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Genistein对耐药卵巢癌细胞SKOV-3增殖、凋亡和顺铂敏感性的影响 被引量:3

Effects of Genistein on Proliferation, Apoptosis and Cisplatin Sensitivity of Drug-resistant Human Ovarian Carcinoma Cell SKOV-3
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摘要 目的探讨Genistein对耐药卵巢癌细胞SKOV3增殖、凋亡和顺铂敏感性的影响。方法采用MTT法检测Genistein单用及合用顺铂对细胞增殖的影响,流式细胞仪分析Genistein及Genistein联合顺铂对细胞周期和凋亡的影响。结果Genistein对SKOV3细胞增殖表现出浓度依赖性的抑制作用,并显著提高了其对顺铂的敏感性(P<0.05);0.625~5μg/ml顺铂与2.5~10μg/mlGenistein合用基本表现为协同作用。5、10μg/mlGenistein均可将细胞阻滞于G2/M期并诱导一定程度的凋亡,10μg/mlGenistein还可进一步的干扰S期进程;当顺铂与Genistein合用时,两种药物在干扰SKOV3细胞周期和诱导凋亡方面表现为显著的协同效应。结论Genistein能够抑制耐药卵巢癌细胞SKOV3的增殖,并显著增强该细胞对顺铂的敏感性。 Objective To study the effects of genistein on proliferation, apoptosis and cisplatin sensitivity of drug-resistant ovarian carcinoma cell skov-3. Methods MTT assay was used to analyze growth inhibitory effect of genistein alone and with cisplatin on SKOV-3 cell. Cell cycle arrest and apoptosis was measured by flow cytometry (FCM). Results Genistein exerted inhibitory effect on SKOV-3 cell in a concen-tration-dependent way and significantly enhanced its sensitivity to cisplatin (P 〈0. 05). Generally, cisplatin (0. 625 -5μg/ml) combined with genistein (2. 5-10μg/ml) resulted in synergistic effect. Both 5μg/ml and 10μg/ml genistein arrested SKOV-3 cell in the G2/M phase and induced apoptosis while 10μg/ml genistein caused additional disturbance on S phase process. Significant synergistic effect between genistein and cisplatin was found in inducing cell cycle arrest and apoptosis. Conclusion Genistein can inhibit the growth of drug-resistant human ovarian carcinoma cell SKOV-3 and enhance its sensitivity to cisplatin significantly.
出处 《肿瘤防治研究》 CAS CSCD 北大核心 2006年第3期187-190,共4页 Cancer Research on Prevention and Treatment
基金 国家自然科学基金资助项目(30472226)
关键词 GENISTEIN 顺铂 卵巢癌 耐药 Genistein Cisplatin Ovarian neoplasms Drug resistance
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  • 1Katdare M,Osborne M,Telang NT.Soy isoflavone genistein modulates cell cycle progression and induces apoptosis in HER-2/neu oncogene expressing human breast epithelial cells [J].Int J Oncol,2002,21(4):809-815.
  • 2Li X,Marani M,Mannucci R.et al.Overexpression of BCL-X(L) underlies the molecular basis for resistance to staurosporine-induced apoptosis in PC-3 cells [J].Cancer Res,2001,61(4):1699-1706.
  • 3Ormerod MG,O′Neill C,Robertson D,et al.cis-Diamminedichloroplatinum(Ⅱ)-induced cell death through apoptosis in sensitive and resistant human ovarian carcinoma cell lines [J].Cancer Chemother Pharmacol,1996,37(5):463-471.
  • 4Gercel-Taylor C,Feitelson AK,Taylor DD.Inhibitory effect of genistein and daidzein on ovarian cancer cell growth [J].Anticancer Res,2004,24(2B):795-800.
  • 5Mansour A,McCarthy B,Schwander SK.et al.genistein induces G2 arrest in malignant B cells by decreasing IL-10 secretion [J].Cell Cycle,2004,3(12):1597-1605.
  • 6Takimoto CH,Glover K,Huang X,et al.Phase Ⅰ pharmacokinetic and pharmacodynamic analysis of unconjugated soy isoflavones administered to individuals with cancer [J].Cancer Epidemiol Biomarkers Prev,2003,12(11 Pt 1):1213-1221.

同被引文献27

  • 1单保恩,郭兰涛,董青,马洪.Syk对三氧化二砷诱导脑瘤细胞周期阻滞的影响[J].癌变·畸变·突变,2005,17(6):346-349. 被引量:2
  • 2袁鹏,黄艳红,辛晓燕,宋晖,田爽,王德堂.染料木黄酮与顺铂联用对耐药卵巢癌细胞SKOV-3的影响[J].第四军医大学学报,2006,27(3):199-201. 被引量:1
  • 3Duffy C. Perez K, Partridge A. Implications of phytoestrogen intake for breast cancer[J].CA Cancer J Clin, 2007, 57 (5) : 260-277.
  • 4Banerjee S, Li Y, Wang Z, el al. Multi-targeted therapy of cancer by genistein[J]. Cancer Lett, 2008,69(2) : 226-242.
  • 5Sarkar FH. Adsule S. Padhye S. et al. The role of genistein and synthetic derivatives of isoflavone in cancer prevention and therapy[J].Mini Rev Med Chem, 2006, 6(4):401-407.
  • 6Buchler P, Gukovskaya AS, Mouria M, et al. Prevention of metastatic pancreatic cancer growth in vivo by induction of apoptosis with genistein, a naturally occurring isoflavonoid[J].Pancreas, 2003, 26(3): 264- 273.
  • 7Sasaki H, Moriyama S, Nakashima Y, et al. Expression of the MTA1 mRNA in advanced lung cancer[J]. Lung Cancer, 2002,35(2) 149-154.
  • 8Toh Y, Ohga T, Endo K, et al. Expression of the metastasis- associated MTA1 protein and its relationship to deacetylation of the histone H4 in esophageal squamous cell carcinomas[J].Int J Cancer, 2004,110(3) :362-367.
  • 9Kawasaki G, Yanamoto S, Yoshitomi I, et al. Overexpression of metastasis-associated MTA1 in oral squamous cell carcino mas: correlation with metastasis and invasion[J]. Int J Oral Maxillofac Surg, 2008,37( 11 ) : 1039-11146.
  • 10Hofer MD, Kuefer R, Varambally S, et al. Expression of MTA1 promotes motility and invasiveness of PANC21 pancreatic carcinoma cells[J]. British J Cancer, 2004, 90(2): 455- 462.

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