临床肿瘤学杂志

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辛伐他汀对人乳腺癌细胞MCF-7的生长抑制作用及机制研究

沈园园1,杜瀛瀛1,袁媛2,潘跃银1   

  1. 1 230022 合肥 安徽医科大学第一附属医院肿瘤科 2 230061安徽省合肥市滨湖医院中心实验室
  • 收稿日期:2014-12-09 修回日期:2015-02-19 出版日期:2015-04-30 发布日期:2015-04-30
  • 通讯作者: 潘跃银

Effect of simvastatin on the proliferation of human breast cancer cell MCF-7 and related mechanisms

SHEN Yuanyuan, DU Yingying, YUAN Yuan, PAN Yueyin.

  

  1. Department of Oncology, the First Affiliated Hospital of Anhui Medical University, Hefei 230022, China
  • Received:2014-12-09 Revised:2015-02-19 Online:2015-04-30 Published:2015-04-30
  • Contact: PAN Yueyin

摘要: 目的 探讨辛伐他汀(SVA)体外对乳腺癌细胞MCF-7的生长抑制作用及其可能的机制。 方法 选用人乳腺癌MCF-7细胞进行体外培养,采用四甲基偶氮唑盐法检测不同浓度SVA(0、3.25、6.25、12.5、25、50和100 μmol/L)处理MCF-7细胞24、48、72 h后的增殖抑制作用,荧光染色法观察SVA(0、2和4 μmol/L)处理MCF-7细胞48 h后的凋亡形态学变化,流式细胞仪测定SVA(0和4 μmol/L)处理MCF-7细胞48 h后的细胞周期变化,免疫印迹法分析SVA(0、2、4和8 μmol/L)处理MCF-7细胞72 h后细胞内Bcl-2和Bax蛋白水平的表达。结果 不同浓度SVA处理不同时间后,MCF-7细胞的增殖明显受到抑制,且增殖抑制作用呈时间和浓度依赖性;荧光显微镜观察发现SVA能够诱导MCF-7细胞出现核固缩、染色质凝集等凋亡形态学改变。流式细胞仪检测细胞周期显示,SVA阻滞MCF-7细胞于G0/G1期。免疫印迹 结果 显示,SVA处理组的Bcl-2蛋白表达水平低于对照组,Bax蛋白表达水平明显高于对照组,且随SVA浓度的增高,Bcl-2蛋白水平逐渐降低,Bax蛋白水平逐渐升高。结论 SVA对人乳腺癌MCF-7细胞具有增殖抑制作用,且呈浓度和时间依赖性,其抗肿瘤机制可能与诱导细胞周期阻滞、下调Bcl-2蛋白及上调Bax蛋白表达有关。

Abstract: Objective To observe the effect of simvastatin(SVA) on the proliferation of MCF-7 cells and elucidate its possible molecular mechanisms. Methods MCF-7 cells were cultured in vitro. The inhibitory effects of different concenrations of SVA(0, 3.25, 6.25, 12.5, 25, 50, 100 μmol/L) on MCF-7 cells were measured by a tetrazolium-based colorimetric assay at 24, 48 and 72 h after treatment. The morphological changes of apoptosis induced by SVA(0, 2, 4, 8 μmol/L) were observed by fluorescence staning under the fluorescence microscope. Cell cycles after treatment with SVA(0, 4 μmol/L) were detected by flow cytometry. In addition, expression of intracellular Bcl-2 and Bax proteins were analyzed at 72 h after treatment with SVA(0, 2, 4, 8 μmol/L) by Western blotting. Results SVA inhibited proliferation of MCF-7 cells significantly in a dose- and time-dependent manner. Flow cytometry showed that the cell cycle was arrested at the G0/G1 phase after the treatment with SVA. Typical apoptotic morphologic changes were observed by fluorescence microscope,such as nuclear condensation and chromatin condensation. Analysis on expressions of intracellular Bcl-2 and Bax protein by Western blotting showed that, with the drug concentration increasing, the expressions of anti-apoptotic protein Bcl-2 were gradually suppressed but the expressions of apoptotic protein Bax were gradually increased. Conclusion SVA has the capabilities of inhibiting proliferation of MCF-7 cells in a dose- and time-dependent manner. Its cytotoxic effects seem to be of inducing cell cycle arrest and down-regulation of Bcl-2 and up-regulation of Bax.

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