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Vitamin D3 constrains estrogen’s effects and influences mammary epithelial organization in 3D cultures
Vitamin D3 (vitD3) and its active metabolite, calcitriol (1,25-(OH)(2)D(3)), affect multiple tissue types by interacting with the vitamin D receptor (VDR). Although vitD3 deficiency has been correlated with increased incidence of breast cancer and less favorable outcomes, randomized clinical trials...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520380/ https://www.ncbi.nlm.nih.gov/pubmed/31092845 http://dx.doi.org/10.1038/s41598-019-43308-1 |
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author | Hasan, Nafis Sonnenschein, Carlos Soto, Ana M. |
author_facet | Hasan, Nafis Sonnenschein, Carlos Soto, Ana M. |
author_sort | Hasan, Nafis |
collection | PubMed |
description | Vitamin D3 (vitD3) and its active metabolite, calcitriol (1,25-(OH)(2)D(3)), affect multiple tissue types by interacting with the vitamin D receptor (VDR). Although vitD3 deficiency has been correlated with increased incidence of breast cancer and less favorable outcomes, randomized clinical trials have yet to provide conclusive evidence on the efficacy of vitD3 in preventing or treating breast cancer. Additionally, experimental studies are needed to assess the biological plausibility of these outcomes. The mammary gland of VDR KO mice shows a florid phenotype revealing alterations of developmental processes that are largely regulated by mammotropic hormones. However, most research conducted on vitD3’s effects used 2D cell cultures and supra-physiological doses of vitD3, conditions that spare the microenvironment in which morphogenesis takes place. We investigated the role of vitD3 in mammary epithelial morphogenesis using two 3D culture models. VitD3 interfered with estrogen’s actions on T47D human breast cancer cells in 3D differently at different doses, and recapitulated what is observed in vivo. Also, vitD3 can act autonomously and affected the organization of estrogen-insensitive MCF10A cells in 3D collagen matrix by influencing collagen fiber organization. Thus, vitD3 modulates mammary tissue organization independent of its effects on cell proliferation. |
format | Online Article Text |
id | pubmed-6520380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65203802019-05-28 Vitamin D3 constrains estrogen’s effects and influences mammary epithelial organization in 3D cultures Hasan, Nafis Sonnenschein, Carlos Soto, Ana M. Sci Rep Article Vitamin D3 (vitD3) and its active metabolite, calcitriol (1,25-(OH)(2)D(3)), affect multiple tissue types by interacting with the vitamin D receptor (VDR). Although vitD3 deficiency has been correlated with increased incidence of breast cancer and less favorable outcomes, randomized clinical trials have yet to provide conclusive evidence on the efficacy of vitD3 in preventing or treating breast cancer. Additionally, experimental studies are needed to assess the biological plausibility of these outcomes. The mammary gland of VDR KO mice shows a florid phenotype revealing alterations of developmental processes that are largely regulated by mammotropic hormones. However, most research conducted on vitD3’s effects used 2D cell cultures and supra-physiological doses of vitD3, conditions that spare the microenvironment in which morphogenesis takes place. We investigated the role of vitD3 in mammary epithelial morphogenesis using two 3D culture models. VitD3 interfered with estrogen’s actions on T47D human breast cancer cells in 3D differently at different doses, and recapitulated what is observed in vivo. Also, vitD3 can act autonomously and affected the organization of estrogen-insensitive MCF10A cells in 3D collagen matrix by influencing collagen fiber organization. Thus, vitD3 modulates mammary tissue organization independent of its effects on cell proliferation. Nature Publishing Group UK 2019-05-15 /pmc/articles/PMC6520380/ /pubmed/31092845 http://dx.doi.org/10.1038/s41598-019-43308-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Hasan, Nafis Sonnenschein, Carlos Soto, Ana M. Vitamin D3 constrains estrogen’s effects and influences mammary epithelial organization in 3D cultures |
title | Vitamin D3 constrains estrogen’s effects and influences mammary epithelial organization in 3D cultures |
title_full | Vitamin D3 constrains estrogen’s effects and influences mammary epithelial organization in 3D cultures |
title_fullStr | Vitamin D3 constrains estrogen’s effects and influences mammary epithelial organization in 3D cultures |
title_full_unstemmed | Vitamin D3 constrains estrogen’s effects and influences mammary epithelial organization in 3D cultures |
title_short | Vitamin D3 constrains estrogen’s effects and influences mammary epithelial organization in 3D cultures |
title_sort | vitamin d3 constrains estrogen’s effects and influences mammary epithelial organization in 3d cultures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520380/ https://www.ncbi.nlm.nih.gov/pubmed/31092845 http://dx.doi.org/10.1038/s41598-019-43308-1 |
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