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2022 | 44 | 231-259

Article title

Anticancer and Antioxidant Phytochemicals as Speed Breakers in Inflammatory Signaling

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Abstracts

EN
A causal association between inflammation and cancer has long been suspected. Multiple lines of compelling evidence from clinical, epidemiologic and laboratory studies support that inflammation plays a critical role in the promotion and progression stages of carcinogenesis. Recent progress in our understanding of the molecular biology of cancer highlights the intracellular signal transduction network, including that involved in mediating the inflammatory response, which often functions abnormally during carcinogenesis. One of the key players in inflammatory signaling is cyclooxygenase-2 (COX-2). Aberrant upregulation of COX-2 is frequently observed in various precancerous and malignant tissues. This seminar write-up highlights the cancer preventive effects of some anti-inflammatory phytochemicals derived from edible plants, and their underlying molecular mechanisms with a focus on representative transcription factors and upstream kinases responsible for COX-2 induction.

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Year

Volume

44

Pages

231-259

Physical description

Contributors

  • Department of Natural Sciences, Faculty of Pure and Applied Sciences, Precious Cornerstone University, Ibadan, Oyo State, Nigeria
  • Department of Biochemistry, Osun State University, Osogbo, Nigeria
  • Department of Natural Sciences, Faculty of Pure and Applied Sciences, Precious Cornerstone University, Ibadan, Oyo State, Nigeria
  • Department of Natural Sciences, Faculty of Pure and Applied Sciences, Precious Cornerstone University, Ibadan, Oyo State, Nigeria

