GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer Journal Article

   


Authors: Pharoah, P. D. P.; Tsai, Y. Y.; Ramus, S. J.; Phelan, C. M.; Goode, E. L.; Lawrenson, K.; Buckley, M.; Fridley, B. L.; Tyrer, J. P.; Shen, H.; Weber, R.; Karevan, R.; Larson, M. C.; Song, H.; Tessier, D. C.; Bacot, F.; Vincent, D.; Cunningham, J. M.; Dennis, J.; Dicks, E.; Aben, K. K.; Anton-Culver, H.; Antonenkova, N.; Armasu, S. M.; Baglietto, L.; Bandera, E. V.; Beckmann, M. W.; Birrer, M. J.; Bloom, G.; Bogdanova, N.; Brenton, J. D.; Brinton, L. A.; Brooks-Wilson, A.; Brown, R.; Butzow, R.; Campbell, I.; Carney, M. E.; Carvalho, R. S.; Chang-Claude, J.; Chen, Y. A.; Chen, Z.; Chow, W. H.; Cicek, M. S.; Coetzee, G.; Cook, L. S.; Cramer, D. W.; Cybulski, C.; Dansonka-Mieszkowska, A.; Despierre, E.; Doherty, J. A.; Dörk, T.; du Bois, A.; Dürst, M.; Eccles, D.; Edwards, R.; Ekici, A. B.; Fasching, P. A.; Fenstermacher, D.; Flanagan, J.; Gao, Y. T.; Garcia-Closas, M.; Gentry-Maharaj, A.; Giles, G.; Gjyshi, A.; Gore, M.; Gronwald, J.; Guo, Q.; Halle, M. K.; Harter, P.; Hein, A.; Heitz, F.; Hillemanns, P.; Hoatlin, M.; Høgdall, E.; Høgdall, C. K.; Hosono, S.; Jakubowska, A.; Jensen, A.; Kalli, K. R.; Karlan, B. Y.; Kelemen, L. E.; Kiemeney, L. A.; Kjaer, S. K.; Konecny, G. E.; Krakstad, C.; Kupryjanczyk, J.; Lambrechts, D.; Lambrechts, S.; Le, N. D.; Lee, N.; Lee, J.; Leminen, A.; Lim, B. K.; Lissowska, J.; Lubinski, J.; Lundvall, L.; Lurie, G.; Massuger, L. F. A. G.; Matsuo, K.; McGuire, V.; Olson, S. H.; Orlow, I.; Pike, M. C.
Article Title: GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer
Abstract: Genome-wide association studies (GWAS) have identified four susceptibility loci for epithelial ovarian cancer (EOC), with another two suggestive loci reaching near genome-wide significance. We pooled data from a GWAS conducted in North America with another GWAS from the UK. We selected the top 24,551 SNPs for inclusion on the iCOGS custom genotyping array. We performed follow-up genotyping in 18,174 individuals with EOC (cases) and 26,134 controls from 43 studies from the Ovarian Cancer Association Consortium. We validated the two loci at 3q25 and 17q21 that were previously found to have associations close to genome-wide significance and identified three loci newly associated with risk: two loci associated with all EOC subtypes at 8q21 (rs11782652, P = 5.5 × 10-9) and 10p12 (rs1243180, P = 1.8 × 10-8) and another locus specific to the serous subtype at 17q12 (rs757210, P = 8.1 × 10-10). An integrated molecular analysis of genes and regulatory regions at these loci provided evidence for functional mechanisms underlying susceptibility and implicated CHMP4C in the pathogenesis of ovarian cancer.
Journal Title: Nature Genetics
Volume: 45
Issue: 4
ISSN: 1061-4036
Publisher: Nature Publishing Group  
Date Published: 2013-04-01
Start Page: 362
End Page: 370
Language: English
PROVIDER: scopus
PUBMED: 23535730
DOI: 10.1038/ng.2564
PMCID: PMC3693183
DOI/URL:

http://www.scopus.com/inward/record.url?eid=2-s2.0-84875707717&partnerID=40&md5=a3e5919f0e53ee0df98942cec36cdac4
Notes: --- - Cited By (since 1996):1 - "Export Date: 1 May 2013" - "CODEN: NGENE" - ":doi 10.1038/ng.2564" - "Source: Scopus"
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MSK Authors
  1. Malcolm Pike
    190 Pike
  2. Sara H Olson
    234 Olson
  3. Irene Orlow
    247 Orlow
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