Chinese Clinical Oncology

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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

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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