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Genome-wide association analysis identifies a meningioma risk locus at 11p15.5

BACKGROUND: Meningiomas are adult brain tumors originating in the meningeal coverings of the brain and spinal cord, with significant heritable basis. Genome-wide association studies (GWAS) have previously identified only a single risk locus for meningioma, at 10p12.31. METHODS: To identify a suscept...

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Detalles Bibliográficos
Autores principales: Claus, Elizabeth B, Cornish, Alex J, Broderick, Peter, Schildkraut, Joellen M, Dobbins, Sara E, Holroyd, Amy, Calvocoressi, Lisa, Lu, Lingeng, Hansen, Helen M, Smirnov, Ivan, Walsh, Kyle M, Schramm, Johannes, Hoffmann, Per, Nöthen, Markus M, Jöckel, Karl-Heinz, Swerdlow, Anthony, Larsen, Signe Benzon, Johansen, Christoffer, Simon, Matthias, Bondy, Melissa, Wrensch, Margaret, Houlston, Richard S, Wiemels, Joseph L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176799/
https://www.ncbi.nlm.nih.gov/pubmed/29762745
http://dx.doi.org/10.1093/neuonc/noy077
Descripción
Sumario:BACKGROUND: Meningiomas are adult brain tumors originating in the meningeal coverings of the brain and spinal cord, with significant heritable basis. Genome-wide association studies (GWAS) have previously identified only a single risk locus for meningioma, at 10p12.31. METHODS: To identify a susceptibility locus for meningioma, we conducted a meta-analysis of 2 GWAS, imputed using a merged reference panel from the 1000 Genomes Project and UK10K data, with validation in 2 independent sample series totaling 2138 cases and 12081 controls. RESULTS: We identified a new susceptibility locus for meningioma at 11p15.5 (rs2686876, odds ratio = 1.44, P = 9.86 × 10(–9)). A number of genes localize to the region of linkage disequilibrium encompassing rs2686876, including RIC8A, which plays a central role in the development of neural crest-derived structures, such as the meninges. CONCLUSIONS: This finding advances our understanding of the genetic basis of meningioma development and provides additional support for a polygenic model of meningioma.