WO2003057201A2

WO2003057201A2 - A nutrient pharmaceutical formulation comprising polyphenols and use in treatment of cancer

Info

Publication number: WO2003057201A2
Application number: PCT/EP2003/000236
Authority: WO
Inventors: Matthias Rath; Shrirang Netke; Aleksandra Niedzwiecki
Original assignee: Individual
Current assignee: Individual
Priority date: 2002-01-11
Filing date: 2003-01-13
Publication date: 2003-07-17
Anticipated expiration: 2004-07-11
Also published as: US20060142212A1; AU2003235762B2; CN1731989A; ZA200405075B; LT5240B; WO2003057201A3; RU2004124384A; HUP0500498A2; BR0302672A; PL371282A1; PL215159B1; HRP20040704A2; HUP0500498A3; LV13248B; ATE382343T1; EP1465614A2; JP2005519055A; HK1086489A1; LT2004076A; DE60318387D1

Abstract

A nutrient pharmaceutical formulation composition comprising ascorbic acid, L-lysine, L-proline and at least one polyphenol compound selected from the group consisting of epigallocatechin gallate, epicatechin gallate, epigallocatechin, epicatechin, catechin and use of treatment in cancer and other tumors is provided. A nutrient pharmaceutical formulation composition of EPICAN FORTETM and its method of use in preventing and treating cancer are disclosed.

Description

A NUTRIENT PHARMACEUTICAL FORMULATION COMPRISING POLYPHENOLS AND USE IN TREATMENT OF CANCER

CROSS-REFERENCE TO RELATED APPLICATION

This application claims the benefit under 35 U.S.C. § 119(e) of U.S. provisional applications Serial No. 60/348,143 filed January 11, 2002, the content of which is incorporated herein by reference in its entirety.

FIELD OF THE INVENTION

The present invention relates to a nutrient pharmaceutical formulation and its use for the treatment of cancer. More specifically, the present invention relates to polyphenol containing pharmaceutical formulations having an effective amount of polyphenols for the treatment of cancer. The formulation of the present invention is used as an agent for the prevention and treatment of cancer comprising ascorbic acid, lysine, proline and at least one polyphenol compound selected from the group consisting of epigallocatechin gallate, epicatechin gallate, epigallocatechin, epicatechin, and catechin.

BACKGROUND OF THE INVENTION

Cancer is one of the leading causes of death in the industrialized world. There exists no specific and causal treatment for cancer and mortality from cancer is among the highest from all diseases. The most widely used treatments - chemotherapy and radiotherapy - do not distinguish between healthy tissue and cancer and are associated with severe side effects. Thus, there is a need for a selective treatment of cancer.

One of the key mechanisms that cancer cells use in order to expand and metastasize in the body involves enzymatic destruction of the surrounding connective tissue. Therapeutic approaches to control this process through specific drugs have not been successful and currently there are no means available to control cancer metastasis. Current treatment protocols with chemotherapy and radio-therapy focus on cancer cell destruction in the body, and they do not address metastasis. Moreover, these treatments are toxic, not specific and associated with severe side effects. Chemotherapy and radiotherapy carry a risk of the development of new cancers and through their destruction of connective tissue in the body can facilitate the invasion of cancer. In order to grow and expand to other parts of the body, cancer cells degrade the extracellular matrix through various matrix metalloproteinases (MMPs) and plasmin, whose activities have been correlated with an aggressiveness of tumor growth. Rath and Pauling (1992) postulated that nutrients such as an amino acid, lysine and ascorbic acid can act as natural inhibitors of extracellular matrix proteolysis and as such they have the potential to modulate tumor growth and expansion. These nutrients can exercise their anti-tumor potential through several mechanisms, among them by inhibition of MMPs and by strengthening of the connective tissue surrounding cancer cells (tumor "encapsulating" effect).

U.S. Pat. No. 5,962,517 discloses a pharmaceutical composition for a different medical indication (acne treatment). The disclosed composition comprises an acne reduction component, at least one of burdock root yellow dock root, or a catechin-based composition; and a skin cell conditioning component comprising a transition metal. The disclosed composition is not shown to have any beneficial value in cancer treatment and/or prevention.

PCT WO 00/76492 discloses a nutrient formulation for disease reduction that contains a catechin compound. However, the bioavailability of catechin compounds has been shown to be small low (Chen L., Lee M.J., Yang C.S. Drug Metab. Dispos. 25:

1045-1050 (1997); Yang C.S., Chen L., Lee M.J., Balentine D.A., Kuo M.C., Schantz S. Cancer Epidemol. Biomark. Prev. 7: 351-35 (1998); Bell J.R., Donovan J.L.,Wong R., Waterhouse H., German J.B., Walzem R.L., Kasim K. Am. J. Clin. Nutr. 71:103-108 (2000); Sherry Chow H.H., Cai Y., Alberts D.S., Hakim I., Dorr R., Shahi F., Crowell J.A., Yang S.C., Hara H. Cancer Epidemol. Biomark. Prev. 10: 53-58 (2001)). and the PCT WO 00/76492 fails to disclose a means to increase the bioavailability as is required in cancer treatment and/or prevention.

Demeule et al. discloses that green tea catechins may have inhibitory effects on matrix metalloproteinase. There is no suggestion or teaching regarding how to use catechins in cancer treatment and/or prevention. Given the fact that the bioavailability of polyphenols in humans is extremely low, the low tissue concentration of catechins greatly reduces the therapeutic value of polyphenols including epigallocatechin gallate (EGCG).

There is a constant need in finding a better nutrient pharmaceutical composition containing polyphenols that is effective in the treatment of neoplastic diseases and other diseases including inflammatory diseases.

There is a need for safe and effective natural approaches that can be used to control the process of cancer expansion in the body. There is also a need for a preventive measure against cancers or benign tumors to develop in human and such measure could be applied to patients without the risk of treatment-related side effects. Nutrient pharmaceutical compositions have become popular, as the incidence of cancer in recent time increases. The requirement of such composition will continue and will likely increase.

SUMMARY OF THE INVENTION

In one object, the present invention provides a nutrient pharmaceutical composition useful in treating cancer, comprising: a) an ascorbic compound; b) a L-lysine compound; c) a L-proline compound; and d) at least one polyphenol compound selected from the group consisting of epigallocatechin gallate, epicatechin gallate, epigallocatechin, epicatechin, and catechin. Compounds of a-c) enhance the polyphenol compound's activity in blocking cancer proliferation and metastasis.

Preferably, the ascorbic compound is selected from the group consisting of ascorbic acid, pharmaceutical acceptable ascorbate salts, ascorbate esters and/or mixture thereof. Preferably, the pharmaceutical acceptable ascorbate salt is calcium ascorbate or magnesium ascorbate. More preferably, the ascorbate ester is ascorbyl palmitate. Preferably, the lysine compound is selected from the group consisting of lysine hydrochloride and lysine pharmaceutically acceptable lysine salts. Preferably, the proline compound is selected from the group consisting of proline hydrochloride and proline pharmaceutical acceptable proline salts.

