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NATURALLY OCCURRING PRODUCTS IN CANCER THERAPY

Rajesh, Leena S. Sankari, L. Malathi, and Jayasri R. Krupaa

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Abstract

Natural products have been used for the treatment of various diseases and are becoming an important research area for drug discovery. These products, especially phytochemicals have been extensively studies and have exhibited anti-carcinogenic activities by interfering with the initiation, development and progression of cancer through the modulation of various mechanisms including cellular proliferation, differentiation, apoptosis, angiogenesis, and metastasis. This concept is gaining attention because it is a cost-effective alternative to cancer treatment. In this article, we have discussed some of the naturally occurring products used in cancer treatment.

KEY WORDS: Carcinogenesis, curcumin, quercetin

Oral cancer is defined as the cancer of mouth and pharynx including cancer of lips, tongue, floor of the mouth, palate, gingiva, alveolar mucosa, buccal mucosa, oropharynx, tonsils, uvula and salivary glands. Cancer is the biggest cause of mortality worldwide, responsible for 8.2 million death/year and rising according to the global scientific report released on the February 5, 2014.[1] Factors such as obesity, poor diet, tobacco, radiation, environmental pollutants, lack of physical activity and age increases cancer risk. These factors may cause cancer by damaging genes directly and/or indirectly in combination with existing genetic mutation within cells.[2]

Epidemiology

Epidemiological studies have shown that diet containing fruits and vegetables reduce the risk of several types of cancer.[3] Intake of fruits and vegetables has been successfully used in the prevention of chronic disease associated with oxidative stress condition including cancer.[4,5] WHO projects 10,000,000 cases of cancer per year worldwide and 6,000,000 deaths from cancer per year worldwide. And it also projected 15 million cases/year in 2020. It is been estimated that 80% of the world population relies on plant-based medicine for primary health care and 75% of all pharmaceuticals were discovered by examining the use of plants in traditional medicine.

Carcinogenesis

The transformation of normal cell to cancer cell occurs through three distinct phases, initiation, promotion, and progression. Initiation of cancer occurs in the normal cells due to exposure of carcinogenic and mutagenic agents. The initiated cells are irreversibly altered and are at greater risk of neoplastic transformation. However, initiation alone is not sufficient for tumor formation.[6] In promotion phase, tumor promoters convert the initiated cells into neoplastic cells.[7,8] Progression involves a stepwise evolution of neoplastic cells into higher degree of malignancy.

Chemopreventive Agents in Oral Carcinogenesis

Various phytochemicals obtained from vegetables, fruits, spices, teas, herbs, and medicinal plants, such as flavonoids carotenoids, phenolic compounds and terpenoids, have been extensively investigated for their anti-cancer activities due to their safety, low toxicity and general availability.[9] In this article we discuss (a) use of phytochemicals, including curcumin, resveratrol, apigenin, quercetin, genistein, lycopene, isothiocyanates (b) their mechanism of action, such as anti-oxidant properties, inhibition of cell cycle, induction of apoptosis, regulation of angiogenesis.

Curcumin

Curcumin (diferuloylmethane), a yellow pigment belongs to the class of polyphenols present in the rhizomes of turmeric is used in cooking in India. It is also used as a cosmetic and in some medical preparations. Multiple therapeutic activities of curcumin have also been considered to be associated with its anti-oxidant and anti-inflammatory properties. The anti-inflammatory effect of curcumin is most likely medicated through its ability to inhibit cyclooxygenase-2, lipoxygenase (LOX), and inducible nitric oxide synthase.[10] Curcumin has the capability to inhibit carcinogen bioactivation via suppression of specific cytochrome P450 isozymes, as well as to induce the activity or expression of phase II carcinogen detoxifyingenzymes.[11] Combination of phenethylisothiocyanate and curcumin caused suppression of epidermal growth factor (EGF) receptor phosphorylation and inhibition of EGF-induced phosphorylation and induction of phosphatidylinositol 3-kinase in prostate cancer-3 cells.[12] It regulates tumor cell growth through multiple cell signaling pathways, including cell proliferation pathway, cell survival pathway, caspase activation pathway, tumor suppressor pathway, death receptor pathway, mitochondrial pathways and protein kinase pathway.

Resveratrol

Resveratrol (trans-3, 5, 4-tryhydroxystilbene) a naturally occurring phytoalexin, is found at a high concentration in the skin of red grapes and red wine. Resveratrol is known to have anti-oxidant, anti-inflammatory and antiproliferative effects on a variety of cancer cells in vitro and in various animal models.[13] Resveratrol has been identified as an effective candidate for cancer prevention based on inhibitory effects on cellular events associated with cancer initiation, promotion, and progression.[14] It has been shown to inhibit tumor necrosis factor-α-mediated matrix metalloproteinase-9 expression in HepG2 cells by down regulation of the nuclear factor-kB signaling pathway.[15] Various studies revealed multiple intracellular targets of resveratrol, which affect cell growth, inflammation, apoptosis, angiogenesis, and invasion and metastasis.[16]

