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癌症睾丸基因CCDC116的顺式表达数量性状基因座(cis-eQTL)遗传变异与多种癌症风险相关。

A cis-eQTL genetic variant of the cancer-testis gene CCDC116 is associated with risk of multiple cancers.

作者信息

Qin Na, Wang Cheng, Lu Qun, Huang Tongtong, Zhu Meng, Wang Lihua, Yu Fei, Huang Mingtao, Jiang Yue, Dai Juncheng, Ma Hongxia, Jin Guangfu, Wu Chen, Lin Dongxin, Shen Hongbing, Hu Zhibin

机构信息

State Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, 210029, China.

Department of Epidemiology and Biostatistics, School of Public Health, Nanjing Medical University, Nanjing, 211166, China.

出版信息

Hum Genet. 2017 Aug;136(8):987-997. doi: 10.1007/s00439-017-1827-2. Epub 2017 Jun 26.

DOI:10.1007/s00439-017-1827-2
PMID:28653172
Abstract

Recent studies have found that cancer-testis (CT) genes, which are expressed predominantly in germ and cancer cells, may be candidate cancer drivers. Because of their crucial roles, genetic variants in these genes may contribute to the development of cancer. Here, we systematically evaluated associations of common variants in CT genes and their promoters for the risk of lung cancer in our initial GWAS (2331 cases and 3077 controls), followed by in silico replication using additional 10,512 lung cancer cases and 9562 controls. We found a significant association between rs3747093 located in the CCDC116 promoter and lung cancer risk (OR = 0.91, P  = 7.81 × 10). Although CCDC116 was expressed at lower levels in somatic tissues compared to the testis, the protective allele A of rs3747093 was associated with decreased CCDC116 expression in many normal tissues, including the lung (P = 8.1 × 10). We subsequently genotyped this variant in another four commonly diagnosed cancers (gastric, esophageal, colorectal, and breast cancers), as we found expression quantitative trait locus (eQTL) signals for rs3747093 and CCDC116 in their corresponding normal tissues. Interestingly, we observed consistent associations between rs3747093 and multiple cancers (gastric cancer: OR = 0.85, P = 2.21 × 10; esophageal cancer: OR = 0.91, P = 2.57 × 10; colorectal cancer: OR = 0.80, P = 1.85 × 10; and breast cancer: OR = 0.87, P = 1.55 × 10). Taken together, the A allele of rs3747093 showed significant protective effects on cancer risk (OR = 0.88, P  = 6.52 × 10) in an Asian population. Moreover, our findings suggest that low abundance expression of CT genes in normal tissues may also contribute to tumorigenesis, providing a new mechanism of CT genes in the development of cancer.

摘要

近期研究发现,主要在生殖细胞和癌细胞中表达的癌-睾丸(CT)基因可能是癌症驱动基因的候选者。由于其关键作用,这些基因中的遗传变异可能有助于癌症的发生发展。在此,我们在最初的全基因组关联研究(GWAS)(2331例病例和3077例对照)中系统评估了CT基因及其启动子中的常见变异与肺癌风险的关联,随后使用另外10512例肺癌病例和9562例对照进行了电子复制分析。我们发现位于CCDC116启动子中的rs3747093与肺癌风险之间存在显著关联(比值比[OR]=0.91,P=7.81×10)。尽管与睾丸相比,CCDC116在体细胞组织中的表达水平较低,但rs3747093的保护性等位基因A与包括肺在内的许多正常组织中CCDC116表达的降低相关(P=8.1×10)。由于我们在相应正常组织中发现了rs3747093和CCDC116的表达数量性状位点(eQTL)信号,随后我们在另外四种常见诊断癌症(胃癌、食管癌、结直肠癌和乳腺癌)中对该变异进行了基因分型。有趣的是,我们观察到rs3747093与多种癌症之间存在一致的关联(胃癌:OR=0.85,P=2.21×10;食管癌:OR=0.91,P=2.57×10;结直肠癌:OR=0.80,P=1.85×10;乳腺癌:OR=0.87,P=1.55×10)。总体而言,在亚洲人群中,rs3747093的A等位基因对癌症风险显示出显著的保护作用(OR=0.

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