Two novel genetic variants in the STK38L and RAB27A genes are associated with glioma susceptibility
Menée en population chinoise à partir de données portant sur 3 097 patients atteints d'un gliome et sur 4 362 témoins, cette étude d'association sur le génome entier identifie deux nouveaux variants des gènes STK38L et RAB27A impliqués dans le développement de la maladie
Glioma is the most common malignant primary brain tumors with poor prognosis. Genome wide association studies (GWAS) of glioma in populations with Western European ancestry were completed in the US and UK. However, our previous results strongly suggest the genetic heterogeneity could be important in glioma risk. To systematically investigate glioma risk–associated variants in Chinese population, we performed a multistage GWAS of glioma in the Han Chinese population, with a total of 3,097 glioma cases and 4,362 controls. In addition to confirming two associations reported in other ancestry groups, this study identified one new risk-associated locus for glioma on chromosome 12p11.23 (rs10842893, Pmeta = 2.33x10-12, STK38L) as well as a promising association at 15q15-21.1 (rs4774756, Pmeta = 6.12x10-8, RAB27A) in 3,097 glioma cases and 4,362 controls. Our findings demonstrate two novel association between the glioma risk region marked by variant rs10842893 and rs4774756) and glioma risk. These findings may advance the understanding of genetic susceptibility to glioma. This article is protected by copyright. All rights reserved.