[1] Li W, Du B, Wang T, et al. Kaempferol induces apoptosis in human HCT116 colon cancer cells via the AtaxiaTelangiectasia Mutatedp53 pathway with the involvement of p53 Upregulated Modulator of Apoptosis. Chem Biol Interact, 2009, 177(2): 121127.
[2] Zhang Q, Zhao XH, Wang ZJ. Cytotoxicity of flavones and flavonols to a human esophageal squamous cell carcinoma cell line (KYSE510) by induction of G2/M arrest and apoptosis. Toxicol In Vitro, 2009, 23(5): 797807.
[3] Kang GY, Lee ER, Kim JH, et al. Downregulation of PLK1 expression in kaempferolinduced apoptosis of MCF7 cells. Eur J Pharmacol, 2009, 611(13): 1721.
[4] Marfe G, Tafani M, Indelicato M, et al. Kaempferol induces apoptosis in two different cell lines via Akt inactivation, Bax and SIRT3 activation, and mitochondrial dysfunction. J Cell Biochem, 2009, 106(4): 643650.
[5] Huang WW, Tsai SC, Peng SF, et al. Kaempferol induces autophagy through AMPK and AKT signaling molecules and causes G2/M arrest via downregulation of CDK1/cyclin B in SKHEP1 human hepatic cancer cells. Int J Oncol, 2013, 42(6): 20692077.
[6] Luo H, Daddysman MK, Rankin GO, et al. Kaempferol enhances cisplatin′s effect on ovarian cancer cells through promoting apoptosis caused by down regulation of cMyc. Cancer Cell Int, 2010, 10: 16.
[7] Luo H, Rankin GO, Li Z, et al. Kaempferol induces apoptosis in ovarian cancer cells through activating p53 in the intrinsic pathway. Food Chem, 2011, 128(2): 513519.
[8] Ria R, Reale A, De Luisi A, et al. Bone marrow angiogenesis and progression in multiple myeloma. Am J Blood Res, 2011, 1(1): 7689.
[9] Luo H, Rankin GO, Juliano N, et al. Kaempferol inhibits VEGF expression and in vitro angiogenesis through a novel ERKNFkappaBcMycp21 pathway. Food Chem, 2012, 130(2): 321328.
[10] Luo H, Rankin GO, Liu L, et al. Kaempferol inhibits angiogenesis and VEGF expression through both HIF dependent and independent pathways in human ovarian cancer cells. Nutr Cancer, 2009, 61(4): 554563.
[11] HadlerOlsen E, Winberg JO, UhlinHansen L. Matrix metalloproteinases in cancer: their value as diagnostic and prognostic markers and therapeutic targets. Tumour Biol, 2013, 34(4): 20412051.
[12] Phromnoi K, Yodkeeree S, Anuchapreeda S, et al. Inhibition of MMP3 activity and invasion of the MDAMB231 human invasive breast carcinoma cell line by bioflavonoids. Acta Pharmacol Sin, 2009, 30(8): 11691176.
[13] Labbe D, Provencal M, Lamy S, et al. The flavonols quercetin, kaempferol, and myricetin inhibit hepatocyte growth factorinduced medulloblastoma cell migration. J Nutr, 2009, 139(4): 646652.
[14] LópezLázaro M. A new view of carcinogenesis and an alternative approach to cancer therapy. Mol Med, 2010, 16(34): 144153.
[15] Lee S, Kim YJ, Kwon S, et al. Inhibitory effects of flavonoids on TNFalphainduced IL8 gene expression in HEK 293 cells. BMB Rep, 2009, 42(5): 265270.
[16] Seibert H, Maser E, Schweda K, et al. Cytoprotective activity against peroxideinduced oxidative damage and cytotoxicity of flavonoids in C6 rat glioma cells. Food Chem Toxicol, 2011, 49(9): 23982407.
[17] Nirmala P, Ramanathan M. Effect of kaempferol on lipid peroxidation and antioxidant status in 1,2dimethyl hydrazine induced colorectal carcinoma in rats. Eur J Pharmacol, 2011, 654(1): 7579.
[18] Mantovani A, Allavena P, Sica A, et al. Cancerrelated inflammation. Nature, 2008, 454(7203): 436444.
[19] Qazi BS, Tang K, Qazi A. Recent advances in underlying pathologies provide insight into interleukin8 expressionmediated inflammation and angiogenesis. Int J Inflam, 2011, 2011: 908468.
[20] Chen SS, Michael A, ButlerManuel SA. Advances in the treatment of ovarian cancer: a potential role of antiinflammatory phytochemicals. Discov Med, 2012, 13(68): 717.
[21] Mukai R, Satsu H, Shimizu M, et al. Inhibition of Pglycoprotein enhances the suppressive effect of kaempferol on transformation of the aryl hydrocarbon receptor. Biosci Biotechnol Biochem, 2009, 73(7): 16351639.
[22] Wang H, Gao M, Wang J. Kaempferol inhibits cancer cell growth by antagonizing estrogenrelated receptor alpha and gamma activities. Cell Biol Int, 2013, In press.
[23] To KK, Yu L, Liu S, et al. Constitutive AhR activation leads to concomitant ABCG2mediated multidrug resistance in cisplatinresistant esophageal carcinoma cells. Mol Carcinog, 2012, 51(6): 449464.
[24] Nakatsuma A, Fukami T, Suzuki T, et al. Effects of kaempferol on the mechanisms of drug resistance in the human glioblastoma cell line T98G. Pharmazie, 2010, 65(5): 379383.
[25] Ahmed F, Toume K, Ohtsuki T, et al. Cryptolepine, isolated from Sida acuta, sensitizes human gastric adenocarcinoma cells to TRAILinduced apoptosis. Phytother Res, 2011, 25(1): 147150.
[26] Geybels MS, Verhage BA, Arts IC, et al. Dietary flavonoid intake, black tea consumption, and risk of overall and advanced stage prostate cancer. Am J Epidemiol, 2013, 177(12): 13881398.
[27] Bobe G, Albert PS, Sansbury LB, et al. Interleukin6 as a potential indicator for prevention of highrisk adenoma recurrence by dietary flavonols in the polyp prevention trial. Cancer Prev Res (Phila), 2010, 3(6): 764775.
[28] Gates MA, Vitonis AF, Tworoger SS, et al. Flavonoid intake and ovarian cancer risk in a populationbased casecontrol study. Int J Cancer, 2009, 124(8): 19181925.
[29] Simons CC, Hughes LA, Arts IC, et al. Dietary flavonol, flavone and catechin intake and risk of colorectal cancer in the Netherlands Cohort Study. Int J Cancer, 2009, 125(12): 29452952.
[30] Wang L, Lee IM, Zhang SM, et al. Dietary intake of selected flavonols, flavones, and flavonoidrich foods and risk of cancer in middleaged and older women. Am J Clin Nutr, 2009, 89(3): 905912. |