Back to Search Start Over

Abstract 3517: A germline variant at 8q24 contributes to familial clustering of prostate cancer in men of African ancestry

Authors :
Victoria L. Stevens
Graham Casey
Rick A. Kittles
Geraldine Cancel-Tassin
Rosalind A. Eeles
Jong Y. Park
Marie-Élise Parent
Jianfeng Xu
Shiv Srivastava
James L. Mohler
Jack A. Taylor
Esther M. John
Sonja I. Berndt
William J. Blot
Stephen J. Chanock
Christopher A. Haiman
Florence Menegaux
Gary J. Smith
Barbara Nemesure
Janet L. Stanford
Jay H. Fowke
Wei Zheng
Benjamin A. Rybicki
Phyllis J. Goodman
Adam S. Kibel
Thomas A. Sellers
Eric A. Klein
Anselm Hennis
Dana C. Crawford
Maureen Sanderson
Olivier Cussenot
Elizabeth T. H. Fontham
William B. Isaacs
Jennifer Cullen
John D. Carpten
Robin J. Leach
Diptasri Mandal
Sue A. Ingles
Burcu F. Darst
Luc Multigner
Laurent Brureau
David V. Conti
Stephen Watya
Ian M. Thompson
Zsofia Kote-Jarai
Jennifer J. Hu
Kathleen A. Cooney
Elaine A. Ostrander
Chad D. Huff
Jeannette T. Bensen
Source :
Cancer Research. 80:3517-3517
Publication Year :
2020
Publisher :
American Association for Cancer Research (AACR), 2020.

Abstract

Germline variation at 8q24 is the strongest risk factor for prostate cancer (PCa) across all racial and ethnic populations. While most 8q24 associations have been observed across populations, rs72725854 [T risk allele frequency ~6%] is only found in men of African ancestry and is the strongest known genome-wide association signal for PCa in this population. We investigated whether the T allele of rs72725854 is associated with PCa family history and age at diagnosis, characteristics known to have a strong genetic component. Analyses were performed using a sample of 9,052 cases and 8,595 controls from the African Ancestry Prostate Cancer (AAPC) GWAS Consortium and the ELLIPSE/PRACTICAL OncoArray Consortium. Participants were unselected for PCa family history. Among cases, 23.7% carried at least one copy of the T allele versus 11.6% of controls. The OR was 2.29 (95% CI=2.10–2.49) for TA heterozygotes and 5.04 (95% CI=3.36–7.55) for TT homozygotes. The percentage of cases carrying the T allele was significantly greater for men with a PCa family history (27.4% vs. 22.7% without a family history, p=0.002) and for men diagnosed 100 ng/ml or death from PCa), 25.4% for high-risk disease (stage T3/T4, Gleason 8-10, or PSA=20-100 ng/ml), 24.6% for intermediate-risk disease (Gleason=7, stage T1/T2, and PSA=10-20 ng/ml), and 21.4% for low-risk disease (Gleason Citation Format: Burcu F. Darst, Jeannette T. Bensen, Sue A. Ingles, Benjamin A. Rybicki, Barbara Nemesure, Esther M. John, Jay H. Fowke, Victoria L. Stevens, Sonja I. Berndt, Chad D. Huff, Jong Y. Park, Wei Zheng, Elaine A. Ostrander, Shiv Srivastava, John Carpten, Thomas A. Sellers, Maureen Sanderson, Dana C. Crawford, Olivier Cussenot, Jennifer Cullen, Rick A. Kittles, Jianfeng Xu, Zsofia Kote-Jarai, Luc Multigner, Marie-Elise Parent, Florence Menegaux, Geraldine Cancel-Tassin, Adam S. Kibel, Eric A. Klein, Phyllis J. Goodman, Jennifer J. Hu, Graham Casey, Anselm J. Hennis, Ian M. Thompson, Robin Leach, James L. Mohler, Elizabeth T. Fontham, Gary J. Smith, Jack A. Taylor, Rosalind A. Eeles, Laurent Brureau, Stephen J. Chanock, Stephen Watya, Janet L. Stanford, Diptasri Mandal, William B. Isaacs, Kathleen A. Cooney, William J. Blot, David V. Conti, Christopher A. Haiman. A germline variant at 8q24 contributes to familial clustering of prostate cancer in men of African ancestry [abstract]. In: Proceedings of the Annual Meeting of the American Association for Cancer Research 2020; 2020 Apr 27-28 and Jun 22-24. Philadelphia (PA): AACR; Cancer Res 2020;80(16 Suppl):Abstract nr 3517.

Details

ISSN :
15387445 and 00085472
Volume :
80
Database :
OpenAIRE
Journal :
Cancer Research
Accession number :
edsair.doi...........6cb4d06fc91a0b8bd49a8143d6a48369
Full Text :
https://doi.org/10.1158/1538-7445.am2020-3517