminescent moiety, a radioactive material, a colorimetric moiety, a nanoparticle having suitable detectable properties, a chromogenic moiety, biotin or an enzyme.

Suitable fluorescent moieties include fluorescent proteins (such as phycoerythrin (PE), peridinin- chlorophyll-protein complex (PerCP) and allophycocyanin (APC)) fluorescent dyes (such as Fluorescein Isothiocyanate (FITC), rhodamines (Rs) and cyanines (Cys)), fluorescent tandem complexes (such as Allophycocyanin-Cyanine 7 (APC-Cy7), Peridinin-Chlorophyll- Protein complex-Cyanine 5 (PerCP-cy5) and Phycoerythrin- Texas Red (PE-TexasRed)),and nanocrystals (such as QDot 525, QDot 545 and QDot 625). The presence of Ambra-1 -ligand and p62-ligand complexes can be detected using fluorescence microscopy via the use of fluorescent ligands or one or more capture agents comprising fluorescent detection moieties.

In embodiments where the detection moiety comprises an enzyme, the presence of the Ambra-1 -ligand complex and the p62-ligand complex can be detected and/or quantified by detecting and/or quantifying the reaction product of a reaction of a substrate catalyzed by the enzyme. In these embodiments, the method further comprises adding a substrate of the enzyme and detecting and/or quantifying the product of the reaction performed on the substrate by the enzyme. For example, the reaction may result in the production of a coloured precipitate, which would be detected using light microscopy. Suitable enzymes include, for example, alkaline phosphatase and horseradish peroxidase. A chromogenic substrate of alkaline phosphatase is PNPP (p-Nitrophenyl Phosphate, Disodium Salt). PNPP produces a yellow water-soluble reaction product that absorbs light at 405 nm. Chromogenic substrates of horseradish peroxidase include ABTS (2,2'-Azinobis [3-ethylbenzothiazoline-6-sulfonic acid]-diammonium salt), which yields a green reaction product, OPD (o-phenylenediamine dihydrochloride) which yields a yellow-orange reaction product, and TMB (3, 3', 5,5'- tetramethylbenzidine) soluble substrates yield a blue colour when detecting HRP. Other suitable enzyme-substrate combinations, methods of detecting the Ambra-1 -ligand and p62- ligand complexes, and suitable detection moieties will be known to those skilled in the art.

In some embodiments, the first and/or second ligand or the capture agent is immobilized on a solid phase surface, for example a microarray, slide, well or bead. In some embodiments, the expression of Ambra-1 and p62 is detected and/or quantified by visual assessment, for example, microscopy. In other embodiments, the expression of Ambra- 1 and p62 is detected and/or quantified by an automated slide scanner.

In certain embodiments, the method of detecting and/or quantifying the Ambra-1 -ligand and/or p62-ligand complex comprises outputting, optionally on a computer, an indication of whether the one or more complexes are present or absent, and this indicates whether the tissue is tumour positive or negative.

Kits

The invention also provides a kit for determining the margin of a tumour in a tissue sample, the kit comprising a ligand against Ambra-1 and/or p62 as described herein.

In certain embodiments, the ligand against Ambra-1 and/or p62 is an anti-Ambra-1 and/or anti- p62 antibody or aptamer as described herein.

In certain embodiments, the kit further comprises instructions for using the kit for determining the margin of a tumour in a tissue sample obtained from a subject with SCC.

In certain embodiments, the kit further comprises at least one capture agent. Typically, a capture agent comprises a detection moiety and/or a binding moiety as described herein.

In certain embodiments, the detection moiety is an enzyme (e.g. alkaline phosphatase) and the kit further comprises a substrate of the enzyme.

Typically, the kit further comprises one or more additional components such as reagents and/or apparatus necessary for carrying out an in vitro assay, e.g. buffers, fixatives, wash solutions, blocking reagents, diluents, chromogens, enzymes, substrates, test tubes, plates, pipettes etc.

The kit of certain embodiments of the invention may advantageously be used for carrying out a method of certain embodiments of the invention and could be employed in a variety of applications, for example in the diagnostic field or as a research tool. It will be appreciated that the parts of the kit may be packaged individually in vials or in combination in containers or multi-container units. Typically, manufacture of the kit follows standard procedures which are known to the person skilled in the art.

Example 1 - Ambra-1 is a biomarker of keratinocyte differentiation

IHC analysis of AMBRA 1 expression in normal skin in vivo revealed increased expression from the basal layer to the stratum corneum in line with increasing keratinocyte differentiation (Figure 1A). Calcium-induced differentiation of CCD1 106 or primary keratinocytes for 5 days in vitro was also reflected by increased expression of AMBRA1 in line with expected changes in other differentiation markers such as loricrin (Fig 1 B/C).

