基础医学与临床 ›› 2009, Vol. 29 ›› Issue (8): 785-788.

• 研究论文 •    下一篇

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

郑红 赵国强 杨洪艳 赵继敏 王尧河 董子明   

  1. 郑州大学基础医学院 郑州大学基础医学院 郑州大学基础医学院
  • 收稿日期:2008-09-23 修回日期:2008-11-05 出版日期:2009-08-20 发布日期:2009-08-20
  • 通讯作者: 董子明

Enhancement of CEA specific RNAi on gene engineering adenovirus H101 treating tumor tissue of nude mice transplanted with human esophageal cancer cells

Hong ZHENG, Guo-qiang ZHAO, Hong-yan YANG, Ji-min ZHAO, Yao-he WANG, Zi-ming DONG   

  1. School of Basic Medical Science, Zhengzhou University Basic Medical College, Zhengzhou University
  • Received:2008-09-23 Revised:2008-11-05 Online:2009-08-20 Published:2009-08-20
  • Contact: Zi-ming DONG

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

Abstract: Objective To study the effect of gene engineering adenovirus H101 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 inhibit the expression of CEA through RNA interference and gene transfection in EC9706 cell, stable CEA gene silencing system were set up, compared with empty vector group and not transfected EC9706 cell, the model of athymic mouse subcutaneous transplantation tumor of human esophagus carcinoma EC9706 cell was established, injection in tumor was done with H101. The mRNA and protein expressions of CEA were detected by real time PCR and immunohistochemistry, the tumors'size were measured. Results Silencing CEA gene by applying RNAi can inhibit CEA mRNA and protein expression in nude mice model with transplanted human esophageal cancer cells, there was no evident influence on speed and volume of forming tumor. After using H101, the tumor size of interfering group was much less than empty vector group and normal control group, (P<0.05).Conclusion Inhibiting CEA expression in esophagus carcinoma EC9706 cell, the sensitivity of H101 can enhance .

Key words: CEA, gene engineering adenovirus, EC9706, nude mice