Horton Julie K, Wilson Samuel H
Laboratory of Structural Biology, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, NC 27709, USA.
DNA Repair (Amst). 2007 Apr 1;6(4):530-43. doi: 10.1016/j.dnarep.2006.10.016. Epub 2006 Nov 20.
Single-base lesions in DNA are repaired predominantly by base excision repair (BER). DNA polymerase beta (pol beta) is the polymerase of choice in the preferred single-nucleotide BER pathway. The characteristic phenotype of mouse fibroblasts with a deletion of the pol beta gene is moderate hypersensitivity to monofunctional alkylating agents, e.g., methyl methanesulfonate (MMS). Increased sensitivity to MMS is also seen in the absence of pol beta partner proteins XRCC1 and PARP-1, and under conditions where BER efficiency is reduced by synthetic inhibitors. PARP activity plays a major role in protection against MMS-induced cytotoxicity, and cells treated with a combination of non-toxic concentrations of MMS and a PARP inhibitor undergo cell cycle arrest and die by a Chk1-dependent apoptotic pathway. Since BER-deficient cells and tumors are similarly hypersensitive to the clinically used chemotherapeutic methylating agent temozolomide, modulation of DNA damage-induced cell signaling pathways, as well as BER, are attractive targets for potentiating chemotherapy.
DNA中的单碱基损伤主要通过碱基切除修复(BER)来修复。DNA聚合酶β(polβ)是首选的单核苷酸BER途径中的聚合酶。缺失polβ基因的小鼠成纤维细胞的特征性表型是对单功能烷化剂(如甲磺酸甲酯,MMS)中度敏感。在缺乏polβ伴侣蛋白XRCC1和PARP-1的情况下,以及在合成抑制剂降低BER效率的条件下,也观察到对MMS的敏感性增加。PARP活性在抵抗MMS诱导的细胞毒性中起主要作用,用无毒浓度的MMS和PARP抑制剂联合处理的细胞会发生细胞周期停滞,并通过Chk1依赖性凋亡途径死亡。由于BER缺陷的细胞和肿瘤对临床使用的化疗甲基化剂替莫唑胺同样敏感,因此调节DNA损伤诱导的细胞信号通路以及BER,是增强化疗效果的有吸引力的靶点。