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NAIF1对肝癌细胞 HepG2 增殖与迁移能力的影响
引用本文:谷愉愉 赵玫 杨梅 王佳,彭华 黄声凯 李佳,桑建利 袁兴华,黄常志.NAIF1对肝癌细胞 HepG2 增殖与迁移能力的影响[J].现代生物医学进展,2015,15(6):1001-1004.
作者姓名:谷愉愉 赵玫 杨梅 王佳  彭华 黄声凯 李佳  桑建利 袁兴华  黄常志
作者单位:北京协和医学院 中国医学科学院肿瘤医院肿瘤研究所 病因及癌变研究室 癌发生及预防分子机理北京市重点实验室 分子肿瘤学国家重点实验室;北京协和医学院 中国医学科学院肿瘤医院肿瘤研究所检验科;北京师范大学生命科学学院;北京协和医学院 中国医学科学院肿瘤医院肿瘤研究所腹部外科
基金项目:国家自然科学基金项目(81472208);北京师范大学细胞增殖及调控生物学教育部重点实验室开放课题资助(201301)
摘    要:目的:在肝癌细胞Hep G2中过表达外源NAIF1(核凋亡诱导因子1),探讨NAIF1的亚细胞定位以及对Hep G2增殖和迁移能力的影响。方法:以真核表达质粒p EGFP-N1为对照组,p EGFP-N1-NAIF1为实验组,瞬时转染肝癌细胞Hep G2,利用免疫印迹方法检测NAIF1蛋白表达效率;以DAPI染核,荧光显微镜下观察绿色荧光蛋白定位,确定NAIF1的亚细胞定位;通过MTT方法绘制细胞增殖曲线;通过transwell小室法检测NAIF1对Hep G2迁移能力的影响。结果:在肝癌细胞Hep G2中,外源表达NAIF1主要定位于细胞核;与对照组Hep G2/p EGFP-N1相比,Hep G2/p EGFP-N1-NAIF1的细胞增殖、迁移能力下降(P<0.05)。结论:外源表达NAIF1蛋白定位于Hep G2细胞核,过表达NAIF1抑制Hep G2的细胞增殖与迁移能力,NAIF1可能作为肝癌治疗的潜在靶点。

关 键 词:NAIF1  HepG2  亚细胞定位  细胞增殖  细胞迁移

Effects of NAIF1 on Cell Proliferation and Migration in Hepatoma Cell HepG2
GU Yu-yu;ZHAO Mei;YANG Mei;WANG Jia;PENG Hua;HUANG Sheng-kai;LI Jia;SANG Jian-li;YUAN Xing-hua;HUANG Chang-zhi.Effects of NAIF1 on Cell Proliferation and Migration in Hepatoma Cell HepG2[J].Progress in Modern Biomedicine,2015,15(6):1001-1004.
Authors:GU Yu-yu;ZHAO Mei;YANG Mei;WANG Jia;PENG Hua;HUANG Sheng-kai;LI Jia;SANG Jian-li;YUAN Xing-hua;HUANG Chang-zhi
Institution:GU Yu-yu;ZHAO Mei;YANG Mei;WANG Jia;PENG Hua;HUANG Sheng-kai;LI Jia;SANG Jian-li;YUAN Xing-hua;HUANG Chang-zhi;Department of Etiology and Carcinogenesis, State Key Laboratory of Molecular Oncology, Cancer Institute and Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College;Department of Clinical Laboratory, Cancer Institute and Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College;Institute of Cell Biology, College of Life Sciences, Beijing Normal University;Department of Abdomen Surgery, Cancer Institute and Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College;
Abstract:Objective:Exogeneous (nuclear apoptosis-inducing factor 1 ) was transfected and expressed in hepatoma cell HepG2, and the localization of as well as the effects of on cell proliferation and cell migration was investigated.Methods:HepG2 cell was transiently transfected with eukaryotic expression plasmid pEGFP-N1 as control group or pEGFP-N1- as test group. Western blot was performed to examine the protein expression levels. Nucleus was stained by DAPI, and the localization of was analyzed by monitoring the GFP using a fluorescence microscope. The ability of cell proliferation was determined by MTT assay. Transwell assay was performed to examine the ability of cell migration.Results:In hepatocma cell HepG2, exogeneous expressed was mainly localized in nucleus. Compared with HepG2/pEGFP-N1 , HepG2/pEGFP-N1- showed decreased ability of cell proliferation and migration (P<0.05).Conclusion:Exogeneous expressed localizes in the nucleus of HepG2. Overexpressed inhibits the cell proliferation and migration of HepG2. may act as a potential target of hepatocarcinoma therapy.
Keywords:HepG2  Subcellular distribution  Cell proliferation  Cell migration
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