References

  • [1] Ogunlana, OO; Ogunlana, OE; Adekunbi, TS; Adetuyi, BO; Adegboye, BE; Iheagwam, FN. Anti-inflammatory Mechanism of Ruzu Bitters on Diet-Induced Nonalcoholic Fatty Liver Disease in Male Wistar Rats. Evidence-Based Complementary and Alternative Medicine, (2020).
  • [2] Hanahan, D.; Weinberg, RA. The hallmarks of cancer. Cell, 100 (1) (2000) 57–70
  • [3] Hanahan, D.; Weinberg, RA. Hallmarks of cancer: the next generation. Cell, 144 (5) (2011) 646–674
  • [4] Jayasekara, H.; MacInnis, RJ.; Room, R.; English, DR. Long-Term Alcohol Consumption and Breast, Upper Aero-Digestive Tract and Colorectal Cancer Risk: A Systematic Review and Meta-Analysis. Alcohol and Alcoholism, 51 (3) (2016) 315–330
  • [5] Adetuyi B.O, Oluwole E.O, Dairo J.O. Biochemical effects of shea butter and groundnut oils on white albino rats, International Journal of Chemistry and Chemical Processes 1(8) (2015) 1-17
  • [6] Kushi, LH.; Doyle, C.; McCullough, M.; Rock, CL.; Demark-Wahnefried, W.; Bandera, EV.; Gapstur, S.; Patel, AV.; Andrews, K.; Gansler, T. American Cancer Society Guidelines on nutrition and physical activity for cancer prevention: reducing the risk of cancer with healthy food choices and physical activity. CA Cancer J Clin, 62 (1) (2012) 30–67
  • [7] Parkin, DM.; Boyd, L.; Walker, LC. 16. The fraction of cancer attributable to lifestyle and environmental factors in the UK in 2010. British Journal of Cancer, 105 (2) (2011) S77–81
  • [8] Adetuyi, BO; Olajide, PA; Adetuyi, AO; Oloke, JK. Preventive Phytochemicals of Cancer as Speed Breakers in Inflammatory Signaling. Research Journal of Life Sciences, Bioinformatics, Pharmaceutical and Chemical Sciences 8 (1) (2022) 30-61
  • [9] Schwarz, J. A.; Viaje, A.; and Siaga, T. J. Fluocinolone acetonide: a potent inhibitor of mouse skin tumor promotion and epidermal DNA synthesis. Chem. Biol. Interact, 17 (1977) 331-347
  • [10] Diamond, L.; McFall, R.; Miller, J.; and Gelboin, H. V. The effects of two isomeric benzoflavones on aryl hydrocarbons. Cancer Res 32 (1972) 731-736
  • [11] Awoyelu EH, Oladipo EK, Adetuyi BO, Senbadejo TY, Oyawoye OM, Oloke JK. Phyloevolutionary analysis of SARS-CoV-2 in Nigeria. New Microbes and New Infections 36 (2020) 100717
  • [12] Jemal, A.; Bray, F.; Center, MM.; Ferlay, J.; Ward, E.; Forman, D. Global cancer statistics. CA Cancer J Clin. 61 (2) (2011) 69–90
  • [13] Manton, K.; Akushevich, I.; Kravchenko, J (28 December 2008). Cancer Mortality and Morbidity Patterns in the U.S. Population: An Interdisciplinary Approach. Springer Science & Business Media. ISBN 978-0-387-78193-8
  • [14] Islami, F.; Goding Sauer, A.; Miller, KD.; Siegel, RL.; Fedewa, SA.; Jacobs, EJ.; McCullough, ML.; Patel, AV.; Ma, J.; Soerjomataram, I.; Flanders, WD.; Brawley, OW.; Gapstur, SM.; Jemal, A. Proportion and number of cancer cases and deaths attributable to potentially modifiable risk factors in the United States. CA Cancer J Clin. 68 (1) (2018) 31–54
  • [15] Chen, S.Y.; Liu, G.H.; Chao, W.Y.; Shi, C.S.; Lin, C.Y.; Lim, Y.P.; Lu, C.H.; Lai, P.Y.; Chen, H.R.; Lee, Y.R. Piperlongumine Suppresses Proliferation of Human Oral Squamous Cell Carcinoma through Cell Cycle Arrest, Apoptosis and Senescence. Int. J. Mol. Sci, 17 (2016) 616
  • [16] Heikkilä, K.; Nyberg, ST.; Theorell, T.; Fransson, EI.; Alfredsson, L.; Bjorner, JB. Work stress and risk of cancer: meta-analysis of 5700 incident cancer events in 116,000 European men and women. BMJ, 346 (2013) f165
  • [17] Tolar, J.; Neglia, JP. Transplacental and other routes of cancer transmission between individuals. Journal of Pediatric Hematology/Oncology, 25 (6) (2003) 430–434
  • [18] Adetuyi, BO; Toloyai, PY; Ojugbeli, ET; Oyebanjo, OT; Adetuyi, OA; Uche, CZ; Olisah, MC; Adumanya, OCU; Jude, C; Chikwendu, JK; Akram, M; Awuchi, CG; Egbuna, C. Neurorestorative Roles of Microgliosis and Astrogliosis in Neuroinflammation and Neurodegeneration. Scicom Journal of Medical and Applied Medical Sciences 1(1) (2021) 1-5
  • [19] James-Okoro, PO; Iheagwam, FN; Sholeye, MI; Umoren, IA; Adetuyi, BO; Ogundipe, AE; Braimah, AA; Adekunbi, TS; Ogunlana, OE; Ogunlana, OO. Phytochemical and in vitro antioxidant assessment of Yoyo bitters World News of Natural Sciences 37 (2021) 1-17
  • [20] Torre, LA.; Bray, F.; Siegel, RL.; Ferlay, J.; Lortet-tieulent, J.; Jemal, A. Global Cancer Statistics, 2012. CA Cancer J Clin, 65(2) (2015) 87–108
