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表达血管内皮生长因子-siRNA及双自杀基因yCDglyTK的联合基因载体构建及其应用研究
引用本文:叶玲,张桂英,刘霆,陈选民,易红,肖志强,冷爱民,彭杰.表达血管内皮生长因子-siRNA及双自杀基因yCDglyTK的联合基因载体构建及其应用研究[J].生物化学与生物物理进展,2010,37(5):503-509.
作者姓名:叶玲  张桂英  刘霆  陈选民  易红  肖志强  冷爱民  彭杰
作者单位:中南大学湘雅医院消化内科;中南大学湘雅医院卫生部肿瘤蛋白质组学重点实验室;
基金项目:国家自然科学基金(30800518); 教育部博士点新教师基金(200805331090)资助项目~~
摘    要:构建了新型联合基因载体pcDNA3.1(-)VEGF-siRNA/yCDglyTK,研究其在人胃癌细胞系SGC7901细胞中的表达和杀伤作用.构建靶向血管内皮生长因子(VEGF)的干扰质粒pGenesil-VEGF-siRNA,采用PCR法从中扩增siRNA表达框(含U6启动子),亚克隆至双自杀基因载体pcDNA3.1(-)CV-yCDglyTK,构建联合基因质粒pcDNA3.1(-)VEGF-siRNA/yCDglyTK;通过酶切、测序等鉴定重组质粒;以磷酸钙纳米颗粒为载体,将干扰质粒、双自杀基因质粒及联合基因质粒转染SGC7901细胞,RT-PCR、Western-blot验证目的基因表达;MTT法检测转染细胞对5-氟胞嘧啶(5-FC)的敏感性.结果表明:酶切及测序证实联合基因载体pcDNA3.1(-)VEGF-siRNA/yCDglyTK构建成功;SGC7901细胞转染联合基因质粒后,RT-PCR、Western-blot证实融合自杀基因表达,而VEGF基因表达下调;在前体药物5-FC作用下,转染联合基因组细胞存活率最低,与其他组比较有统计学差异.成功构建联合基因载体pcDNA3.1(-)VEGF-si...

关 键 词:RNA干扰  自杀基因  胃癌  联合基因治疗  
收稿时间:2009/10/13 0:00:00
修稿时间:2010/1/23 0:00:00

Construction of Combination Gene Vector Expressing VEGF-siRNA and Fusion Suicide Gene yCDglyTK and Its Application
YE Ling,ZHANG Gui-Ying,LIU Ting,CHEN Xuan-Min,YI Hong,XIAO Zhi-Qiang,LENG Ai-Min and PENG Jie.Construction of Combination Gene Vector Expressing VEGF-siRNA and Fusion Suicide Gene yCDglyTK and Its Application[J].Progress In Biochemistry and Biophysics,2010,37(5):503-509.
Authors:YE Ling  ZHANG Gui-Ying  LIU Ting  CHEN Xuan-Min  YI Hong  XIAO Zhi-Qiang  LENG Ai-Min and PENG Jie
Institution:YE Ling1),ZHANG Gui-Ying1),LIU Ting1),CHEN Xuan-Min1),YI Hong2),XIAO Zhi-Qiang2),LENG Ai-Min1),PENG Jie1) (1) Department of Gastroenterology,Xiangya Hospital of Central South University,Changsha 410008,China,2) Key Laboratory of Cancer Proteomics of Ministry of Health of China,Xiangya Hospital,Central South University,China)
Abstract:This research aimed to construct a new combination gene vector: pcDNA3.1 (-)VEGF-siRNA/ yCDglyTK, study its expression quality and lethal effet in human gastric cancer cell line SGC7901. First, RNA interference (RNAi) targeting vascular endothelial growth factor (VEGF) was applied to construct interfering plasmid pGenesil-VEGF-siRNA. Then, the siRNA expression cassette (including U6 promotor ) was amplified by PCR and subcloned into pcDNA3.1 (-)CV-yCDglyTK to build a new combination gene plasmid: pcDNA3.1 (...
Keywords:RNA interference  suicide gene  gastric cancer  combination gene therapy  
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