Tu Lin, Yan Bin, Peng Zhiyong
Department of General Surgery Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, 1630 Dongfang Road, Shanghai, 200127, People's Republic of China.
Mol Genet Genomics. 2015 Jun;290(3):901-12. doi: 10.1007/s00438-014-0970-x. Epub 2014 Dec 5.
Several genome-wide association studies on colorectal cancer (CRC) have reported similar findings of a new susceptibility locus, 15q13.3. After that, a number of studies have reported that the rs4779584 and rs10318 polymorphisms at chromosome 15q13.3 have been implicated in CRC and colorectal adenoma (CRA) risk; however, these studies have yielded inconsistent results. To investigate this inconsistency, we performed a meta-analysis of 22 studies involving a total of 48,468 CRC cases, 4,189 CRA cases, and 85,105 controls for the two polymorphisms to evaluate its effect on genetic susceptibility for CRC/CRA. Potential sources of heterogeneity and publication bias were also systematically explored. Overall, the summary odds ratio (OR) of rs4779584-T variant for CRC was 1.13 (95 % CI 1.09-1.16, P < 10(-5)) and 1.15 (95 % CI 1.04-1.28, P = 0.006) for CRA. After stratified by ethnicity, significantly increased CRC risks were found for rs4779584 polymorphism among East Asians and Caucasians, while no significant associations were detected among African American and other ethnic populations. A meta-analysis of studies on the rs10318 polymorphism also showed significant overall association with CRC, yielding a per-allele OR of 1.13 (95 % CI 1.02-1.24, P = 0.02). In the subgroup analysis by ethnicity, significantly increased CRC risks were found in Caucasians; whereas no significant associations were found among East Asians and African Americans. This meta-analysis demonstrated that the rs4779584 and rs10318 polymorphism at 15q13.3 is a risk factor associated with increased CRC/CRA susceptibility, but these associations vary in different ethnic populations.
多项针对结直肠癌(CRC)的全基因组关联研究报告了一个新的易感位点15q13.3的相似研究结果。此后,多项研究报告称,15号染色体q13.3区域的rs4779584和rs10318多态性与结直肠癌和结直肠腺瘤(CRA)风险相关;然而,这些研究结果并不一致。为了探究这种不一致性,我们对22项研究进行了荟萃分析,这些研究共纳入了48468例结直肠癌病例、4189例结直肠腺瘤病例以及85105例对照,以评估这两种多态性对结直肠癌/结直肠腺瘤遗传易感性的影响。还系统地探讨了异质性和发表偏倚的潜在来源。总体而言,rs4779584 - T变异体对结直肠癌(CRC)的汇总比值比(OR)为1.13(95%可信区间1.09 - 1.16,P < 10⁻⁵),对结直肠腺瘤(CRA)为1.15(95%可信区间1.04 - 1.28,P = 0.006)。按种族分层后,东亚人和白种人中rs4779584多态性的结直肠癌风险显著增加,而在非裔美国人和其他种族人群中未检测到显著关联。对rs10318多态性研究的荟萃分析也显示与结直肠癌存在显著的总体关联,每个等位基因的OR为1.13(95%可信区间1.02 - 1.24,P = 0.02)。在按种族进行的亚组分析中,白种人的结直肠癌风险显著增加;而东亚人和非裔美国人中未发现显著关联。这项荟萃分析表明,15q13.3处的rs4779584和rs10318多态性是与结直肠癌/结直肠腺瘤易感性增加相关的危险因素,但这些关联在不同种族人群中有所不同。