BACKGROUND OF THE INVENTION Plants may undergo instances of stress, which result in activation of complex genetic pathways that bring about physiological responses appropriate to the stress source. Common stresses to which plants are subjected include extreme UV radiation, osmotic shock, heat shock and pathogen attack. Stress hormones have evolved in plants, which are released in such times of stress and initiate various cascades which end in appropriate responses. Jasmonic acid (JA) and methyl jasmonate (MJ), belong to the group of natural plant stress hormones named"jasmonates" (Sembdner and Parthier, Annu. Rev. Physiol. Plant Mol. Biol., 44,569-589,1993). Jasmonic acid is crucial to intracellular signaling in response to injury and methyl jasmonate causes induction of a proteinase inhibitor that accumulates at low concentrations in response to wounding or pathogenic attacks (Farmer and Ryan, Proc. Natl. Acad. Sci., 87, 7713-7716,1990). Jasmonates have been patented for a variety of uses in plant growth and crop improvement. Application of jasmonates can have a wide range of contradictory effects on virtually all plants. These effects range from inhibition of plant development to promotion of plant processes. U. S. Patent No. 6,114,284 discloses use of jasmonic acid ester and giberellin to synergistically enhance plant growth and development. U. S. Patent No. 5,436,226 discloses use of a jasmonate to inhibit sprouting and darkening in tubers after they have been picked, and U. S. Patent No.

5,118,711 discloses use of methyl jasmonate to repel insects.

Sodium salicylate (SA) is a plant stress hormone of another family, and a central mediator of plant defense responses to pathogens and to injury (Ryals et al., Plant Cell., 8,1809-1819,1996).

One typical response plants use when attacked by a microbial pathogen, may be, for instance, programmed cell death termed the hypersensitive response (HR) which results in the formation of a zone of dead cells around the infection site. The layers of dead cells that surround the site of pathogen entry are thought to function as a physical barrier that inhibits further proliferation and spread of the pathogen. A subsequent step of the process involves synthesis of the plant stress hormone sodium salicylate, and accumulation of antimicrobial agents, such as pathogenesis-related proteins and phytoalexins (Dangl et al., Plant Cell, 8,1793-1807,1996; Mitler and Lam, Trends.

Microbiol., 4,10-15 1996).

This programmed cell death in response to pathogen attack is reminiscent of programmed cell death known to occur in mammalian cells. Mammalian cells can die by"unscheduled"necrosis, which is caused by outside damage and results in cell explosion, or in the more organized manner of apoptosis, also termed"programmed cell death"or"cellular suicide" (Willingham, J. Histochem. Cytochem., 47,1101-1109, 1999). In apoptosis, biochemical and morphological events are usually organized in a cascade of very specific and controlled steps, which include fragmentation of the nucleus and shrinkage of the cell, and end with complete splitting of the cell contents to apoptotic bodies (Stewart, J. Cancer Inst., 86,1286-1295,1994).

The process of apoptosis is slower then necrosis and happens in a few hours or days, depending on the inducer. This kind of death may be regarded as"cell suicide" (Willingham, J. Histochem. Cytochem., 47,1101-1109,1999).

Surprisingly enough, the plant stress hormone SA was able to induce intracellular biochemical events typical of a stress response in mammalian cells as well (Schwenger et al., Proc. Natl. Acad. Sci. USA, 4,2869-2873,1997; Schwenger et al., J. Cell.

Physiol., 179,109-114,1999), and was able to induce apoptosis (programmed cell death) in cell lines of human myeloid leukemia, through activation of Caspase-3 (a mammalian cytoplasmic protease essential for the final steps of apoptosis) (Klampfer et al., Blood., 93,2386-2394,1999; Willingham, J. Histochem. Cytochem., 47, 1101-1109, 1999; Porter and Janicke, Cell Death Differ., 6,99-104 1999). SA was likewise able to induce apoptosis in mammalian FS-4 fibroblasts (Schwenger et al., Proc. Natl. Acad. Sci. USA, 4,2869-2873,1997), and in human pancreatic cancer (McDade et al., J. Surg. Res., 83,56-61 1999). The family of drugs of which salicylic acid is a member, non-steroidal anti-inflammatory drugs (NSAID), have potent chemopreventive activity (Morgan, Gut., 38,646-648 1996; Peleg et al., Dig. Dis. Sci., 41,1319-1326 1996; Vainio et al., Cancer Epidemiol. Biomarkers Prev., 6,749-753, 1997).

