Genomic Epidemiology Group, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Int J Cancer. 2012 Dec 15;131(12):2920-8. doi: 10.1002/ijc.27567. Epub 2012 Jul 3.
ATP-binding cassette (ABC) transporter expression and genetic heterogeneity have been implicated in response to anticancer therapy. This study characterized genetic variability of the ABCB1 (also known as MDR1), ABCC2 (MRP2) and ABCG2 (BCRP) genes, which are key players in the metabolism of many chemotherapeutic agents including those used in the treatment of lung cancer. We genotyped 53 polymorphisms in the candidate genes in genomic DNA samples of 171 cases of small cell lung carcinoma (SCLC) and 206 cases of non-small cell lung carcinoma (NSCLC), and studied their impact on early response to chemotherapy, progression-free survival and overall survival. SNP rs717620 in ABCC2 was moderately associated with a poor response to chemotherapy but strongly with shorter progression-free survival and overall survival in SCLC but not NSCLC patients, indicating that ABCC2 genetic variation is an important factor in SCLC survival after chemotherapy.
三磷酸腺苷结合盒(ABC)转运蛋白的表达和遗传异质性与抗癌治疗的反应有关。本研究对 ABCB1(也称为 MDR1)、ABCC2(MRP2)和 ABCG2(BCRP)基因的遗传变异性进行了特征描述,这些基因是许多化疗药物代谢的关键因子,包括用于治疗肺癌的药物。我们对 171 例小细胞肺癌(SCLC)和 206 例非小细胞肺癌(NSCLC)的基因组 DNA 样本中的 53 个候选基因多态性进行了基因分型,并研究了它们对化疗早期反应、无进展生存期和总生存期的影响。ABCC2 中的 SNP rs717620 与化疗反应不良中度相关,但与 SCLC 患者而非 NSCLC 患者的无进展生存期和总生存期较短密切相关,表明 ABCC2 遗传变异是 SCLC 化疗后生存的一个重要因素。