In another object, the present nutrient pharmaceutical composition further comprises a trace element selected from the group consisting of selenium, copper, manganese, calcium and magnesium. In another object, the present nutrient pharmaceutical composition further comprises an amino acid. Preferably, the amino acid is arginine. More preferably, the present nutrient pharmaceutical composition further comprises N-acetyl cysteine.

In another object, the present invention provides a nutrient pharmaceutical composition useful in treating cancer, comprising: a) an ascorbic compound; b) a L-lysine compound; c) a L-proline compound; d) N-acetyl cysteine; and e) at least one polyphenol compound selected from the group consisting of epigallocatechin gallate, epicatechin gallate, epigallocatechin, epicatechin, and catechin. The a-d) compounds enhance the polyphenol compound's activity in blocking cancer proliferation and metastasis.

In another object, the present invention provides a nutrient pharmaceutical composition comprising 250 mg ascorbic acid, 250 mg calcium ascorbate, 250 mg magnesium ascorbate, 250 mg ascorbyl palmitate, 1,000 mg polyphenols, 200 mg N- acetyl-cysteine, 1,000 mg lysine, 750 mg proline, 500 mg arginine, 30 meg selenium, 2 mg copper, and 1 mg manganese.

In another object, the present invention provides a nutrient pharmaceutical composition comprising 25 mg ascorbic acid, 25 mg calcium ascorbate, 25 mg magnesium ascorbate, 25 mg ascorbyl palmitate, 200 mg polyphenols, 10 mg N-acetyl- cysteine, 50 mg lysine, 25 mg proline, 50 mg arginine, 1 meg selenium, 20 meg copper, and 50 meg manganese.

In another object, the present invention provides a nutrient pharmaceutical composition comprising 5,000 mg ascorbic acid, 5,000 mg calcium ascorbate, 5,000 mg magnesium ascorbate, 5,000 mg ascorbyl palmitate, 5,000 mg. polyphenols, 1,500 mg N- acetyl-cysteine, 5,000 mg lysine, 3,000 mg proline, 3,000 mg arginine, 200 meg selenium, 9 mg copper, and 10 mg manganese.

In another object, the present invention provides a nutrient pharmaceutical composition comprising 250 mg ascorbic acid, 250 mg calcium ascorbate, 250 mg magnesium ascorbate, 250 mg ascorbyl palmitate, 1,000 mg polyphenols, 200 mg N- acetyl-cysteine, 1,000 mg lysine, 750 mg proline, 500 mg arginine, 100 meg selenium, 2 mg copper, 1 mg manganese, 500 mg calcium, and 400 mg magnesium. In another object, the present invention provides a nutrient pharmaceutical composition comprising 250 mg ascorbic acid, 250 mg calcium ascorbate, 250 mg magnesium ascorbate, 250 mg ascorbyl palmitate, 1,000 mg polyphenols, 200 mg N- acetyl-cysteine, 1,000 mg lysine, 750 mg proline, 500 mg arginine, 100 meg selenium, 2 mg copper, 1 mg manganese, 500 mg calcium, 400 magnesium, and 200 citrus biofavonoids.

In yet another object, the present invention provides a nutrient pharmaceutical composition useful in treating cancer, comprising: L-lysine, L-proline, L-arginine, ascorbic acid, calcium, magnesium, polyphenols, N-acetyl-cysteine, selenium, copper, and manganese.

In another object, the present invention provides a nutrient pharmaceutical composition comprising 1,000 mg L-lysine, 750 mg L-proline, 500 mg L-arginine, 710 mg ascorbic acid, 22 mg calcium, 50 mg magnesium, 1,000 mg polyphenols, 200 mg, N- acetyl cysteine, 30 meg selenium, 2 mg copper, and 1 mg manganese.

In another object, the present invention provides a method of treating cancer in an individual, comprising the step of administering to the individual the nutrient pharmaceutical compositions as disclosed. Preferably, the cancer is selected from the group consisting of melanoma cancer, breast cancer, colon cancer, lung cancer and brain cancer.

In another object, the present invention provides a method of treating an inflammatory disease in an individual, comprising the step of administering to the individual the nutrient pharmaceutical composition as disclosed. Preferably, the inflammatory disease is osteoarthritis.

BRIEF DESCRIPTION OF DRAWINGS Fig. 1 depicts the inhibitory effects of polyphenols, ascorbate, proline and lysine on migration behavior of human breast cancer cells. Fig. 2 depicts the inhibitory effects of polyphenols, ascorbate, proline, and lysine on migration behavior of human colon cancer cells.

Fig. 3 depicts the inhibitory effects of polyphenols, ascorbate, proline, and lysine on migration behavior of human melanoma cells. Fig. 4 depicts the inhibitory effects of polyphenol, ascorbate, proline, and lysine on apoptosis of human melanoma cells.

Fig. 5 depicts the inhibitory effects of ascorbic acid, proline, lysine and various amounts of EGCG on cell proliferation of human melanoma cells (A 2058).

Fig. 6 depicts the inhibitory effects of EGCG on cell proliferation of human breast cancer cells (MDA-MB 231).

Fig. 7 depicts the effects of supplementation of basal medium with ascorbic acid, proline, lysine with various amounts of EGCG on cell proliferation of human breast cancer cells

(MDA-MB 231).

Fig. 8 depicts the effects of supplementation of basal medium with ascorbic acid, proline, lysine and various amounts of EGCG on cell proliferation of human colon cancer cells

(HCT 116).

Fig. 9 depicts the effects of supplementation of basal medium with ascorbic acid, proline, lysine and various amounts of EGCG on expression of matrix metalloproteinases (MMP) in human melanoma cells. Fig. 10 depicts the effects of supplementation of basal medium with ascorbic acid, proline, lysine and various amounts of EGCG on Matrigel invasion by human breast cancer cells (MDA-MB 231).

Fig. 11 depicts the effects of supplementation of basal medium with ascorbic acid, proline, lysine and various amounts of EGCG on Matrigel invasion by human colon cancer cells (HTC 116).

Fig. 12 depicts the effects of supplementation of basal medium with ascorbic acid, proline, lysine and various amounts of EGCG on reducing the number of invading cells in human melanoma cells (A 2058).

DETAILED DESCRIPTION OF THE INVENTION

As used herein, "lysine" is used interchangeable with L-lysine, "proline" is used interchangeable with L-proline, "arginine" is used interchangeable with "L-arginine";

"vitamin C" is used interchangeable with ascorbic acid, and may include ascorbate salts or ascorbate esters. "MMPs" refers to matrix metalloproteinases; e.g., MMP-1, MMP-2, MMP-3, MMP-4, MMP-5, MMP-6, MMP7, MMP-8, MMP-8, MMP-9, MMP-10, MMP- 11 etc. "EGCG" refers to (-)-epigallocatechin-3 -gallate which is the major polyphenolic constitutents present in green tea. "NHDF" refers to normal human dermal fibroblast, including human chondrocytes and human stromal cells.

The present invention provides a nutrient pharmaceutical composition ascorbic acid, lysine, proline and at least one polyphenol compound. Preferably, ascorbate compound is selected from the group consisting of ascorbic acid, ascorbate salts and ascorbate esters. Preferably, lysine is lysine hydrochloride or pharmaceutically acceptable lysine salts. Preferably, proline is proline hydrochloride or pharmaceutically acceptable proline salts thereof.

