Most men diagnosed with prostate cancer will experience indolent disease; hence, discovering genetic variants that distinguish aggressive from nonaggressive prostate cancer is of critical clinical importance for disease prevention and treatment. In a multistage, case-only genome-wide association study of 12,518 prostate cancer cases, we identify two loci associated with Gleason score, a pathological measure of disease aggressiveness: rs35148638 at 5q14.3 (RASA1, P=6.49 × 10(-9)) and rs78943174 at 3q26.31 (NAALADL2, P=4.18 × 10(-8)). In a stratified case-control analysis, the SNP at 5q14.3 appears specific for aggressive prostate cancer (P=8.85 × 10(-5)) with no association for nonaggressive prostate cancer compared with controls (P=0.57). The proximity of these loci to genes involved in vascular disease suggests potential biological mechanisms worthy of further investigation.

Two susceptibility loci identified for prostate cancer aggressiveness.

Campa, D;
2015-01-01

Abstract

Most men diagnosed with prostate cancer will experience indolent disease; hence, discovering genetic variants that distinguish aggressive from nonaggressive prostate cancer is of critical clinical importance for disease prevention and treatment. In a multistage, case-only genome-wide association study of 12,518 prostate cancer cases, we identify two loci associated with Gleason score, a pathological measure of disease aggressiveness: rs35148638 at 5q14.3 (RASA1, P=6.49 × 10(-9)) and rs78943174 at 3q26.31 (NAALADL2, P=4.18 × 10(-8)). In a stratified case-control analysis, the SNP at 5q14.3 appears specific for aggressive prostate cancer (P=8.85 × 10(-5)) with no association for nonaggressive prostate cancer compared with controls (P=0.57). The proximity of these loci to genes involved in vascular disease suggests potential biological mechanisms worthy of further investigation.
2015
Berndt, Si; Wang, Z; Yeager, M; Alavanja, Mc; Albanes, D; Amundadottir, L; Andriole, G; Beane Freeman, L; Campa, D; Cancel-Tassin, G; Canzian, F; Cornu, Jn; Cussenot, O; Diver, Wr; Gapstur, Sm; Grönberg, H; Haiman, Ca; Henderson, B; Hutchinson, A; Hunter, Dj; Key, Tj; Kolb, S; Koutros, S; Kraft, P; Le Marchand, L; Lindström, S; Machiela, Mj; Ostrander, Ea; Riboli, E; Schumacher, F; Siddiq, A; Stanford, Jl; Stevens, Vl; Travis, Rc; Tsilidis, Kk; Virtamo, J; Weinstein, S; Wilkund, F; Xu, J; Lilly Zheng, S; Yu, K; Wheeler, W; Zhang, H; African, Ancestry Prostate Cancer GWAS Consortium; Sampson, J; Black, A; Jacobs, K; Hoover, Rn; Tucker, M; Chanock, Sj. Ingles SA; Kittles, Ra; Strom, Ss; Rybicki, Ba; Nemesure, B; Isaacs, Wb; Zheng, W; Pettaway, Ca; Yeboah, Ed; Tettey, Y; Biritwum, Rb; Adjei, Aa; Tay, E; Truelove, A; Niwa, S; Chokkalingam, Ap; John, Em; Murphy, Ab; Signorello, Lb; Carpten, J; Leske, Mc; Wu, Sy; Hennis, Aj; Neslund-Dudas, C; Hsing, Aw; Chu, L; Goodman, Pj; Klein, Ea; Witte, Js; Casey, G; Kaggwa, S; Cook, Mb; Stram, Do; Blot, Wj.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/779527
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