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Characterizing Genetic Risk at Known Prostate Cancer Susceptibility Loci in African Americans

GWAS of prostate cancer have been remarkably successful in revealing common genetic variants and novel biological pathways that are linked with its etiology. A more complete understanding of inherited susceptibility to prostate cancer in the general population will come from continuing such discover...

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Autores principales: Haiman, Christopher A., Chen, Gary K., Blot, William J., Strom, Sara S., Berndt, Sonja I., Kittles, Rick A., Rybicki, Benjamin A., Isaacs, William B., Ingles, Sue A., Stanford, Janet L., Diver, W. Ryan, Witte, John S., Chanock, Stephen J., Kolb, Suzanne, Signorello, Lisa B., Yamamura, Yuko, Neslund-Dudas, Christine, Thun, Michael J., Murphy, Adam, Casey, Graham, Sheng, Xin, Wan, Peggy, Pooler, Loreall C., Monroe, Kristine R., Waters, Kevin M., Le Marchand, Loic, Kolonel, Laurence N., Stram, Daniel O., Henderson, Brian E.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102736/
https://www.ncbi.nlm.nih.gov/pubmed/21637779
http://dx.doi.org/10.1371/journal.pgen.1001387
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author Haiman, Christopher A.
Chen, Gary K.
Blot, William J.
Strom, Sara S.
Berndt, Sonja I.
Kittles, Rick A.
Rybicki, Benjamin A.
Isaacs, William B.
Ingles, Sue A.
Stanford, Janet L.
Diver, W. Ryan
Witte, John S.
Chanock, Stephen J.
Kolb, Suzanne
Signorello, Lisa B.
Yamamura, Yuko
Neslund-Dudas, Christine
Thun, Michael J.
Murphy, Adam
Casey, Graham
Sheng, Xin
Wan, Peggy
Pooler, Loreall C.
Monroe, Kristine R.
Waters, Kevin M.
Le Marchand, Loic
Kolonel, Laurence N.
Stram, Daniel O.
Henderson, Brian E.
author_facet Haiman, Christopher A.
Chen, Gary K.
Blot, William J.
Strom, Sara S.
Berndt, Sonja I.
Kittles, Rick A.
Rybicki, Benjamin A.
Isaacs, William B.
Ingles, Sue A.
Stanford, Janet L.
Diver, W. Ryan
Witte, John S.
Chanock, Stephen J.
Kolb, Suzanne
Signorello, Lisa B.
Yamamura, Yuko
Neslund-Dudas, Christine
Thun, Michael J.
Murphy, Adam
Casey, Graham
Sheng, Xin
Wan, Peggy
Pooler, Loreall C.
Monroe, Kristine R.
Waters, Kevin M.
Le Marchand, Loic
Kolonel, Laurence N.
Stram, Daniel O.
Henderson, Brian E.
author_sort Haiman, Christopher A.
collection PubMed
description GWAS of prostate cancer have been remarkably successful in revealing common genetic variants and novel biological pathways that are linked with its etiology. A more complete understanding of inherited susceptibility to prostate cancer in the general population will come from continuing such discovery efforts and from testing known risk alleles in diverse racial and ethnic groups. In this large study of prostate cancer in African American men (3,425 prostate cancer cases and 3,290 controls), we tested 49 risk variants located in 28 genomic regions identified through GWAS in men of European and Asian descent, and we replicated associations (at p≤0.05) with roughly half of these markers. Through fine-mapping, we identified nearby markers in many regions that better define associations in African Americans. At 8q24, we found 9 variants (p≤6×10(−4)) that best capture risk of prostate cancer in African Americans, many of which are more common in men of African than European descent. The markers found to be associated with risk at each locus improved risk modeling in African Americans (per allele OR = 1.17) over the alleles reported in the original GWAS (OR = 1.08). In summary, in this detailed analysis of the prostate cancer risk loci reported from GWAS, we have validated and improved upon markers of risk in some regions that better define the association with prostate cancer in African Americans. Our findings with variants at 8q24 also reinforce the importance of this region as a major risk locus for prostate cancer in men of African ancestry.