Polyphenol compounds are extracts of green tea. They are also known as catechins. Polyphenols are present in green tea and have been suggested to provide protection against variety of illnesses including cancer (Mukhtar H., Ahmed N. Am. J. Clin. Nutr. 71 : 1698S-1702S (2000)). Oral administration of green tea enhanced the tumor-inhibitory effects of doxorubicin in mice. The potential anti-cancer activity of catechins may relate to their effects on several factors involved in proliferation of cancer cells and their metastasis. Catechins are known to cause cell cycle arrest in human carcinoma cells (Ahmad N., Feyes D.K., Nieminen A.L., Agarwal R., Mukhtar H.J. Natl. Cancer Inst. 89: 1881-1886 (1997)). Polyphenolic fraction from green tea is also implicated to protect against inflammation and cytokines induced by tumors.

Polyphenolic compounds present as 30% dry weight in green tea. They include flavanols, flavandiols, flavonoids, and phenolic acids. Flavanols are the most abundant among the polyphenols in green tea and are commonly known as catechins. There are four major catechins in green tea: 1) (-)-epicatechin, 2) (-)-epicatechin-3 -gallate, 3) (-)- epigallocatechin, and 4) (-)-epigallocatechin-3 -gallate (EGCG). Among the catechins, EGCG is the major polyphenolic constitutents present in green tea. EGCG is a potent anti-oxidant compound and may attribute to the anti-cancer activity of green tea. Catechin compounds were reported to exercise its anti-metastatic activity by preventing the angiogenesis process (Cao Y., Cao R. Nature 398:381 (1999)). EGCG has also been shown to interfere with the activity of urokinase (u-plasminogen activator) (Jankun J., Selman S.H., Swiercz R., Skrzypczak J.E. Nature: 387-567 (1997)), one of the most frequently expressed enzymes in human cancers. EGCG is a preferred polyphenol compound.

Preferably, polyphenol compound is selected from the group consisting of epigallocatechin gallate, epicatechin gallate, epigallocatechin, epicatechin, catechin and other pharmaceutically acceptable polyphenol salts and/or mixtures thereof.

One of the main therapeutic target of this patent application is the prevention of the digestion of the extracellular matrix and its restoration. Ascorbic acid or its salt (i.e., ascorbate) is required for the synthesis of collagen, elastin and other key extracellular matrix molecules.

Preferably, a combination of ascorbic acid, proline and lysine is used to enhance the anti-cancer activity of polyphenol compounds. More preferably, the combination enhances the polyphenol compounds including epigallocatechin gallate, epicatechin gallate, epigallocatechin, epicatechin, catechin in such a manner that the polyphenol compound is effective in reducing invasion of cancer cells or completely blocking the invasion.

Without bound by any theory, the present nutrient pharmaceutical formulation contains a mixture of ingredients including polyphenols and the mixture is found to function effectively in blocking proliferation and metastasis processes. We found that the present nutrient formulation composition significantly reduces the invasion of cancer cells or blocks the metastasis of cancer cells completely. Thus, this composition effectively prevented these cancer cells from spreading. The therapeutic use of the compound claimed is an effective, selective and safe treatment for cancer of the breast, colon and of other organs. Preferably, the disclosed nutrient pharmaceutical composition may contain two of the components that are covalently bound.

Preferably, the efficacy of the nutrient composition is enhanced by including compounds known to beneficially affect growth and invasion of cancer and other tumors, including L-arginine and/or arginine-containing compounds. More preferably, N-acetyl- cysteine is used. More preferably, a selenium salt, a copper salt, and a manganese salt are used that are effective to prevent and treat cancer and other tumors. This composition may also include one or more compounds needed as a coenzyme in the Krebs-Cycle, the respiration chain, or for other metabolic functions of cells in an amount effective to prevent and treat cancer and other tumors.

The present nutrient pharmaceutical composition may be administered to a patient in form of capsules, tablets, powders, pills, injections, infusions, inhalations, suppositories or other pharmaceutically acceptable carriers and/or means of delivery for the prevention and treatment of cancer and other tumors. Preferably, the nutrient pharmaceutical composition is administered as capsules, tablets or powders. More preferably, it is administered as capsules.

The present nutrient pharmaceutical composition can be used in preventing and treating cancer and other tumors in a selected patient where the tumor or cancer is located in the breast, ovaries, cervix or other organs of the female reproductive system, lung, liver, skin, gastrointestinal system, brain, bones or other organs of the body. Preferably, the composition is used in lung cancer and brain cancer.

The present nutrient pharmaceutical composition can also be used in preventing and treating the infectious diseases, atherosclerosis, restenosis, other cardiovascular diseases and inflammatory diseases. Preferably, the inflammatory disease is osteoarthritis.

MMP -Mediated Plasmin Activation: It is speculated that MMPs activity can be affected by lysine through plasmin-mediated mechanisms although other mechanisms are not excluded. The MMPs are secreted as proenzymes and their activation is mediated partially by plasmin and its completion requires active form of MMP-3. The mechanism of activation of various MMPs detailed by Nagase (1997) indicates that MMP-3 also requires the conversion of plasminogen to its active form, plasmin. Plasminogen active binding center has the sites where lysine gets specifically attached. Therefore lysine can interfere with activation of plasminogen into plasmin by plasminogen activator (Rath and

Pauling, 1992), by binding to plasminogen active sites, tranexamic acid, a synthetic lysine analog has been used to inhibit plasmin induced proteolysis through this mechanism. Since plasmin activity is essential to induce several tissue MMPs, lysine can interfere with conversion of plasminogen to plasmin and thereby it can inhibit the activation of almost all MMPs. In addition, EGCG may exert an inhibitory effect on extracellular matrix degradation through inhibition of MMP-2.

Cancer Invasion and Role of Matrix: It is also possible to affect cancer cell matrix invasion by increasing the stability and strength of the connective tissue surrounding cancer cells, and contributing to the "encapsulation" of the tumor. This requires optimizing the synthesis and structure of collagen fibrils, for which the hydroxylation of hydroxyproline and hydroxylysine residues in collagen fibers is essential. Ascorbic acid may be essential for hydroxylation of these amino acids. Ascorbic acid and L-lysine are not normally produced in the human body; therefore, suboptimal level of these nutrients is possible in various pathological stages as well as through inadequate diets. Although proline can be synthesized from arginine, its synthesis and or hydroxylation may be affected at pathological conditions. As such, it has been shown that hydroxyproline content of metastatic tumor tissue is much lower than non-metastatic tumor tissue (Chubainskaia et al., 1989). A variety of drugs that reduced metastasis also increased the hydroxyproline content of the tissues (Chubinskaia et al.,1989). The urinary hydroxyproline content of cancer patients has been found to be higher than that in healthy persons or non-cancer patients (Okazaki et al., 1992). All these findings suggest adverse effects of cancer cells on metabolism of proline and possible conditioned deficiency of proline in cancer patients.

