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全基因组关联研究鉴定出 12p11.23 上肾细胞癌的新易感位点。

A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23.

机构信息

Department of Epidemiology, Division of Cancer Prevention and Population Sciences, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.

出版信息

Hum Mol Genet. 2012 Jan 15;21(2):456-62. doi: 10.1093/hmg/ddr479. Epub 2011 Oct 18.

Abstract

Renal cell carcinoma (RCC) is the most lethal urologic cancer. Only two common susceptibility loci for RCC have been confirmed to date. To identify additional RCC common susceptibility loci, we conducted an independent genome-wide association study (GWAS). We analyzed 533 191 single nucleotide polymorphisms (SNPs) for association with RCC in 894 cases and 1516 controls of European descent recruited from MD Anderson Cancer Center in the primary scan, and validated the top 500 SNPs in silico in 3772 cases and 8505 controls of European descent involved in the only published GWAS of RCC. We identified two common variants in linkage disequilibrium, rs718314 and rs1049380 (r(2) = 0.64, D ' = 0.84), in the inositol 1,4,5-triphosphate receptor, type 2 (ITPR2) gene on 12p11.23 as novel susceptibility loci for RCC (P = 8.89 × 10(-10) and P = 6.07 × 10(-9), respectively, in meta-analysis) with an allelic odds ratio of 1.19 [95% confidence interval (CI): 1.13-1.26] for rs718314 and 1.18 (95% CI: 1.12-1.25) for rs1049380. It has been recently identified that rs718314 in ITPR2 is associated with waist-hip ratio (WHR) phenotype. To our knowledge, this is the first genetic locus associated with both cancer risk and WHR.

摘要

肾细胞癌(RCC)是最致命的泌尿系统癌症。迄今为止,仅确认了两个常见的 RCC 易感性基因座。为了鉴定额外的 RCC 常见易感性基因座,我们进行了独立的全基因组关联研究(GWAS)。我们在原发性扫描中分析了 894 例 RCC 病例和 1516 例欧洲裔对照的 533191 个单核苷酸多态性(SNP)与 RCC 的关联,并在仅发表的 RCC GWAS 中涉及的 3772 例欧洲裔病例和 8505 例对照中对前 500 个 SNP 进行了计算机验证。我们在 12p11.23 上的肌醇 1,4,5-三磷酸受体,2 型(ITPR2)基因中鉴定出两个连锁不平衡的常见变体 rs718314 和 rs1049380(r(2) = 0.64,D = 0.84),它们是 RCC 的新易感基因座(在荟萃分析中,rs718314 和 rs1049380 的 P 值分别为 8.89×10(-10)和 6.07×10(-9)),其等位基因优势比为 1.19 [95%置信区间(CI):1.13-1.26]rs718314 和 1.18(95%CI:1.12-1.25)rs1049380。最近发现,ITPR2 中的 rs718314 与腰围-臀围比(WHR)表型相关。据我们所知,这是第一个与癌症风险和 WHR 相关的遗传基因座。

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