Multiple loci on 8q24 associated with prostate cancer susceptibility

被引:230
作者
Al Olama, Ali Amin [1 ]
Kote-Jarai, Zsofia [2 ]
Giles, Graham G. [3 ,4 ]
Guy, Michelle [2 ]
Morrison, Jonathan [1 ]
Severi, Gianluca [3 ,4 ]
Leongamornlert, Daniel A. [2 ]
Tymrakiewicz, Malgorzata [2 ]
Jhavar, Sameer [2 ]
Saunders, Ed [2 ]
Hopper, John L. [4 ]
Southey, Melissa C. [5 ]
Muir, Kenneth R. [6 ]
English, Dallas R. [4 ]
Dearnaley, David P. [2 ,7 ]
Ardern-Jones, Audrey T. [7 ]
Hall, Amanda L. [2 ,7 ]
O'Brien, Lynne T. [2 ]
Wilkinson, Rosemary A. [2 ]
Sawyer, Emma [2 ]
Lophatananon, Artitaya [6 ]
Horwich, Alan [2 ,7 ]
Huddart, Robert A. [2 ,7 ]
Khoo, Vincent S. [2 ,7 ]
Parker, Christopher C. [2 ,7 ]
Woodhouse, Christopher J. [7 ]
Thompson, Alan [7 ]
Christmas, Tim [7 ]
Ogden, Chris [7 ]
Cooper, Colin [2 ]
Donovan, Jenny L. [8 ]
Hamdy, Freddie C. [9 ]
Neal, David E. [7 ,10 ,11 ,12 ]
Eeles, Rosalind A. [2 ]
Easton, Douglas F. [1 ]
机构
[1] Univ Cambridge, Canc Res UK Genet Epidemiol Unit, Cambridge, England
[2] Inst Canc Res, Surrey, England
[3] Canc Council Victoria, Canc Epidemiol Ctr, Carlton, Vic, Australia
[4] Univ Melbourne, Ctr Mol Environm Genet & Analyt Epidemiol, Carlton, Vic 3053, Australia
[5] Univ Melbourne, Dept Pathol, Genet Epidemiol Lab, Parkville, Vic 3052, Australia
[6] Univ Nottingham, Sch Med, Queens Med Ctr, Nottingham, England
[7] Royal Marsden Natl Hlth Serv Fdn Trust, Surrey, England
[8] Univ Bristol, Dept Social Med, Bristol, Avon, England
[9] Univ Oxford, Nuffield Dept Surg, Oxford, England
[10] Li Ka Shing Ctr, Canc Res UK Cambridge Res Inst, Cambridge, England
[11] Univ Cambridge, Addenbrookes Hosp, Dept Oncol, Cambridge CB2 2QQ, England
[12] Univ Cambridge, Addenbrookes Hosp, Dept Surg, Cambridge CB2 2QQ, England
基金
英国医学研究理事会;
关键词
GENOME-WIDE ASSOCIATION; RISK LOCUS; COLORECTAL-CANCER; RS6983267; AMERICANS; VARIANTS; MYC;
D O I
10.1038/ng.452
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Previous studies have identified multiple loci on 8q24 associated with prostate cancer risk. We performed a comprehensive analysis of SNP associations across 8q24 by genotyping tag SNPs in 5,504 prostate cancer cases and 5,834 controls. We confirmed associations at three previously reported loci and identified additional loci in two other linkage disequilibrium blocks (rs1006908: per-allele OR = 0.87, P = 7.9 x 10(-8); rs620861: OR = 0.90, P = 4.8 x 10(-8)). Eight SNPs in five linkage disequilibrium blocks were independently associated with prostate cancer susceptibility.
引用
收藏
页码:1058 / 1060
页数:3
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