期刊
DNA REPAIR
卷 35, 期 -, 页码 126-136出版社
ELSEVIER
DOI: 10.1016/j.dnarep.2015.10.003
关键词
BER; Cisplatin; MMR; Resistance; ATPase
资金
- National Institutes of Health [GM088249, ES008786, CA148629]
Mismatch repair (MMR) deficiency gives rise to cisplatin resistance and can lead to poor prognosis in cancers. Various models have been proposed to explain this low level of resistance caused due to loss of MMR proteins. We have shown that MMR proteins are required to maintain cisplatin interstrand cross-links (ICLs) on the DNA leading to increased cellular sensitivity. In our previous studies, we have shown that BER processing of the cisplatin ICLs is mutagenic. Polymerase beta (Pol beta) can generate mismatches which leads to the activation and the recruitment of mismatch repair proteins. In this paper, we distinguished between the requirement of different downstream MMR proteins for maintaining cisplatin sensitivity. We show that the MutS alpha (MSH2-MSH6) heterocomplex is required to maintain cisplatin sensitivity, whereas the Muts beta complex has no effect. These results can be correlated with the increased repair of cisplatin ICLs and ICL induced DNA double strand breaks (DSBs) in the resistant cells. Moreover, we show that MLH1 proficient cells displayed a cisplatin sensitive phenotype when compared with the MLH1 deficient cells and the ATPase activity of MLH1 is essential to mediate this effect. Based on these results, we propose that MutS alpha as well as the downstream MMR pathway proteins are essential to maintain a cisplatin sensitive phenotype as a consequence of processing Pol beta induced mismatches at sites flanking cisplatin ICLs. (C) 2015 Elsevier B.V. All rights reserved.
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