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携带Kallistatin的溶瘤腺病毒载体构建及其对肝癌细胞的体外杀伤效应
引用本文:夏玉龙,马步云,肖睿娟,雷文,杨远勤,王毅刚. 携带Kallistatin的溶瘤腺病毒载体构建及其对肝癌细胞的体外杀伤效应[J]. 浙江丝绸工学院学报, 2012, 0(4): 594-598
作者姓名:夏玉龙  马步云  肖睿娟  雷文  杨远勤  王毅刚
作者单位:浙江理工大学生命科学学院新元医学与生物技术研究所,杭州310018
基金项目:国家自然科学基金项目(30800093);浙江省大学生科技创新计划课题(2010R406036);浙江理工大学科研启动基金项目(1016845-Y,1016834-Y)
摘    要:采用靶向基因-病毒治疗策略,通过同源重组的方式构建了携带Kallistatin(KAL)的重组溶瘤腺病毒ZD55-KAL,并研究其对肝癌细胞的杀伤作用。通过PCR方法鉴定病毒构建正确;MTT法检测病毒对肝癌细胞的杀伤能力和对正常细胞的安全性;结晶紫染色观察细胞凋亡现象。结果显示:经目的病毒ZD55-KAL感染后肝癌细胞出现明显的病变和生长抑制,而正常细胞未出现病变现象,表明目的病毒具有较高的安全性和对肿瘤细胞的特异性杀伤能力。此外ZD55-KAL感染肝癌细胞后引起凋亡,所携带的治疗基因KAL能通过促进肿瘤的凋亡达到抑制肿瘤细胞生长的效果。

关 键 词:ZD55-KAL  MTT  结晶紫染色  靶向基因-病毒治疗

Construction of Oncolytic Adenovirus Vector Carrying Kallistatin and Its Killing-Effect to Liver Cancer Cells in Vitro
XIA Yu-long,MA Bu yun,XIAO Rui-juan,LEI Wen,YANG Yuan-qin,WANG Yi-gang. Construction of Oncolytic Adenovirus Vector Carrying Kallistatin and Its Killing-Effect to Liver Cancer Cells in Vitro[J]. , 2012, 0(4): 594-598
Authors:XIA Yu-long  MA Bu yun  XIAO Rui-juan  LEI Wen  YANG Yuan-qin  WANG Yi-gang
Affiliation:(Xinyuan Institute of Medicine and Biochnology, School of Life Sciences, Zhejiang Sci-Tech University, Hangzhou 310018, China)
Abstract:Here the authors use targeting gene-virotherapy strategy to construct recombinant oncolytic adenovirus ZD55-KAL harboring Kallistatin(KAL) gene by homologous recombination method, and inves- tigate its antitumor effect to liver cancer ceils. Subsequently, PCR for identification of recombinant virus, MTT assay and crystal violet staining for detection of tumor killing-effect and safe to normal cells is per- formed. The results show that the hepatoma cells have apparent lesions and growth inhibition effect after infection by ZD55 KAL, while no impact on the normal cells showing its high security. In addition, infection by the therapeutic viruses causes apoptosis of hepatoma cells by carrying the KAL gene, indicating the perfect security ability and the effect of inhibition of tumor cell growth.
Keywords:ZD55-KAL  MTT  crystal violet staining  targeted gene-virus therapy
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