Cancer patients may have insufficient levels of ascorbic acid. Ascorbic acid may be cytotoxic to malignant cell lines and exerts anti-metastatic action. The present invention discloses that a combination of ascorbic acid, proline, lysine and at least one poyphenol compound exerts a potent anti-proliferative and anti-metastatic effect on cancer cell lines. Preferably, the present nutrient pharmaceutical formulation is effective against melanoma, breast cancer and colon cancer cells. Most preferably, the present pharmaceutical formulation is effective against human colon cancer cells.

Polyphenol Compounds (Catechins): EGCG represents one of the catechins in green tea extract and may have growth inhibitory effects against human cancer cells. The exact underlying mechanism is unclear. The present invention discloses a surprising synergy in the nutrient pharmaceutical formulation comprising ascorbic acid, proline and lysine and at least one polyphenol compound in effectively blocking proliferation and metastasis of cancer cells.

The nutrient pharmaceutical composition of the present invention effectively block the invasion of cancer of the breast, colon, skin (melanoma), and other forms of cancer. The ingredients present in the nutrient formulation are naturally occurring compounds; and when used in the claimed range as disclosed in the application, they are shown to have no toxic side effects. Thus, this composition can also be used prophylactically, i./e. the effective prevention of cancer and other tumors in the body.

Since viral cells and other invasive microorganisms use similar proteases that cancer cells for spreading of the infection through the body, the composition claimed in this patent may be used in the effective prevention and treatment of viral diseases and other infectious diseases.

Similar mechanism of activation of matrix metalloproteinases that cancer cells use for matrix invasion also contributes to destabilization of atherosclerotic plaques leading to myocardial infarctions and stroke. Therefore, the composition claimed in this patent can also be used in the effective prevention and treatment of atherosclerosis, restenosis and other cardiovascular complications.

Activation of matrix metalloproteinases that cancer cells use for matrix invasion is a key component in various inflammatory conditions. Therefore, the composition claimed in this patent can also be used in the effective prevention and treatment of diseases, such as rheumatoid arthritis, emphysema, allergies, osteoarthritis and other conditions that include inflammatory aspects.

The nutrient pharmaceutical composition of the present invention can be provided to a patient in form of tablets, pills, injections, infusions, inhalations, suppositories or other pharmaceutically acceptable carriers and/or means of delivery. EXAMPLES

The effects of ascorbic acid, lysine, proline, and at least one polyphenol compound were studied for their anti-proliferative and anti- invasive potential in various human cancer cell lines. More particularly, one of the green tea extract ingredient (i.e., epigallochatechin gallate (EGCG)) was examined. Materials and Methods

Human breast cancer cells MDA-MB-231, human colon cancer cells HCT 116, human melanoma cell line A2058 were obtained from ATCC. Normal human dermal fibroblasts were obtained from GICBO. Where not indicated, the culture media obtained from ATCC were used.

In cancer cell proliferation studies each treatment was replicated eight times. In the invasion assays, each treatment was performed in three or four replicates.

Cell Proliferation Studies

In these studies 5X10 breast cancer cells were grown in Liebovitz's medium with 10%) fetal bovine serum (FBS) in 24-well plates. The medium was used as such (basal) or with designated supplements. Plates were incubated in an air-circulating incubator (without supplemental CO₂) for four days. The colon cancer cells HCT116 were grown in McCoy's 5 A media and maintained in a 5% CO₂ -air circulating incubator. At the end of the incubation period, the media were withdrawn and the cells in the wells were washed with PBS followed by incubation for 3 hours with MTT stain. Dimethyl-sulfoxide (DMSO, 1ml) was added to each well. The plates with DMSO were allowed to stand at room temperature for 15 minutes with gently agitation and then OD of the solution in each well was measured at 550 nm. The OD₅₅₀ of the DMSO solution in the well was considered to be directly proportional to the number of cells. The OD₅₅₀ of treatment that did not contain any supplement (Basal) was considered as 100.

Matrigel Invasion Studies The studies were conducted using Matrigel (Becton Dickinson) inserts in compatible 24-well plates. Fibroblasts were seeded and grown in the wells of the plate using DMEM. When fibroblasts reached confluence, the medium was withdrawn and replaced with 750 μl of the media designated for the treatment. The cancer cells (5X 10⁴) suspended in 250 μl of the medium supplemented with nutrients as specified in the design of the experiment were seeded on the insert in the well. Thus both the medium on the insert and in the well contained the same supplements. The plates with the inserts were then incubated (in air-circulating incubator for MDA-MB-231 cells and 5% CO₂ incubator for colon cancer cells and melanoma cells) for 18-20 hours. After incubation, the media from the wells was withdrawn. The cells on the upper surface of the inserts were gently scrubbed away with cotton swab. The cells that had penetrated the Matrigel membrane and had migrated on the lower surface of the Matrigel were stained with hemacolor stain (EM Sciences) and were visually counted under the microscope. The results were subjected to ANOVA and all the possible pairs were tested for significance at p< 0.05.

The media in different studies were supplemented with ascorbic acid, proline, lysine and EGCG at concentrations as indicated.

Gelatinase Zymography

Gelatinase zymography was performed in 10% Novex pre-cast polyacrylamide gel (Invitrogen) in the presence of 0.1% gelatin. Culture media (20μl) was loaded and SDS- PAGE was performed with tris-glysine SDS buffer. After electrophoresis, the gels were washed with 5% Triton X-100 for 30 minutes and stained. Protein standards were run concurrently and approximate molecular weights were determined.

Example 1

MDA-MB 231 (ATCC) breast cancer cells were seeded on Matrigel insert in an improved Matrigel Invasion Chamber (BD). Conditioned media from normal human dermal fibroblast (Clonetics) supplemented with various agents (as indicated on Fig.l) were added to the well. The chamber was incubated for 24 hours and the cells that had invaded the Matrigel membrane and had migrated into the lower surface of the membrane were counted. These data show the inhibitory effect of epigallocatechin gallate and the combination of ascorbic acid, proline and lysine on Matrigel invasion and migration by MDA-MB 231 human breast cancer cells.

Example 2 HTCT116 (ATCC) human colon cancer cells were seeded on Matrigel insert in an improved Matrigel Invasion Chamber (BD). Conditioned media from Normal Human Dermal Fibroblast (Clonetics) supplemented with various agents (as indicated on Fig. 2) were added to the well. The chamber was incubated for 24 hours and the cells that had invaded the Matrigel membrane and had migrated into the lower surface of the membrane were counted. These data show an inhibitory effect of epigallocatechin gallate and the combination of ascorbic acid, proline and lysine on Matrigel invasion and migration by

HCT116 human colon cancer cells.

Example 3

A2058 (ATCC) human melanoma cells were seeded on Matrigel insert in improved Matrigel Invasion Chamber (BD). Conditioned media from Normal Human

Dermal Fibroblast (Clonetics) supplemented with various agents was added to the well.

The chamber was incubated for 24 hours and the cells that had invaded the Matrigel membrane and had migrated into the lower surface of the membrane were counted.

These data show an inhibitory effect of epigallocatechin gallate and the combination of ascorbic acid, proline and lysine on Matrigel invasion and migration by A2058 human melanoma cells.