  • [21] Cohen, S.; Murphy, ML.; Prather, AA. Ten Surprising Facts About Stressful Life Events and Disease Risk. Annual Review of Psychology, 70 (2019) 577–597
  • [22] Adetuyi, BO; Olajide, PA; Awoyelu, EH; Adetuyi, OA; Adebisi, OA; Oloke, JK. Epidemiology and Therapeutic measure for COVID-19; A review. African Journal of Reproductive Health June 2020 (Special Edition on COVID-19); 24 (2) (2020) 142
  • [23] Kabir, A.; Bukar, M.; Nggada, HA.; Rann, HB.; Gidado, A.; Musa, AB. Prevalence of human papillomavirus genotypes in cervical cancer in Maiduguri, Nigeria. Pan Afr Med J, 33 (2019) 284
  • [24] Howitt, BE.; Herfs, M.; Tomoka, T.; Kamiza, S.; Gheit, T.; Tommasino, M. Comprehensive Human Papillomavirus Genotyping in Cervical Squamous Cell Carcinomas and Its Relevance to Cervical Cancer Prevention in Malawian Women. J Glob Oncol, 3(3) (2017) 227–234
  • [25] Cordon-Cardo, C.; Prives, C. At the crossroads of inflammation and tumorigenesis. J Exp Med, 190 (1999) 1367–70
  • [26] Okolo, C.; Franceschi, S.; Adewole, I.; Thomas, JO.; Follen, M.; Snijder, PJF. Human papillomavirus infection in women with and without cervical cancer in Ibadan, Nigeria. Infect Agents Cancer, 5(1) (2010) 24
  • [27] Lowy, DR.; Solomon, D.; Hildesheim, A.; Schiller, JT.; Schiffman, M. Human papillomavirus infection and the primary and secondary prevention of cervical cancer. Cancer, 113(7) (2008) 1980–1993
  • [28] Liu, G.; Sharma, M.; Tan, N.; Barnabas, RV. HIV-positive women have higher risk of human papilloma virus infection, precancerous lesions, and cervical cancer. AIDS 32(6) (2018) 795–808
  • [29] Looker, KJ.; Rönn, MM.; Brock, PM.; Brisson, M.; Drolet, M.; Mayaud, P. Evidence of synergistic relationships between HIV and Human Papillomavirus (HPV): systematic reviews and meta-analyses of longitudinal studies of HPV acquisition and clearance by HIV status, and of HIV acquisition by HPV status. J Int AIDS Soc 21(6) (2018) e25110
  • [30] Massad, LS.; Xie, X.; D’Souza, G.; Darragh, TM.; Minkoff, H.; Wright, R. Incidence of cervical precancers among HIV-seropositive women. Am J Obstet Gynecol, 212(5) (2015) 606. 1–8
  • [31] Siegel, RL.; Miller, KD.; Jemal, A. Cancer statistics, 2020. CA Cancer J Clin, 70(1) (2020) 7–30
  • [32] Ogunlana, OO; Ogunlana, OE; Popoola, JO; Adetuyi, BO; Adekunbi, TS; David, OL; Adeleye, OJ; Udeogu, SA; Adeyemi, AO. Twigs of Andrographis paniculata (Burn. F) Nees attenuates Carbon Tetrachloride (CCl4) Induced Liver Damage in Wistar Albino Rats. RASAYAN Journal of Chemistry 14(4) (2021) 2598-2603
  • [33] Howlader, N.; Noone, AM.; Krapcho, M.; Miller, D.; Bishop, K.; Altekruse, SF. SEER cancer statistics review, 1975–2013. Bethesda, MD: National Cancer Institute (2016).
  • [34] Cumbera, S.; Nchanji, K.; Tsoka-Gwegweni, J. Breast cancer among women in sub-Saharan Africa: prevalence and a situational analysis. South Afr J Gyn Onc 9(2): (2017) 35–7
  • [35] Didunyemi, MO; Adetuyi, BO; Oyewale, IA. Inhibition of lipid peroxidation and in-vitro antioxidant capacity of aqueous, acetone and methanol leaf extracts of green and red Acalypha wilkesiana Muell Arg. Int J Biol Med Res 11(3) (2020) 7089-7094
  • [36] Smyth, MJ.; Cretney, E.; Kershaw, MH.; Hayakawa, Y. Cytokines in cancer immunity and immunotherapy. Immunol Rev, 202 (2004) 275–293
  • [37] Naylor, MS.; Stamp, GW.; Foulkes, WD.; Eccles, D.; Balkwill, FR. Tumor necrosis factor and its receptors in human ovarian cancer. Potential role in disease progression. J Clin Invest, 91 (1993) 2194–2206
  • [38] Wang, X.; Lin, Y. Tumor necrosis factor and cancer, buddies or foes? Acta Pharmacol Sin, 29 (2008) 1275–1288
  • [39] Vidal-Vanaclocha, F.; Fantuzzi, G.; Mendoza, L.; Fuentes, AM.; Anasagasti, MJ.; Martín, J. IL-18 regulates IL-1beta-dependent hepatic melanoma metastasis via vascular cell adhesion molecule-1. Proc Natl Acad Sci USA 97 (2000) 734–739
  • [40] Hassuneh, MR.; Nagarkatti, M.; Nagarkatti, PS. Role of interleukin-10 in the regulation of tumorigenicity of a T cell lymphoma. Leuk Lymphoma, 54 (2013) 827–834
  • [41] Ahmad, N.; Ammar, A.; Storr, SJ.; Green, AR.; Rakha, E.; Ellis, IO. IL-6 and IL-10 are associated with good prognosis in early stage invasive breast cancer patients. Cancer Immunol Immunother, 67 (2018) 537–549
