首页 | 本学科首页   官方微博 | 高级检索  
     

微小RNA-21对宫颈癌HeLa细胞程序性细胞死亡4蛋白表达及细胞增殖的影响
引用本文:戴桂红,李国利,钱华,袁冬兰,焦霞,梅佳,朱晓蔚,于鸿. 微小RNA-21对宫颈癌HeLa细胞程序性细胞死亡4蛋白表达及细胞增殖的影响[J]. 江苏大学学报(医学版), 2013, 23(4): 288-291
作者姓名:戴桂红  李国利  钱华  袁冬兰  焦霞  梅佳  朱晓蔚  于鸿
作者单位:(1.泰州市人民医院病理科, 江苏 泰州 225300; 2.扬州大学医学院, 江苏 扬州 225000; 3.泰州市人民医院妇产科, 江苏 泰州 225300; 4. 解放军第81医院病理科, 江苏 南京 210001)
基金项目:江苏省"333工程"培养资金资助项目(项目编号:200924)南通大学自然科学基金资助项目(项目编号:10Z088)
摘    要:摘要目的: 探讨微小RNA-21(miR-21)对宫颈癌HeLa细胞中程序性细胞死亡4(programmed cell death, PDCD4)基因表达及细胞增殖的影响,为应用miR-21对宫颈癌进行基因治疗提供一定的依据。方法: 用脂质体转染的方法,将pre-miR-21、pre-miR-21阴性对照、anti-miR-21、anti-miR-21阴性对照瞬时转染HeLa细胞。实时荧光定量PCR(qRT-PCR)法检测miR-21相对表达量;MTT法检测宫颈癌HeLa细胞增殖的变化;蛋白质印迹法检测PDCD4蛋白表达情况;荧光素酶报告基因法验证miR-21的靶位点。 结果: pre-miR-21上调miR-21的表达,抑制PDCD4蛋白表达,促进HeLa细胞增殖;而anti-miR-21下调miR-21的表达,增加PDCD4蛋白的表达,抑制HeLa细胞增殖。pMIR-Luc-PDCD4-3′UTR与pre-miR-21共转染后,荧光素酶活性下降,而与anti-miR-21共转染后,荧光素酶活性升高。 结论: PDCD4基因是miR-21的靶基因;miR-21通过调节PDCD4基因的表达调控细胞增殖。

关 键 词:宫颈癌  HeLa细胞  微小RNA-21  程序性细胞死亡4  
收稿时间:2013-02-26

Effect of microRNA-21 transfection on PDCD4 expression and cell proliferation in cervical cancer cells
DAI Gui-hong,LI Guo-li,QIAN Hua,YUAN Dong-lan,JIAO Xia,MEI Jia,ZHU Xiao-wei,YU Hong. Effect of microRNA-21 transfection on PDCD4 expression and cell proliferation in cervical cancer cells[J]. Journal of Jiangsu University Medicine Edition, 2013, 23(4): 288-291
Authors:DAI Gui-hong  LI Guo-li  QIAN Hua  YUAN Dong-lan  JIAO Xia  MEI Jia  ZHU Xiao-wei  YU Hong
Affiliation:(1.Department of Pathology, Taizhou People′s Hospital, Taizhou Jiangsu 225000; 2. School of Medical College, Yangzhou University, Yangzhou Jiangsu 225000; 3. Department of Gynaecology, Taizhou People′s Hospital, Taizhou Jiangsu 225300; 4. Department of Pathology, PLA No.81 Hospital, Nanjing Jiangsu 210001, China)
Abstract:Objective: To investigate the effect of miR-21 transfection on the expression of programmed cell death 4(PDCD4) and cell proliferation in cervical cancer cell line HeLa cells,and to provide experimental foundation for miR-21 gene therapy of cervical cancer.Methods: Lipid-mediated transfection was used to transfect pre-miR-21,pre-miR-21 negative control and anti-miR-21,anti-miR-21 negative control into HeLa cervical cancer cells.The miR-21 expression was measured by quantitative real-time PCR(qRTPCR).The cellular growth activity was determined by MTT assay.The protein expression of PDCD4 was measured by western blotting.Detection of the target sites of miR-21 was analyzed by luciferase report gene assays.Results: In pre-miR-21 transfected cells,the cellular growth activity increased,and the expression of PDCD4 protein decreased.Conversely,in anti-miR-21 transfected cells,the cellular growth activity decreased,and the expression of PDCD4 protein increased.pMIR-Luc-PDCD4-3' UTR co-transfected with pre-miR-21,luciferase activity decreased;while it co-transfected with anti-miR-21,luciferase activity increased.Conclusion: PDCD4 gene was the target gene of miR-21,which suggested the potential possibility of miR-21 as a target gene for cervical cancer therapy.
Keywords:cervical cancer  HeLa cell  microRNA-21  programmed cell death 4
本文献已被 维普 万方数据 等数据库收录!
点击此处可从《江苏大学学报(医学版)》浏览原始摘要信息
点击此处可从《江苏大学学报(医学版)》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号