摘要
目的 探讨ErbB-2转录因子1 (TOB1)对人类肺癌A549细胞放射敏感性的影响并探讨其机制.方法 通过脂质体介导的重组质粒转染及G418筛选,建立TOB1高表达的肺癌A549细胞稳定转染株;采用克隆形成实验检测TOB1对A549细胞放射敏感性的影响;采用单细胞凝胶电泳实验检测TOB1对电离辐射引起的DNA损伤修复的影响;同时采用Western blot实验检测TOB1对DNA损伤修复相关蛋白表达的调控作用.结果 通过重组质粒转染及G418筛选,成功建立TOB1的肺癌A549细胞稳定转染株;克隆形成实验证实外源性TOB1高表达显著增加肺癌A549细胞的放射敏感性,采用单击多靶模型拟合细胞存活曲线,细胞的放射增敏比(SER)为1.63;单细胞凝胶电泳实验证实接受6Gy的X线照射后,A549/TOB1细胞的尾矩分别为(25.71±4.32)%,明显高于A549细胞[(14.26±1.21)%,P<0.05].Western blot实验证实与A549母细胞比较,X线照射后A549/TOB1细胞中共济失调毛细血管扩张症突变基因(ATM)、06-甲基鸟嘌呤-DNA甲基转移酶(MGMT)、DNA依赖性蛋白激酶催化亚单位(DNA-PKcs)、Ku70、Ku80、DNA双链断裂修复基因X线修复交叉互补4(XRCC4)蛋白的表达水平明显降低.结论 TOB1高表达增加肺癌A549细胞的放射敏感性,其机制可能与TOB1抑制DNA损伤修复相关蛋白的表达,从而抑制DNA损伤的修复有关.
Objective To evaluate the effect of transducer of ErbB2.1 (TOB1) on radiosensitivity of human lung cancer cell line A549 and investigate the related mechanisms.Methods The lipofectamine mediated TOB1 recombinant plasmid transfection and selective G418 cell culture were performed to obtain lung cancer cell line A549 with over-expressed TOB1.The effects on lung cancer cell radiosensitivity in vitro were evaluated by clonogenic survival analysis,and comet DNA damage assay was used to understand the molecular mechanisms of radiosensitization of TOB1 and investigate its effects on the initial DNA damage response to irradiation.Western blotting analysis was performed to determine the related mechanisms.Results Using Lipofectamine and G418-mediated plasmid stable transfection,multiple clones stably transfected with TOB1 were selected.As compared with parental and mock transfected cells,enhanced radiosensitivity was detected in A549/TOB1 cells and the sensitizing enhancement ratio was 1.63.Comet DNA damage assay revealed that the tail moment of A549/TOB1 cells were (25.71 ± 4.32) %,which was significantly higher than that of A549 cells.Western blotting analysis revealed that TOB1 could down-regulate the expression of ATM,MGMT,DNA-PKcs,Ku70,Ku80 and XRCC4 as compared with parental cells.Conclusion Overexpression of TOB1 enhanced the radiosensitivity of A549 cells in vitro,at least by its potential function as an expression regulator of DNA damage repair related proteins,as well as its regulation on DNA damage repair.
出处
《中华实验外科杂志》
CAS
CSCD
北大核心
2014年第3期584-586,共3页
Chinese Journal of Experimental Surgery
基金
昆山市社会发展计划资助项目(KS1224)