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SWI/SNF 染色质重塑因子亚基下调调节顺铂细胞毒性。

Downregulation of SWI/SNF chromatin remodeling factor subunits modulates cisplatin cytotoxicity.

机构信息

Department of Biochemistry and Cancer Biology, University of Toledo-Health Science Campus, Toledo, OH 43614, USA.

出版信息

Exp Cell Res. 2012 Oct 1;318(16):1973-86. doi: 10.1016/j.yexcr.2012.06.011. Epub 2012 Jun 18.

Abstract

Chromatin remodeling complex SWI/SNF plays important roles in many cellular processes including transcription, proliferation, differentiation and DNA repair. In this report, we investigated the role of SWI/SNF catalytic subunits Brg1 and Brm in the cellular response to cisplatin in lung cancer and head/neck cancer cells. Stable knockdown of Brg1 and Brm enhanced cellular sensitivity to cisplatin. Repair kinetics of cisplatin DNA adducts revealed that downregulation of Brg1 and Brm impeded the repair of both intrastrand adducts and interstrand crosslinks (ICLs). Cisplatin ICL-induced DNA double strand break repair was also decreased in Brg1 and Brm depleted cells. Altered checkpoint activation with enhanced apoptosis as well as impaired chromatin relaxation was observed in Brg1 and Brm deficient cells. Downregulation of Brg1 and Brm did not affect the recruitment of DNA damage recognition factor XPC to cisplatin DNA lesions, but affected ERCC1 recruitment, which is involved in the later stages of DNA repair. Based on these results, we propose that SWI/SNF chromatin remodeling complex modulates cisplatin cytotoxicity by facilitating efficient repair of the cisplatin DNA lesions.

摘要

染色质重塑复合物 SWI/SNF 在包括转录、增殖、分化和 DNA 修复在内的许多细胞过程中发挥重要作用。在本报告中,我们研究了 SWI/SNF 催化亚基 Brg1 和 Brm 在肺癌和头颈部癌细胞对顺铂的细胞反应中的作用。Brg1 和 Brm 的稳定敲低增强了细胞对顺铂的敏感性。顺铂 DNA 加合物的修复动力学表明,下调 Brg1 和 Brm 会阻碍链内加合物和链间交联 (ICLs) 的修复。在 Brg1 和 Brm 耗尽的细胞中,顺铂 ICL 诱导的 DNA 双链断裂修复也减少。在 Brg1 和 Brm 缺陷细胞中观察到细胞检查点激活改变,凋亡增加,染色质松弛受损。下调 Brg1 和 Brm 不影响 DNA 损伤识别因子 XPC 向顺铂 DNA 损伤的募集,但影响 ERCC1 的募集,后者参与 DNA 修复的后期阶段。基于这些结果,我们提出 SWI/SNF 染色质重塑复合物通过促进顺铂 DNA 损伤的有效修复来调节顺铂的细胞毒性。

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