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p21蛋白激活激酶4在乳腺癌上皮间质转化中的作用研究 被引量:6

Study of PAK4 induces epithelial-mesenchymal transition of breast cancer cells
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摘要 目的:探讨p21蛋白激活激酶4(PAK4)在乳腺癌细胞上皮间质转化中的作用。方法:在乳腺癌MCF7细胞中超表达PAK4,而在乳腺癌MDA-MB-231细胞中干扰PAK4表达,通过迁移和侵袭实验检测其对乳腺癌细胞迁移侵袭的影响,荧光定量法和免疫印迹分析检测PAK4、E-Cadherin、N-Cadherin、Vimentin mRNA和蛋白质表达量变化,免疫印迹法检测EMT相关转录激活因子Snail、Slug表达量变化。结果:MCF7细胞超表达PAK4后,细胞的迁移侵袭能力显著增加,并且上皮标志分子E-Cadherin蛋白表达下调,而间质标志分子N-Cadherin和Vimentin蛋白则表达上调,EMT相关转录激活因子Slug表达量增加;MDA-MB-231细胞中,抑制内源PAK4表达能显著降低细胞的迁移侵袭能力,上调E-Cadherin蛋白表达,下调NCadherin、Vimentin和Slug蛋白的表达。结论:PAK4通过上调Slug促进乳腺癌发生上皮间质转化,可作为抑制乳腺癌转移的分子靶点。 [Abstartc] Objetcive: To analyze the effect of p21 protein activated kinase 4( PAK4) on epithelial-mesenchymal transition of breast cancer cells.Met hods: The mRNA and protein expression of PAK4,E-Cadherin,N-Cadherin and Vimentin were detected by qRTP-CR and Western blot in breast cancer cells transfected with pcDNA -PAK4 or siRNA PAK4;The biology behaviors of MCF-7 cells and MDA-MB-231 cells transfected with pcDNA-PAK4 or siRNA PAK4 were analysed by cell migration assay ,invasion assay.Results:Overexpressing PAK4 could significant increase in the migration and invasion compared with vector-infected cells, decrease the expression of epithelial marker E-cadherin and upregulate the expression of mesenchymal markers N-cadherin and Vimentin in detached MCF7 cells.Silenced PAK4 gene in detached MDA-MB-231 cells could suppress the migration and invasion ,decrease the levels of the mesenchymal markers and increased the levels of the epithelial markers at both mRNA and protein levels .Conclusion:PAK4 plays a key role in EMT of breast cancer cells ,and its promoting EMT effect associated with upregulating the expression of Slug .
作者 米旭光 李首庆 刘磊 芦小单 方艳秋 谭岩 MI Xu-Guang;LI Shou-Qing;LIU Lei;LU Xiao-Dan;FANG Yan-Qiu;TAN Yan
出处 《中国免疫学杂志》 CAS CSCD 北大核心 2017年第12期1771-1773,1778,共4页 Chinese Journal of Immunology
基金 吉林省科技发展计划项目(20150520047JH) 吉林省科技厅重点实验室建设专项基金(20150622024JC 20160622008JC)
关键词 乳腺癌 p21蛋白激活激酶4 上皮间质转化 Breast cancer p21 protein activated kinase 4 Epithelial-mesenchymal transition
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