Kaewbubpa Walennee, Areepium Nutthada, Sriuranpong Virote
Department of Pharmacy Practice, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok, Thailand. Email:
Asian Pac J Cancer Prev. 2016 Nov 1;17(11):4917-4920. doi: 10.22034/APJCP.2016.17.11.4917.
For advanced non-small-cell lung cancer (NSCLC) cases, a platinum-based regimen is the first-line chemotherapy treatment. The excision repair cross-complementing group 1 (ERCC1) plays an important role in DNA repair and has been related to resistance to platinum chemotherapy. This study aimed to investigate the effects of the ERCC1 (C118T) polymorphism on treatment response in 26 Thai advanced NSCLC patients receiving first line platinum-based chemotherapy during January to July 2015 at King Chulalongkorn Memorial Hospital (KCMH). DNA was extracted from peripheral blood lymphocytes and the single nucleotide polymorphism of ERCC1 was genotyped using a realtime PCR method with the TaqMan assay. The distribution of C/C, C/T and T/T genotypes was 57.7 %, 34.6 % and 7.7 %, respectively. The response rate to platinum-based chemotherapy in the wild type (C/C) of ERCC1 (C118T) was better than with the variant types (C/T and T/T) but the difference was not statistically significant (29.7% vs 9.1%, P=0.274). The results showed that a genetic polymorphism in ERCC1 might influence patient response to platinumbased chemotherapy. Further multicenter studies are now required to confirm the results of our study.
对于晚期非小细胞肺癌(NSCLC)病例,铂类方案是一线化疗治疗方法。切除修复交叉互补组1(ERCC1)在DNA修复中起重要作用,并且与铂类化疗耐药相关。本研究旨在调查2015年1月至7月期间在朱拉隆功国王纪念医院(KCMH)接受一线铂类化疗的26例泰国晚期NSCLC患者中,ERCC1(C118T)基因多态性对治疗反应的影响。从外周血淋巴细胞中提取DNA,并使用TaqMan分析法通过实时PCR方法对ERCC1的单核苷酸多态性进行基因分型。C/C、C/T和T/T基因型的分布分别为57.7%、34.6%和7.7%。ERCC1(C118T)野生型(C/C)对铂类化疗的反应率优于变异型(C/T和T/T),但差异无统计学意义(29.7%对9.1%,P = 0.274)。结果表明,ERCC1基因多态性可能影响患者对铂类化疗的反应。现在需要进一步的多中心研究来证实我们的研究结果。