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CEA特异性RNAi增强基因工程腺病毒H101治疗人食管癌裸鼠皮下移植瘤
引用本文:郑红,赵国强,杨洪艳,赵继敏,王尧河,董子明.CEA特异性RNAi增强基因工程腺病毒H101治疗人食管癌裸鼠皮下移植瘤[J].基础医学与临床,2009,29(8):785-788.
作者姓名:郑红  赵国强  杨洪艳  赵继敏  王尧河  董子明
作者单位:1. 郑州大学基础医学院病理及病理生理学教研室,河南,郑州,450052
2. 郑州大学基础医学院微生物免疫学教研室,河南,郑州,450052
3. 郑州大学基础医学院病理学教研室,河南,郑州,450052
基金项目:教育部科技创新工程重点项目
摘    要:目的 研究癌胚抗原(CEA)特异性基因沉默对基因工程腺病毒H101杀伤食管癌EC9706细胞作用的影响,以探讨影响H101敏感性的内在因素。方法 利用RNA干扰(RNAi) 技术,构建针对人食管癌EC9706细胞的CEA siRNA载体,通过基因转染, 在EC9706细胞中建立稳定的CEA基因沉默体系,并以空载体转染和未进行转染的EC9706细胞作对照,建立人食管癌细胞裸鼠皮下移植瘤模型, H101瘤内注射。用RT-PCR和免疫组化法检测CEA在移植瘤中的表达,测量肿瘤体积。结果 降低CEA在mRNA和蛋白质水平的表达,对人食管癌EC9706细胞裸鼠皮下移植瘤成瘤时间和大小无明显影响,H101瘤内注射后,干扰组肿瘤体积显著低于空载体组和对照组(P<0.05)。结论 抑制食管癌EC9706细胞中CEA的表达, 能增强H101的敏感性。

关 键 词:癌胚抗原  基因工程腺病毒  EC9706  裸鼠
收稿时间:2008-9-23
修稿时间:2008-11-5

Enhancement of CEA specific RNAi on gene engineering adenovirus H101 for treatment of tumor tissue of nude mice transplanted with human esophageal cancer cells
ZHENG Hong,ZHAO Guoq-iang,YANG Hong-yan,ZHAO Ji-min,WANG Yao-he,DONG Zi-ming.Enhancement of CEA specific RNAi on gene engineering adenovirus H101 for treatment of tumor tissue of nude mice transplanted with human esophageal cancer cells[J].Basic Medical Sciences and Clinics,2009,29(8):785-788.
Authors:ZHENG Hong  ZHAO Guoq-iang  YANG Hong-yan  ZHAO Ji-min  WANG Yao-he  DONG Zi-ming
Institution:ZHENG Hong1,ZHAO Guo-qiang2,YANG Hong-yan1,ZHAO Ji-min1,WANG Yao-he3,DONG Zi-ming1(1.Department of Pathologic Physiology,2.Department of Microbiology and Immunology,3.Department of Pathology,School of Basic Medical Sciences,Zhengzhou University,Zhengzhou 450052,China)
Abstract:Objective To study the effect of gene engineering adenovirus H101 for treating esophagus carcinoma EC9706 induced by CEA gene specific silencing and to explore internal influential factor of H101 sensitivity. Methods To construct the siRNA expression vector of CEA and to inhibit the expression of CEA through RNA interference and gene transfection in EC9706 cell,stable CEA gene silencing system was set up,compared with empty vector group and non-transfected EC9706 cell,the model of athymic mouse subcutaneous...
Keywords:EC9706
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