Cytotoxic effects of peanut phenolic compounds possessing histone deacetylase inhibitory activity on human colon cancer cell lines

Cytotoxic effects of peanut phenolic compounds possessing histone deacetylase inhibitory activity on human colon cancer cell lines

Phenolic compounds present in our diet play an important role in colon cancer chemoprevention. Previous results demonstrated that peanut testa extract inhibited both histone deacetylase (HDAC) activity and the growth of colon cancer cells. In this study, four identified phenolic compounds in peanut testae (resveratrol, p-coumaric acid, ferulic acid, and sinapinic acid) were investigated for their HDAC inhibitory and anticancer activities against colon cancer cell lines. In vitro study revealed that resveratrol exhibited the greatest HDAC inhibitory activity. Molecular docking studies demonstrated that all four compounds could bind both HDAC1 and HDAC2. Resveratrol exhibited the most effective antiproliferative activity against both human colon adenocarcinoma (HT29) and human colorectal carcinoma (HCT116) cells. Apoptosis induction by ferulic acid and resveratrol appeared to be associated with p53 activation in HCT116 cells. However, resveratrol, p-coumaric acid, ferulic acid, and sinapinic acid induced apoptosis of HT29 cells in a p53-independent manner. Low-concentration treatments of p-coumaric and ferulic acids resulted in cell cycle arrest of HCT116 cells. In contrast, high-concentration treatments of p-coumaric and ferulic acids showed cell death activation as evidenced by increased sub-G1 fractions. The induction of p21 by p-coumaric acid and resveratrol correlated well with the decreased CDK4 levels and cell cycle arrest. Resveratrol, p-coumaric acid, ferulic acid, and sinapinic acid caused activation of pERK1/2 in HCT116 cells, whereas ferulic and sinapinic acids caused downregulation of pERK1/2 in HT29 cells. These results suggest that these peanut phenolics may be potential antineoplastic agents for colon cancer chemoprevention/chemotherapy.

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  • Agrawal S, Agarwal ML, Chatterjee-Kishore M, Stark GR, Chisolm GM (2002). Stat1-dependent, p53-independent expression of p21waf1 modulates oxysterol-induced apoptosis. Mol Cell Biol 22: 1981-1992.
  • Arai K, Lee SR, van Leyen K, Kurose H, Lo EH (2004). Involvement of ERK MAP kinase in endoplasmic reticulum stress in SHSY5Y human neuroblastoma cells. J Neurochem 89: 232-239.
  • Asgar A, Senawong G, Sripa B, Senawong T (2016). Synergistic anticancer effects of cisplatin and histone deacetylase inhibitors (SAHA and TSA) on cholangiocarcinoma cell lines. Int J Oncol 48: 409-420.
  • Bagriacik EU, Uslu K, Yurtcu E, Stefek M, Karasu C (2007). Stobadine inhibits doxorubicin-induced apoptosis through a caspase-9 dependent pathway in P815 mastocytoma cells. Cell Biol Int 31: 979-984.
  • Banin S, Moyal L, Shieh S, Taya Y, Anderson CW, Chessa L, Ziv Y (1998). Enhanced phosphorylation of p53 by ATM in response to DNA damage. Science 281: 1674-1677.
  • Benitez DA, Pozo-Guisado E, Alvarez-Barrientos A, FernandezSalguero PM, Castellon EA (2007). Mechanisms involved in resveratrol-induced apoptosis and cell cycle arrest in prostate cancer-derived cell lines. J Androl 28: 282-293.
  • Center MM, Jemal A, Smith RA, Ward E (2009). Worldwide variations in colorectal cancer. CA Cancer J Clin 59: 366-378.
  • Chang JC, Lai YH, Djoko B, Wu PL, Liu CD, Liu YW, Chiou RY (2006). Biosynthesis enhancement and antioxidant and antiinflammatory activities of peanut (Arachis hypogaea L.) arachidin-1, arachidin-3, and isopentadienylresveratrol. J Agric Food Chem 54: 10281-10287.
  • Cho JW, Jeong YW, Kim KS, Oh JY, Park JC, Lee JC, Suh MH (2001). p21WAF1 is associated with CDK2 and CDK4 protein during HL-60 cell differentiation by TPA treatment. Cell Prolif 34: 267-274.
  • Dhillon AS, Hagan S, Rath O, Kolch W (2007). MAP kinase signalling pathways in cancer. Oncogene 26: 3279-3290.
  • Drummond DC, Noble CO, Kirpotin DB, Guo Z, Scott GK, Benz CC (2005). Clinical development of histone deacetylase inhibitors as anticancer agents. Ann Rev Pharmacol Toxicol 45: 495-528.
