Résumé
Genome-wide association studies (GWAS) have identified 76 variants associated with prostate cancer risk predominantly in populations of European ancestry. To identify additional susceptibility loci for this common cancer, we conducted a meta-analysis of >10 million SNPs in 43,303 prostate cancer cases and 43,737 controls from studies in populations of European, African, Japanese and Latino ancestry. Twenty-three new susceptibility loci were identified at association P < 5 × 10 â '8; 15 variants were identified among men of European ancestry, 7 were identified in multi-ancestry analyses and 1 was associated with early-onset prostate cancer. These 23 variants, in combination with known prostate cancer risk variants, explain 33% of the familial risk for this disease in European-ancestry populations. These findings provide new regions for investigation into the pathogenesis of prostate cancer and demonstrate the usefulness of combining ancestrally diverse populations to discover risk loci for disease.
langue originale | Anglais |
---|---|
Pages (de - à) | 1103-1109 |
Nombre de pages | 7 |
journal | Nature Genetics |
Volume | 46 |
Numéro de publication | 10 |
Les DOIs | |
état | Publié - 26 sept. 2014 |
Modification externe | Oui |
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Dans: Nature Genetics, Vol 46, Numéro 10, 26.09.2014, p. 1103-1109.
Résultats de recherche: Contribution à un journal › Article › Revue par des pairs
TY - JOUR
T1 - A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer
AU - Olama, Ali Amin Al
AU - Kote-Jarai, Zsofia
AU - Berndt, Sonja I.
AU - Conti, David V.
AU - Schumacher, Fredrick
AU - Han, Ying
AU - Benlloch, Sara
AU - Hazelett, Dennis J.
AU - Wang, Zhaoming
AU - Saunders, Ed
AU - Leongamornlert, Daniel
AU - Lindstrom, Sara
AU - Jugurnauth-Little, Sara
AU - Dadaev, Tokhir
AU - Tymrakiewicz, Malgorzata
AU - Stram, Daniel O.
AU - Rand, Kristin
AU - Wan, Peggy
AU - Stram, Alex
AU - Sheng, Xin
AU - Pooler, Loreall C.
AU - Park, Karen
AU - Xia, Lucy
AU - Tyrer, Jonathan
AU - Kolonel, Laurence N.
AU - Marchand, Loic Le
AU - Hoover, Robert N.
AU - Machiela, Mitchell J.
AU - Yeager, Merideth
AU - Burdette, Laurie
AU - Chung, Charles C.
AU - Hutchinson, Amy
AU - Yu, Kai
AU - Goh, Chee
AU - Ahmed, Mahbubl
AU - Govindasami, Koveela
AU - Guy, Michelle
AU - Tammela, Teuvo L.J.
AU - Auvinen, Anssi
AU - Wahlfors, Tiina
AU - Schleutker, Johanna
AU - Visakorpi, Tapio
AU - Leinonen, Katri A.
AU - Xu, Jianfeng
AU - Aly, Markus
AU - Donovan, Jenny
AU - Travis, Ruth C.
AU - Key, Tim J.
AU - Siddiq, Afshan
AU - Canzian, Federico
AU - Khaw, Kay Tee
AU - Takahashi, Atsushi
AU - Kubo, Michiaki
AU - Pharoah, Paul
AU - Pashayan, Nora
AU - Weischer, Maren
AU - Nordestgaard, Borge G.
AU - Nielsen, Sune F.
AU - Klarskov, Peter
AU - Røder, Martin Andreas
AU - Iversen, Peter
AU - Thibodeau, Stephen N.
AU - McDonnell, Shannon K.
AU - Schaid, Daniel J.
AU - Stanford, Janet L.
AU - Kolb, Suzanne
AU - Holt, Sarah
AU - Knudsen, Beatrice
AU - Coll, Antonio Hurtado
AU - Gapstur, Susan M.
AU - Diver, W. Ryan
AU - Stevens, Victoria L.
AU - Maier, Christiane
AU - Luedeke, Manuel
AU - Herkommer, Kathleen
AU - Rinckleb, Antje E.
AU - Strom, Sara S.
AU - Pettaway, Curtis
AU - Yeboah, Edward D.
AU - Tettey, Yao
AU - Biritwum, Richard B.
AU - Adjei, Andrew A.
AU - Tay, Evelyn
AU - Truelove, Ann
AU - Niwa, Shelley
AU - Chokkalingam, Anand P.
AU - Cannon-Albright, Lisa
AU - Cybulski, Cezary
AU - Wokołorczyk, Dominika
AU - Kluźniak, Wojciech
AU - Park, Jong
AU - Sellers, Thomas
AU - Lin, Hui Yi
AU - Isaacs, William B.
