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作 者:陈衍[1] 刘文超[1] 秦鸿雁[2] 张瑞[3] 韩骅[2]
机构地区:[1]第四军医大学西京医院肿瘤科,陕西西安710032 [2]第四军医大学医学遗传和发育教研室,陕西西安710032 [3]第四军医大学生物化学和分子生物学教研室,陕西西安710032
出 处:《现代肿瘤医学》2007年第12期1701-1704,共4页Journal of Modern Oncology
基 金:国家自然科学基金资助项目(编号:30572100);陕西省自然科学基金资助项目(编号:2004C222)
摘 要:目的:构建脂肪酸合成酶(FAS)启动子驱动下的单纯疱疹病毒胸苷激酶(HSV-TK)重组腺病毒,研究其对乳腺癌细胞SKBR3的靶向杀伤作用。方法:以AdEasyTM腺病毒系统为载体,构建FAS启动子驱动下的HSV-TK重组腺病毒载体Ad-FAS-TK,将线性化的Ad-FAS-TK在AD-293细胞中包装,经过大量扩增和纯化,得到重组腺病毒。MTT法检测重组腺病毒Ad-FAS-TK与前体药物更昔洛韦(GCV)对SKBR3细胞的靶向杀伤作用。TUNEL法检测细胞凋亡。结果:成功构建FAS启动子驱动下的HSV-TK重组腺病毒载体Ad-FAS-TK,经包装、扩增和纯化得到约1010pfu/ml的重组腺病毒。MTT法和TUNEL检测结果显示,FAS启动子驱动下的HSV-TK重组腺病毒与GCV能够诱导SKBR3细胞凋亡,产生靶向细胞毒作用。结论:FAS启动子驱动下的HSV-TK重组腺病毒联合GCV对SKBR3细胞具有靶向杀伤作用,FAS启动子可以作为肿瘤靶向基因治疗的工具。Objective:To construct the recombinant adenovirus carrying herpes simplex virus thymidine kinase (HSV -TK) driven by human fatty acid synthase (FAS) promoter and analyze its selective cytotoxic effect in vitro on human breast cancer cell line SKBR3 combined with ganciclovir (GCV). Methods: To construct the recombinant adenovirus carrying HSV -TK driven by human FAS promoter (Ad -FAS -TK) based on AdEasyTM adenoviral system and analyze the selective cytotoxic effect of the recombinant adenovirus on SKBR3 breast cancer cells combined with prodrug GCV by MTT and TUNEL assays. Results : We successfully constructed the adenoviral vector Ad - FAS -TK. After packing, amplification and purification, we harvested 10^10 pfu/ml recombinant adenovirus. The recombinant adenovirus combined with GCV treatment could evidently inhibit the proliferation of SKBR3 breast cancer cells and induce cell apoptosis, but showed low activity in normal fibroblast cells. Conclusion: Adenoviral - mediated suicide gene therapy controlled by FAS promoter could induce specific cytotoxic effect on SKBR3 breast cancer cells, suggesting FAS promoter can serve as a useful tool for transcriptional targeting of breast cancer gene therapy.
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