Many plant genes that respond to environmental and developmental changes are regulated by jasmonic acid, which is derived from linolenic acid by an octadecanoid pathway. Plant defense responses to certain wavelengths of ultraviolet radiation require activation of the octadecanoid defense signaling pathway (Conconi et al., Nature, 383, 826-829,1996). The release of linolenic acid from the membrane into the cell, and its subsequent conversion to JA, is analogous to signaling pathways in mammalian cells, where releasing of arachidonic acid from the membrane results in synthesis of eicosanoids, such as prostaglandins (Needleman et al., Ann. Rev. Biochem., 55,69-102 1986). Prostaglandins of the A and J series, which contain a cyclopentanone ring structure, are potent inhibitors of cell proliferation in vitro and are able to suppress tumorigenicity in vivo (D\'Onofrio et al., Int. J. Cancer., 51,481-488,1992; Gorospe et al., Mol. Cell. Biol., 16,762-770,1996). The ability of prostaglandins to arrest growth in a diverse range of tumor cell lines has raised the possibility that they might be useful for treatment of human cancer (Sasaki and Fukushima, Anti-Cancer Drugs, 5,131-138, 1994). Structural similarity exists between jasmonates and prostaglandins, since both are cyclopentanons, which suggests that JA and MJ may be potent against cancer cells.

The present invention discloses use of members of the plant stress hormone family termed"jasmonates", for suppressing and killing mammalian cancer cells that represent major types of human malignancies. To the best of the applicant\'s knowledge, jasmonates were never studied as anti-cancer agents. Since chemotherapeutic drugs for use in mammalian systems usually work by induction of apoptosis in cancer cells (Bailly et al., Leukemia., 11,1523-1532,1997), and jasmonates are thought to be involved in an apoptotic response to plant stress, the applicants tested the ability of jasmonates to suppress replication of mammalian cancer cell lines of clinical importance. The cytotoxicity of jasmonates was compared to that of the plant stress hormone sodium salicylate, which is known to be cytotoxic to mammalian cancer cells.

Chemotherapeutic drugs are often so highly toxic as to leave the patient with numerous side-effects that seriously diminish the patient\'s quality of life and impair his function. Chemotherapy regimens can last several months and can be performed repeatedly in cases of relapse, leaving even an ambulatory patient with repeated periods of partial impairment of function. The need exists, therefore, for chemotherapeutic drugs with undiminished potency, yet with a higher degree of specificity towards malignant cells, and fewer side-effects. The present invention discloses use of jasmonate compounds to treat malignancies. Jasmonates are commonly found in minute quantities in many edible plants (Sembdner and Parthier, Annu. Rev. Physiol.

Plant Mol. Biol., 44,569-589 1993), such as tomato, potato, and pumpkin seeds, and thus are non-toxic. Jasmonates are shown by the applicants to be highly specific; inducing apoptosis in clinically important types of cancer cells, yet not effecting the proliferation of normal human cells, such as healthy lymphocytes. Jasmonates are additionally shown by the applicants to be effective in the treatment of lymphoma in a cancer model in mice.

It is the object of the present invention to propose jasmonate compounds as a potent chemotherapeutic drug, with a high degree of specificity towards malignant cells. These and other objects of the present invention will become more apparent from the detailed description of the preferred embodiments, that follows below.

In the present invention, the term"jasmonates"is intended to include the natural plant hormones jasmonic acid and methyl jasmonate, as well as any natural or synthetic derivative and isomers of jasmonic acid and of jasmone. These derivatives have: 1) a lower acyl side chain at C3 (free acid or ester or conjugate) 2) a keto or hydroxy (free hydroxy or ester) moiety at the C6 carbon 3) an n-pentenyl or n-pentyl side chain at C7.

A variety of jasmonates may be used, and include but are not limited to those having the formula: wherein n is 0,1, or 2; Ri is OH, alkoxy, O-glucosyl, or imino, R2 is OH, O, alkoxy or O-glucosyl, R3, R4 and Rs are H, OH, alkoxy or O-glucosyl, and/or wherein Ri and R2, or R, and R4 together form a lactone, and further wherein the bonds between C3 : C7, C4: Cs, and Cg : Clo may be double or single bonds.

