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刘书哲, 檀艳丽, 高伟敏, 薛娟, 杨永滨. 金雀异黄素对胶质瘤细胞株细胞生长周期影响[J]. 中国公共卫生, 2011, 27(10): 1277-1279. DOI: 10.11847/zgggws-2011-27-10-25
引用本文: 刘书哲, 檀艳丽, 高伟敏, 薛娟, 杨永滨. 金雀异黄素对胶质瘤细胞株细胞生长周期影响[J]. 中国公共卫生, 2011, 27(10): 1277-1279. DOI: 10.11847/zgggws-2011-27-10-25
LIU Shu-zhe, TAN Yan-li, GAO Wei-min, . Effects of genistein on cell cycle of human glioma cell line U251MG[J]. Chinese Journal of Public Health, 2011, 27(10): 1277-1279. DOI: 10.11847/zgggws-2011-27-10-25
Citation: LIU Shu-zhe, TAN Yan-li, GAO Wei-min, . Effects of genistein on cell cycle of human glioma cell line U251MG[J]. Chinese Journal of Public Health, 2011, 27(10): 1277-1279. DOI: 10.11847/zgggws-2011-27-10-25

金雀异黄素对胶质瘤细胞株细胞生长周期影响

Effects of genistein on cell cycle of human glioma cell line U251MG

  • 摘要: 目的 研究金雀异黄素(genistein)对人胶质瘤U251MG细胞生长和细胞周期的影响。方法 采用噻唑蓝(MTT)比色法观察不同浓度genistein在不同作用时间下对U251MG细胞生长的影响,用流式细胞仪分析细胞周期分布,蛋白免疫印迹(western blotting)技术检测细胞周期素B1(cyclin B1)和细胞周期素依赖性蛋白激酶1(CDK1)蛋白表达。结果 Genistein对胶质瘤细胞生长有明显抑制作用,使细胞生长停滞于G22/M期,并使细胞cyclin B1、CDK1蛋白表达下降(均P<0.01),且呈剂量依赖性。结论 Genistein对U251MG细胞生长有明显抑制作用,诱导G22/M期阻滞可能与下调cyclinB1和CDK1蛋白表达有关。

     

    Abstract: Objective To investigate the effects of genistein on the growth and cell cycle of human glioma cell line U251MG.Methods The growth inhibition of U251MG cells was measured with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenytetrazolium bromide(MTT)assay.Phase distribution of cell cycle was analyzed with flow cytometry.The expression of cyclin B1 and cyclin-dependent protein kinase 1(CDK1)were determined with western blotting.Results Genistein inhibited the grow th of U251MG cells significantly in a dose-and time-dependent manner.When U251MG cells were treated with genistein for 48 hours,the cell cycle was arrested in the G22/M phase and cyclin B1,CDK1 protein expressions were significantly decreased in a dose-dependent manner(P<0.01,P<0.01).Conclusion Genistein can inhibit the grow th of U251MG cells significantly.G22/M arrest of U251MG cells after treated with genistein may be related to the decreased protein expression of cyclin B1 and CDK1.

     

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