Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma
Law, M.H., Bishop, D.T., Lee, J.E., Brossard, M., Martin, N.G., Moses, E.K., Song, F., Barrett, J.H., Kumar, R., Easton, D.F., Pharoah, P.D.P., Swerdlow, A.J., Kypreou, K.P., Taylor, J.C., Harland, M., Randerson-Moor, J., Akslen, L.A., Andresen, P.A., Avril, M.-F., Azizi, E., Scarrà, G.B., Brown, K.M., Dȩbniak, T., Duffy, D.L., Elder, D.E., Fang, S., Friedman, E., Galan, P., Ghiorzo, P., Gillanders, E.M., Goldstein, A.M., Gruis, N.A., Hansson, J., Helsing, P., Hočevar, M., Höiom, V., Ingvar, C., Kanetsky, P.A., Chen, W.V., Landi, M.T., Lang, J., Lathrop, G.M., Lubiński, J., Mackie, R.M., Mann, G.J., Molven, A., Montgomery, G.W., Novaković, S., Olsson, H., Puig, S., Puig-Butille, J.A., Qureshi, A.A., Radford-Smith, G.L., Van Der Stoep, N., Van Doorn, R., Whiteman, D.C., Craig, J.E., Schadendorf, D., Simms, L.A., Burdon, K.P., Nyholt, D.R., Pooley, K.A., Orr, N., Stratigos, A.J., Cust, A.E., Ward, S.V., Hayward, N.K., Han, J., Schulze, H.-J., Dunning, A.M., Bishop, J.A.N., Demenais, F., Amos, C.I., MacGregor, S., & Iles, M.M. (2015) Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Nature Genetics, 47(9), pp. 987-995.
Thirteen common susceptibility loci have been reproducibly associated with cutaneous malignant melanoma (CMM). We report the results of an international 2-stage meta-analysis of CMM genome-wide association studies (GWAS). This meta-analysis combines 11 GWAS (5 previously unpublished) and a further three stage 2 data sets, totaling 15,990 CMM cases and 26,409 controls. Five loci not previously associated with CMM risk reached genome-wide significance (P < 5 × 10−8), as did 2 previously reported but unreplicated loci and all 13 established loci. Newly associated SNPs fall within putative melanocyte regulatory elements, and bioinformatic and expression quantitative trait locus (eQTL) data highlight candidate genes in the associated regions, including one involved in telomere biology.
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|Item Type:||Journal Article|
|Keywords:||cytochrome P450 1B1, Article, bioinformatics, cancer risk, chromosome 10q, chromosome 11q, chromosome 15q, chromosome 6p, chromosome 7p, chromosome 9q, controlled study, cutaneous malignant melanoma, cutaneous melanoma, enhancer region, gene expression, gene identification, gene locus, genetic association, genetic susceptibility, human, keratinocyte, major clinical study, melanocyte, meta analysis, nevus, phenotype, priority journal, quantitative trait locus, single nucleotide polymorphism, skin pigmentation, telomere, transcription initiation site, cancer genetics, comparative study, DNA repair, excision repair, genetic association, heritability, promoter region, skin carcinogenesis, systematic review, telomere homeostasis|
|Divisions:||Current > Schools > School of Biomedical Sciences
Current > QUT Faculties and Divisions > Faculty of Health
Current > Institutes > Institute of Health and Biomedical Innovation
|Copyright Owner:||Copyright 2015 Nature America, Inc.|
|Deposited On:||12 Jan 2016 00:50|
|Last Modified:||12 Jan 2016 22:54|
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