SUMMARY OF THE INVENTION The present invention relates to a pharmaceutical composition useful for the treatment of cancer in mammals, comprising as an active ingredient a therapeutically effective amount of a jasmonate compound of the formula I : Formula I wherein: n is 0, 1, or 2 ; Ri is OH, alkoxy, O-glucosyl, or imino, R2 is OH, O, alkoxy or O-glucosyl, R3, R4 and Rs are H, OH, alkoxy or O-glucosyl, and/or wherein Rl and R2, or Rl and R4 together form a lactone, and further wherein the bonds between C3 : C7, C4: Cs, and C9 : Clo may be double or single bonds; or a derivative of said formula, wherein the derivative has at least one of the following: a lower acyl side chain at C3 (free acid or ester or conjugate), a keto or hydroxy (free hydroxy or ester) moiety at the C6 carbon, or an n-pentenyl or n-pentyl side chain at C7.

According to a preferred embodiment of the present invention, the jasmonate is selected from methyl jasmonate, jasmonic acid, jasmone, 7-iso-jasmonic acid, 9,10-dihydrojasmonic acid, 2,3-didehydrojasmonic acid, 3,4-didehydrojasmonic acid, 3,7-didehydrojasmonic acid, 4,5-didehydrojasmonic acid, 4,5-didehydro-7-iso-jasmonic acid, cucurbic acid, 6-epi-cucurbic acid, 6-epi-cucurbic-acid-lactone, 12-hydroxy-jasmonic acid, 12-hydroxy-jasmonic-acid-lactone, 11-hydroxy-jasmonic acid, 8-hydroxy-jasmonic acid, homo-jasmonic acid, dihomo-jasmonic acid, 11-hydroxy-dihomo-jasmonic acid, 8-hydroxy-dihomo-jasmonic acid, tuberonic acid, tuberonic acid-0-p-glucopyranoside, cucurbic acid-0-p-glucopyranoside, 5,6-didehydrojasmonic acid, 6,7-didehydrojasmonic acid, 7,8-didehydrojasmonic acid, cis-jasmone, methyldihydroisojasmonate, dihydrojasmone, amino acid conjugates of jasmonic acid, and the lower alkyl esters, the carrier ligand conjugates and the sterioisomers thereof.

Further, according to a preferred embodiment of the present invention, the cancer to be treated is selected from prostate cancer, breast cancer, skin cancer, colon cancer, lung cancer, pancreatic cancer, lymphoma, leukemia, head and neck cancer, kidney cancer, ovarian cancer, bone cancer, liver cancer or thyroid cancer.

Moreover, in accordance with a preferred embodiment of the present invention, the active ingredient is dissolved in any acceptable lipid carrier.

Still further, in accordance with a preferred embodiment of the present invention, the composition additionally comprises at least one other chemotherapeutic agent.

Additionally in accordance with a preferred embodiment of the present invention the composition is prepared for oral administration. In such embodiments, the composition is in a form selected from an emulsion, a solution, a capsule, a tablet.

In another embodiment of the present invention, the composition is prepared for administration by injection. The composition is prepared so as to be suitable for injection intra-muscularly, intra-peritoneally, or intraveneously.

Still further, in certain embodiments, the composition is prepared for topical administration. According to these embodiments, the composition is in a form selected from an ointment, a gel, or a cream.

Moreover, in some embodiments of the present invention, the composition is prepared for administration by inhalation. In other embodiments, the composition is prepared for administration via a suppository.

The present invention further discloses use of a therapeutically effective amount of a jasmonate compound of Formula I : Formula I wherein: n is 0, 1, or 2 ; R, is OH, alkoxy, O-glucosyl, or imino, R2 is OH, O, alkoxy or O-glucosyl, R3, R4 and Rs are H, OH, alkoxy or O-glucosyl, and/or wherein Ri and R2, or R, and R4 together form a lactone, and further wherein the bonds between C3 : C7, C4: C5, and Cg : Clo may be double or single bonds; or a derivative of said formula, wherein the derivative has at least one of the following: a lower acyl side chain at C3 (free acid or ester or conjugate), a keto or hydroxy (free hydroxy or ester) moiety at the C6 carbon, or an n-pentenyl or n-pentyl side chain at C7; or any pharmaceutically acceptable salt thereof, in the preparation of a pharmaceutical composition useful for treatment of prostate cancer, breast cancer, skin cancer, colon cancer, lung cancer, pancreatic cancer, lymphoma, leukemia, head and neck cancer, kidney cancer, ovarian cancer, bone cancer, liver cancer or thyroid cancer, in mammals.