  • [42] Negus, RP.; Stamp, GW.; Relf, MG.; Burke, F.; Malik, ST.; Bernasconi, S. The detection and localization of monocyte chemoattractant protein-1 (MCP-1) in human ovarian cancer. J Clin Invest, 95 (1995) 2391–2396
  • [43] Maini, RN.; Taylor, PC. Anti-cytokine therapy for rheumatoid arthritis. Annu Rev Med, 51 (2000) 207–229
  • [44] Haghnegahdar, H.; Du, J.; Wang, D.; Strieter, RM.; Burdick, MD.; Nanney, LB. The tumorigenic and angiogenic effects of MGSA/GRO proteins in melanoma. J Leukoc Biol, 67 (2000) 53–62
  • [45] Tricot, G. New insights into role of microenvironment in multiple myeloma. Lancet, 355 (2000) 248–250
  • [46] Thun, MJ.; Namboodiri, MM.; Calle, EE.; Flanders, WD.; Heath, CW., Jr Aspirin use and risk of fatal cancer. Cancer Res, 53 (1993) 1322–7
  • [47] Zhao, X.; Xu, Z.; Li, H. NSAIDs use and reduced metastasis in cancer patients: Results from a meta-analysis. Sci Rep, 7 (2017) 1875
  • [48] Mirvish, S. S. Ascorbic acid inhibition of N-nitroso compound formation in chemical, food and biological systems. In: M. S. Zedeck and M. Lipkin (eds.), Inhibition of Tum Induction and Development, 1981, pp. 101-126. New York: Plenum Publishing Corp.
  • [49] Mirvish, S. S. Inhibition of the formation of carcinogenic N-nitroso compounds by ascorbic acid and other compounds. In: J. H. Burchenal and H. F. Oettgen (eds.), Cancer Achievements, Challenges and Prospects for the 1980’s. 1981, pp. 557-588. New York: Grune and Stratton.
  • [50] Newmark, H. and Mergens, W. α-Tocopherol (vitamin E) and its relationship to tumor induction. In: M. S. Zedeck and M. Lipken (eds.), Inhibition of Tumor Induction and Development. 1981, pp. 127-168. New York: Plenum Publishing Corp.
  • [51] Kuenzig, W.; Chau, J.; Norkus, E.; Holowaschenko, H.; Newmark, H.; Mergens, W.; and Conney, A. N. Caffeic and ferulic acid as blockers of nitrosamine formation. Carcinogenesis (Lond.), 5 (1984) 309-314
  • [52] Lesca, P. Protective effects of ellagic acid and other plant phenols on benzo(a)pyrene-induced neoplasia in mice. Carcinogenesis (Lond.), 4 (1983) 1651-1653
  • [53] Parkin, DM.; Boyd, L.; Walker, LC. 16. The fraction of cancer attributable to lifestyle and environmental factors in the UK in 2010. British Journal of Cancer, 105 (2) (2011) S77–81
  • [54] Wattenberg, L. Inhibitors of chemical carcinogenesis. In: P. Emmelot and E. Kriek (eds.), Environmental Carcinogenesis, 1979, pp. 241-264. Amsterdam: Elsevier/North-Holland Biomedical Press.
  • [55] Wattenberg, L. W. Inhibition of carcinogenic effects of polycyclic hydrocarbons by benzyl isothiocyanate and related compounds. J. Natl. Cancer Inst, 58 (1977) 395-398
  • [56] Dhillon, H.; Chikara, S.; Reindl, K.M. Piperlongumine induces pancreatic cancer cell death by enhancing reactive oxygen species and DNA damage. Toxicol. Rep, 1 (2014) 309–318
  • [57] Wattenberg, L. W.; and Lam, L. K. T. Protective effects of coffee constituents on carcinogenesis in experimental animals. In: Banbury Report 17: Coffee and Health, 1984, pp. 137-145. Cold Spring Harbor, NY: Cold Spring harbor Press.
  • [58] Wattenberg, L. W. Inhibitors of chemical carcinogens. Adv. Cancer Res, 26 (1978) 197-226
  • [59] Wattenberg, L. Inhibitors of chemical carcinogens. In: J. H. Burchenal (ed.), Cancer: Achievements, Challenges and Prospects for the 1980’s, 1981, pp. 517-539. New York: Grune and Stratton.
  • [60] Yamamoto, R. S.; Weisburger, J. H.; and Weisburger, E. K. Controlling factors in urethane carcinogenesis in mice: effect of enzyme inducers and metabolic inhibitors. Cancer Res, 31 (1971) 483-486
  • [61] Sporn, M. B., and Roberts, A. B. The role of retinoids in differentiation and carcinogenesis. Cancer Res, 43 (1983) 3034-3040
  • [62] Seifter, E.; Rettura, G.; and Levenson, S. M. Dietary β-carotene is an effective tumor preventive agent. In: Proceedings of the Thirteenth International Cancer Congress, Seattle, WA, September 8-15, (1982) p. 30
  • [63] Adetuyi, BO; Ogundipe, AE; Ogunlana, OO; Egbuna, C; Estella, OU; Mishra, AP; Akram, M; Achar, RR. (2022). Banana Peel as a Source of Nutraceuticals. Food and Agricultural Byproducts as Important Source of Valuable Nutraceuticals.1st ed. (2022) Springer, Berlin. xxx, 400 p. Gebunden. ISBN 978-3-030-98759-6
  • [64] Hozumi, M.; Ogawa, M.; Sugimura, T.; Takeuchi, T.; and Umezawa, H. Inhibition of tumorigenesis in mouse skin by leupeptin, a protease inhibitor from Actinmycetes. Cancer Res, 32 (1972) 1725-1728
