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EGFRvⅢ的siRNA对胶质瘤细胞凋亡和增殖的影响[J]. 肿瘤防治研究, 2011, 38(09): 975-978. DOI: 10.3971/j.issn.1000-8578.2011.09.001
引用本文: EGFRvⅢ的siRNA对胶质瘤细胞凋亡和增殖的影响[J]. 肿瘤防治研究, 2011, 38(09): 975-978. DOI: 10.3971/j.issn.1000-8578.2011.09.001
Effect of EGFRvⅢ siRNA on Apoptosis and Growth of Glioma Cell Line[J]. Cancer Research on Prevention and Treatment, 2011, 38(09): 975-978. DOI: 10.3971/j.issn.1000-8578.2011.09.001
Citation: Effect of EGFRvⅢ siRNA on Apoptosis and Growth of Glioma Cell Line[J]. Cancer Research on Prevention and Treatment, 2011, 38(09): 975-978. DOI: 10.3971/j.issn.1000-8578.2011.09.001

EGFRvⅢ的siRNA对胶质瘤细胞凋亡和增殖的影响

Effect of EGFRvⅢ siRNA on Apoptosis and Growth of Glioma Cell Line

  • 摘要: 目的研究EGFRvⅢ的siRNA对U87-EGFRvⅢ胶质瘤细胞中EGFRvⅢ的表达及其对细胞增殖和凋亡的影响。 方法化学方法合成特异针对EGFRvⅢ的siRNA,转染U87-EGFRvⅢ细胞后,利用半定量RT-PCR法检测细胞中EGFRvⅢ的mRNA表达,采用蛋白印迹法和免疫荧光法检测细胞中EGFRvⅢ的蛋白表达水平,MTT法检测siRNA对胶质瘤细胞增殖的作用,Annexin V-FITC/PI法检测siRNA对细胞凋亡的作用。结果RT-PCR、蛋白印迹法和免疫荧光法均可显示EGFRvⅢ siRNA可使EGFRvⅢ的基因和蛋白表达显著下降,48 h内可使蛋白含量下降(75.7±3.1)%;MTT法和Annexin V-FITC/PI检测结果显示siRNA可抑制U87-EGFRvⅢ细胞的增殖并促进其凋亡。 结论EGFRvⅢ siRNA可特异地抑制EGFRvⅢ在胶质瘤细胞中的表达,抑制细胞增殖、促进细胞凋亡。

     

    Abstract: ObjectiveTo study the effect of the EGFRvⅢ siRNA on the expression of EGFRvⅢ and the apoptosis and cell growth in the U87-EGFRvⅢ cell line. Methods The EGFRvⅢ siRNA was synthesized by the chemical method.The gene expression of EGFRvⅢ was detected by RT-PCR and the protein expression was detected by Western blot and immunofluorescence.MTT and Annexin V-FITC/PI assays were used to detect the inhibitory effect on cell proliferation and the apoptosis effect. Results The results of RT-PCR and Western blot showed that the gene and protein expression of EGFRvⅢ was decreased significantly by EGFRvⅢ siRNA,which could be reduced (75.7±3.1)% after transfected with siRNA for 48 h.The results of the MTT and Annexin V-FITC/PI assays showed that siRNA could suppress the cell growth of glioma cell line and induce apoptosis of the glioma cell. ConclusionEGFRvⅢ siRNA could significantly inhibit EGFRvⅢ gene,protein expression and the proliferation,as well as induced apoptosis of U87-EGFRvⅢ cells.

     

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