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Seven novel prostate cancer susceptibility loci identified by a multi-stage genome-wide association study
- Source :
- Kote-Jarai, Z, Olama, A A A, Giles, G G, Severi, G, Schleutker, J, Weischer, M, Campa, D, Riboli, E, Key, T, Gronberg, H, Hunter, D J, Kraft, P, Thun, M J, Ingles, S, Chanock, S, Albanes, D, Hayes, R B, Neal, D E, Hamdy, F C, Donovan, J L, Pharoah, P, Schumacher, F, Henderson, B E, Stanford, J L, Ostrander, E A, Dalsgaard Sorensen, K, Dörk, T, Andriole, G, Dickinson, J L, Cybulski, C, Lubinski, J, Spurdle, A, Clements, J A, Chambers, S, Aitken, J, Gardiner, R A F, Thibodeau, S N, Schaid, D, John, E M, Vogel, W, Cooney, K A, Park, J Y, Cannon-Albright, L, Brenner, H, Habuchi, T, Zhang, H-W, Lu, Y-J, Kaneva, R, Ørntoft, T F, Borre, M & The UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons' Section of Oncology 2011, ' Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study ', Nature Genetics, vol. 43, no. 8, pp. 785-791 . https://doi.org/10.1038/ng.882, Nature Genetics; Vol 43
- Publication Year :
- 2011
-
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 425% of the familial risk in this disease, have now been identified. © 2011 Nature America, Inc. All rights reserved.
- Subjects :
- Oncology
Adult
Male
medicine.medical_specialty
Genotype
Genome-wide association study
Single-nucleotide polymorphism
Biology
urologic and male genital diseases
Polymorphism, Single Nucleotide
Article
Cohort Studies
03 medical and health sciences
Prostate cancer
0302 clinical medicine
Internal medicine
Genetics
medicine
SNP
Chromosomes, Human
Humans
Genotyping
Telomerase
030304 developmental biology
Aged
Randomized Controlled Trials as Topic
Aged, 80 and over
0303 health sciences
Genome, Human
Haplotype
Cancer
Prostatic Neoplasms
Middle Aged
medicine.disease
3. Good health
030220 oncology & carcinogenesis
Case-Control Studies
Immunology
Disease Susceptibility
Genome-Wide Association Study
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Kote-Jarai, Z, Olama, A A A, Giles, G G, Severi, G, Schleutker, J, Weischer, M, Campa, D, Riboli, E, Key, T, Gronberg, H, Hunter, D J, Kraft, P, Thun, M J, Ingles, S, Chanock, S, Albanes, D, Hayes, R B, Neal, D E, Hamdy, F C, Donovan, J L, Pharoah, P, Schumacher, F, Henderson, B E, Stanford, J L, Ostrander, E A, Dalsgaard Sorensen, K, Dörk, T, Andriole, G, Dickinson, J L, Cybulski, C, Lubinski, J, Spurdle, A, Clements, J A, Chambers, S, Aitken, J, Gardiner, R A F, Thibodeau, S N, Schaid, D, John, E M, Vogel, W, Cooney, K A, Park, J Y, Cannon-Albright, L, Brenner, H, Habuchi, T, Zhang, H-W, Lu, Y-J, Kaneva, R, Ørntoft, T F, Borre, M & The UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons' Section of Oncology 2011, ' Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study ', Nature Genetics, vol. 43, no. 8, pp. 785-791 . https://doi.org/10.1038/ng.882, Nature Genetics; Vol 43
- Accession number :
- edsair.doi.dedup.....5df5842449a1acb83bf28bb70dd8a97c
- Full Text :
- https://doi.org/10.1038/ng.882