  • [65] Lowe, N. J.; Connor, M. J.; Breeding, J.; and Chalet, M. Inhibition of ultraviolet-B epidermal ornithine decarboxylase induction and skin carcinogenesis in hairless mice by topical indomethacin and triamcinolone acetonide. Cancer Res, 42 (1982) 3941-3943
  • [66] Wattenberg, L. W. Inhibition of carcinogen-induced neoplasia by sodium cyanate, tert-butylisocyanate and benzyl isothiocyanate administered subsequent to carcinogen exposure. Cancer Res. 41 (1981) 2991-2994
  • [67] Wattenberg, L. W.; and Lam, L. K. T. Phenolic antioxidants as protective agents in chemical carcinogenesis. In: O. F. Nygaard and M. G. Simig (eds.), Radioprotectors and anticarcinogens, (1983) pp. 461-469. New York: Academic Press, Inc.
  • [68] Chen, S.Y.; Huang, H.Y.; Lin, H.P.; Fang, C.Y. Piperlongumine induces autophagy in biliary cancer cells via reactive oxygen species-activated Erk signaling pathway. Int. J. Mol. Med, 44 (2019) 1687–1696
  • [69] Nomura, T.; Hata, S.; Enomoto, T.; Tanaka, H.; and Shibata, K. Inhibiting effects of antipain on urethane-induced lung neoplasia in mice. Br. J. Cancer, 42 (1980) 624-626
  • [70] Kuroda, K.; Kanisawa, M.; and Akao, M. Inhibitory effect of fumaric acid on forestomach and lung carcinogenesis by a 5-nitrofuran naphthyridine derivative in mice. J. Natl. Cancer Inst, 69 (1982) 1317-1320
  • [71] Miller, E. C. Some current perspectives on chemical carcinogenesis in human and experimental animals. Cancer Res, 38 (1978) 1479-1496
  • [72] Miller, J. A., and Miller, E. C. The metabolic activation of carcinogenic aromatic amines and amides. Prog. Expp. Tumor Res, 11 (1969) 273- 301
  • [73] Wood, A. W.; Huang, M. T.; Chang, R. L.; Newmark, H. L.; Lehr, R. E.; Yagi, H.; Sayer, J. M.; Jerina, D. M.; and Conney, A. H. Inhibition of the mutagenicity of bay-region diol epoxides of polycyclic aromatic hydrocarbons by naturally occurring plant phenols: exceptional activity of ellagic acid. Proc. Natl. Acad. Sci. USA, 1982, 79: 5513-5517.
  • [74] Moon, R. C.; McCormick, D. L.; and Mehta, R. G. Inhibition of carcinogenesis by retinoids. Cancer Res, (Suppl.), 43 (1983) 2469s-2475s
  • [75] Izabela Jęśkowiak, Stanisław Ryng, Novel potential anticancer agents. World Scientific News 93 (2018) 40-49
  • [76] Sporn, M. B. Retinoids and suppression of carcinogenesis. Hosp. Pract. 1983, 18: 83-98
  • [77] Jacobs, M. M. Inhibitory effects of selenium on 1,2-dimethylhyrazine and methylazoxymethanol colon carcinogenesis. Cancer (Phila.), 40 (1977) 2557-2564
  • [78] Slaga, T. J.; Solanki, W.; and Logani, M. Studies on the mechanism of action of antitumor promoting agents: suggestive evidence for the involvement of free radicals in promotion. In: O. F. Nygaard and M. G. Simic (eds.), Radioprotectors and Anticarcinogens, (1983) pp. 417-485. New York: Academic Press, Inc.
  • [79] Troll, W. Blocking of tumor promotion by protease inhibitors. In: P. N. Magee et al. (eds.), Fundamentals in Cancer prevention, (1976) pp. 41-55. Baltimore: University Park Press.
  • [80] Kensler, T. W.; Bush, D. M.; and Kozumbo, W. J. Inhibition of tumor promotion by a biomimetic superoxide dismutase. Science (Wash DC), 221 (1983) 75-77
  • [81] Solanki, V.; Yotti, L.; Logani, M. K.; and Slaga, T. J. The reduction of tumor initiating activity and cell mediated mutagenicity of dimethylbenz(a)anthracene by a copper coordination compound. Carcinogenesis (Lond.), (1984) 129-131
  • [82] Verma, A. K.; Garcia, C. T.; Ashendel, C. L.; and Boutwell, R. K. Inhibition of 7-bromoethylbenz(a)anthracene-promoted mouse skin tumor formation by retinoic acid and dexamethasone. Cancer Res, 43 (1983) 3045-3049
  • [83] Verma, A. K.; Shapas, B. G.; Ric, H. M.; and Boutwell, R. K. Correlation of the inhibition by retinoids of tumor promoter-induced mouse epidermal ornithine decarboxylase activity and of skin tumor ppromotion. Cancer Res, 39 (1979) 419-425
  • [84] Troll, W.; Klassen, A.; and Janoff, A. Tumorigenesis in mouse skin: inhibition by synthetic inhibitors of proteases. Science (Wash DC), 169 (1970) 1211-1213
  • [85] Adetuyi, BO; Adebisi, OA; Adetuyi, OA; Ogunlana, OO; Toloyai, P; Egbuna, C; Uche, CZ; Khan, J; Adumanya, OCU; Patrick-Iwuanyanwu, KC. Ficus exasperata Attenuates Acetaminophen-Induced Hepatic Damage via NF-κB Signaling Mechanism in Experimental Rat Model BioMed Research International, (2022). https://doi.org/10.1155/2022/6032511