BRIEF DESCRIPTION OF THE DRAWINGS The present invention is herein described, by way of example only, with reference to the accompanying drawings, wherein: Fig. 1 is a graph illustrating the cytotoxicity of plant hormones methyl jasmonate and jasmonic acid, compared with salicylic acid, as a measure of their concentration.

Table 1 is a comparison of the level of toxicity effected by jasmonic acid, methyl jasmonate and salicylic acid on four malignant cell lines.

Fig. 2 is a graph illustrating the cytotoxicity of the plant hormone cis-jasmone, as a measure of its concentration.

Fig. 3 is a graph illustrating the activity levels of the apoptotic marker protein Caspase-3, in Molt-4 cells treated with jasmonic acid and methyl jasmonate.

Fig 4 illustrates fluorescence microscopy pictures depicting apoptotic changes in morphology of Molt-4 cells, after treatment with jasmonic acid and methyl jasmonate.

Fig. 5 is a graph illustrating the specificity of the cytotoxic effect jasmonates exert on malignant cells, versus no effect on normal lymphocytes from healthy donors.

Fig. 6 is a graph illustrating the cumulative percentage of survival of mice treated with jasmonates to prevent the formation of lymphomas, versus untreated mice.

DETAILED DESCRIPTION OF THE INVENTION It is appreciated that the detailed description that follows is intended only to illustrate certain preferred embodiments of the present invention. It is in no way intended to limit the scope of the invention, as set out in the claims.

The present invention describes use of jasmonates to prevent proliferation and induce death of malignant cells.

Particularly preferred jasmonates include jasmonic acid [ (-)-JA and/or (+)-7-iso-JA], methyl jasmonate, jasmone, and 9,10-dihydrojasmonic acid and its lower alkyl ester. Other preferred jasmonates include 4,5-didehydro-7-iso-JA, 3,7-didehydro-JA, cucurbic acid (CA), 6-epi-CA, 6-epi-CA-lactone, 12-hydroxy-JA, 12-hydroxy-JA-lactone, 11-hydroxy-JA, 8-hydroxy-JA, homo-JA, dihomo-JA, 11-hydroxy-dihomo-JA, 8-hydroxy-dihomo-JA, tuberonic acid (TA), TA-O-ß-glucopyranoside, CA-O-ß-glucopyranoside, amino acid conjugates of JA, as well as the corresponding lower alkyl esters of each of these acids.

The applicants have proven below, that two jasmonates, methyl jasmonate and jasmonic acid, have a positive therapeutic effect on malignant cells, yet do not harm normal cells such as normal circulatory lymphocytes. The following examples demonstrate that jasmonates are cytotoxic to four different types of malignant cells in culture, in doses that would be considered safe and attainable in mammals, and do not inhibit growth of healthy lymphocytes. The applicants have additionally proven, in Example 7, that jasmonates are effective in prolonging the lifetime of mice injected with lymphoma cells, resulting in a survival rate that is significantly higher than that of untreated mice (2. 25 times the number of survivors than in the untreated group).

Example 1-Plant Stress Hormones Are Cytotoxic For Four Human Transformed Cell Lines Four transformed cell lines of different histological lineages were exposed to one of three plant stress hormones. The cell lines chosen represent four types of cancer of widespread clinical importance. Molt-4 is a human T lymphoblastic leukemia cell line, SK-28 are human melanoma cells. LNCaP is an androgen-responsive human prostate adenocarcinoma cell line, and MCF7 is a human breast carcinoma cell line.

All cell lines were purchased from ATCC (Rockville, MD). All reagents were purchased from Sigma Chemicals (St. Louis, MO) unless otherwise stated. JA and MJ were dissolved in ethanol. All cell cultures were performed in RPMI-1640 with 10% fetal calf serum (Biological Industries, Beit-Haemek, Israel), and cells (except for Molt-4 and lymphocytes from the peripheral blood) were allowed to adhere prior to every treatment mentioned below.

