Turchi John J, Woods Derek S, VanderVere-Carozza Pamela
Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana. Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana.
Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana.
Cancer Discov. 2014 Oct;4(10):1118-9. doi: 10.1158/2159-8290.CD-14-0893.
DNA repair has been shown to affect the cellular response to platinum-based therapy in a variety of cancers; however, translating this knowledge to the clinic has proven difficult and yielded mixed results. In this issue of Cancer Discovery, Van Allen and colleagues have analyzed responders and nonresponders to neoadjuvant platinum-based therapy with locally advanced urothelial cancer and identified a series of mutations in the nucleotide excision repair (NER) gene ERCC2 that correlate with the response to platinum-based therapy. This work provides evidence that defects in NER can be exploited to maximize the efficacy of conventional platinum-based chemotherapy.
DNA修复已被证明会影响多种癌症对铂类疗法的细胞反应;然而,将这一认识转化到临床实践中已被证明是困难的,且结果不一。在本期《癌症发现》中,范·艾伦及其同事分析了局部晚期尿路上皮癌新辅助铂类疗法的反应者和无反应者,并在核苷酸切除修复(NER)基因ERCC2中鉴定出一系列与铂类疗法反应相关的突变。这项工作提供了证据,表明可以利用NER缺陷来最大化传统铂类化疗的疗效。