  • [86] Viaje, A.; Siaga, T. J.; Wigler, M.; and Weinstein, B. Effects of anti-inflammatory agents on mouse skin tumor promotion, epidermal DNA synthesis, phorbool ester-induced cellular proliferation, and production of plasminogen activator. Cancer Res, 37 (1977) 1530-1536
  • [87] Nakadate, T.; Yamamoto, S.; Ishii, M.; and Kato, R. Inhibition of 12-tetradecanoylphorbol-13-acetate-induced epidermal ornithine decarboxylase activity by lipoxygenase inhibitors: possible role of product(s) of lipoxygenase pathway. Carcinogenesis (Lond.), 3 (1982) 1411-1414
  • [88] Perchellet, J. P. and Boutwell, R. K. Comparison of the effects of 30isobutyl-1-methylxanthine and adenosine cyclic 3’:5’-monophosphatae on the induction of skin tumors by the initiation-promotion protocol and by the complete carcinogenesis process. Carcinogenesis (Lond.), 3 (1982) 53-60
  • [89] Weekes, R. G.; Verma, A. K.; and Boutwell, R. K. Inhibition by putrescine of the induction of epidermal ornithine decarboxylase activivty and tumor promotion caused by 12-O-tetradecanoylphorbol-13-acetate. Cancer Res, 40 (1980) 4013-4018
  • [90] Wood, A. W.; Chang, R. L.; Huang, M. T.; Uskokovic, M.; and Conney, A. H. 1α-25-dihydroxyvitamin D3 inhibits phorbol ester-dependent chemical carcinogenesis in mouse skin. Biochem. Biophys. Res. Commun, 116 (1983) 605-611
  • [91] Kato, R.; Nakadate, T.; Yamamoto, S.; and Sugimura, T. Inhibition of 12-O-tetradecanoylphorbol-13-acetate-induced tumor promotion and ornithine decarboxylase activity by quercetin: possible involvement of lipoxygenase inhibition. Carcinogenesis (Lond.), 4 (1983) 1301-1305
  • [92] Takigawa, M.; Verma, A. K.; Simsiman, R. C.; and Boutwell, R. K. Inhibition of mouse skin tumor promotion and of promoter-stimulated epidermal polyamine biosynthesis by α-difluoromethylornithine. Cancer Res, 43 (1983) 3732-3738
  • [93] Pramanik, K.C.; Fofaria, N.M.; Gupta, P.; Ranjan, A.; Kim, S.H.; Srivastava, S.K. Inhibition of beta-catenin signaling suppresses pancreatic tumor growth by disrupting nuclear beta-catenin/TCF-1 complex: Critical role of STAT-3. Oncotarget, 6 (2015) 11561–11574
  • [94] Sung, B.; Prasad, S.; Yadav, V.R.; Aggarwal, B.B. Cancer cell signaling pathways targeted by spice-derived nutraceuticals. Nutr. Cancer, 64 (2012) 173–197
  • [95] Venier, N.A.; Colquhoun, A.J.; Sasaki, H.; Kiss, A.; Sugar, L.; Adomat, H.; Fleshner, N.E.; Klotz, L.H.; Venkateswaran, V. Capsaicin: A novel radio-sensitizing agent for prostate cancer. Prostate, 75 (2015) 113–125
  • [96] Oyagbemi, A.A.; Saba, A.B.; Azeez, O.I. Capsaicin: A novel chemopreventive molecule and its underlying molecular mechanisms of action. Indian J. Cancer, 47 (2010) 53–58
  • [97] Guedes, V.; Castro, J.P.; Brito, I. Topical capsaicin for pain in osteoarthritis: A literature review. Reumatol. Clin, 14 (2018) 40–45
  • [98] Swami, S. Inhibition of prostaglandin synthesis and actions by genistein in human prostate cancer cells and by soy isoflavones in prostate cancer patients. Int. J. Cancer, 124 (2009) 2050–2059
  • [99] Baron, J. A. Aspirin and NSAIDs for the prevention of colorectal cancer. Recent Results Cancer Res, 181 (2009) 223–229
  • [100] Gaber E. Batiha, Dina A Awad, Abdelazeem M. Algamma, Richard Nyamota, Mir I Wahed, Muhammad Ajmal Shah, Mohammad Nurul Amin, Babatubde O. Adetuyi, Helal F. Hetta, Natalia Cruz-Marins, Niranjan Koirala, Arabinda Ghosh, Jean-Marc Sabatier (2021). Diary-derived and Egg White Proteins inEnhancing Immune System against COVID-19. Frontiers in Nutritionr. (Nutritional Immunology) 8 (2021) 629440
  • [101] Adetuyi, BO; Adebayo, PF; Olajide, PA; Atanda, OO; Oloke, JK. Involvement of Free Radicals in the Ageing of Cutaneous Membrane. World News of Natural Sciences 43 (2022) 11-37
  • [102] Adetuyi B.O, Oluwole E.O Dairo J.O (2015). Chemoprotective Potential of Ethanol Extract of Ganoderma Lucidum on Liver and Kidney Parameters in Plasmodium Beghei-Induced Mice. International Journal of Chemistry and Chemical Processes 1(8) (2015)29-36
  • [103] Rao, A.V.; Ray, M.R.; Rao, L.G. Lycopene. Adv. Food Nutr. Res, 51 (2006) 99–164
  • [104] Didunyemi MO, Adetuyi BO, Oyebanjo OO (2019). Morinda lucida attenuates acetaminophen-induced oxidative damage and hepatotoxicity in rats, Journal of Biomedical Sciences 8(2:5) (2019) 1-7