LNCaP, MCF7 and SK-28 cells (at 4x 103/well) and Molt-4 cells (at 1. 5xl04/well) were seeded in 96-well plates and incubated overnight. Plant stress hormone at increasing concentrations was added as indicated below, and toxicity was measured after 24 hours using the CellTiter 96 Aqueous Non-Radioactive Cell Proliferation Assay (Promega, Madison, WI); an assay in which viable cells produce a colored product (for details on the protocol of this assay, see below). This assay is quantitative, as the amount of color produced is read using an ELISA reader.

The highest non-toxic pharmacological concentration used in humans, of the nonsteroidal anti-inflammatory drug SA, is approximately 3mM (Katzung, Lange Medical Book, Stamford, 1998). In order to compare the additional plant stress hormones JA (jasmonic acid) and MJ (methyl jasmonate) with SA, the same range of concentrations (0.5-3mM) was chosen. These compounds at the aforementioned concentrations are not toxic for mice. Each cell line was incubated with each of these hormones at a concentration ranging from 0.5-3mM for 24 hours, after which cytotoxicity was measured. The statistical significance of the results was determined (where appropriate) by two-tailed student\'s t-test, n=3. Results are presented as means standard deviation.

In reference to Fig. 1, the cytotoxicity of each one of three plant hormones is plotted as a measure of its concentration. diamonds = Molt-4 lymphoblastic leukemia cells; squares = SK28 melanoma cells; triangles = LNCaP androgen-responsive prostate adenocarcinoma cells, circles = MCF7 breast carcinoma cells.

Referring to Fig. 1A, all cell lines responded in a dose-dependent fashion to SA.

Cytotoxicity of SA was significant, P <0.05, in Molt-4 lymphoblastic leukemia cells, SK28 melanoma cells and MCF7 breast carcinoma cells at all concentrations, and in LNCaP human prostate adenocarcinoma cells, from 1 mM and higher. SA was shown here to inhibit cell proliferation of different cancer cells from 20 to 40%, depending on the cell line. This finding is in agreement with similar reported observations, where SA inhibited growth of breast cancer cell lines, rat hepatoma and human fibroblasts cultures (Sotiriou et al., Anticancer Res., 19,2997-3006 1999; Hial et al., J. Pharmacol.

Exp. Ther., 202,446-454 1977). A possible interpretation of this data is that SA causes stress in cancer cells, resulting in suppression of proliferation in those cells.

JA and MJ were studied in comparison to SA in order to determine whether the effects of SA on cancer cells are common to plant stress hormones, and whether jasmonates would be deemed more effective than salicylic acid at targeting and inhibiting the growth of malignant cells.

Referring to Fig. 1B, the responsiveness to JA was dose-dependent. The cytotoxicity of JA was significant, P <0.05, in Molt-4 cells from 1 mM and higher, in LNCaP and SK28 cells from 2 mM and higher, and in MCF7 cells at 3 mM. The order of sensitivity to JA was Molt-4> SK-28> LNCaP> MCF7.

Referring to Fig. 1C, cytotoxicity of MJ was significant, P <0.01, in Molt-4 cells at all concentrations and in MCF7 cells at 3 mM; and at P <0.05 in LNCaP and SK28 cells from 2 mM and higher.

The results presented here show that MJ caused the highest level of cytotoxicity.

For instance, 0.5 mM of MJ induced 87.52% cytotoxicity in Molt-4 cells. The other cell lines responded to MJ in a dose-dependent way. The order of sensitivity was Molt-4>LNCaP>SK28>MCF7.

Appropriate controls established that ethanol (in which JA and MJ were dissolved) by itself did not induce any cytotoxicity.

Example 1 demonstrates that while cancer cells from various origins responded to plant stress hormones, their response was differential. Among the cell lines examined, Molt-4 responded strongly to JA (90% cytotoxicity at 3 mM) and MJ (90% cytotoxicity at 0.5 mM).

Cytotoxicity Assay Used In Examples Inhibition of cell proliferation was determined by the CellTiter 96 Aqueous Non-Radioactive Cell Proliferation Assay (Promega, Madison, WI) : Upon completion of a given experiment, MTS (a tetrazolium compound) at 333 pg/ml + phenazine methosulfate (at 25 uM) was added to each well of the 96-well plate for 1 hour at 37°C.

