Genistein对人卵巢癌细胞系3AO抑制增殖的作用及机制的探讨
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《第四军医大学学报》
料木黄酮;卵巢肿瘤;细胞系;细胞凋亡,,染料木黄酮;卵巢肿瘤;细胞系;细胞凋亡,1材料和方法,2结果,3讨论
Inhibitory effects of genistein on proliferation in human ovarian carcinoma cell line 3AO and related mechanismTIAN Shuang1, XIN XiaoYan1, HUANG YanHong1, GAO Xu2, ZHANG Wei1,YUAN Peng1
1Department of Obstetrics and Gynaecology, Xijing Hospital, Fourth Military Medical University, Xian 710033, China, 2Department of Neurosurgery, Tangdu Hospital, Fourth Military Medical University, Xian 710038,China
【Abstract】 AIM: To investigate the effects of genistein on proliferation inhibition and apoptosis induction in human ovarian carcinoma cell line 3AO and to explore its anticancer mechanism. METHODS: After cultured with different doses of genistein for different time periods, the cells were tested by MTT assay. Study on the ultrastructure of 3AO cells was performed by transmission electron microscope (TEM) after the administration of genistein. Apoptosis was detected by means of terminal deoxynucleotidyl transferase mediated dUTPbiotin nick end labeling (TUNEL) method. Apoptosis rate and cell cycle distribution of 3AO cells were measured by flow cytometry (FCM). The expression of estrogen receptor β protein was measured by immunocytochemical technique. RESULTS: After 3AO cells were treated with different concentrations of genistein, dose and timedependent growth inhibition was demonstrated. Inhibition percentage in cells exposed to 10 mg/L and 20 mg/L genistein for 72 h were, respectively, 54.24% and 65.99%. Also, genistein could block 3AO cells in the G2/M phase of cell cycle, and a typical subdiploid apoptosis peak was demonstrated before G1/G2 phase. Moreover the apoptosis was timedependent. The characteristic morphological changes of apoptosis in genisteintreated 3AO cells were observed by TEM. TUNEL staining revealed apoptosispositive cells. Genistein could upregulate the expression of ERβ. CONCLUSION: Genistein can dose and timedependently inhibit growth and induce apoptosis in ovarian carcinoma cell line 3AO the potential pathway of ERβ. ......
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