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全基因组关联研究鉴定出汉族人群肺鳞癌 12q23.1 上的一个新的易感位点。

Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese.

机构信息

Department of Epidemiology and Biostatistics and Ministry of Education, MOE Key Lab for Modern Toxicology, School of Public Health, Nanjing Medical University, Nanjing, China.

出版信息

PLoS Genet. 2013;9(1):e1003190. doi: 10.1371/journal.pgen.1003190. Epub 2013 Jan 17.

Abstract

Adenocarcinoma (AC) and squamous cell carcinoma (SqCC) are two major histological subtypes of lung cancer. Genome-wide association studies (GWAS) have made considerable advances in the understanding of lung cancer susceptibility. Obvious heterogeneity has been observed between different histological subtypes of lung cancer, but genetic determinants in specific to lung SqCC have not been systematically investigated. Here, we performed the GWAS analysis specifically for lung SqCC in 833 SqCC cases and 3,094 controls followed by a two-stage replication in additional 2,223 lung SqCC cases and 6,409 controls from Chinese populations. We found that rs12296850 in SLC17A8-NR1H4 gene region at12q23.1 was significantly associated with risk of lung SqCC at genome-wide significance level [additive model: odds ratio (OR) = 0.78, 95% confidence interval (CI) = 0.72-0.84, P = 1.19×10(-10)]. Subjects carrying AG or GG genotype had a 26% (OR = 0.74, 95% CI = 0.67-0.81) or 32% (OR = 0.68, 95% CI = 0.56-0.83) decreased risk of lung SqCC, respectively, as compared with AA genotype. However, we did not observe significant association between rs12296850 and risk of lung AC in a total of 4,368 cases with lung AC and 9,486 controls (OR = 0.96, 95% CI = 0.90-1.02, P = 0.173). These results indicate that genetic variations on chromosome 12q23.1 may specifically contribute to lung SqCC susceptibility in Chinese population.

摘要

腺癌(AC)和鳞状细胞癌(SqCC)是肺癌的两种主要组织学亚型。全基因组关联研究(GWAS)在理解肺癌易感性方面取得了相当大的进展。已经观察到不同组织学亚型的肺癌之间存在明显的异质性,但尚未系统地研究特定于肺 SqCC 的遗传决定因素。在这里,我们针对 833 例肺 SqCC 病例和 3094 例对照进行了 GWAS 分析,随后在中国人群中对另外 2223 例肺 SqCC 病例和 6409 例对照进行了两阶段复制。我们发现 12q23.1 上 SLC17A8-NR1H4 基因区域的 rs12296850 与肺 SqCC 的风险显著相关,达到全基因组显著水平[加性模型:比值比(OR)=0.78,95%置信区间(CI)=0.72-0.84,P=1.19×10(-10)]。与 AA 基因型相比,携带 AG 或 GG 基因型的个体患肺 SqCC 的风险分别降低了 26%(OR=0.74,95%CI=0.67-0.81)或 32%(OR=0.68,95%CI=0.56-0.83)。然而,我们没有观察到 rs12296850 与总计 4368 例肺 AC 病例和 9486 例对照之间的肺 AC 风险之间存在显著关联(OR=0.96,95%CI=0.90-1.02,P=0.173)。这些结果表明,染色体 12q23.1 上的遗传变异可能特异性地导致中国人群中肺 SqCC 的易感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6a2/3547794/64fdf809c11f/pgen.1003190.g001.jpg

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