  • Edwards BK, Ward E, Kohler BA, Eheman C, Zauber AG, Anderson RN, Ries LA (2010). Annual report to the nation on the status of cancer, 1975-2006, featuring colorectal cancer trends and impact of interventions (risk factors, screening, and treatment) to reduce future rates. Cancer 116: 544-573.
  • Gartel AL (2005). The conflicting roles of the cdk inhibitor p21(CIP1/ WAF1) in apoptosis. Leuk Res 29: 1237-1238.
  • Hassig CA, Tong JK, Fleischer TC, Owa T, Grable PG, Ayer DE, Schreiber SL (1998). A role for histone deacetylase activity in HDAC1-mediated transcriptional repression. P Natl Acad Sci USA 95: 3519-3524.
  • Jaganathan SK, Supriyanto E, Mandal M (2013). Events associated with apoptotic effect of p-coumaric acid in HCT-15 colon cancer cells. World J Gastroenterol 19: 7726-7734.
  • Jemal A, Center MM, DeSantis C, Ward EM (2010). Global patterns of cancer incidence and mortality rates and trends. Cancer Epidemiol Biomarkers Prev 19: 1893-1907.
  • Joe AK, Liu H, Suzui M, Vural ME, Xiao D, Weinstein IB (2002). Resveratrol induces growth inhibition, S-phase arrest, apoptosis, and changes in biomarker expression in several human cancer cell lines. Clin Cancer Res 8: 893-903.
  • Johnson R, Spiegelman B, Hanahan D, Wisdom R (1996). Cellular transformation and malignancy induced by ras require c-jun. Mol Cell Biol 16: 4504-4511.
  • Khaopha S, Jogloy S, Patanothai A, Senawong T (2015). Histone deacetylase inhibitory activity of peanut testa extracts against human cancer cell lines. J Food Biochem 39: 263-273.
  • Khaopha S, Senawong T, Jogloy S, Patanothai A (2012). Comparison of total phenolic content and composition of individual phenolic acids in testae and testa-removed kernels of 15 Valencia-type peanut (Arachis hypogaea L.) genotypes. Afr J Biotechnol 11: 15923-15930.
  • Kim YJ, Greer CB, Cecchini KR, Harris LN, Tuck DP, Kim TH (2013). HDAC inhibitors induce transcriptional repression of high copy number genes in breast cancer through elongation blockade. Oncogene 32: 2828-2835.
  • Lee B, Moon SK (2005). Resveratrol inhibits TNF-alpha-induced proliferation and matrix metalloproteinase expression in human vascular smooth muscle cells. J Nutr 135: 2767-2773.
  • Li TM, Chen GW, Su CC, Lin JG, Yeh CC, Cheng KC, Chung JG (2005). Ellagic acid induced p53/p21 expression, G1 arrest and apoptosis in human bladder cancer T24 cells. Anticancer Res 25: 971-979.
  • Link A, Balaguer F, Goel A (2010). Cancer chemoprevention by dietary polyphenols: promising role for epigenetics. Biochem Pharmacol 80: 1771-1792.
  • Marks PA, Richon VM, Rifkind RA (2000). Histone deacetylase inhibitors: inducers of differentiation or apoptosis of transformed cells. J Natl Cancer Inst 92: 1210-1216.
  • Mates JM, Segura JA, Alonso FJ, Marquez J(2008). Intracellular redox status and oxidative stress: implications for cell proliferation, apoptosis, and carcinogenesis. Arch Toxicol 82: 273-299.
  • Martindale JL, Holbrook NJ (2002). Cellular response to oxidative stress: signaling for suicide and survival. J Cell Physiol 192: 1-15.
  • Mordret G (1993). MAP kinase kinase: a node connecting multiple pathways. Biol Cell 79: 193-207.
  • Nakajima Y, Nishida H, Matsugo S, Konishi T (2009). Cancer cell cytotoxicity of extracts and small phenolic compounds from Chaga [Inonotus obliquus (persoon) Pilat]. J Med Food 12: 501- 507.
  • Narayanan BA, Geoffroy O, Willingham MC, Re GG, Nixon DW (1999). p53/p21(WAF1/CIP1) expression and its possible role in G1 arrest and apoptosis in ellagic acid treated cancer cells. Cancer Lett 136: 215-221
  • Ong PS, Wang XQ, Lin HS, Chan SY, Ho PC (2012). Synergistic effects of suberoylanilide hydroxamic acid combined with cisplatin causing cell cycle arrest independent apoptosis in platinum-resistant ovarian cancer cells. Int J Oncol 40: 1705- 1713.
  • Park H, Lee J, Lee S (2006). Critical assessment of the automated AutoDock as a new docking tool for virtual screening. Proteins 65: 549-554.
