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Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study
Authors:Kote-Jarai Zsofia  Olama Ali Amin Al  Giles Graham G  Severi Gianluca  Schleutker Johanna  Weischer Maren  Campa Daniele  Riboli Elio  Key Tim  Gronberg Henrik  Hunter David J  Kraft Peter  Thun Michael J  Ingles Sue  Chanock Stephen  Albanes Demetrius  Hayes Richard B  Neal David E  Hamdy Freddie C  Donovan Jenny L  Pharoah Paul  Schumacher Fredrick  Henderson Brian E  Stanford Janet L  Ostrander Elaine A  Sorensen Karina Dalsgaard  Dörk Thilo  Andriole Gerald  Dickinson Joanne L  Cybulski Cezary  Lubinski Jan  Spurdle Amanda  Clements Judith A  Chambers Suzanne  Aitken Joanne  Gardiner R A Frank  Thibodeau Stephen N
Affiliation:The Institute of Cancer Research, Sutton, Surrey, UK.
Abstract:
Prostate cancer (PrCa) is the most frequently diagnosed male cancer in developed countries. We conducted a multi-stage genome-wide association study for PrCa and previously reported the results of the first two stages, which identified 16 PrCa susceptibility loci. We report here the results of stage 3, in which we evaluated 1,536 SNPs in 4,574 individuals with prostate cancer (cases) and 4,164 controls. We followed up ten new association signals through genotyping in 51,311 samples in 30 studies from the Prostate Cancer Association Group to Investigate Cancer Associated Alterations in the Genome (PRACTICAL) consortium. In addition to replicating previously reported loci, we identified seven new prostate cancer susceptibility loci on chromosomes 2p11, 3q23, 3q26, 5p12, 6p21, 12q13 and Xq12 (P = 4.0 × 10(-8) to P = 2.7 × 10(-24)). We also identified a SNP in TERT more strongly associated with PrCa than that previously reported. More than 40 PrCa susceptibility loci, explaining ~25% of the familial risk in this disease, have now been identified.
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