This allowed for development of a color reaction in which dehydrogenases reduce the MTS in metabolically active cells. Since the cells were not washed before the addition of MTS, there were no potentially loosely adherent or non-adherent cells that could have been problematic. Soluble MTS formazan product was measured at a wavelength of 490nm using a CERES 900 HDI ELISA reader (Bio-Tek Instruments, Inc, Highland Park, VT). Optical density is directly proportional to the number of living cells in culture. Cytotoxicity (%) was calculated in the following way: [ (OD of control cells- OD of drug-treated cells)/OD of control cells] x 100.

Example 2-Cis-Jasmone, An Additional Jasmonate Compound, Is Cytotoxic For Three Human Transformed Cell Lines Three transformed cells lines, out of those described in Example 1, were exposed to cis-jasmone, which is an additional jasmonate compound (in addition to JA and MJ), in order to study its cytotoxicity towards cancer cell lines. The experiment was performed as described in Example 1.

Referring to Figure 2, cis-jasmone is a potent cytotoxic agent which affects the cells dose-dependently. The effect of cis-jasmone on every cell line was significant at every concentration used, (with the statistical significance being P <0.01 as determined by t-test). The only result not deemed significant was that measured when the lowest dosage of cis-jasmone used, 0.5 mM, was applied to LNCaP cells. Cytotoxicity exceeded 50% of cells in all cell lines studied, when cis-jasmone was applied at concentrations of 2 mM and above. At the highest concentration used, cis-jasmone was cytotoxic for 75-85% of transformed cells in each plate.

Example 3-Characterization Of The Damage Induced By Jasmonates Since the same number of cells was aliquoted into each well initially, decreased optical density as measured in wells containing treated cells (above) reflects cellular death and/or decrease in the rate of proliferation. To distinguish between these two possibilities we employed an additional cytotoxicity assay which detects cell death by lack of trypan blue exclusion. Cells were incubated with 0.1% trypan blue for 2-5 minutes and the percentage of dead cells (those, which did not exclude the dye) was determined microscopically.

Referring to Table 1, among the plant hormones tested, MJ induced death most effectively in every cell line. MJ is more effective in killing human transformed cell lines than its non-methylated form JA (Fig. lB, 1C and Table 1). SA suppressed proliferation in all cell lines, while JA induced death in lymphoblastic leukemia cells and suppression of proliferation in the other cells. In terms of relative susceptibility, Molt-4 cells are followed by SK28, LNCaP and MCF7 cells, in that order. Differential susceptibility of the different cell lines to the plant stress hormones suggests a specificity of the influence of those compounds on the cells.

It is important to note the difference between SA and jasmonates in their influence on cancer cell lines. SA causes inhibition of cell proliferation in the tested cell lines, JA causes cell death in Molt-4 cells and inhibition of cell proliferation in SK28, LNCaP and MCF7 cells, whereas MJ causes death in all cell lines. These differences could be explained by different structures of plant stress hormones and/or by difference in biochemical events that those compounds induce in the cells.

Example 4-Jasmonates Induce Apoptosis In Molt-4 Cells Elevated levels of Caspase-3 are a specific marker of the apoptosis process (Porter and Janicke, Cell Death Differ., 6,99-104,1999). In order to definitively determine that the cause of cell death was apoptosis, the level of Caspase-3 activity was measured in cells after treatment with JA and MJ.

Molt-4 cells were incubated with JA and MJ for 2,4 and 14 hours, and levels of activity of the apoptosis-mediating protease, Caspase-3, were determined using the Caspase-3 (CPP32) protease assay kit (PharMingen, San Diego, CA) as suggested by the manufacturer. Briefly, 2x 106 cells were lysed and resuspended in 100 uL of reaction buffer containing a fluorogenic Caspase-3 (CPP32) substrate Ac-DEVD-AMC.

Reactions were incubated at 37°C for 2 hours and samples were assayed at excitation wavelength of 360 nm and emission wavelength of 460 nm, in the FL600 Microplate Fluorescence Reader (Bio-Tek Instruments, Winooski, Vermont, USA).

Referring to Fig. 3, dose-dependent elevation of Caspase-3 activity was observed: (Diamonds=2 hours, squares = 4 hours, triangles=14 hours.) As can be seen in Fig. 3, JA and MJ increased Caspase-3 activity significantly, P <0.05, at all concentrations and times.

Referring to Fig. 3A, incubation with JA for 2 hours didn\'t induce an elevation in the level of Caspase-3.

