基础医学与临床 ›› 2007, Vol. 27 ›› Issue (8): 881-885.

• 研究论文 • 上一篇    下一篇

三羟异黄酮诱导人肝癌细胞凋亡及对相关基因的影响

魏思枕 白文元 王军民 姚冬奇 姚金锋 戴胜兰   

  1. 河北医科大学第二医院消化内科 河北医科大学第二医院消化内科 河北医科大学第二医院消化内科 河北医科大学第二医院消化内科 河北医科大学第二医院消化内科 河北医科大学第二医院消化内科
  • 收稿日期:2006-08-31 修回日期:2006-11-01 出版日期:2007-08-25 发布日期:2007-08-25
  • 通讯作者: 白文元

Effect of GENISTEIN on apoptosis and apoptosis related genes in hepatocarcinoma cells

Si-chen Wei Wen-yuan Bai Jun-min Wang Dong-qi Yao Jin-feng Yao Sheng-lan Dai   

  • Received:2006-08-31 Revised:2006-11-01 Online:2007-08-25 Published:2007-08-25
  • Contact: Wen-yuan Bai

摘要: 目的 探讨三羟异黄酮(genistein)对人肝癌细胞凋亡的诱导作用及其机制。方法 将三羟异黄酮作用于体外培养的人肝癌细胞(SMMC-7721),MTT法检测增殖抑制率,光镜下观察凋亡细胞的形态,凝胶电泳分析DNA改变;通过免疫组化技术检测凋亡基因蛋白P53、SURVIVIN和CASPASE-3的表达。结果 三羟异黄酮呈浓度和时间依赖性抑制人肝癌细胞的增殖,5、10 和20μg/ mL作用48h对肝癌细胞的抑制率分别为9.86%、19.13%和25.64%。形态学显示三羟异黄酮能诱导SMMC-7721细胞凋亡,细胞DNA电泳出现典型梯状条带;且凋亡相关基因蛋白SURVIVIN表达明显减少,而P53和CASPASE-3的表达增加。结论 三羟异黄酮能诱导SMMC-7721细胞凋亡,其凋亡机制之一可能是下调SURVIVIN蛋白表达,增强P53和CASPASE-3的表达。

Abstract: Objective To study the apoptosis of human hepatocarcinoma cells induced by genistein and its mechanism. Methods Human hepatocarcinoma SMMC-7721 cells cultured in vitro were treated with genistein. MTT test was used to examine the proliferation inhibitory rate, The morphology of apoptotic cells was observed by microscopy. DNA fragmentation was examined by gel electrophoresis. The expressions of apoptotic gene of P53、SURVIVIN and CASPASE-3 were examined by immunohistochemstry method. Results Genistein could inhibit the proliferation of human hepatoma cells in dose and time-dependent manner, The inhibitory rates were 9.86%、19.13% and 25.64% differently in 5,10 and 20μg /mL for 48h. It also could induce the apoptosis of SMMC-7721 cells, The DNA of cells presented "ladder" break. The expression of apoptosis related protein SURVIVIN was down regulated, the expressions of P53 and CASPASE-3 were up regulated. Conclusions Genistein can induce the apoptosis of SMMC-7721 cells. One of the molecular mechanisms of genistein might decrease apoptosis related protein expression of SURVIVIN and increase the expressions of P53 and CASPASE-3.