Furthermore, siRNA mediated knockdown of AMBRA1 in primary calcium induced differentiated keratinocytes results in deregulated differentiation, as evidenced by decreased loricrin mRNA and protein expression (Figure 2). These observations are also associated with an increase in keratinocyte proliferation and collectively highlight the critical role for Ambra-1 in normal keratinocyte differentiation as well as suppression of excessive cellular proliferation.

Example 2 - loss of Ambra-1 expression in cSCC tumours results in loss of terminal differentiation leading to more aggressive phenotypes

IHC analysis of a retrospective cohort of cSCC sub-type biopsies confirmed increased Ambra- 1 expression in normal epidermis in-line with epidermal differentiation. However, within the cSCC tumour itself a distinct difference in Ambra-1 expression was observed between“well- differentiated” and “poorly-differentiated” tumours; with “poorly-differentiated” tumours exhibiting markedly reduced/absent Ambra-1 expression compared to the normal epidermis, or well-differentiated tumours. Similar reductions in Ambra-1 expression were also detected in dysplastic cells comprising actinic keratoses or Bowen’s disease (Figure 3).

Taken together, these data show loss of Ambra-1 expression in cSCC results in loss of terminal differentiation leading to a more aggressive phenotype.

Example 3 - Loss of AMBRA1 and increased p62 expression in cSCC is associated with poorly differentiated cSCC

To confirm a potential relationship of AMBRA1 expression with differentiation status and to explore the potential of both AMBRA1 and p62 as prognostic biomarkers for cSCC, IHC expression of AMBRA1 and p62 was analysed in a cohort of in situ , poorly or well differentiated cSCCs (Figure 4). Results revealed loss of AMBRA1 expression and increased cytoplasmic expression of p62 were associated with poorly differentiated cSCCs (Fig 4G & H).

Example 4 - Nuclear p62 expression is a marker for epidermal dysplasia

IHC analysis of nuclear and cytoplasmic p62 expression in normal epidermis and the adjacent epidermis to cSCCs or cSCC in situ revealed a step wise progression from normal epidermis to in-situ carcinoma is associated with increased nuclear p62 (Figure 5). These data suggest that the absence of nuclear p62 represents normal epidermis and a potential tumour excision margin. In particular, increased nuclear p62 expression is observed in dysplastic keratinocytes in the normal epidermis immediately adjacent to the tumour which declined distally in the epidermis from the cSCC (Figure 5). This observation supports the hypothesis that autophagy blockade is an early tumour initiating factor and the use of p62 as a marker to aid mohs surgery in defining excision margin adequacy.

Collectively these data suggests that Ambra-1 plays an important role in keratinocyte differentiation and proliferation. Variation of Ambra-1 and p62 expression in cSCC biopsies thus represents a diagnostic biomarker highlighting the presence of dysplastic cells, as well as being a prognostic biomarker of disease risk; thus allowing refinement of patient management in terms of surgical aggression, excision margin adequacy and patient follow up regimes.

Example 5 - Materials and Methods

Western blotting was used to detect AMBRA1 , Loricrin and GAPDH protein expression in primary keratinocytes or the CCD1 106 keratinocyte cell line in vitro in the presence or absence of calcium-induced (1 3mM) differentiation for 5 days.

Western blotting or RT-qPCR were used to determine protein (relative to GAPDH/p-actin) or mRNA levels (relative to RPL13A) of AMBRA1 or Loricrin in primary keratinocytes in the presence /absence of AMBRA1 siRNA and subsequent calcium induced differentiation in vitro for 5 days.

Keratinocyte proliferation in vitro was assessed by standard sulphorhodamine assay.

Pre-optimised semi-quantitative automated IHC was used to determine expression of AMBRA1 and p62 in FFPE tissue derived from a cohort of primary well or poorly differentiated cSCCs.

Immunohistochemistrv for Ambra-1 or p62

A staining protocol for the Ambra-1 or p62 antibodies is described briefly below:

Antigen retrieval buffer 10mM Tris HCL Ph 9.

Positive control: normal skin section adjacent primary carcinoma sections.

Negative controls: Null primaries of normal skin and all tumours.

Use research antibody for Ambra-1 Abeam Ab69501 1 /2500 1 hr room temperature, Use research antibody for p62 Abeam Ab96134 1/100 to 1/1000 1 hr room temperature,

- secondary anti-rabbit 1/200 from Rabbit VECTASTAIN Elite ABC HRP Kit (VECTOR laboratories). - Test conditions: Ambra-1 antibodies chosen at 20ug/ml 1 hr room temperature. Secondary antibody used Sigma anti-flag HRP A8592 at 1/200 concentration as optimised for each antibody.

