Division of Cancer Epidemiology and Genetics, National Cancer Institute NCI, US National Institutes of Health, US Department of Health and Human Services, Bethesda, Maryland, USA.
Nat Genet. 2013 Jun;45(6):680-5. doi: 10.1038/ng.2634. Epub 2013 May 12.
We conducted a meta-analysis to identify new susceptibility loci for testicular germ cell tumor (TGCT). In the discovery phase, we analyzed 931 affected individuals and 1,975 controls from 3 genome-wide association studies (GWAS). We conducted replication in 6 independent sample sets comprising 3,211 affected individuals and 7,591 controls. In the combined analysis, risk of TGCT was significantly associated with markers at four previously unreported loci: 4q22.2 in HPGDS (per-allele odds ratio (OR) = 1.19, 95% confidence interval (CI) = 1.12-1.26; P = 1.11 × 10(-8)), 7p22.3 in MAD1L1 (OR = 1.21, 95% CI = 1.14-1.29; P = 5.59 × 10(-9)), 16q22.3 in RFWD3 (OR = 1.26, 95% CI = 1.18-1.34; P = 5.15 × 10(-12)) and 17q22 (rs9905704: OR = 1.27, 95% CI = 1.18-1.33; P = 4.32 × 10(-13) and rs7221274: OR = 1.20, 95% CI = 1.12-1.28; P = 4.04 × 10(-9)), a locus that includes TEX14, RAD51C and PPM1E. These new TGCT susceptibility loci contain biologically plausible genes encoding proteins important for male germ cell development, chromosomal segregation and the DNA damage response.
我们进行了一项荟萃分析,以确定睾丸生殖细胞肿瘤(TGCT)的新易感基因座。在发现阶段,我们分析了来自 3 项全基因组关联研究(GWAS)的 931 名受影响个体和 1975 名对照。我们在 6 个独立样本集中进行了复制,其中包括 3211 名受影响个体和 7591 名对照。在综合分析中,TGCT 的风险与四个以前未报道的基因座的标记显著相关:HPGDS 中的 4q22.2(每个等位基因的优势比(OR)=1.19,95%置信区间(CI)=1.12-1.26;P=1.11×10(-8)),MAD1L1 中的 7p22.3(OR=1.21,95%CI=1.14-1.29;P=5.59×10(-9)),RFWD3 中的 16q22.3(OR=1.26,95%CI=1.18-1.34;P=5.15×10(-12))和 17q22(rs9905704:OR=1.27,95%CI=1.18-1.33;P=4.32×10(-13)和 rs7221274:OR=1.20,95%CI=1.12-1.28;P=4.04×10(-9)),该基因座包含编码对雄性生殖细胞发育、染色体分离和 DNA 损伤反应至关重要的蛋白质的生物学上合理的基因。这些新的 TGCT 易感基因座包含编码对雄性生殖细胞发育、染色体分离和 DNA 损伤反应至关重要的蛋白质的生物学上合理的基因。