Referring to Fig. 3B, after 14 hours of exposure to MJ, the extent of death at 1 mM and above was such that Caspase-3 activity could not be determined.

These results suggested that JA and MJ induced apoptotic death in Molt-4 cells.

To confirm this fact, Molt-4 cells were treated with JA (2 mM) and MJ (0.5 mM) for 14 hours, and analyzed by fluorescence microscopy in order to detect essential morphological characteristics of apoptosis such as condensation and fragmentation of chromatin.

Referring to Fig 4, fluorescence microscopy pictures are shown depicting changes in cellular morphology within the nuclei of Molt-4 cells, after treatment with plant stress hormones JA or MJ. 5x105 cells/sample were harvested, then fixated by addition of a solution of phosphate-buffered saline (PBS) containing [3% paraformaldehyde and 0.1% Triton X-100], for one hour. Cells were stained for 10 minutes with DAPI (1 llg/ml). Nuclei were analyzed by fluorescence microscopy, (using a fluorescence microscope model Ax70 TRF, made by Olympus Optical, Japan) at a magnification of 1: 400. Characteristic apoptotic nuclei are marked with arrows.

Referring to Fig. 4A, untreated Molt-4 cells are shown.

Referring to Fig. 4B, Molt-4 cells were treated with JA at 2 mM for 14 hours.

Treatment with JA induced condensation and fragmentation of chromatin.

Referring to Fig. 4C, Molt-4 cells were treated with MJ at 0.5 mM for 14 hours.

Treatment with MJ completely destroyed nuclear morphology in almost all cells.

These results confirm that JA and MJ caused apoptotic death in Molt-4 cells, based on the rise in caspase-3 activity, which is one of the features of apoptosis, and on characteristic morphological changes.

SA was reported to induce apoptosis and activation of caspases in myeloid leukemia cell lines and in B-cell chronic lymphocytic leukemia cells. There is also evidence that SA enhances apoptosis and causes apoptosis in FS-4 cells via p38 (Schwenger et al., Proc. Natl. Acad. Sci. USA, 4,2869-2873,1997). In those studies different cell lines undergo apoptosis on incubation with concentrations of salicylates higher than those achieved in plasma of patients treated for inflammatory disorders. In the present invention, concentrations of salicylates were used, that are comparable to those achieved in the plasma. This can explain the difference between studies where SA induced apoptosis, and our results.

Example 5-Jasmonates Are Not Harmful To Normal Lymphocytes The results shown above prove that plant stress hormones possess the ability to adversely affect cancer cells. The effect of these plant products was tested on normal cells, to determine if jasmonates have an adverse cytotoxic effect on non-cancerous cells as well.

Normal lymphocytes were separated from peripheral blood, as follows: Mononuclear cells (MNC) from venous blood of healthy donors were collected by Ficoll-Hypaque (Phamacia Fine Chemicals, Uppsala, Sweden) density gradient centrifugation. The resultant mononuclear cell preparation was allowed to adhere to plastic dishes to remove contaminant macrophages. The non-adherent peripheral blood lymphocytes were selected for use.

Prior to treatment with JA and MJ, normal lymphocytes were stimulated by TPA (5 ng/ml) and PHA (0.8 g/ml) for 48 hours, to cause the lymphocytes to proliferate (and so, be comparable to the immortal malignant cells). Normal lymphocytes and Molt-4 cells were seeded (at 1.5xlO4/well) in 96-well plates.

Jasmonates or salicylic acid were added at a concentration of 1 mM or 3 mM, and cells were incubated for 24 hours. Optical density representing viable cells was determined by the CellTiter 96 Aqueous Non-Radioactive Cell Proliferation Assay.

Each plant stress hormone induced significant cytotoxicity in Molt-4 cells, P< 0. 05, while non of the hormones induced any significant cytotoxicity in normal lymphocytes.

Referring to Fig. 5, normal blood lymphocytes (represented by solid bars) were practically not influenced by plant stress hormones, contrary to the Molt-4 transformed lymphoblastic leukemia cells (represented by open bars).

Figure 5A shows treatment with SA at concentrations of 1mM and 3mM.

Fig. 5B shows treatment with JA at concentrations of 1mM and 3mM, and Fig. 5C shows treatment with MJ at concentrations of 1mM and 3mM.

Refer to Table 1 as well, which illustrates the selectivity of jasmonates for malignant cells versus healthy cells.