- All tissue sections formalin fixed paraffin embedded, cut at 5mm and baked.

Deparaffinise Sections:

1 . Place slides in metal rack and incubate in Histoclear 20 mins.

2. Dip slides in: 100% ethanol for 5 secs, 75% for 5 secs, 50% for 5 secs, dH20 for 5 secs. Antigen Retrieval:

3. Place slides in plastic rack, with blank slides around the edges to even out the heat.

4. Place in buffer (10Mm Tris HCI PH 9 ) and heat in microwave.

5. Allow to cool slowly in buffer solution for 15 minutes.

Permeabiiize Cells:

6. Place slides on flat metal tray, draw around sections with hydrophobic pen and allow to dry.

7. Incubate sections with PBS/T (PBS + 0.05% Tween 20) for 3 mins to rehydrate sections.

8. Incubate slides in 0.2% Triton X-100 in PBS/T for 10 mins.

Block Endogenous Peroxidase:

9. Wash with PBS/T

10. Incubate with 3% H202 in water for 10 min

Endogenous Avidin/Biotin Blocking Step:

1 1 . Wash with PBS/T

12. Block endogenous Avidin (Vector Labs Avidin/Biotin Blocking kit) for 15 mins

13. Wash with PBS/T

14. Block endogenous Biotin (Vector Labs Avidin/Biotin Blocking kit) for 15 mins

Protein Blocking Step:

15. Wash with PBS/T

16. Incubate with appropriate 2% serum in PBS/T (2 drops in 5 ml) Normal mouse/goat serum (Sigma/Vector Labs) for 20mins

17. Wash with PBS/T

Primary Antibody:

1 . Incubate with anti-Ambra-1 primary antibody (in PBS/ 2% serum) or anti-p62 primary antibody 1 hr room temperature. Incubate positive control slide with research antibody abCam ab176322, ab69501 (PBS/ 2% serum) 1 hr room temperature.

2. 3x Wash with PBS/T

Secondary Antibody:

3. Incubate with biotinylated anti rabbit/anti-flag secondary antibody. 4. Prepare ABC Reagent from Vectastain Elite kit, leave at room temperature for 30 min a. 2.5 ml PBS + 1 drop A + 1 drop B

5. 3x Wash with PBS/T

Staining:

6. Incubate with ABC reagent for 30 mins.

7. 3x Wash with PBS/T.

8. Prepare DAB substrate as per manufacturer’s instructions (Vector, ImmPACT DAB EqV peroxidase substrate SK-4103). Mix an equal volume of DAB reagent 1 and 2, mix well before use (working solution can be stored for 1 week at 2-8 ^s C).

9. Incubate tissue sections with DAB substrate for 2 mins.

10. Rinse slides in water for 5 mins to stop peroxidase reaction.

1 1 . Incubate in Meyer’s Haemalum (hematoxylin) for 10 minutes.

12. Wash 10 min with frequent changes

13. Put slides in: 75% ethanol for 5 secs (blot firmly), 100% ethanol for 5 secs

14. Put slides in Histoclear to clean sections for 2 minutes.

15. Allow slides to dry and mount cover slips with DPX.

Development of anti-Ambra- 1 or o62 antibodies

Antibodies against Ambra-1 were produced using BioRad HuCAL PLATINUM ^® antibody generation technology and CysDisplay ^® technology. HUCAL stands for‘Human Combinatorial antibody library’, which is a synthetic (generated by de novo gene synthesis) antibody library containing human antibody gene sequences covering more than 95% of the human structural gene repertoire (45 billion antibodies) that are cloned in E. coli phagemid vectors. Each E. coli phage contains one of the 45 billion antibody genes and displays the corresponding antibody on their surface in Fab format, by means of a disulfide linkage between Fab and gene III protein (CysDisplay).

Antigens of Ambra-1 (a synthesized peptide) were used to isolate the antibodies described herein. The antigens were immobilized on to a solid support (i.e., ELISA microtiter plates or covalently coupled to magnetic beads), before the HuCAL library presented on phage was incubated with the antigens. Non-specific antibodies were removed by washing and specific antibody phages eluted by adding a reducing agent.

CysDisplay technology, where the Fab antibody fragment is linked to the phage by a disulphide bond that is easily cleavable rather than a conventional peptide bond, was used to allow more efficient elution of high affinity phages with reducing agents during antibody selection (Bio-Rad). This ensured that high affinity antibodies were not lost during selection, a common problem with more traditional panning phage display methods.

The specific antibody phages were used to infect an E. coli culture along with helper phages, allowing the enriched antibody phage library to be used for subsequent rounds of panning (usually 2 - 3 rounds of enrichment panning).

