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Admixture Mapping of African–American Women in the AMBER Consortium Identifies New Loci for Breast Cancer and Estrogen-Receptor Subtypes

Recent genetic admixture coupled with striking differences in incidence of estrogen receptor (ER) breast cancer subtypes, as well as severity, between women of African and European ancestry, provides an excellent rationale for performing admixture mapping in African American women with breast cancer...

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Autores principales: Ruiz-Narváez, Edward A., Sucheston-Campbell, Lara, Bensen, Jeannette T., Yao, Song, Haddad, Stephen, Haiman, Christopher A., Bandera, Elisa V., John, Esther M., Bernstein, Leslie, Hu, Jennifer J., Ziegler, Regina G., Deming, Sandra L., Olshan, Andrew F., Ambrosone, Christine B., Palmer, Julie R., Lunetta, Kathryn L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030764/
https://www.ncbi.nlm.nih.gov/pubmed/27708667
http://dx.doi.org/10.3389/fgene.2016.00170
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author Ruiz-Narváez, Edward A.
Sucheston-Campbell, Lara
Bensen, Jeannette T.
Yao, Song
Haddad, Stephen
Haiman, Christopher A.
Bandera, Elisa V.
John, Esther M.
Bernstein, Leslie
Hu, Jennifer J.
Ziegler, Regina G.
Deming, Sandra L.
Olshan, Andrew F.
Ambrosone, Christine B.
Palmer, Julie R.
Lunetta, Kathryn L.
author_facet Ruiz-Narváez, Edward A.
Sucheston-Campbell, Lara
Bensen, Jeannette T.
Yao, Song
Haddad, Stephen
Haiman, Christopher A.
Bandera, Elisa V.
John, Esther M.
Bernstein, Leslie
Hu, Jennifer J.
Ziegler, Regina G.
Deming, Sandra L.
Olshan, Andrew F.
Ambrosone, Christine B.
Palmer, Julie R.
Lunetta, Kathryn L.
author_sort Ruiz-Narváez, Edward A.
collection PubMed
description Recent genetic admixture coupled with striking differences in incidence of estrogen receptor (ER) breast cancer subtypes, as well as severity, between women of African and European ancestry, provides an excellent rationale for performing admixture mapping in African American women with breast cancer risk. We performed the largest breast cancer admixture mapping study with in African American women to identify novel genomic regions associated with the disease. We conducted a genome-wide admixture scan using 2,624 autosomal ancestry informative markers (AIMs) in 3,629 breast cancer cases (including 1,968 ER-positive, 1093 ER-negative, and 601 triple-negative) and 4,658 controls from the African American Breast Cancer Epidemiology and Risk (AMBER) Consortium, a collaborative study of four large geographically different epidemiological studies of breast cancer in African American women. We used an independent case-control study to test for SNP association in regions with genome-wide significant admixture signals. We found two novel genome-wide significant regions of excess African ancestry, 4p16.1 and 17q25.1, associated with ER-positive breast cancer. Two regions known to harbor breast cancer variants, 10q26 and 11q13, were also identified with excess of African ancestry. Fine-mapping of the identified genome-wide significant regions suggests the presence of significant genetic associations with ER-positive breast cancer in 4p16.1 and 11q13. In summary, we identified three novel genomic regions associated with breast cancer risk by ER status, suggesting that additional previously unidentified variants may contribute to the racial differences in breast cancer risk in the African American population.
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spelling pubmed-50307642016-10-05 Admixture Mapping of African–American Women in the AMBER Consortium Identifies New Loci for Breast Cancer and Estrogen-Receptor Subtypes Ruiz-Narváez, Edward A. Sucheston-Campbell, Lara Bensen, Jeannette T. Yao, Song Haddad, Stephen Haiman, Christopher A. Bandera, Elisa V. John, Esther M. Bernstein, Leslie Hu, Jennifer J. Ziegler, Regina G. Deming, Sandra L. Olshan, Andrew F. Ambrosone, Christine B. Palmer, Julie R. Lunetta, Kathryn L. Front Genet Genetics Recent genetic admixture coupled with striking differences in incidence of estrogen receptor (ER) breast cancer subtypes, as well as severity, between women of African and European ancestry, provides an excellent rationale for performing admixture mapping in African American women with breast cancer risk. We performed the largest breast cancer admixture mapping study with in African American women to identify novel genomic regions associated with the disease. We conducted a genome-wide admixture scan using 2,624 autosomal ancestry informative markers (AIMs) in 3,629 breast cancer cases (including 1,968 ER-positive, 1093 ER-negative, and 601 triple-negative) and 4,658 controls from the African American Breast Cancer Epidemiology and Risk (AMBER) Consortium, a collaborative study of four large geographically different epidemiological studies of breast cancer in African American women. We used an independent case-control study to test for SNP association in regions with genome-wide significant admixture signals. We found two novel genome-wide significant regions of excess African ancestry, 4p16.1 and 17q25.1, associated with ER-positive breast cancer. Two regions known to harbor breast cancer variants, 10q26 and 11q13, were also identified with excess of African ancestry. Fine-mapping of the identified genome-wide significant regions suggests the presence of significant genetic associations with ER-positive breast cancer in 4p16.1 and 11q13. In summary, we identified three novel genomic regions associated with breast cancer risk by ER status, suggesting that additional previously unidentified variants may contribute to the racial differences in breast cancer risk in the African American population. Frontiers Media S.A. 2016-09-21 /pmc/articles/PMC5030764/ /pubmed/27708667 http://dx.doi.org/10.3389/fgene.2016.00170 Text en Copyright © 2016 Ruiz-Narváez, Sucheston-Campbell, Bensen, Yao, Haddad, Haiman, Bandera, John, Bernstein, Hu, Ziegler, Deming, Olshan, Ambrosone, Palmer and Lunetta. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Ruiz-Narváez, Edward A.
Sucheston-Campbell, Lara
Bensen, Jeannette T.
Yao, Song
Haddad, Stephen
Haiman, Christopher A.
Bandera, Elisa V.
John, Esther M.
Bernstein, Leslie
Hu, Jennifer J.
Ziegler, Regina G.
Deming, Sandra L.
Olshan, Andrew F.
Ambrosone, Christine B.
Palmer, Julie R.
Lunetta, Kathryn L.
Admixture Mapping of African–American Women in the AMBER Consortium Identifies New Loci for Breast Cancer and Estrogen-Receptor Subtypes
title Admixture Mapping of African–American Women in the AMBER Consortium Identifies New Loci for Breast Cancer and Estrogen-Receptor Subtypes
title_full Admixture Mapping of African–American Women in the AMBER Consortium Identifies New Loci for Breast Cancer and Estrogen-Receptor Subtypes
title_fullStr Admixture Mapping of African–American Women in the AMBER Consortium Identifies New Loci for Breast Cancer and Estrogen-Receptor Subtypes
title_full_unstemmed Admixture Mapping of African–American Women in the AMBER Consortium Identifies New Loci for Breast Cancer and Estrogen-Receptor Subtypes
title_short Admixture Mapping of African–American Women in the AMBER Consortium Identifies New Loci for Breast Cancer and Estrogen-Receptor Subtypes
title_sort admixture mapping of african–american women in the amber consortium identifies new loci for breast cancer and estrogen-receptor subtypes
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030764/
https://www.ncbi.nlm.nih.gov/pubmed/27708667
http://dx.doi.org/10.3389/fgene.2016.00170
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