Example 4

In this experiment A2058 (ATCC) human melanoma cells were seeded on Matrigel insert in an improved Matrigel Invasion Chamber (BD) in the presence of:

A: conditioned media from Normal Human Dermal Fibroblast (Clonetics) and B: the same media supplemented with various nutrients as indicated in the Fig.4 legends. After 24 hours of incubation the cells that invaded the Matrigel membrane and migrated to the lower surface of the membrane were examined under the microscope and counted.

These data show an apoptotic effect of epigallocatechin gallate and the combination of ascorbic acid + proline + lysine on A2058. A; Human Melanoma Cells in tissue culture medium. B: Human Melanoma Cells in tissue culture medium containing ascorbic acid (100 μM), proline (140 μM), lysine (400 μM) and EGCG (20 μg/ml). Note: the cells were destroyed. Example 5

Cancer Cells Proliferation Study

Melanoma A2058 Cells

Figure 5 shows the effect of 10, 20 and 50 μg/ml of EGCG without and with lysine, proline, and ascorbic acid supplementation on the proliferation of melanoma cells. Neither lysine, proline, and ascorbic acid nor EGCG at 10 and 20 μg/ml had any significant effect on cell proliferation. However, EGCG at 50 μg/ml significantly reduced the cell number to 30%. A similar effect was observed with lysine, proline and ascorbic acid.

Breast Cancer MDA-MB-231 Cells h these experiments, the basal media was supplemented with 0, 10, 20, 50,100 or 200 μg/ml of EGCG (Figure 6). The results show that supplementation of the basal media with 50, 100 and 200 μg/ml of EGCG significantly reduced the cell number to 66.1 ± 5.3, 33.6 ± 2 and 29.6 ± 0.8 % compared to unsupplemented controls respectively.

EGCG concentrations in the cellular media up to 20 μg/ml did not have any significant inhibitory effect on cell proliferation.

We also studied the effects of ascorbic acid, lysine, proline and different concentrations of EGCG on proliferation of cancer cells. Figure 7 shows non- significantly reduced the cell number to 86.1+ 1.93% with ascorbic acid, lysine and proline. Further addition of 20, 50 and lOOμg EGCG to this combination significantly reduced the cell number to 74 ± 5.8, 64.8 ± 1.6 and 22 ± 5 % compared to the control group respectively.

Colon cancer HCT116 cells

While the inhibitory effect of ascorbic acid, proline and lysine on cell proliferation of colon cancer cells was not pronounced, the combination of ascorbic acid, proline and lysine with 20μg/ml EGCG significantly decreased the cell number to 69 ± 0.5 % (Figure 8). A higher level of EGCG in this combination (50 μg/ml) drastically reduced the cell number to 4.6 ± 0.3%. The anti-proliferative activity of the nutrient combinations used in these studies varied with the type of cancer cells. In breast cancer cells, the combination of ascorbic acid, proline and lysine with EGCG had higher anti-proliferative effects than when these nutrients were used individually. In melanoma and colon cancer cells exposed to the combination of ascorbic acid, proline, lysine did not affect their proliferation. However, combining these nutrients with 20 μg/ml EGCG resulted in a significant reduction in the number of colon cancer cells but not in melanoma cells. The colon cancer cells appeared to be more sensitive than the breast cancer cells and melanoma cells the least to the combination of ascorbic acid, proline, lysine and EGCG. The proliferation of the colon cancer cells was almost completely reduced (4.6%>) when ascorbic acid, proline and lysine was given with 50μg/ml of EGCG.

Example 6

Geltinase Zymo graph Studies The effect of EGCG on melanoma cells with basal and ascorbic acid, proline, and lysine supplementation on expression of MMPs is depicted in figure 9 by gelatinase zymography. Melanoma cells showed two bands corresponding to MMP-2 and MMP-9. Ascorbic acid, lysine and proline combination has no effect on the expression of MMPs bands as compared to the basal. However, EGCG inhibits the expression of both MMP-2 and MMP-9 in a dose dependent manner. The intensity of bands for basal and ascorbic acid, lysine and proline combination were the same.

Example 7

Extracellular Matrix Invasion and Migration Studies The inhibitory effects of a combination of ascorbic acid, proline and lysine used separately and together with various concentrations of EGCG were examined. The effects of these combinations on extracellular matrix using pre-formed Matrigel matrices, routinely used to assess invasive potential of various cancer cell lines were studied.

Breast cancer MDA-MB-231 Cells

Figure 10 shows the results of Matrigel invasion of breast cancer cells incubated in the presence of ascorbic acid, proline and lysine. Invasion of cancer cells incubated in a combination of ascorbic acid, proline and lysine was reduced to 48.1 ± 22.1 %_> compared to cells incubated in non-supplemented media. In the media supplemented with 20 μg/ml of EGCG only, the number of invading cells decreased to 69.5 ± 27.4%. The complete inhibition of matrix invasion by breast cancer cells was achieved in the presence of higher EGCG concentrations (50μg/ml and lOOμg/ml).

In another series of studies, supplementation of media with 100 μM ascorbic acid reduced the invasion by 36%. Supplementation with ascorbic acid and 140 μM proline further reduced the invasion by 47%. Using 400 μM lysine in addition to ascorbic acid and proline in the supplement further reduced the invasion to 67%; lysine shows a linear response in enhancing the effects of ascorbic acid and proline up to 800 μM level.

Figure 10 also shows that the combination of ascorbic acid, proline and lysine as well as 20μg/ml of EGCG was effective in a complete stopping of the invasion of cancer cells through the extracellular matrix. This combination made it possible to achieve the maximum inhibitory effect on cancer cells invasion without the necessity of using high concentrations of individual nutrients. As such, ascorbic acid, proline and lysine along with EGCG made it possible to stop matrix invasion of breast cancer cells completely at lower level of EGCG (20μg/ml).

Colon cancer HCT116 Cells Figure 11 shows that the combination of ascorbic acid, proline and lysine significantly reduced the invasion of colon cancer cells to 67.2 ± 3.7 %. The EGCG used alone at 20μg/ml reduced the invasion to 44.9 ± 3.3%>, while the combination of ascorbic acid, proline and lysine and 20 μg/ml of EGCG had a synergistic effect reducing colon cancer cells invasion to 24.9 ± 4.6%>.

Melanoma A2058 Cells

Figure 12 shows that the combination of ascorbic acid, proline, and lysine was effective in reducing the number of invading cells to 88.2 ± 4%>, however this decrease was not statistically significant. Combining these nutrients with as little as 20 μg/ml of EGCG was effective in reducing the number of invading cells to zero.

The results show that the use of ascorbic acid, proline and lysine with EGCG enabled us to obtain drastic reduction in the number of cells invading and migrating through Matrigel membrane at lower levels of EGCG. The invasion was reduced to zero using as low a level as 20μg/ml EGCG with ascorbic acid, proline and lysine in breast cancer cells and melanoma cells. The benefits of the combination results were not as spectacular with colon cancer cells as obtained with breast cancer cells. The level of EGCG had to be at 50 μg/ml to obtain 90% reduction in invasion by these cells. In this study, no alteration in MMPs expression in melanoma cells was observed, although EGCG has an inhibitory effect on their expression in a dose dependent fashion.