After panning, the phagemid DNA encoding the enriched antibody population was isolated as a pool and subcloned into a Fab expression vector containing antibiotic resistance. The vector format chosen was a bivalent Fab (Fab-A-FH) formed with dimerization of bacterial alkaline phosphatase, with two tags Flag (DYKDDDK) and His 6 (His6). E. coli was then transformed with the Fab expression vector ligation mixture and plated on agar plates containing antibiotic. Each growing colony represents a monoclonal antibody and was picked and grown in a 384 well microtiter plate. Antibody expression was induced and the culture harvested and lysed to release the antibodies.

Culture lysates were screened primarily for specific antigen binding to antigens by indirect ELISA. 95 ELISA-positive antibody clones, derived from the primary screening, were ranked according to their binding strength (koff-rate determination; ‘secondary screening’) as measured by Bio-Layer Interferometry using the Pall ForteBio Octet ^® System. Antibodies were then selected according to both antigen specificity and binding strength. Hits from the primary or secondary antibody screening procedures were sequenced to identify unique antibodies. The Fab antibodies with unique sequences were expressed in E. coli and purified using one-step affinity chromatography. Purified antibodies were tested by QC ELISA for required specificity. This QC ELISA screen was performed on native as well as denatured antigen due to the final antibody application of immunohistochemistry, where antigens during the tissue processing may be denatured, as well as immobilized control proteins Glutathione S-transferase, BSA (carrier protein), N1 -CD33-His6 (the ectodomain of human CD33 fused to the N1 domain of the g3p filamentous phage M13) used for calculation of background. Purity was assessed by Coomassie® staining of a sodium dodecyl sulfate-polyacrylamide gel (SDS- PAGE) and concentration measured by UV absorbance at 280 nm.

Ambra-1 recombinant monoclonal antibody Fab fragments were obtained and used for subsequent validation.

The recombinant human HuCAL antibody fragment antibodies were validated in the first instance using immunohistochemistry protocols on normal skin tissue (where Ambra-1 is expressed or p62 is lost) and in a selection of SCC tissue (where expression of Ambra-1 is lost or p62 is expressed). In all instances the staining of the HuCAL antibodies were compared to commercially available Ambra-1 antibodies by Abeam in the same tissue. Negative control of omitting the primary antibody and using anti-Flag (HuCAL antibodies) or anti-Rabbit (Abeam antibodies) secondary antibodies was also included in each instance.

Antibodies against p62 were produced in a similar way to that described above for antibodies against Ambra-1.

Example 6 - epitope mapping of anti-Ambra-1 antibodies

Epitopes of Ambra-1 recognized by anti-Ambra-1 antibodies were mapped using linear, conformational and replacement analysis epitope mapping (Pepscan Presto BV) using established techniques (Timmerman et al (2007). J. Mol. Recognit. 20: 283-299; Langedijk et al. (201 1 ) Analytical Biochemistry 417: 149-155).

The anti-Ambra-1 antibody was tested on arrays with overlapping linear peptides and looped peptides, based on the C-terminal sequence of Ambra-1 :

VSLPSAEGPTLHCELTNNNHLLDGGSSRGDAAGPRGEPRNR (SEQ ID NO: 63)

The core epitope, based on overlapping peptides in the linear and looped arrays, was determined to be sequence ₃₇ EPR _39. A second binding site is apparent only in specific length peptides, and more pronounced in the looped peptide array. Binding to these residues may require a very specific conformation, which in the LOOP1 1 peptide mimics is provided readily, and can only be induced with the specific residue content in the LIN1 1 peptides. If so, this suggests that a secondary structure may be formed for recognition of these residues. This recognition occurs only in this length peptide. Thus, it is possible that specific residues need to be aligned precisely to be recognized. This may represent a structure such as a beta turn, in which some residues on opposite strands are required for the formation, allowing the proper positioning of the two identified residues in the loop tip. The location of the two residues in the center of the 1 1 -mers also corroborates such a possibility. In conclusion, the main residues for binding are ₃₇ EPR _39, which may be aided by ₂₃ DG ₂₄ in a specific conformation.

Details of the epitope information is summarized in the Table below. Core binding sites are listed based on overlap of peptides. Underlined sequence highlights the key residues deducted from the replacement analysis (REPNET):

The reader’s attention is directed to all papers and documents which are filed concurrently with or before this specification in connection with this application and which are open to public inspection with this specification, and the contents of all such papers and documents are incorporated herein by reference.

The reader’s attention is directed to all papers and documents which are filed concurrently with or before this specification in connection with this application and which are open to public inspection with this specification, and the contents of all such papers and documents are incorporated herein by reference.