In this example, the influence of plant stress hormones on transformed lymphocytes (Molt-4 cells) was compared, versus their influence on normal lymphocytes extracted from peripheral blood. Normal lymphocytes (that had been stimulated by TPA/PHA to induce proliferation), were not influenced by SA and jasmonates, contrary to transformed lymphocytes. This data supports the potential use of plant stress hormones as selective anti-cancer agents.

Example 6-Jasmonates Are Not Harmful To Normal Erythrocytes The effect of jasmonic acid, methyl jasmonate and cis-jasmone, was studied on normal human erythrocytes. To that end, an assay was established which evaluates damage to erythrocytes by the release of hemoglobin. The latter was measured spectrophotometrically at 412nm. As a positive control, distilled water was used to induce total hemolysis and generate the release of hemoglobin. None of the jasmonates caused hemoglobin release from normal human erythrocytes of three different donors.

This, when jasmonates were applied at concentrations at which they cause cytotxic effects in cancer cells (0.5-3 mM). Thus, in addition to their not harming normal human lymphocytes (as shown in Example 5), jasmonates are not harmful to erythrocytes, further exhibiting their selective effect against cancer cells.

Example 7-In-Vivo Experiments In Mice Syngeneic lymphoma cells were injected into a test group and a control group of mice (strain C57BL). The injections were administered either sub-cutaneously, or intra-peritoneally. Methyl jasmonate was administered orally, by injection directly into the resultant tumor or into the peritoneum, and the effect on tumor progression and on the rate of survival, were analyzed.

400,000 EL-4 lymphoma cells were injected intra-peritoneally into 20 test mice, or 19 control mice, of the C57BL strain.

Preliminary experiments had shown that methyl jasmonate at a dosage of 236-472 mg/kg. body weight was appropriate for prevention of tumoral growth.

Therefore, methyl jasmonate was dissolved in a lipid carrier (0.4% Lipofundin, manufactured by B. Brown, Melsunger, Germany) and administered orally at a dosage of 236 mg/kg body weight. Administration was daily, via the drinking water, beginning with the day of injection of the lymphoma cells.

19 control mice received the lipid carrier only (0.4% Lipofundin), with no methyl jasmonate dissolved within.

The survival time of each group of mice was measured (in days), and analyzed.

Referring to Fig. 6, a Kaplan & Meier Survivorship Function graph is shown, illustrating the cumulative percentage of survival in each group, as the experiment progressed. Survival rates were significantly higher for the treated group (represented by crosses, and by the letter"T"), versus the control group (represented by circles, and by the letter"C"); as can be seen, for example, in the plateau of 50% survival reached by the treated group on the 33rd day, as opposed to the plateau of 20% survival reached by the control group.

The significance of these results was analyzed statistically, using two highly stringent statistical means of analysis, the Log-Rank Test and the Cox-Mantel Test.

Each of these tests weighs numerically the importance of a death within one of the two groups of mice, on a given day, compared to the number of surviving mice in the whole.

The significance of the results was deemed to be high, p=0.01492 for the Log-Rank Test, and p=0. 00953 for the Cox-Mantel Test (wherein a result is considered significant if p< 0. 05).

In conclusion, Examples 1-7 elucidate the effect of the structurally-diverse plant stress hormones, jasmonates and salicylate, on cell proliferation and viability in several diverse cancer cell lines. There were four major findings. Firstly, all the stress hormones investigated share the ability to adversely affect proliferation of cancer cells.

Jasmonic acid (JA) induced death in lymphoblastic leukemia cells and caused suppression of cell proliferation in the other human cancer cells mentioned above.

Methyl jasmonate (MJ) induced death in each of the cell lines. The plant hormones acted dose-dependently in the following order of sensitivity: lymphoblastic leukemia > prostate cancer > melanoma > breast cancer. Secondly, death caused by jasmonates in Molt-4 cells was determined as apoptotic, similar to the mechanism most chemotherapeutic drugs employ at the cellular level. Thirdly, jasmonates do not cause damage to normal lymphocytes or erythrocytes. Fourthly, jasmonates are effective not only in vitro, but also in an animal model of lymphoma, significantly increasing the survival rate (by 2.25 times), using a dosage deemed safe in mice.

These findings suggest that plant stress hormones may be used as a novel class of anti-cancer drugs.