Yang Jin, Chen Wentao, Fan Yanfeng, Zhang Huitao, Wang Wubin, Zhang Hongjie
Department of Occupational Health, School of Public Health, Shanxi Medical University, 030001, Taiyuan, People's Republic of China.
J Biochem Mol Toxicol. 2016 Oct;30(10):481-488. doi: 10.1002/jbt.21811. Epub 2016 Apr 20.
Previous studies in our laboratory demonstrated that Ring2 may affect DNA damage and repair through pathways other than through regulating the expression of the nucleotide excision repair protein. In a series of experiments using wild-type cell (16HBE and WI38) and small interfering RNA (siRNA) Ring2 cells exposed to benzo[a]pyrene (BaP), we evaluated the cell cycle and DNA damage. The benzo(a)pyrene-7,8-dihydrodiol-9,10-epoxide (BPDE-DNA) adduct assay demonstrated that in vitro exposure to BaP increased DNA damage in a time- and dose-dependent manner in wild-type and siRNA Ring2 cells. Analysis of covariance showed that a decrease of Ring2 caused DNA hypersensitivity to BaP. Flow cytometry results and proliferating cell nuclear antigen levels indicated that inhibition of Ring2 attenuated the effect of BaP on S-phase arrest. Taken together, these data implied that the lower proportion of cells in the S phase induced by inhibition of Ring2 may play an important role in DNA hypersensitivity to BaP.
我们实验室之前的研究表明,Ring2可能通过调节核苷酸切除修复蛋白表达以外的途径影响DNA损伤和修复。在一系列使用野生型细胞(16HBE和WI38)和暴露于苯并[a]芘(BaP)的小干扰RNA(siRNA)Ring2细胞的实验中,我们评估了细胞周期和DNA损伤。苯并(a)芘-7,8-二氢二醇-9,10-环氧化物(BPDE-DNA)加合物检测表明,体外暴露于BaP会使野生型和siRNA Ring2细胞中的DNA损伤呈时间和剂量依赖性增加。协方差分析表明,Ring2的减少导致DNA对BaP超敏。流式细胞术结果和增殖细胞核抗原水平表明,抑制Ring2可减弱BaP对S期阻滞的作用。综上所述,这些数据表明,抑制Ring2诱导的S期细胞比例降低可能在DNA对BaP的超敏反应中起重要作用。