AU - Partin, Alan W.
AU - Brenner, Hermann
AU - Dieffenbach, Aida Karina
AU - Stegmaier, Christa
AU - Chen, Constance
AU - Giovannucci, Edward L.
AU - Ma, Jing
AU - Stampfer, Meir
AU - Penney, Kathryn L.
AU - Mucci, Lorelei
AU - John, Esther M.
AU - Ingles, Sue A.
AU - Kittles, Rick A.
AU - Murphy, Adam B.
AU - Pandha, Hardev
AU - Michael, Agnieszka
AU - Kierzek, Andrzej M.
AU - Blot, William
AU - Signorello, Lisa B.
AU - Zheng, Wei
AU - Albanes, Demetrius
AU - Virtamo, Jarmo
AU - Weinstein, Stephanie
AU - Nemesure, Barbara
AU - Carpten, John
AU - Leske, Cristina
AU - Wu, Suh Yuh
AU - Hennis, Anselm
AU - Kibel, Adam S.
AU - Rybicki, Benjamin A.
AU - Neslund-Dudas, Christine
AU - Hsing, Ann W.
AU - Chu, Lisa
AU - Goodman, Phyllis J.
AU - Klein, Eric A.
AU - Zheng, S. Lilly
AU - Batra, Jyotsna
AU - Clements, Judith
AU - Spurdle, Amanda
AU - Teixeira, Manuel R.
AU - Paulo, Paula
AU - Maia, Sofia
AU - Slavov, Chavdar
AU - Kaneva, Radka
AU - Mitev, Vanio
AU - Witte, John S.
AU - Casey, Graham
AU - Gillanders, Elizabeth M.
AU - Seminara, Daniella
AU - Riboli, Elio
AU - Hamdy, Freddie C.
AU - Coetzee, Gerhard A.
AU - Li, Qiyuan
AU - Freedman, Matthew L.
AU - Hunter, David J.
AU - Muir, Kenneth
AU - Gronberg, Henrik
AU - Neal, David E.
AU - Southey, Melissa
AU - Giles, Graham G.
AU - Severi, Gianluca
AU - Cook, Michael B.
AU - Nakagawa, Hidewaki
AU - Wiklund, Fredrik
AU - Kraft, Peter
AU - Chanock, Stephen J.
AU - Henderson, Brian E.
AU - Easton, Douglas F.
AU - Eeles, Rosalind A.
AU - Haiman, Christopher A.
N1 - Publisher Copyright: © 2014 Nature America, Inc. All rights reserved.
PY - 2014/9/26
Y1 - 2014/9/26
N2 - Genome-wide association studies (GWAS) have identified 76 variants associated with prostate cancer risk predominantly in populations of European ancestry. To identify additional susceptibility loci for this common cancer, we conducted a meta-analysis of >10 million SNPs in 43,303 prostate cancer cases and 43,737 controls from studies in populations of European, African, Japanese and Latino ancestry. Twenty-three new susceptibility loci were identified at association P < 5 × 10 â '8; 15 variants were identified among men of European ancestry, 7 were identified in multi-ancestry analyses and 1 was associated with early-onset prostate cancer. These 23 variants, in combination with known prostate cancer risk variants, explain 33% of the familial risk for this disease in European-ancestry populations. These findings provide new regions for investigation into the pathogenesis of prostate cancer and demonstrate the usefulness of combining ancestrally diverse populations to discover risk loci for disease.
AB - Genome-wide association studies (GWAS) have identified 76 variants associated with prostate cancer risk predominantly in populations of European ancestry. To identify additional susceptibility loci for this common cancer, we conducted a meta-analysis of >10 million SNPs in 43,303 prostate cancer cases and 43,737 controls from studies in populations of European, African, Japanese and Latino ancestry. Twenty-three new susceptibility loci were identified at association P < 5 × 10 â '8; 15 variants were identified among men of European ancestry, 7 were identified in multi-ancestry analyses and 1 was associated with early-onset prostate cancer. These 23 variants, in combination with known prostate cancer risk variants, explain 33% of the familial risk for this disease in European-ancestry populations. These findings provide new regions for investigation into the pathogenesis of prostate cancer and demonstrate the usefulness of combining ancestrally diverse populations to discover risk loci for disease.
UR - http://www.scopus.com/inward/record.url?scp=84922011640&partnerID=8YFLogxK
U2 - 10.1038/ng.3094
DO - 10.1038/ng.3094
M3 - Article
C2 - 25217961
AN - SCOPUS:84922011640
SN - 1061-4036
VL - 46
SP - 1103
EP - 1109
JO - Nature Genetics
JF - Nature Genetics
IS - 10
ER -