These series of studies conclusively demonstrate that the present nutrient pharmaceutical formulation comprising ascorbic acid, proline, lysine and at least one polyphenol compound exerts an effective anti-proliferative and anti-invasive effects on cancer cells.

Example 8

The following nutrient pharmaceutical formulations (Tables 1-5) and EPIC AN FORTE™ (Table 6) are illustrated for their preparations. These formulations comprising ascorbic acid, proline, lysine and at least one polyphenol compound are found to be effective in blocking invasion of cancer cells and metastasis of cancer cells.

Table 1 Formulation 1

Biochemical Substances Amount %

Ascorbic Acid 250 mg 5.6

Calcium Ascorbate 250 mg 5.6

Magnesium Ascorbate 250 mg 5.6

Ascorbyl Palmitate 250 mg 5.6

Polyphenols 1,000 mg 22.5

N-Acetyl-Cysteine 200 mg 4.5

Lysine 1,000 mg 22.5

Proline 750 mg 16.8

Arginine 500 mg 11.2

Selenium 30 meg <0.01

Copper 2 mg 0.04

Manganese l mg 0.02 mg = milligrams meg = micrograms

'%" refers to % weight of individual ingredient over total weight of formulation Table 2 Formulation 2

Biochemical Substances Amount %

Ascorbic Acid 25 mg 5.7

Calcium Ascorbate 25 mg 5.7

Magnesium Ascorbate 25 mg 5.7

Ascorbyl Palmitate 25 mg 5.7

Polyphenols - 50%o 200 mg 46.0

N-Acetyl-Cysteine 10 mg 2.3

Lysine 50 mg 11.5

Proline 25 mg 5.7

Arginine 50 mg 11.5

Selenium 1 meg <0.001

Copper 20 meg O.001

Manganese 50 meg O.001 mg = milligrams meg = micrograms "%" refers to % weight of individual ingredient over total weight of formulation

Table 3 Formulation 3

Biochemical Substances Amount %

Ascorbic Acid 5,000 mg 13.3

Calcium Ascorbate 5,000 mg 13.3

Magnesium Ascorbate 5,000 mg 13.3

Ascorbyl Palmitate 5,000 mg 13.3

Polyphenols - 100% 5,000 mg 13.3

N-Acetyl-Cysteine 1,500 mg 4.0

Lysine 5,000 mg 13.3

Proline 3,000 mg 8.0

Arginine 3,000 mg 8.0

Selenium 200 meg O.001

Copper 9 mg 0.02

Manganese 10 mg 0.002 mg = milligrams meg = micrograms "%" refers to % weight of individual ingredient over total weight of formulation

Table 4 Formulation 4

Biochemical Substances Amounτ Yo

Ascorbic Acid 250 mg 4.7 Calcium Ascorbate 250 mg 4.7 Magnesium Ascorbate 250 mg 4.7 Ascorbyl Palmitate 250 mg 4.7 Polyphenols - 98%) 1,000 mg 18.7 N-Acetyl-Cysteine 200 mg 3.7 Lysine 1,000 mg 18.7 Proline 750 mg 14.0

Arginine 500 mg 9.3

Selenium 100 meg O.002

Copper 2 mg 0.04

Manganese l mg 0.02

Calcium 500 mg 9.3

Magnesium 400 mg „ 7.5 mg = milligrams meg = micrograms "%" refers to % weight of individual ingredient over total weight of formulation

Table 5 FormulatioB L 5

Biochemical Substances Amount %

Ascorbic Acid 250 mg 4.5

Calcium Ascorbate 250 mg 4.5

Magnesium Ascorbate 250 mg 4.5

Ascorbyl Palmitate 250 mg 4.5

Polyphenols - 98% 1,000 mg 18

N-Acetyl-Cysteine 200 mg 3.6

Lysine 1,000 mg 18

Proline 750 mg 13.5

Arginine 500 mg 9

Selenium 100 meg O.002

Copper 2 mg <0.04

Manganese l mg <0.02

Calcium 500 mg 9

Magnesium 400 mg 7.2

Citrus Bioflavonoids 200 mg 3.6 g = milligrams meg = micrograms

"%" refers to % weight of individual ingredient over total weight of fo

Table 6 Formulation for EPICAN FORTE™

Serving size: 6 Capsules (Suggested use: two capsules three times daily preferably with meals)

mg = milligrams meg = micrograms

EPICAN FORTE™ is a trademark name in a pending U.S. application. Other ingredients: Vetetarian capsules (hydroxypropyl methycellulose), silicon dioxide, cellulose and magnesium stearate.

Example 9

Effects of EPICAN FORTE™ on Human Cancer Cells The effects of EPICAN FORTE™ on human cancer cells were studied. Metastatic parameters such as expression of matrix metalloproteinases (MMPs) by gelatinase zymography, invasion potential through Matrigel and proliferation growth by MTT assays were studied. The protocols for these assays are described in detail as above. Several human cancer cell lines were used: skin cancer - melanoma cells 2058, liver cancer- HepG2 cells, fibrosarcoma - HT 1080 cells, colon cancer - HCT 116, breast cancer ER+/- MCF-7 and breast cancer ER-/- MDA-MB-231.

The following tables (Tables 7 and 8) summarize the results:

Effects of EPICAN FORTE™ on Proliferation/Growth of Human Cancer Cell

Lines:

Table 7 Treatment Doses of EPICAN FORTE™ (ug/mlV. Percent of Control

Cancer Cells 0 10 50 100 500 1000

Melanoma 100% 98 - 105 - 50

Hep G2 100% 92 - 138 - 85

HT-1080 100 % 100 - 97 80 63

Colon

(HCT 116) 100 % 119 125 141 120 106

MCF-7 100% 93 88 92 97 77

MDA-MB-231 100% 103 - 82 - 25 Effects of EPICAN FORTE™ on Matrigel Invasion and Migration by Human

Cancer Cells:

Table 8 Treatment Doses of EPICAN FORTE™ (μe/mϊ): Percent hihibition

Cancer Cell 0 10 50 100 500 1000

Melanoma 0% 80 98 100

HepG2 0% 15 25 50 95 100

HT-1080 0% 90 50 70 100

Colon

(HCT 116) 0% 20 50 80 100

MDA-MB-231 0% 50 98

MCF-7 Non-invasive

Effects of EPICAN FORTE™ on the Expression of Matrix Metalloproteinases (MMPs^') by Human Cancer Cell Lines: Melanoma Cells: Melanoma cells exhibited two bands on gelatinase zymography corresponding to MMP-2 and MMP-9. EPICAN FORTE™ inhibited the expression of

MMP-2 and -9 in a dose dependent fashion. The expression of MMP-2 and -9 was significantly inhibited with a concentration of 100 μg/ml of EPICAN FORTE™ and virtually undetectable with a concentration of 1000 μg/ml.

HepG2 Cells: Like melanoma cell, HepG2 cell also expressed two bands corresponding to MMP-2 and MMP-9. EPICAN FORTE™ inhibited the expression of

MMP-2 and-9 at 500 and 1000 μg/ml concentration.