  • [105] Yang, T.; Liu, J.; Yang, M.; Huang, N.; Zhong, Y.; Zeng, T.; Wei, R.; Wu, Z.; Xiao, C.; Cao, X.; et al. Cucurbitacin B exerts anti-cancer activities in human multiple myeloma cells in vitro and in vivo by modulating multiple cellular pathways. Oncotarget, 8 (2017) 5800–5813
  • [106] Yar Saglam, A.S.; Alp, E.; Elmazoglu, Z.; Menevse, S. Treatment with cucurbitacin B alone and in combination with gefitinib induces cell cycle inhibition and apoptosis via EGFR and JAK/STAT pathway in human colorectal cancer cell lines. Hum. Exp. Toxicol, 35 (2016) 526–543
  • [107] Zhang, M.; Bian, Z.G.; Zhang, Y.; Wang, J.H.; Kan, L.; Wang, X.; Niu, H.Y.; He, P. Cucurbitacin B inhibits proliferation and induces apoptosis via STAT3 pathway inhibition in A549 lung cancer cells. Mol. Med. Rep, 10 (2014) 2905–2911
  • [108] Zheng, Q.; Liu, Y.; Liu, W.; Ma, F.; Zhou, Y.; Chen, M.; Chang, J.; Wang, Y.; Yang, G.; He, G. Cucurbitacin B inhibits growth and induces apoptosis through the JAK2/STAT3 and MAPK pathways in SHSY5Y human neuroblastoma cells. Mol. Med. Rep, 10 (2014) 89–94
  • [109] Ma, W.; Xiang, Y.; Yang, R.; Zhang, T.; Xu, J.; Wu, Y.; Liu, X.; Xiang, K.; Zhao, H.; Liu, Y.; et al. Cucurbitacin B induces inhibitory effects via the CIP2A/PP2A/C-KIT signaling axis in t(8;21) acute myeloid leukemia. J. Pharmacol. Sci, 139 (2019) 304–310
  • [110] Zhang, M.; Sun, C.; Shan, X.; Yang, X.; Li-Ling, J.; Deng, Y. Inhibition of pancreatic cancer cell growth by cucurbitacin B through modulation of signal transducer and activator of transcription 3 signaling. Pancreas, 39 (2010) 923–929
  • [111] Gupta, P.; Srivastava, S.K. Inhibition of Integrin-HER2 signaling by Cucurbitacin B leads to in vitro and in vivo breast tumor growth suppression. Oncotarget 5 (2014) 1812–1828
  • [112] Wu, X.; Zhou, Q.H.; Xu, K. Are isothiocyanates potential anti-cancer drugs? Acta Pharmacol. Sin, 30 (2009) 501–512
  • [113] Lai, K.C.; Huang, A.C.; Hsu, S.C.; Kuo, C.L.; Yang, J.S.; Wu, S.H.; Chung, J.G. Benzyl isothiocyanate ( BITC ) inhibits migration and invasion of human colon cancer HT29 cells by inhibiting matrix metalloproteinase-2/-9 and urokinase plasminogen (uPA) through PKC and MAPK signaling pathway. J. Agric. Food Chem, 58 (2010) 2935–2942
  • [114] Wang, L.G.; Chiao, J.W. Prostate cancer chemopreventive activity of phenethyl isothiocyanate through epigenetic regulation (review). Int. J. Oncol, 37 (2010) 533–539
  • [115] Prasad, S.; Tyagi, A.K. Historical Spice as a Future Drug: Therapeutic Potential of Piperlongumine. Curr. Pharm. Des, 22 (2016) 4151–4159
  • [116] Anand, P.; Kunnumakkara, AB.; Sundaram, C.; Harikumar, KB.; Tharakan, ST.; Lai, OS.; Sung, B.; Aggarwal, BB. Cancer is a preventable disease that requires major lifestyle changes. Pharmaceutical Research, 25 (9) (2008) 2097–2116
  • [117] Yao, Y.; Sun, Y.; Shi, M.; Xia, D.; Zhao, K.; Zeng, L.; Yao, R.; Zhang, Y.; Li, Z.; Niu, M.; et al. Piperlongumine induces apoptosis and reduces bortezomib resistance by inhibiting STAT3 in multiple myeloma cells. Oncotarget, 7 (2016) 73497–73508
  • [118] N Munir, M Hasnain, H Waqif, BO Adetuyi, C Egbuna, MC Olisah. Gelling Agents, Micro and Nanogels in Food System Applications. Application of Nanotechnology in Food Science, Processing and Packaging, (2022) 153-167
  • [119] Denny, L.; Adewole, I.; Anorlu, R.; Dreyer, G.; Moodley, M.; Smith, T. Human papillomavirus prevalence and type distribution in invasive cervical cancer in sub-Saharan Africa. Int J Cancer, 134(6) (2014) 1389–1398
  • [120] Han, J.G.; Gupta, S.C.; Prasad, S.; Aggarwal, B.B. Piperlongumine chemosensitizes tumor cells through interaction with cysteine 179 of IkappaBalpha kinase, leading to suppression of NF-kappaB-regulated gene products. Mol. Cancer Ther 13 (2014) 2422–2435
  • [121] Randhawa, H.; Kibble, K.; Zeng, H.; Moyer, M.P.; Reindl, K.M. Activation of ERK signaling and induction of colon cancer cell death by piperlongumine. Toxicol In Vitro, 27 (2013) 1626–1633
  • [122] Chen, J.; O’Donoghue, A.; Deng, Y.F.; Zhang, B.; Kent, F.; O’Hare, T. The effect of lycopene on the PI3K/Akt signalling pathway in prostate cancer. Anticancer Agents Med. Chem, 14 (2014) 800–805
  • [123] Li, Q.; Chen, L.; Dong, Z.; Zhao, Y.; Deng, H.; Wu, J.; Wu, X.; Li, W. Piperlongumine analogue L50377 induces pyroptosis via ROS mediated NF-kappaB suppression in non-small-cell lung cancer. Chem. Biol. Interact, 313 (2019) 108820
