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作 者:李子博[1] 曾赵军[2] 孙开胜[1] 罗洁[1]
机构地区:[1]长沙医学院医学检验系,湖南长沙410219 [2]中南大学生物科学与技术学院分子生物学研究中心,湖南长沙410078
出 处:《现代生物医学进展》2009年第8期1424-1427,共4页Progress in Modern Biomedicine
基 金:湖南省教育厅基金资助项目(L07C151)
摘 要:目的:构建携带受Tet-On以及VEGF启动子双调控自杀基因HSVtk的重组腺相关病毒载体,研究其在乳腺癌细胞MCF-7中的可调控表达。方法:用PCR方法扩增VEGF启动子,将其插入pAAV/TRE/HSVtk/Tet-On中形成重组载体pAAV/VEGF/TRE/HSVtk/Tet-On质粒。进行病毒包装后得到了rAAV/VEGF/TRE/HSVtk/Tet-On重组腺相关病毒。用重组腺相关病毒感染乳腺癌细胞株MCF-7和正常乳腺HBL-100细胞,用MTT法及RT-PCR检测在Dox诱导下,GCV对rAAV感染的MCF-7细胞和HBL-100细胞的杀伤作用以及HSVtk基因在MCF-7细胞内的表达情况。结果:在rAAV+Dox+GCV组,GCV对rAAV感染的MCF-7细胞的杀伤作用明显高于rAAV+Dox组,rAAV+Dox组以及HBL-100组,并且RT-PCR结果显示经Dox诱导HSVtk表达较明显。结论:成功构建了携带双调控自杀基因的重组腺相关病毒载体,该病毒载体能有效的感染乳腺癌细胞MCF-7,并能联合GCV治疗,抑制肿瘤细胞生长,而且具有靶向性。Objective: To construct the recombinant adeno-associated virus (rAAV) vector containing suicide gene HSVtk controlled by Tet-On gene regulation system and VEGF promoter and to detect the expression of HSVtk in the MCF-7 cells. Methods: VEGF promoter was inserted into the plasmid pAAV/TRE/HSVtk/Tet-On and the recombinant plasmid pAAV/VEGF/TRE/HSVtk/Tet-On was constructed ,and rAAV were then harvested. Purified rAAV was used to infect breast cancer cell strain MCF-7 and normal cell sWain HBL-100, killing effects of GCV on MCF-7 cells infected with rAAV and expression of HSVtk gene in the infected MCF-7 cells were detected using MTT method and RT-PCR assay under doxycycline(Dox) induction. Results: The viruses infected MCF-7 cell showed that the mortality of MCF-7 cells in the rAAV+Dox+GCV group was obviously higher than that in rAAV+GCV group,rAAV+Dox group, as well as HBL-100 group (p〈0.05) and HSVtk gene express obviously in MCF-7 cells under Dox induction,which suggests Dox-induction enhanced tumor killing effects of GCV and expression of HSVtk gene. Conclusions: The constructed rAAV/VEGF/TRE/HSVtk/Tet-On can effective enhance efficacy ofGCV antitumor, inhibit the tumor cell growth, and the gene can specifically express at the turnor cell.
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