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New insights into fetal mammary gland morphogenesis: differential effects of natural and environmental estrogens
An increased breast cancer risk during adulthood has been linked to estrogen exposure during fetal life. However, the impossibility of removing estrogens from the feto-maternal unit has hindered the testing of estrogen’s direct effect on mammary gland organogenesis. To overcome this limitation, we d...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244390/ https://www.ncbi.nlm.nih.gov/pubmed/28102330 http://dx.doi.org/10.1038/srep40806 |
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author | Speroni, Lucia Voutilainen, Maria Mikkola, Marja L. Klager, Skylar A. Schaeberle, Cheryl M. Sonnenschein, Carlos Soto, Ana M. |
author_facet | Speroni, Lucia Voutilainen, Maria Mikkola, Marja L. Klager, Skylar A. Schaeberle, Cheryl M. Sonnenschein, Carlos Soto, Ana M. |
author_sort | Speroni, Lucia |
collection | PubMed |
description | An increased breast cancer risk during adulthood has been linked to estrogen exposure during fetal life. However, the impossibility of removing estrogens from the feto-maternal unit has hindered the testing of estrogen’s direct effect on mammary gland organogenesis. To overcome this limitation, we developed an ex vivo culture method of the mammary gland where the direct action of estrogens can be tested during embryonic days (E)14 to 19. Mouse mammary buds dissected at E14 and cultured for 5 days showed that estrogens directly altered fetal mammary gland development. Exposure to 0.1 pM, 10 pM, and 1 nM 17 β-estradiol (E2) resulted in monotonic inhibition of mammary buds ductal growth. In contrast, Bisphenol-A (BPA) elicited a non-monotonic response. At environmentally relevant doses (1 nM), BPA significantly increased ductal growth, as previously observed in vivo, while 1 μM BPA significantly inhibited ductal growth. Ductal branching followed the same pattern. This effect of BPA was blocked by Fulvestrant, a full estrogen antagonist, while the effect of estradiol was not. This method may be used to study the hormonal regulation of mammary gland development, and to test newly synthesized chemicals that are released into the environment without proper assessment of their hormonal action on critical targets like the mammary gland. |
format | Online Article Text |
id | pubmed-5244390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52443902017-01-23 New insights into fetal mammary gland morphogenesis: differential effects of natural and environmental estrogens Speroni, Lucia Voutilainen, Maria Mikkola, Marja L. Klager, Skylar A. Schaeberle, Cheryl M. Sonnenschein, Carlos Soto, Ana M. Sci Rep Article An increased breast cancer risk during adulthood has been linked to estrogen exposure during fetal life. However, the impossibility of removing estrogens from the feto-maternal unit has hindered the testing of estrogen’s direct effect on mammary gland organogenesis. To overcome this limitation, we developed an ex vivo culture method of the mammary gland where the direct action of estrogens can be tested during embryonic days (E)14 to 19. Mouse mammary buds dissected at E14 and cultured for 5 days showed that estrogens directly altered fetal mammary gland development. Exposure to 0.1 pM, 10 pM, and 1 nM 17 β-estradiol (E2) resulted in monotonic inhibition of mammary buds ductal growth. In contrast, Bisphenol-A (BPA) elicited a non-monotonic response. At environmentally relevant doses (1 nM), BPA significantly increased ductal growth, as previously observed in vivo, while 1 μM BPA significantly inhibited ductal growth. Ductal branching followed the same pattern. This effect of BPA was blocked by Fulvestrant, a full estrogen antagonist, while the effect of estradiol was not. This method may be used to study the hormonal regulation of mammary gland development, and to test newly synthesized chemicals that are released into the environment without proper assessment of their hormonal action on critical targets like the mammary gland. Nature Publishing Group 2017-01-19 /pmc/articles/PMC5244390/ /pubmed/28102330 http://dx.doi.org/10.1038/srep40806 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Speroni, Lucia Voutilainen, Maria Mikkola, Marja L. Klager, Skylar A. Schaeberle, Cheryl M. Sonnenschein, Carlos Soto, Ana M. New insights into fetal mammary gland morphogenesis: differential effects of natural and environmental estrogens |
title | New insights into fetal mammary gland morphogenesis: differential effects of natural and environmental estrogens |
title_full | New insights into fetal mammary gland morphogenesis: differential effects of natural and environmental estrogens |
title_fullStr | New insights into fetal mammary gland morphogenesis: differential effects of natural and environmental estrogens |
title_full_unstemmed | New insights into fetal mammary gland morphogenesis: differential effects of natural and environmental estrogens |
title_short | New insights into fetal mammary gland morphogenesis: differential effects of natural and environmental estrogens |
title_sort | new insights into fetal mammary gland morphogenesis: differential effects of natural and environmental estrogens |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5244390/ https://www.ncbi.nlm.nih.gov/pubmed/28102330 http://dx.doi.org/10.1038/srep40806 |
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