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Title: Common Variation at 1q24.1 (ALDH9A1) Is a Potential Risk Factor for Renal Cancer.
Authors: Henrion MY,  Purdue MP,  Scelo G,  Broderick P,  Frampton M,  Ritchie A,  Meade A,  Li P,  McKay J,  Johansson M,  Lathrop M,  Larkin J,  Rothman N,  Wang Z,  Chow WH,  Stevens VL,  Diver WR,  Albanes D,  Virtamo J,  Brennan P,  Eisen T,  Chanock S,  Houlston RS
Journal: PLoS One
Date: 2015
Branches: BB, CGR, LTG, NEB, OD, OEEB
PubMed ID: 25826619
PMC ID: PMC4380462
Abstract: So far six susceptibility loci for renal cell carcinoma (RCC) have been discovered by genome-wide association studies (GWAS). To identify additional RCC common risk loci, we performed a meta-analysis of published GWAS (totalling 2,215 cases and 8,566 controls of Western-European background) with imputation using 1000 Genomes Project and UK10K Project data as reference panels and followed up the most significant association signals [22 single nucleotide polymorphisms (SNPs) and 3 indels in eight genomic regions] in 383 cases and 2,189 controls from The Cancer Genome Atlas (TCGA). A combined analysis identified a promising susceptibility locus mapping to 1q24.1 marked by the imputed SNP rs3845536 (Pcombined =2.30x10-8). Specifically, the signal maps to intron 4 of the ALDH9A1 gene (aldehyde dehydrogenase 9 family, member A1). We further evaluated this potential signal in 2,461 cases and 5,081 controls from the International Agency for Research on Cancer (IARC) GWAS of RCC cases and controls from multiple European regions. In contrast to earlier findings no association was shown in the IARC series (P=0.94; Pcombined =2.73x10-5). While variation at 1q24.1 represents a potential risk locus for RCC, future replication analyses are required to substantiate our observation.