Gao Rui, Price Douglas K, Sissung Tristan, Reed Eddie, Figg William D
Molecular Pharmacology Section, Center for Cancer Research, National Cancer Institute/NIH, Bethesda, MD 20892, USA.
Mol Cancer Ther. 2008 May;7(5):1246-50. doi: 10.1158/1535-7163.MCT-07-2206.
Nucleotide excision repair (NER) and base excision repair (BER) pathways are DNA repair pathways that are important in carcinogenesis and in response to DNA-damaging chemotherapy. ERCC1 and ERCC2 are important molecular markers for NER; XRCC1 and PARP1 are important molecular markers for BER. Functional polymorphisms have been described that are associated with altered expression levels of these genes and with altered DNA repair capability. We assayed genomic DNA from 156 Americans of European descent and 164 Americans of African descent for the allelic frequencies of specific polymorphisms of ERCC1 N118N (500C>T), ERCC1 C8092A, ERCC2 K751Q (2282A>C), XRCC1 R399Q (1301G>A), XRCC1 R194W (685C>T), and PARP1 V762A (2446T>C). Differences were observed between Americans of European descent and Americans of African descent in the allelic frequencies of the ERCC1 N118N polymorphism (P < 0.000001). Differences were also observed between these two ethnic groups for ERCC2 K751Q (P = < 0.006675), XRCC1 R399Q (P < 0.000001), and PARP1 V762A (P = 0.000001). The ERCC1 N118N polymorphic variant that is seen most commonly in Americans of European descent is associated with a measurable reduction in NER function. ERCC1-mediated reduction in NER functionality affects the repair of cisplatin-DNA lesions.
核苷酸切除修复(NER)和碱基切除修复(BER)途径是DNA修复途径,在致癌作用以及对DNA损伤化疗的反应中起重要作用。ERCC1和ERCC2是NER的重要分子标志物;XRCC1和PARP1是BER的重要分子标志物。已描述了与这些基因表达水平改变以及DNA修复能力改变相关的功能多态性。我们检测了156名欧洲裔美国人和164名非洲裔美国人的基因组DNA,以确定ERCC1 N118N(500C>T)、ERCC1 C8092A、ERCC2 K751Q(2282A>C)、XRCC1 R399Q(1301G>A)、XRCC1 R194W(685C>T)和PARP1 V762A(2446T>C)特定多态性的等位基因频率。在欧洲裔美国人和非洲裔美国人之间观察到ERCC1 N118N多态性的等位基因频率存在差异(P<0.000001)。在这两个种族群体之间还观察到ERCC2 K751Q(P =<0.006675)、XRCC1 R399Q(P<0.000001)和PARP1 V762A(P = 0.000001)存在差异。在欧洲裔美国人中最常见的ERCC1 N118N多态变异与NER功能的可测量降低有关。ERCC1介导NER功能的降低会影响顺铂-DNA损伤的修复。