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鉴定出子宫内膜癌的 9 个新的易感性位点。

Identification of nine new susceptibility loci for endometrial cancer.

机构信息

Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, 4006, QLD, Australia.

Department of Obstetrics and Gynecology, University Hospitals KU Leuven, University of Leuven, Division of Gynecologic Oncology, Leuven, 3000, Belgium.

出版信息

Nat Commun. 2018 Aug 9;9(1):3166. doi: 10.1038/s41467-018-05427-7.

Abstract

Endometrial cancer is the most commonly diagnosed cancer of the female reproductive tract in developed countries. Through genome-wide association studies (GWAS), we have previously identified eight risk loci for endometrial cancer. Here, we present an expanded meta-analysis of 12,906 endometrial cancer cases and 108,979 controls (including new genotype data for 5624 cases) and identify nine novel genome-wide significant loci, including a locus on 12q24.12 previously identified by meta-GWAS of endometrial and colorectal cancer. At five loci, expression quantitative trait locus (eQTL) analyses identify candidate causal genes; risk alleles at two of these loci associate with decreased expression of genes, which encode negative regulators of oncogenic signal transduction proteins (SH2B3 (12q24.12) and NF1 (17q11.2)). In summary, this study has doubled the number of known endometrial cancer risk loci and revealed candidate causal genes for future study.

摘要

子宫内膜癌是发达国家女性生殖道最常见的癌症。通过全基因组关联研究(GWAS),我们先前已经确定了 8 个子宫内膜癌风险位点。在这里,我们对 12906 例子宫内膜癌病例和 108979 例对照(包括 5624 例新的基因型数据)进行了扩展的荟萃分析,并确定了 9 个新的全基因组显著位点,包括先前通过子宫内膜癌和结直肠癌的荟萃 GWAS 确定的 12q24.12 上的一个位点。在五个位点上,表达数量性状基因座(eQTL)分析确定了候选因果基因;这些位点中的两个风险等位基因与编码致癌信号转导蛋白的负调节剂的基因表达降低相关(SH2B3(12q24.12)和 NF1(17q11.2))。总之,这项研究将已知的子宫内膜癌风险位点数量增加了一倍,并揭示了候选因果基因,以供进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/354e/6085317/e31bb9285ac4/41467_2018_5427_Fig1_HTML.jpg

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