Apigenin

Apigenin, a naturally occurring plant flavone, abundantly present in common fruits and vegetables possesses anti-oxidant, anti-mutagenic, anti-carcinogenic, anti-inflammatory, anti-growth, and anti-progression properties.[17] Apigenin is effective in carcinogenesis, topical application of apigenin inhibited dimethyl benzanthracene-induced skin tumors,[18] and also diminished ultraviolet-induced cancer incidence and increased tumor free survival experiment.[19]

Earlier studies demonstrated that the apigenin promotes metal chelation, scavenges free radicals and stimulates phase II detoxification enzymes in cell culture and in vivo tumor models.[20]

Quercetin

Quercetin is a dietary flavonoid abundant in variety of foods including apples, berries, brassica vegetables, grapes, onions, shallots, tea, and tomatoes as well as many seeds, nuts, barks and leaves.[21] It usually occurs as o-glycosides with D-glucose as glycosides have been identified.[22] Among polyphenols, quercetin is one of the most potent anti-oxidants, as demonstrated in different studies.[23,24] It has been shown to inhibit oxidative species generating enzymes such as xanthine oxidase, LOX, and nicotinamide adenine dinucleotide phosphate oxidase.[25] It is a potent anti-cancer agent, exhibiting different activities such as cell cycle regulation, interaction with type II estrogen binding sites and tyrosine kinase inhibition.[26]

Isothicyanates

Isothiocyanates (ITCs) are electrophilic compounds that play a major role in potential chemopreventive effects associated with high intake of cruciferous vegetables such as watercress, brussel sprouts, broccoli, cabbage, horseradish, radish, and turnip.[27] Cruciferous vegetables have been widely accepted as potential diet components that may decrease the risk of cancer.[28] Epidemiological studies show that the dietary intake of ITCs I associated with reduced risk of certain human cancers.[29] ITCS display anti-carcinogenic activity by reducing the activation of carcinogens and increase their detoxification.

Genistein and ursolic acid

Genistein is an isoflavone compound found in soybean and related products such as tofu, soy milk and soy sauce.[30] And is a promising cancer chemotherapeutic agent.[31] It inhibits the growth of cancer by increasing apoptosis, including cell cycle delays and modulating intercellular signaling pathways.[32]

Ursolic acid is a pentacyclic triterpene compound widely found in food, medicinal herbs, apple peel and is able to exhibit a wide range of pharmacological functions, including anti-oxidant, anti-tumor, anti-inflammatory activities.[33]

Conclusion

Natural products play a major role in chemotherapy drugs, and primarily target proliferating tumor cells. Chemoprevention by phytochemicals is of great interest and is considered to be an inexpensive, readily applicable, acceptable, and accessible approach to cancer control and management. Several phytochemicals are in preclinical or clinical trials for cancer chemoprevention. Epidemiological studies have shown that high dietary consumption of vegetables and fruits reduced the risk of cancer. Severe toxicity is a major drawback in conventional radiotherapy and chemotherapy.

Footnotes

Source of Support: Nil

Conflict of Interest: None declared.

