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Pathway-based analysis of GWAs data identifies association of sex determination genes with susceptibility to testicular germ cell tumors

机译:基于通路的GWA数据分析可确定性别决定基因与睾丸生殖细胞肿瘤易感性的关联

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摘要

Genome-wide association (GWA) studies of testicular germ cell tumor (TGCT) have identified 18 susceptibility loci, some containing genes encoding proteins important in male germ cell development. Deletions of one of these genes, DMRT1, lead to male-to-female sex reversal and are associated with development of gonadoblastoma. To further explore genetic association with TGCT, we undertook a pathway-based analysis of SNP marker associations in the Penn GWAs (349 TGCT cases and 919 controls). We analyzed a custom-built sex determination gene set consisting of 32 genes using three different methods of pathway-based analysis. The sex determination gene set ranked highly compared with canonical gene sets, and it was associated with TGCT (FDRG = 2.28 × 10−5, FDRM = 0.014 and FDRI = 0.008 for Gene Set Analysis-SNP (GSA-SNP), Meta-Analysis Gene Set Enrichment of Variant Associations (MAGENTA) and Improved Gene Set Enrichment Analysis for Genome-wide Association Study (i-GSEA4GWAS) analysis, respectively). The association remained after removal of DMRT1 from the gene set (FDRG = 0.0002, FDRM = 0.055 and FDRI = 0.009). Using data from the NCI GWA scan (582 TGCT cases and 1056 controls) and UK scan (986 TGCT cases and 4946 controls), we replicated these findings (NCI: FDRG = 0.006, FDRM = 0.014, FDRI = 0.033, and UK: FDRG = 1.04 × 10−6, FDRM = 0.016, FDRI = 0.025). After removal of DMRT1 from the gene set, the sex determination gene set remains associated with TGCT in the NCI (FDRG = 0.039, FDRM = 0.050 and FDRI = 0.055) and UK scans (FDRG = 3.00 × 10−5, FDRM = 0.056 and FDRI = 0.044). With the exception of DMRT1, genes in the sex determination gene set have not previously been identified as TGCT susceptibility loci in these GWA scans, demonstrating the complementary nature of a pathway-based approach for genome-wide analysis of TGCT.
机译:睾丸生殖细胞肿瘤(TGCT)的全基因组关联(GWA)研究确定了18个易感基因座,其中一些包含编码对男性生殖细胞发育重要的蛋白质的基因。这些基因之一DMRT1的缺失会导致男女性别逆转,并与性腺母细胞瘤的发展有关。为了进一步探索与TGCT的遗传关联,我们对Penn GWA(349 TGCT病例和919对照)中的SNP标记关联进行了基于路径的分析。我们使用三种不同的基于途径的分析方法分析了由32个基因组成的定制性别决定基因集。性别决定基因组与规范基因组相比排名很高,并且与TGCT相关(FDRG = 2.28×10 −5 ,FDRM = 0.014,FDRI = 0.008,用于基因组分析-SNP(GSA) -SNP),变异关联的荟萃分析基因集富集(MAGENTA)和全基因组关联研究的改良基因集富集分析(i-GSEA4GWAS)。从基因组中删除DMRT1后,关联仍然存在(FDRG = 0.0002,FDRM = 0.055和FDRI = 0.009)。使用来自NCI GWA扫描(582 TGCT病例和1056对照)和UK扫描(986 TGCT病例和4946对照)的数据,我们重复了这些发现(NCI:FDRG = 0.006,FDRM = 0.014,FDRI = 0.033,和UK:FDRG = 1.04×10 -6 ,FDRM = 0.016,FDRI = 0.025)。从基因组中删除DMRT1后,性别决定基因组仍与NCI(FDRG = 0.039,FDRM = 0.050和FDRI = 0.055)和UK扫描(FDRG = 3.00×10 −5 ,FDR M = 0.056和FDR I = 0.044)。除DMRT1外,性别确定基因集中的基因先前尚未在这些GWA扫描中鉴定为TGCT易感基因座,这证明了基于途径的TGCT全基因组分析方法的互补性质。

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