Identification of seven new prostate cancer susceptibility loci through a genome-wide association study

R.A. Eeles*, Z. Kote Jarai, A.A. Al Olama, G.G. Giles, M. Guy, G. Severi, K. Muir, J.L. Hopper, B.E. Henderson, C.A. Haiman, J. Schleutker, F.C. Hamdy, D.E. Neal, J.L. Donovan, J.L. Stanford, E.A. Ostrander, S.A. Ingles, E.M. John, S.N. Thibodeau, D. SchaidJ.Y. Park, A. Spurdle, J. Clements, J.L. Dickinson, C. Maier, W. Vogel, T. Dork, T.R. Rebbeck, K.A. Cooney, L. Cannon Albright, P.O. Chappuis, P. Hutter, M. Zeegers, R. Kaneva, H.W. Zhang, Y.J. Lu, WD. Foulkes, D.R. English, D.A. Leongamornlert, M. Tymrakiewicz, J. Morrison, A.T. Ardern Jones, A.L. Hall, L.T. O'Brien, R.A. Wilkinson, E.J. Saunders, E.C. Page, E.J. Sawyer, S.M. Edwards, D.P. Dearnaley, A. Horwich, R.A. Huddart, V.S. Khoo, C.C. Parker, N. Van As, C.J. Woodhouse, A. Thompson, T. Christmas, C. Ogden, C.S. Cooper, M.C. Southey, A. Lophatananon, J.F. Liu, L.N. Kolonel, L. Le Marchand, T. Wahlfors, T.L. Tammela, A. Auvinen, S.J. Lewis, A. Cox, L.M. FitzGerald, J.S. Koopmeiners, D.M. Karyadi, E.M. Kwon, M.C. Stern, R. Corral, A.D. Joshi, A. Shahabi, S.K. McDonnell, T.A. Sellers, J. Pow Sang, S. Chambers, J. Aitken, R.A. Gardiner, J. Batra, M.A. Kedda, F. Lose, A. Polanowski, B. Patterson, J. Serth, A. Meyer, M. Luedeke, K. Stefflova, A.M. Ray, E.M. Lange, J. Farnham, H. Khan, C. Slavov, A. Mitkova

*Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review


    Prostate cancer (PrCa) is the most frequently diagnosed cancer in males in developed countries. To identify common PrCa susceptibility alleles, we previously conducted a genome-wide association study in which 541,129 SNPs were genotyped in 1,854 PrCa cases with clinically detected disease and in 1,894 controls. We have now extended the study to evaluate promising associations in a second stage in which we genotyped 43,671 SNPs in 3,650 PrCa cases and 3,940 controls and in a third stage involving an additional 16,229 cases and 14,821 controls from 21 studies. In addition to replicating previous associations, we identified seven new prostate cancer susceptibility loci on chromosomes 2, 4, 8, 11 and 22 (with P = 1.6 x 10(-8) to P = 2.7 x 10(-33)).
    Original languageEnglish
    Pages (from-to)1116-21
    JournalNature Genetics
    Issue number10
    Publication statusPublished - 1 Jan 2009

    Cite this