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siRNA-TRF2对人乳腺癌MCF-7细胞增殖的影响[J]. 肿瘤防治研究, 2010, 37(09): 1010-1012. DOI: 10.3971/j.issn.1000-8578.2010.09.009
引用本文: siRNA-TRF2对人乳腺癌MCF-7细胞增殖的影响[J]. 肿瘤防治研究, 2010, 37(09): 1010-1012. DOI: 10.3971/j.issn.1000-8578.2010.09.009
Effects of siRNA-TRF2 on Cell Proliferation of Human Breast Cancer Cell Line MCF-7[J]. Cancer Research on Prevention and Treatment, 2010, 37(09): 1010-1012. DOI: 10.3971/j.issn.1000-8578.2010.09.009
Citation: Effects of siRNA-TRF2 on Cell Proliferation of Human Breast Cancer Cell Line MCF-7[J]. Cancer Research on Prevention and Treatment, 2010, 37(09): 1010-1012. DOI: 10.3971/j.issn.1000-8578.2010.09.009

siRNA-TRF2对人乳腺癌MCF-7细胞增殖的影响

Effects of siRNA-TRF2 on Cell Proliferation of Human Breast Cancer Cell Line MCF-7

  • 摘要: 目的 构建表达端粒重复序列结合因子2基因小干扰RNA的腺病毒表达载体(rAd-shRNA-TRF2),探讨其对人乳腺癌MCF-7细胞增殖的影响。方法 根据预实验筛选出的针对人TRF2 mRNA的特异性siRNA靶序列,构建表达siRNA-TRF2的重组腺病毒载体rAd-shRNA-TRF2,转染人乳腺癌MCF-7细胞后,用MTT比色法检测MCF-7细胞增殖情况,流式细胞仪检测细胞周期分布情况。结果 rAd-shRNA-TRF2转染MCF-7细胞后,MCF-7细胞增殖抑制、细胞周期阻滞于G0/G1期、增殖指数显著下降。结论 通过RNAi抑制TRF2基因表达进而抑制人乳腺癌MCF-7细胞增殖的方法有望成为肿瘤基因治疗的一个新策略。

     

    Abstract: Objective Constructed recombinant adenovirus vector for the express of small interfering RNA targeting telomeric repeatbinding factor2,i.e.rAd-shRNA-TRF2 and to investi gate the effects of rAd-shRNA-TRF2 on cell proliferation of human breast cancer MCF-7 cells.Methods Constructed recombinant adenovirus vector (rAd-shRNA-TRF2) expressing siRNA -TRF2 was constructed by selecting, siRNA witch can specifically and effectively express TRF2 mRNA based on preliminary experiments.After rAd-shRNA-TRF2 was transfected into MCF-7 cells, the cell growth were detected by MTT assay and the cell cycle was observed by means of flow cytometry.Results The cell proliferation of MCF-7 was inhibited.The cell cycle of MCF-7 was at G0/G1 phase and the cell proliferation index(PI) was breakdown significantly after rAd-shRNA-TRF2 was transfected into MCF-7 cells.Conclusion The cell proliferation of MCF-7 is prohibited by inhibiting the TRF2 express,which maybe become a new gene therapy strategy for the tumor treatment.

     

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