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References

  1. Cancer Report worldwide. Press Release WCD 2014, Crisis of Cancer Impact Worldwide. 2014
  2. Anand P, Kunnumakkara AB, Sundaram C, Harikumar KB, Tharakan ST, Lai OS, et al. Cancer is a preventable disease that requires major lifestyle changes. Pharm Res. 2008;25:2097–116. [PMC free article] [PubMed]
  3. Donaldron MS. Nutrition and cancer. A review of the evidence for an anticancer diet. Nutrition journal. 2004;3:1–21.
  4. Riboli E, Norat T. Epidemiological evidence of the protective effect of fruit and vegetables on cancer risk. Am J Clin Nutr. 2003;78(3 suppl):559–69s. [PubMed]
  5. Nichenametla SN, Taruscio TG, Barney DL, Exon JH. A review of the effects and mechanisms of polyphenolics in cancer. Crit Rev Food Sci Nutr. 2006;46:161–83. [PubMed]
  6. Hollman PC, Katan MB. Dietary flavonoids: Intake, health effects and bioavailability. Food Chem Toxicol. 1999;37:937–42. [PubMed]
  7. Di Carlo G, Mascolo N, Izzo AA, Capasso F. Flavonoids: Old and new aspects of a class of natural therapeutic drugs. Life Sci. 1999;65:337–53. [PubMed]
  8. Cragg GM, Newman DJ. Maryland: National Cancer Institute; 2007. Natural products branch. Developmental therapeutics program, Division of cancer, treatment and diagnosis; pp. 461–77.
  9. Amin AR, Kucuk O, Khuri FR, Shin DM. Perspectives for cancer prevention with natural compounds. J Clin Oncol. 2009;27:2712–25. [PMC free article] [PubMed]
  10. Menon VP, Sudheer AR. Antioxidant and anti-inflammatory properties of curcumin. In: Aggarwal BB, Surh YJ, Shishodia S, editors. The Molecular Targets and Therapeutic Uses of Urcumin in Health and Disease. US, Texas: Springer; 2007. pp. 105–25.
  11. Surh YJ, Chun KS. Cancer chemopreventive effects of curcumin. In: Aggarwal BB, Surh YJ, Shishodia S, editors. The Molecular Targets and Therapeutic Uses of Urcumin in Health and Disease. London: Springer; 2007. pp. 149–72.
  12. Kim JH, Xu C, Keum YS, Reddy B, Conney A, Kong AN. Inhibition of EGFR signaling in human prostate cancer PC-3 cells by combination treatment with beta-phenylethyl isothiocyanate and curcumin. Carcinogenesis. 2006;27:475–82. [PubMed]
  13. Gagliano N, Aldini G, Colombo G, Rossi R, Colombo R, Gioia M, et al. The potential of resveratrol against human gliomas. Anticancer Drugs. 2010;21:140–50. [PubMed]
  14. Huang X, Zhu HL. Resveratrol and its analogues: Promising antitumor agents. Anticancer Agents Med Chem. 2011;11:479–90. [PubMed]
  15. Yu HB, Pan CE, Wu WJ, Zhao SH, Zhang HF. Effects of resveratrol on matrix metalloproteinase-9 expression in hepatoma cells. Zhong Xi Yi Jie He Xue Bao. 2008;6:270–3. [PubMed]
  16. Athar M, Back JH, Kopelovich L, Bickers DR, Kim AL. Multiple molecular targets of resveratrol: Anti-carcinogenic mechanisms. Arch Biochem Biophys. 2009;486:95–102. [PMC free article] [PubMed]
  17. Patel D, Shukla S, Gupta S. Apigenin and cancer chemoprevention: Progress, potential and promise (review) Int J Oncol. 2007;30:233–45. [PubMed]
  18. Wei H, Tye L, Bresnick E, Birt DF. Inhibitory effect of apigenin, a plant flavonoid, on epidermal ornithine decarboxylase and skin tumor promotion in mice. Cancer Res. 1990;50:499–502. [PubMed]
  19. Birt DF, Mitchell D, Gold B, Pour P, Pinch HC. Inhibition of ultraviolet light induced skin carcinogenesis in SKH-1 mice by apigenin, a plant flavonoid. Anticancer Res. 1997;17:85–91. [PubMed]
  20. Middleton E, Jr, Kandaswami C, Theoharides TC. The effects of plant flavonoids on mammalian cells: Implications for inflammation, heart disease, and cancer. Pharmacol Rev. 2000;52:673–751. [PubMed]
  21. Kelly GS. Quercetin. Monograph. Altern Med Rev. 2011;16:172–94. [PubMed]
  22. Yang CS, Landau JM, Huang MT, Newmark HL. Inhibition of carcinogenesis by dietary polyphenolic compounds. Annu Rev Nutr. 2001;21:381–406. [PubMed]
  23. Bors W, Heller W, Michel C, Saran M. Flavonoids as antioxidants: Determination of radical-scavenging efficiencies. Methods Enzymol. 1990;186:343–55. [PubMed]
  24. Prior RL. Fruits and vegetables in the prevention of cellular oxidative damage. Am J Clin Nutr. 2003;78:570–8S. [PubMed]
  25. Day AJ, Bao Y, Morgan MR, Williamson G. Conjugation position of quercetin glucuronides and effect on biological activity. Free Radic Biol Med. 2000;29:1234–43. [PubMed]
  26. Lamson DW, Brignall MS. Antioxidants and cancer, part 3: Quercetin. Altern Med Rev. 2000;5:196–208. [PubMed]
  27. Cavell BE, Alwi SS, Donlevy A, Packham G. Antiangiogenic effects of dietary isothiocyanates; mechanisms of action and implications for human health. Biochem Pharmacol. 2010;81:327–36. [PubMed]
  28. Lam TK, Gallicchio L, Lindsley K, Shiels M, Hammond E, Tao XG, et al. Cruciferous vegetable consumption and lung cancer risk: A systematic review. Cancer Epidemiol Biomarkers Prev. 2009;18:184–95. [PMC free article] [PubMed]
  29. Mi L, Di Pasqua AJ, Chung FL. Proteins as binding targets of isothiocyanates in cancer prevention. Carcinogenesis. 2011;32:1405–13. [PMC free article] [PubMed]
  30. Fotsis T, Pepper M, Adlercreutz H, Hase T, Montesano R, Schweigerer L. Genistein, a dietary ingested isoflavonoid, inhibits cell proliferation and in vitro angiogenesis. J Nutr. 1995;125:790–7S. [PubMed]
  31. Li W, Frame LT, Hirsch S, Cobos E. Genistein and hematological malignancies. Cancer Lett. 2010;296:1–8. [PubMed]
  32. Barnes S. Effect of genistein on in vitro and in vitro models of cancer. J Nutr. 1995;125(3 Suppl):777–83S. [PubMed]
  33. Mizushina Y, Iida A, Ohta K, Sugawara F, Sakaguchi K. Novel triterpenoids inhibit both DNA polymerase and DNA topoisomerase. Biochem J. 2000;350:757–63. [PMC free article] [PubMed]