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Estrogenic activity, race/ethnicity, and Indigenous American ancestry among San Francisco Bay Area women
Estrogens play a significant role in breast cancer development and are not only produced endogenously, but are also mimicked by estrogen-like compounds from environmental exposures. We evaluated associations between estrogenic (E) activity, demographic factors and breast cancer risk factors in Non-L...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6433244/ https://www.ncbi.nlm.nih.gov/pubmed/30908519 http://dx.doi.org/10.1371/journal.pone.0213809 |
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author | Sanchez, Sylvia S. Tachachartvanich, Phum Stanczyk, Frank Z. Gomez, Scarlett L. John, Esther M. Smith, Martyn T. Fejerman, Laura |
author_facet | Sanchez, Sylvia S. Tachachartvanich, Phum Stanczyk, Frank Z. Gomez, Scarlett L. John, Esther M. Smith, Martyn T. Fejerman, Laura |
author_sort | Sanchez, Sylvia S. |
collection | PubMed |
description | Estrogens play a significant role in breast cancer development and are not only produced endogenously, but are also mimicked by estrogen-like compounds from environmental exposures. We evaluated associations between estrogenic (E) activity, demographic factors and breast cancer risk factors in Non-Latina Black (NLB), Non-Latina White (NLW), and Latina women. We examined the association between E activity and Indigenous American (IA) ancestry in Latina women. Total E activity was measured with a bioassay in plasma samples of 503 women who served as controls in the San Francisco Bay Area Breast Cancer Study. In the univariate model that included all women with race/ethnicity as the independent predictor, Latinas had 13% lower E activity (p = 0.239) and NLBs had 35% higher activity (p = 0.04) compared to NLWs. In the multivariable model that adjusted for demographic factors, Latinas continued to show lower E activity levels (26%, p = 0.026), but the difference between NLBs and NLWs was no longer statistically significant (p = 0.431). An inverse association was observed between E activity and IA ancestry among Latina women (50% lower in 0% vs. 100% European ancestry, p = 0.027) consistent with our previously reported association between IA ancestry and breast cancer risk. These findings suggest that endogenous estrogens and exogenous estrogen-like compounds that act on the estrogen receptor and modulate E activity may partially explain racial/ethnic differences in breast cancer risk. |
format | Online Article Text |
id | pubmed-6433244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64332442019-04-08 Estrogenic activity, race/ethnicity, and Indigenous American ancestry among San Francisco Bay Area women Sanchez, Sylvia S. Tachachartvanich, Phum Stanczyk, Frank Z. Gomez, Scarlett L. John, Esther M. Smith, Martyn T. Fejerman, Laura PLoS One Research Article Estrogens play a significant role in breast cancer development and are not only produced endogenously, but are also mimicked by estrogen-like compounds from environmental exposures. We evaluated associations between estrogenic (E) activity, demographic factors and breast cancer risk factors in Non-Latina Black (NLB), Non-Latina White (NLW), and Latina women. We examined the association between E activity and Indigenous American (IA) ancestry in Latina women. Total E activity was measured with a bioassay in plasma samples of 503 women who served as controls in the San Francisco Bay Area Breast Cancer Study. In the univariate model that included all women with race/ethnicity as the independent predictor, Latinas had 13% lower E activity (p = 0.239) and NLBs had 35% higher activity (p = 0.04) compared to NLWs. In the multivariable model that adjusted for demographic factors, Latinas continued to show lower E activity levels (26%, p = 0.026), but the difference between NLBs and NLWs was no longer statistically significant (p = 0.431). An inverse association was observed between E activity and IA ancestry among Latina women (50% lower in 0% vs. 100% European ancestry, p = 0.027) consistent with our previously reported association between IA ancestry and breast cancer risk. These findings suggest that endogenous estrogens and exogenous estrogen-like compounds that act on the estrogen receptor and modulate E activity may partially explain racial/ethnic differences in breast cancer risk. Public Library of Science 2019-03-25 /pmc/articles/PMC6433244/ /pubmed/30908519 http://dx.doi.org/10.1371/journal.pone.0213809 Text en © 2019 Sanchez et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Sanchez, Sylvia S. Tachachartvanich, Phum Stanczyk, Frank Z. Gomez, Scarlett L. John, Esther M. Smith, Martyn T. Fejerman, Laura Estrogenic activity, race/ethnicity, and Indigenous American ancestry among San Francisco Bay Area women |
title | Estrogenic activity, race/ethnicity, and Indigenous American ancestry among San Francisco Bay Area women |
title_full | Estrogenic activity, race/ethnicity, and Indigenous American ancestry among San Francisco Bay Area women |
title_fullStr | Estrogenic activity, race/ethnicity, and Indigenous American ancestry among San Francisco Bay Area women |
title_full_unstemmed | Estrogenic activity, race/ethnicity, and Indigenous American ancestry among San Francisco Bay Area women |
title_short | Estrogenic activity, race/ethnicity, and Indigenous American ancestry among San Francisco Bay Area women |
title_sort | estrogenic activity, race/ethnicity, and indigenous american ancestry among san francisco bay area women |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6433244/ https://www.ncbi.nlm.nih.gov/pubmed/30908519 http://dx.doi.org/10.1371/journal.pone.0213809 |
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