Fibrosarcoma HT-1080: HT-1080 cells exhibited two bands for MMP-2 and -9.

EPICAN FORTE™ also inhibited the expression of both the bands in a dose dependent fashion. Very faint bands were seen at 500 and 1000 μg/ml concentration.

Colon cancer HCT 116: Colon cancer cells showed only one band on zymography corresponding to MMP-2 which totally disappeared at 100 μg/ml concentration.

MCF-7 and MDA-MB-231 : These cancer cell lines did not any MMPs bands under our experimental concentration, which were similar to the other cancer cell lines.

Invasion of MDA-MB-231 through Matrigel was inhibited by 50, 60 and 95% by 10, 50 and 100 μg/ml of EPICAN FORTE™ respectively. EPICAN FORTE™ was not toxic to MDA-MB-231 at lOμg/ml, showed slight toxicity at lOOμg/ml. However, it exhibited significant toxicity at 1000 μg/ml. Neither MMP-2 nor MMP-9 was expressed by zymography. In contrast, EPICAN FORTE™ was not toxic to MCF-7 even at 500 μg/ml, and exhibited slight toxicity at 1000 μg/ml. MCF-7 was not invasive and did not express MMPs activities.

EPICAN FORTE™ inhibits the expression of MMP-2 and MMP-9 in a dose- dependent fashion. The expression of MMP-2 and MMP-9 was significantly inhibited with a concentration of 100 μg/ml of EPICAN FORTE™ and virtually undetectable with a concentration of 100 μg/ml. EPICAN FORTE™ used at 10 and 100 μg/ml concentrations did not significantly affect the cells viability, and at 100 μg/ml it showed cytotoxicity at the range of 10-40 percent, depending on cell type. The invasion of melanoma cells, MDA-MB-231 cells, and a co-culture of melanoma cells withNHDF through Matrigel was significantly reduced in a dose-dependent manner. Invasion of HT- 1080 cells thought Matrigel was inhibited by 10%, 50%, 70% and 100% at 10, 100, 200 and 1000 μg/ml respectively. Interestingly, EPICAN FORTE™ was not toxic to HT- 1080 cells at 100 μg/ml. These results demonstrate that EPICAN FORTE™ is very effective for several cancer cell lines and also in co-culture. These observations reveal that EPICAN FORTE™ may provide a natural therapeutic basis that makes it a valuable and promising candidate for the treatment of human cancers.

Example 10

Effects of EPICAN FORTE™ on Human Normal Cell Lines The effects of EPICAN FORTE™ on normal human cells was studied. Parameters similar to those of cancer cell lines were employed; namely zymography for MMPs expression, invasion through Matrigel and proliferation/growth by MTT assays. Several normal human dermal fibroblast (NHDF) were used, including: human chondrocytes and human stromal cells.

The following tables (Tables 9, 10 and 11) summarize the effects of EPICAN FORTE™ on proliferation/growth, metastasis invasion and MMP production in normal human cells: Table 9 Effects of EPICAN FORTE™ on Proliferation/Growth of Normal Human Cells. Treatment Doses of EPICAN FORTE™ (μg/ml : Percent of Control

Normal Cells 0 10 50 100 500 100

NHDF 100% 118 135 - 90

Chondrocytes 100% 113 148 76 82

Stromal Cells 100% 100 116 115 98 64

Table 10 Effects of EPICAN FORTE™ on Matrigel Invasion by Normal Human Cells. Treatment Doses of EPICAN FORTE™ (μg/mlV Percent Inhibition

Normal Cell 0 10 50 100 200 1000

NHDF 0% 67% 89% 100% -

Chondrocytes 0% 45% 85% 95% 100%

Stromal Cells 0% 0% - 95% 100%

The effects of EPICAN FORTE™ on the expression of matrix metalloproteinases (MMPs) by normal human cells are summarized as followed:

NHDF: NHDF expressed only one band on zymography corresponding to MMP- 2, which virtually disappeared at 1000 μg/ml concentration of EPICAN FORTE™.

Chondrocytes: Chondrocytes also showed only one band corresponding to MMP- 2. EPICAN FORTE™ inhibited the expression of MMP-2 in a dose dependent manner. The expression of MMP-2 was significantly inhibited at a concentration of 100 μg/ml of EPICAN FORTE™ and totally disappeared at 200 μg/ml concentration of EPICAN FORTE™.

Stromal Cells: Stromal cells also exhibited only one band corresponding to MMP-2. EPICAN FORTE™ inhibited the expression of MMP-2 in a dose dependent fashion. Very faint band was seen at 50 and 100 μg/ml concentration which was undetected at 200 and 500 μg/ml concentration.

hi summary, the results indicated that EPICAN FORTE™ inhibits the expression of MMP-2 in a dose-dependent manner. The expression of MMP-2 was significantly inhibited at a concentration of 100 μg/ml of EPICAN FORTE™ and virtually not detected at a concentration of 200 μg/ml. hi addition, it was also found that invasion of chondrocytes through Matrigel was inhibited by 50%, 85%> and 95% at 10 μg/ml, 100 μg/ml and 200 μg/ml. At 500 μg/ml the invasion was totally reduced to 0%. EPICAN FORTE™ was not toxic to chrondrocytes even at a concentration of 200 μg/ml. h fact, EPICAN FORTE™ exerted a cell proliferation effect, a 70% increase in cell proliferation with 200 μg/ml, 70%> more over the control. Slight toxic effect was seen only at 500 μg/ml. These results demonstrate that EPICAN FORTE™ is effective in inhibiting the MMP-2 expression and that EPICAN FORTE™ represents a novel anti- inflammatory nutrient formulation as a natural approach to inhibit MMP production and extracellular matrix degradation in osteoarthritis and other related disorders including excessive cartilage degradation.

Although in vivo test lines of Epican-Forte have just started to be carried out two cases proving the validity of Epican-Forte as a medicament for treating cancer have been reported.

A female patient with diagnosed brain tumour was treated with chemo- and radiotherapy without success at the end of April 2002 she was given up. By chance she started to be treated with Epican-Forte with dosages as recommended. At the end of August 2002 MRTS showed that the tumour had vanished.

A male patient of 64 years having a markedly elevated level of the tumour marker

PSA in May 2002 (59,9 μg/1) was diagnosed having metastasis prostate carcinoma along the lymphatic vessels of the aorta. He started treatment with Epican-Forte at recommended dosage. Three months later the PSA level fell to 0,9 μg/1. CT check-up at the end of October 2002 showed that the previously visible lymphatic metastasis was no longer apparent and his prostate was of normal size.

A number of embodiments of the invention have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of the invention.

Claims

WHAT IS CLAIMED IS:

1. A nutrient phaπnaceutical composition useful in treating cancer, comprising: a) an ascorbic compound; b) a L-lysine compound; c) a L-proline compound; and d) at least one polyphenol compound selected from the group consisting of epigallocatechin gallate, epicatechin gallate, epigallocatechin, epicatechin, and catechin, wherein the compounds of a-c) enhance the polyphenol compound's activity in blocking cancer proliferation and metastasis.