  • [124] Zhang P, Shi L, Zhang T, Hong L, He W, Cao P, Shen X, Zheng P, Xia Y, Zou P. Piperlongumine potentiates the antitumor efficacy of oxaliplatin through ROS induction in gastric cancer cells. Cell Oncol (Dordr). 2019 Dec; 42(6): 847-860. doi: 10.1007/s13402-019-00471-x
  • [125] Olubanke O. Ogunlana, Babatunde O. Adetuyi, Miracle Rotimi, Iohor Esalomi, Alaba Adeyemi, Julie Akinyemi, Oluseyi Ogunlana, Oluwatosin Adetuyi, Oluseun Adebisi, Edward Okpata, Roua Baty, Gaber Batiha. Hypoglycemic Activities of Ethanol Seed Extract of Hunteria umbellate (Hallier F.) on Streptozotocin-induced Diabetic Rats. Clinical Phytoscience 7 (1) (2021) 1-9
  • [126] Kong, E.H.; Kim, Y.J.; Kim, Y.J.; Cho, H.J.; Yu, S.N.; Kim, K.Y.; Chang, J.H.; Ahn, S.C. Piplartine induces caspase-mediated apoptosis in PC-3 human prostate cancer cells. Oncol. Rep, 20 (2008) 785–792
  • [127] Wang, D. & Dubois, R. N. Eicosanoids and cancer. Nat. Rev. Cancer 10 (2010) 181–193.
  • [128] Adetuyi BO, Dairo JO, Didunyemi MO. Anti-Hyperglycemic Potency of Jatropha Gossypiifolia in Alloxan Induced Diabetes. Biochem Pharmacol (Los Angel) 4(5) (2015) 193
  • [129] Adetuyi, BO; Okeowo, TO; Adetuyi, OA; Adebisi, OA; Ogunlana, O; Oretade, OJ; Marraiki, N; Beshbishy, AM; Welson, NN; Batiha, GE. Ganoderma lucidum from red mushroom attenuates formaldehyde- induced liver damage in experimental male rat model. Biology, 9(10) (2020) 313
  • [130] Grosser, T.; Ricciotti, E. & FitzGerald, G. A. The cardiovascular pharmacology of nonsteroidal anti-inflammatory drugs. Trends Pharmacol. Sci, 38 (2017) 733–748
  • [131] Patrignani, P. & Patrono, C. Aspirin and cancer. J. Am. Coll. Cardiol, 68 (2016) 967–976
  • [132] Sala, A.; Proschak, E.; Steinhilber, D. & Rovati, G. E. Two-pronged approach to anti-inflammatory therapy through the modulation of the arachidonic acid cascade. Biochem. Pharmacol, 158 (2018) 161–173
  • [133] Adetuyi, BO; Omolabi, FK; Olajide, PA; Oloke, JK. Pharmacological, Biochemical and Therapeutic Potential of Milk Thistle (Silymarin): A Review World News of Natural Sciences 37 (2021) 75-91
  • [134] Yarla, N. S. Targeting arachidonic acid pathway by natural products for cancer prevention and therapy. Semin. Cancer Biol. (2016) 40-41, 48–81
  • [135] Grivennikov, S. I.; Greten, F. R. & Karin, M. Immunity, inflammation, and cancer. Cell, 140 (2010) 883–899.
  • [136] Nazir, A; Itrat, N; Shahid, A; Mushtaq, Z; Abdulrahman, SA; Egbuna, C; Adetuyi, BO; Khan, J; Uche, CZ; Toloyai, PY. Orange Peel as a Source of Nutraceuticals. Food and Agricultural Byproducts as Important Source of Valuable Nutraceuticals.1st ed. (2022) Springer, Berlin. xxx, 400 p. Gebunden. ISBN 978-3-030-98759-6
  • [137] Grivennikov, S. IL-6 and Stat3 are required for survival of intestinal epithelial cells and development of colitis-associated cancer. Cancer Cell, 15 (2009) 103–113
  • [138] Wang, X.; Baek, S. J. & Eling, T. COX inhibitors directly alter gene expression: role in cancer prevention? Cancer Metastasis Rev, 30 (2011) 641–657
  • [139] Prieto, P. Interplay between post-translational cyclooxygenase-2 modifications and the metabolic and proteomic profile in a colorectal cancer cohort. World J. Gastroenterol, 25 (2019) 433–446
  • [140] Swami, S. Inhibition of prostaglandin synthesis and actions by genistein in human prostate cancer cells and by soy isoflavones in prostate cancer patients. Int. J. Cancer, 124 (2009) 2050–2059
  • [141] Agarwal, S.; Rao, A.V. Tomato lycopene and its role in human health and chronic diseases. Can. Med. Assoc. J, 163 (2000) 739–744
  • [142] Iwama, T. NSAIDs and colorectal cancer prevention. J. Gastroenterol, 44(19) (2009) 72–76
  • [143] BO Adetuyi, OA Adebisi, EH Awoyelu, OA Adetuyi, OO Ogunlana. Phytochemical and Toxicological effect of Ethanol extract of Heliotropium indicum on Liver of Male Albino Rats. Letters in Applied NanoBioscience 10(2) (2020) 2085-2095
  • [144] Olsen, J. H. Use of NSAIDs, smoking and lung cancer risk. Br. J. Cancer, 98 (2008) 232–237
  • [145] Zhao, Y. S. Association between NSAIDs use and breast cancer risk: a systematic review and meta-analysis. Breast Cancer Res. Treat, 117 (2009) 141–150
  • [146] Piazza, G. A. A novel sulindac derivative that does not inhibit cyclooxygenases but potently inhibits colon tumor cell growth and induces apoptosis with antitumor activity. Cancer Prev. Res. (Philos.), 2 (2009) 572–580

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