Supportive evidence for FOXP1, BARX1, and FOXF1 as genetic risk loci for the development of esophageal adenocarcinoma

作者: Jessica Becker , Andrea May , Christian Gerges , Mario Anders , Lothar Veits

DOI: 10.1002/CAM4.500

关键词:

摘要: The Barrett's and Esophageal Adenocarcinoma Consortium (BEACON) recently performed a genome-wide association study (GWAS) on esophageal adenocarcinoma (EAC) esophagus. They identified significant for variants at three genes, namely CRTC1, FOXP1, BARX1. Furthermore, they replicated an the FOXF1 gene that has been previously found in GWAS We aimed further replicating these other loci showed suggestive with P < 10(-4) BEACON sample. In total, we tested 88 SNPs independent sample consisting of 1065 EAC cases 1019 controls German descent. could replicate BARX1, nominal significance thereby confirm genetic genes confer risk. addition, near XRCC2 GATA6 were strongly (P 10(-5) ) although not significantly associated GWAS. Therefore, both corresponding represent promising candidates future studies samples.

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