刘 唯,吴素慧,史晓峰.RNA干扰沉默MIF基因对宫颈癌SiHa细胞上皮细胞间质变的影响[J].中国肿瘤,2014,23(11):956-960.
RNA干扰沉默MIF基因对宫颈癌SiHa细胞上皮细胞间质变的影响
Effects of Silencing Migration Inhibitory Factor Gene by RNA Interference on Expression of EMT-associated Protein in Human Cervical Carcinoma SiHa Cell
投稿时间:2014-02-24  
DOI:10.11735/j.issn.1004-0242.2014.11.A018
中文关键词:  RNA干扰  上皮细胞间质转化  巨噬细胞移动抑制因子  宫颈癌
英文关键词:RNA interference  epithelial-mesenchymal transition(EMT)  MIF  cervical cancer
基金项目:山西省自然科学基金资助项目(2010011047-3);
作者单位
刘 唯 山西医科大学 
吴素慧 山西医学科学院山西大医院 
史晓峰 山西医科大学 
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中文摘要:
      摘 要:[目的] 探讨巨噬细胞移动抑制因子(MIF)对人宫颈癌SiHa细胞上皮间质转化(EMT)的影响。[方法] 构建并鉴定重组真核表达质粒Genesil-MIF siRNA,转染人宫颈癌细胞SiHa细胞。RT-PCR检测各组细胞中MIF、E-cadherin、Vimentin mRNA表达水平。免疫细胞化学法组检测E-cadherin、Vimentin蛋白表达水平。[结果] 重组质粒Genesil-MIF siRNA成功构建并转染至人宫颈癌SiHa细胞。RT-PCR法证实实验组细胞中E-cadherin mRNA相对高表达(P<0.05),而Vimentin、MIF mRNA相对低表达(P<0.05)。免疫细胞化学法证实实验组细胞中E-cadherin蛋白表达水平升高,Vimentin蛋白表达水平明显降低。[结论] MIF沉默通过促进SiHa细胞中E-cadherin表达,抑制Vimentin表达从而抑制EMT发生。
英文摘要:
      Abstract:[Purpose] To investigate the effect of RNA interference(RNAi) targeting macrophage migration inhibitory factor (MIF) on epithelial-mesenchymal transition(EMT)-associated proteins in human cervical carcinoma SiHa cells.[Methods] Recombinant eukaryotic expression plasmid pGenesil-MIF siRNA was constructed and identified,then transfected into human cervical cancer cells SiHa using a liposome approach. Real-time PCR was used to detect the silencing efficacy of MIF mRNA and the expression of E-cadherin、Vimentin mRNA.The protein expression of E-cadherin and Vimentin was detected by immunocytochemistry.[Results] The recombinant plasmid pEGFP-N1-MIF was constructed successfully and transfected into SiHa cells. In experimental group,the mRNA expression of Vimentin decreased,whereas E-cadherin expression increased. Immunocytochemical staining showed that expression of E-cadherin increased,whereas Vimentin expression decreased.[Conclusion] RNA interference of MIF suppresses epithelial-mesenchymal transition in SiHa cells by decreasing the expression of E-cadherin and increasing the expression of Vimentin.
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