检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:苏国强[1] 黄宗海[1] 苏刚[2] 俞金龙[1] 厉周[1] 范应方[1] 周广军[1] 林荣凯[1] 陈建雄[1]
机构地区:[1]南方医科大学珠江医院普外科,广州510282 [2]华中科技大学同济医学院附属协和医院心血管外科
出 处:《中华实验外科杂志》2005年第6期692-694,i002,共4页Chinese Journal of Experimental Surgery
基 金:国家863计划资助项目(2001AA217171);广东省自然科学基金项目(013072)
摘 要:目的腺病毒介导KDR启动子驱动的CDglyTK融合基因(AdKDRCDglyTK)体系对实体肿瘤细胞及血管内皮细胞靶向杀伤作用。方法分别将KDR和CMV启动子融合基因腺病毒体外感染表达KDR的ECV304、MCF7、MGC803及SW620细胞株和不表达KDR的LS174T细胞株,并给予不同浓度的前药5FC和/或GCV,观察其对各细胞株的杀伤效应及其旁观者效应。结果两种腺病毒对各细胞的感染率随腺病毒滴度的递增而增加,当MOI为200时,各细胞株均达约100%感染;感染AdCMVCDglyTK的各组细胞和感染AdKDRCDglyTK的ECV304、MCF7、MGC803及SW620对前药具有较高的敏感性,且其敏感性差异无统计学意义(P均>0.05);与其他细胞相比,感染AdKDRCDglyTK的LS174T细胞对前药不敏感(P<0.01);且观察到该体系明显的旁观者效应。结论KDR基因启动子调控的CDglyTK融合基因体系可选择性杀伤实体肿瘤细胞及血管内皮细胞。Objective To evaluate the selectively killing effect of adenovirus (Ad) mediated double suicide gene under the regulation of KDR promoter on vein endothelial cells and some sorts of solid tumor cells.Methods KDR producing cells (ECV304,MCF7,MGC803 and SW620) and the KDR nonproducing cells (LS174T) were infected by the two Ads (AdEasy-KDR-CDglyTK and AdEasy-CMV-CDglyTK,),followed by treatment with 5-FC and GCV.Then their killing effects on various kinds of cells were evaluated and their bystander effects were analyzed.Results The infection rate of the two resultant recombinant Ads to all the cells was increased gradually with the addition of multiple of infection (MOI) of Ads.All the cells infected with Ad-CMV-CDglyTK and some cells (ECV304,MCF7,MGC803 and SW620) infected with Ad-KDR-CDglyTK were sensitive highly to the prodrugs,and there were no significant differences among them (P> 0.05).Compared with the others,the LS174T cells infected with Ad-KDR-CDglyTK appeared to be unsensitive to the two prodrugs (P< 0.01).In addition,they all had considerable bystander effect.Conclusion The CD/TK fusion gene driven by KDR promoter has selectively killing effect on the KDR-expressing endothelial cells and solid tumor cells.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.43