  • Peart MJ, Smyth GK, van Laar RK, Bowtell DD, Richon VM, Marks PA, Johnstone RW (2005). Identification and functional significance of genes regulated by structurally different histone deacetylase inhibitors. P Natl Acad Sci USA 102: 3697-3702.
  • Peng CC, Chyau CC, Wang HE, Chang CH, Chen KC, Chou KY, Peng RY (2013). Cytotoxicity of ferulic acid on T24 cell line differentiated by different microenvironments. Biomed Res Int 2013: 579859.
  • Poolman RA, Brooks G (1998). Expressions and activities of cell cycle regulatory molecules during the transition from myocyte hyperplasia to hypertrophy. J Mol Cell Cardiol 30: 2121-2135.
  • Richon VM, Sandhoff TW, Rifkind RA, Marks PA (2000). Histone deacetylase inhibitor selectively induces p21WAF1 expression and gene-associated histone acetylation. P Natl Acad Sci USA 97: 10014-10019.
  • Roberts CW, Leroux MM, Fleming MD, Orkin SH (2002). Highly penetrant, rapid tumorigenesis through conditional inversion of the tumor suppressor gene Snf5. Cancer Cell 2: 415-425.
  • Roy M, Chakraborty S, Siddiqi M, Bhattacharya RK (2002). Induction of apoptosis in tumor cells by natural phenolic compounds. Asian Pac J Cancer Prev 3: 61-67.
  • Senawong T, Khaopha S, Misuna S, Komaikul J, Senawong G, Wongphakham P, Yunchalard S (2014). Phenolic acid composition and anticancer activity against human cancer cell lines of the commercially available fermentation products of Houttuynia cordata. ScienceAsia 40: 420-427.
  • Senawong T, Misuna S, Khaopha S, Nuchadomrong S, Sawatsitang P, Phaosiri C, Sripa B (2013). Histone deacetylase (HDAC) inhibitory and antiproliferative activities of phenolicrich extracts derived from the rhizome of Hydnophytum formicarum Jack.: sinapinic acid acts as HDAC inhibitor. BMC Compl Altern Med 13: 232.
  • Shen J, Huang C, Jiang L, Gao F, Wang Z, Zhang Y, Bai J, Zhou H, Chen Q (2007). Enhancement of cisplatin induced apoptosis by suberoylanilide hydroxamic acid in human oral squamous cell carcinoma cell lines. Biochem Pharmacol 73: 1901-1909.
  • Sherr CJ (1994). G1 phase progression: cycling on cue. Cell 79: 551- 555.
  • Sherr CJ, McCormick F (2002). The RB and p53 pathways in cancer. Cancer Cell 2: 103-112.
  • Shin GC, Kim C, Lee JM, Cho WS, Lee SG, Jeong M, Lee K (2009). Apigenin-induced apoptosis is mediated by reactive oxygen species and activation of ERK1/2 in rheumatoid fibroblast-like synoviocytes. Chem Biol Interact 182: 29-36.
  • Tan BJ, Chiu GN (2013). Role of oxidative stress, endoplasmic reticulum stress and ERK activation in triptolide-induced apoptosis. Int J Oncol 42: 1605-1612.
  • te Poele RH, Okorokov AL, Jardine L, Cummings J, Joel SP (2002). DNA damage is able to induce senescence in tumor cells in vitro and in vivo. Cancer Res 62: 1876-1883.
  • Udenigwe CC, Ramprasath VR, Aluko RE, Jones PJ (2008). Potential of resveratrol in anticancer and anti-inflammatory therapy. Nutr Rev 66: 445-454.
  • Warrener R, Beamish H, Burgess A, Waterhouse NJ, Giles N, Fairlie D, Gabrielli B (2003). Tumor cell-selective cytotoxicity by targeting cell cycle checkpoints. FASEB J 1: 1550-1552.
  • Yang CS, Landau JM, Huang MT, Newmark HL (2001). Inhibition of carcinogenesis by dietary polyphenolic compounds. Ann Rev Nutr 21: 381-406.
  • Yi WG, Fischer J, Krewer G, Akoh CC (2005). Phenolic compounds from blueberries can inhibit colon cancer cell proliferation and induce apoptosis. J Agric Food Chem 53: 7320-7329.
  • Zhao Y, Lu S, Wu L, Chai G, Wang H, Chen Y, Zhu WG (2006). Acetylation of p53 at lysine 373/382 by the histone deacetylase inhibitor depsipeptide induces expression of p21(Waf1/Cip1). Mol Cell Biol 26: 2782-2790
Turkish Journal of Biology-Cover
  • ISSN: 1300-0152
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
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