2. The nutrient pharmaceutical composition of claim 1, wherein the ascorbic compound is selected from the group consisting of ascorbic acid, pharmaceutical acceptable ascorbate salts, ascorbate esters and/or mixture thereof.

3. The nutrient composition of claim 2, wherein the pharmaceutical acceptable ascorbate salt is calcium ascorbate or magnesium ascorbate.

4. The nutrient composition of claim 2, wherein the ascorbate ester is ascorbyl palmitate.

5. The nutrient pharmaceutical composition of claim 1, wherein the lysine compound is selected from the group consisting of lysine hydrochloride and lysine pharmaceutically acceptable lysine salts.

6. The nutrient pharmaceutical composition of claim 1 , wherein the proline compound is selected from the group consisting of proline hydrochloride and proline pharmaceutical acceptable proline salts.

7. The nutrient pharmaceutical composition of claim 1, further comprises a trace element selected from the group consisting of selenium, copper, manganese, calcium and magnesium.

8. The nutrient pharmaceutical composition of claim 1, further comprises an amino acid.

9. The nutrient pharmaceutical composition of claim 8, wherein the amino acid is arginine.

10. The nutrient pharmaceutical composition of claim 1, further comprises N-acetyl cysteine.

11. A nutrient pharmaceutical composition useful in treating cancer, comprising: a) an ascorbic compound; b) a L-lysine compound; c) a L-proline compound; 5 d) N-acetyl cysteine; and e) at least One polyphenol compound selected from the group consisting of epigallocatechin gallate, epicatechin gallate, epigallocatechin, epicatechin, and catechin, wherein the compounds of a-d) enhance the polyphenol compound's activity in o blocking cancer proliferation and metastasis.

12. The nutrient pharmaceutical composition of claim 11, wherein the ascorbic compound is selected from the group consisting of ascorbic acid, pharmaceutical acceptable ascorbate salts, ascorbate esters and/or mixture thereof.

13. The nutrient composition of claim 12, wherein the pharmaceutical acceptable 5 ascorbate salt is calcium ascorbate or magnesium ascorbate.

14. The nutrient composition of claim 12, wherein the ascorbate ester is ascorbyl palmitate.

15. The nutrient pharmaceutical composition of claim 11, wherein the lysine compound is selected from the group consisting of lysine hydrochloride and lysine 0 pharmaceutically acceptable lysine salts.

16. The nutrient pharmaceutical composition of claim 11, wherein the proline compound is selected from the group consisting of proline hydrochloride and proline pharmaceutical acceptable proline salts.

17. The nutrient pharmaceutical composition of claim 11, wherein the composition 5 further comprises a trace element selected from the group consisting of selenium, copper, manganese, calcium and magnesium.

18. The nutrient pharmaceutical composition of claim 11, further comprises an amino acid.

19. The nutrient pharmaceutical composition of claim 18, wherein the amino acid is 0 arginine.

20. A nutrient pharmaceutical composition useful in treating cancer, comprising: ascorbic acid, calcium ascorbate, magnesium ascorbate, ascorbyl palmitate, polyphenols, N- acetyl-cysteine, lysine, proline, arginine, selenium, copper, and manganese.

21. The nutrient pharmaceutical composition of claim 20, wherein the composition 5 comprises 250 mg ascorbic acid, 250 mg calcium ascorbate, 250 mg magnesium ascorbate, 250 mg ascorbyl palmitate, 1,000 mg polyphenols, 200 mg N-acetyl- cysteine, 1,000 mg lysine; 750 mg proline, 500 mg arginine, 30 meg selenium, 2 mg copper, and 1 mg manganese.

22. The nutrient pharmaceutical composition of claim 20, wherein the composition comprises 25 mg ascorbic acid, 25 mg calcium ascorbate, 25 mg magnesium ascorbate, 25 mg ascorbyl palmitate, 200 mg polyphenols, 10 mg N-acetyl-cysteine,

50 mg lysine, 25 mg proline, 50 mg arginine, 1 meg selenium, 20 meg copper, and 50 meg manganese.

23. The nutrient pharmaceutical composition of claim 20, wherein the composition comprises 5,000 mg ascorbic acid, 5,000 mg calcium ascorbate, 5,000 mg magnesium ascorbate, 5,000 mg ascorbyl palmitate, 5,000 mg polyphenols, 1,500 mg N-acetyl- cysteine, 5,000 mg lysine, 3,000 mg proline, 3,000 mg arginine, 200 meg selenium, 9 mg copper, and 10 mg manganese.

24. The nutrient pharmaceutical composition of claim 20, wherein the composition comprises 250 mg ascorbic acid, 250 mg calcium ascorbate, 250 mg magnesium ascorbate, 250 mg ascorbyl palmitate, 1,000 mg polyphenols, 200 mg N-acetyl- cysteine, 1,000 mg lysine, 750 mg proline, 500 mg arginine, 100 meg selenium, 2 mg copper, 1 mg manganese, 500 mg calcium, and 400 mg magnesium.

25. The nutrient pharmaceutical composition of claim 20, wherein the composition comprises 250 mg ascorbic acid, 250 mg calcium ascorbate, 250 mg magnesium ascorbate, 250 mg ascorbyl palmitate, 1,000 mg polyphenols, 200 mg N-acetyl- cysteine, 1,000 mg lysine, 750 mg proline, 500 mg arginine, 100 meg selenium, 2 mg copper, 1 mg manganese, 500 mg calcium, 400 magnesium, and 200 citrus biofavonoids.

26. A nutrient pharmaceutical composition useful in treating cancer, comprising: L-lysine, L-proline, L-arginine, ascorbic acid, calcium, magnesium, polyphenols, N-acetyl- cysteine, selenium, copper, and manganese.

27. The nutrient pharmaceutical composition of claim 26, wherein the composition comprises 1,000 mg L-lysine, 750 mg L-proline, 500 mg L-arginine, 710 mg ascorbic acid, 22 mg calcium, 50 mg magnesium, 1,000 mg polyphenols, 200 mg, N-acetyl cysteine, 30 meg selecium, 2 mg copper, and 1 mg manganese.

28. The nutrient pharmaceutical composition of claim 27, wherein the ascorbic acid is selected from the group consisting of ascorbic acid, calcium ascorbate, mangesium ascorbate and ascorbyl palmitate.

29. The nutrient pharmaceutical composition of claim 27, wherein the polyphenol is selected from the group consisting of epigallocatechin gallate, epicatechin gallate, epigallocatechin, epicatechin, catechin and other pharmaceutically acceptable polyphenol salts and/or mixture thereof. 5

30. A method for treating cancer in an individual, comprising the step of administering to the individual the nutrient pharmaceutical composition of any of claims 1-29.

31. The method of claim 30 wherein the cancer is selected from the group consisting of melanoma cancer, breast cancer, colon cancer, lung cancer and brain cancer.

32. A method for treating an inflammatory disease in an individual, comprising the step o of administering to the individual the nutrient pharmaceutical composition of any of claims 1-29.

33. The method of claim 32, wherein the inflammatory disease is osteoarthritis.