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一项针对接受伊立替康联合顺铂化疗的小细胞肺癌患者生存情况的全基因组关联研究。

A genome-wide association study of survival in small-cell lung cancer patients treated with irinotecan plus cisplatin chemotherapy.

作者信息

Han J-Y, Lee Y-S, Shin E Soon, Hwang J-A, Nam S, Hong S-H, Ghang H Young, Kim J Young, Yoon S Jin, Lee J Soo

机构信息

Center for Lung Cancer, Research Institute and Hospital, National Cancer Center, Goyang, Republic of Korea.

Functional Genomic Branch, Research Institute and Hospital, National Cancer Center, Goyang, Republic of Korea.

出版信息

Pharmacogenomics J. 2014 Feb;14(1):20-7. doi: 10.1038/tpj.2013.7. Epub 2013 Mar 12.

Abstract

We conducted a genome-wide association study (GWAS) to identify single nucleotide polymorphisms (SNPs) influencing overall survival (OS) of small-cell lung cancer (SCLC) patients. We prospectively collected blood samples from 139 SCLC patients who participated in phase II studies of irinotecan and cisplatin (IP) chemotherapy as first-line therapy. Among 334 127 SNPs, which passed quality control, seven showed significant association with OS. The rs16950650CT, rs7186128AG or GG, rs17574269AG, rs8020368CC, rs4655567CC, rs2166219TT or rs2018683TT showed shorter OS compared with control alleles. Among the seven SNPs, rs4655567, rs8020368 and rs2018683 were significantly associated with a resistant relapse (RR). In the multivariate analysis, rs8020368CC was significantly associated with higher risk of RR (odds ratio=16.7, P=0.007). In vitro and in silico analysis showed that SNPs in C14orf49 might be associated with epithelial-to-mesenchymal transition. This exploratory GWAS identified candidate SNPs that may be predictive of the clinical outcome of SCLC patients receiving IP.

摘要

我们开展了一项全基因组关联研究(GWAS),以鉴定影响小细胞肺癌(SCLC)患者总生存期(OS)的单核苷酸多态性(SNP)。我们前瞻性地收集了139例参与伊立替康和顺铂(IP)化疗II期研究作为一线治疗的SCLC患者的血样。在通过质量控制的334127个SNP中,有7个与OS显著相关。与对照等位基因相比,rs16950650CT、rs7186128AG或GG、rs17574269AG、rs8020368CC、rs4655567CC、rs2166219TT或rs2018683TT显示出较短的OS。在这7个SNP中,rs4655567、rs8020368和rs2018683与耐药性复发(RR)显著相关。在多变量分析中,rs8020368CC与RR的较高风险显著相关(优势比=16.7,P=0.007)。体外和计算机模拟分析表明,C14orf49中的SNP可能与上皮-间质转化相关。这项探索性GWAS鉴定出了可能预测接受IP治疗的SCLC患者临床结局的候选SNP。

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