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spelling pubmed-31027362011-06-02 Characterizing Genetic Risk at Known Prostate Cancer Susceptibility Loci in African Americans Haiman, Christopher A. Chen, Gary K. Blot, William J. Strom, Sara S. Berndt, Sonja I. Kittles, Rick A. Rybicki, Benjamin A. Isaacs, William B. Ingles, Sue A. Stanford, Janet L. Diver, W. Ryan Witte, John S. Chanock, Stephen J. Kolb, Suzanne Signorello, Lisa B. Yamamura, Yuko Neslund-Dudas, Christine Thun, Michael J. Murphy, Adam Casey, Graham Sheng, Xin Wan, Peggy Pooler, Loreall C. Monroe, Kristine R. Waters, Kevin M. Le Marchand, Loic Kolonel, Laurence N. Stram, Daniel O. Henderson, Brian E. PLoS Genet Research Article GWAS of prostate cancer have been remarkably successful in revealing common genetic variants and novel biological pathways that are linked with its etiology. A more complete understanding of inherited susceptibility to prostate cancer in the general population will come from continuing such discovery efforts and from testing known risk alleles in diverse racial and ethnic groups. In this large study of prostate cancer in African American men (3,425 prostate cancer cases and 3,290 controls), we tested 49 risk variants located in 28 genomic regions identified through GWAS in men of European and Asian descent, and we replicated associations (at p≤0.05) with roughly half of these markers. Through fine-mapping, we identified nearby markers in many regions that better define associations in African Americans. At 8q24, we found 9 variants (p≤6×10(−4)) that best capture risk of prostate cancer in African Americans, many of which are more common in men of African than European descent. The markers found to be associated with risk at each locus improved risk modeling in African Americans (per allele OR = 1.17) over the alleles reported in the original GWAS (OR = 1.08). In summary, in this detailed analysis of the prostate cancer risk loci reported from GWAS, we have validated and improved upon markers of risk in some regions that better define the association with prostate cancer in African Americans. Our findings with variants at 8q24 also reinforce the importance of this region as a major risk locus for prostate cancer in men of African ancestry. Public Library of Science 2011-05-26 /pmc/articles/PMC3102736/ /pubmed/21637779 http://dx.doi.org/10.1371/journal.pgen.1001387 Text en This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Haiman, Christopher A.
Chen, Gary K.
Blot, William J.
Strom, Sara S.
Berndt, Sonja I.
Kittles, Rick A.
Rybicki, Benjamin A.
Isaacs, William B.
Ingles, Sue A.
Stanford, Janet L.
Diver, W. Ryan
Witte, John S.
Chanock, Stephen J.
Kolb, Suzanne
Signorello, Lisa B.
Yamamura, Yuko
Neslund-Dudas, Christine
Thun, Michael J.
Murphy, Adam
Casey, Graham
Sheng, Xin
Wan, Peggy
Pooler, Loreall C.
Monroe, Kristine R.
Waters, Kevin M.
Le Marchand, Loic
Kolonel, Laurence N.
Stram, Daniel O.
Henderson, Brian E.
Characterizing Genetic Risk at Known Prostate Cancer Susceptibility Loci in African Americans
title Characterizing Genetic Risk at Known Prostate Cancer Susceptibility Loci in African Americans
title_full Characterizing Genetic Risk at Known Prostate Cancer Susceptibility Loci in African Americans
title_fullStr Characterizing Genetic Risk at Known Prostate Cancer Susceptibility Loci in African Americans
title_full_unstemmed Characterizing Genetic Risk at Known Prostate Cancer Susceptibility Loci in African Americans
title_short Characterizing Genetic Risk at Known Prostate Cancer Susceptibility Loci in African Americans
title_sort characterizing genetic risk at known prostate cancer susceptibility loci in african americans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102736/
https://www.ncbi.nlm.nih.gov/pubmed/21637779
http://dx.doi.org/10.1371/journal.pgen.1001387
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