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Reversion of breast epithelial polarity alterations caused by obesity
Molecular links between breast cancer risk factors and pro-oncogenic tissue alterations are poorly understood. The goal of this study was to characterize the impact of overweight and obesity on tissue markers of risk, using normal breast biopsies, a mouse model of diet-induced obesity, and cultured...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10170133/ https://www.ncbi.nlm.nih.gov/pubmed/37160903 http://dx.doi.org/10.1038/s41523-023-00539-w |
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author | Holmes, Julia Gaber, Mohamed Jenks, Mónica Z. Wilson, Adam Loy, Tucker Lepetit, Cassandra Vitolins, Mara Z. Herbert, Brittney-Shea Cook, Katherine L. Vidi, Pierre-Alexandre |
author_facet | Holmes, Julia Gaber, Mohamed Jenks, Mónica Z. Wilson, Adam Loy, Tucker Lepetit, Cassandra Vitolins, Mara Z. Herbert, Brittney-Shea Cook, Katherine L. Vidi, Pierre-Alexandre |
author_sort | Holmes, Julia |
collection | PubMed |
description | Molecular links between breast cancer risk factors and pro-oncogenic tissue alterations are poorly understood. The goal of this study was to characterize the impact of overweight and obesity on tissue markers of risk, using normal breast biopsies, a mouse model of diet-induced obesity, and cultured breast acini. Proliferation and alteration of epithelial polarity, both necessary for tumor initiation, were quantified by immunostaining. High BMI (>30) and elevated leptin were associated with compromised epithelial polarity whereas overweight was associated with a modest increase in proliferation in human and mice mammary glands. Human serum with unfavorable adipokine levels altered epithelial polarization of cultured acini, recapitulating the effect of leptin. Weight loss in mice led to metabolic improvements and restored epithelial polarity. In acini cultures, alteration of epithelial polarity was prevented by antioxidants and could be reverted by normalizing culture conditions. This study shows that obesity and/or dietary factors modulate tissue markers of risk. It provides a framework to set target values for metabolic improvements and to assess the efficacy of interventional studies aimed at reducing breast cancer risk. |
format | Online Article Text |
id | pubmed-10170133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-101701332023-05-11 Reversion of breast epithelial polarity alterations caused by obesity Holmes, Julia Gaber, Mohamed Jenks, Mónica Z. Wilson, Adam Loy, Tucker Lepetit, Cassandra Vitolins, Mara Z. Herbert, Brittney-Shea Cook, Katherine L. Vidi, Pierre-Alexandre NPJ Breast Cancer Article Molecular links between breast cancer risk factors and pro-oncogenic tissue alterations are poorly understood. The goal of this study was to characterize the impact of overweight and obesity on tissue markers of risk, using normal breast biopsies, a mouse model of diet-induced obesity, and cultured breast acini. Proliferation and alteration of epithelial polarity, both necessary for tumor initiation, were quantified by immunostaining. High BMI (>30) and elevated leptin were associated with compromised epithelial polarity whereas overweight was associated with a modest increase in proliferation in human and mice mammary glands. Human serum with unfavorable adipokine levels altered epithelial polarization of cultured acini, recapitulating the effect of leptin. Weight loss in mice led to metabolic improvements and restored epithelial polarity. In acini cultures, alteration of epithelial polarity was prevented by antioxidants and could be reverted by normalizing culture conditions. This study shows that obesity and/or dietary factors modulate tissue markers of risk. It provides a framework to set target values for metabolic improvements and to assess the efficacy of interventional studies aimed at reducing breast cancer risk. Nature Publishing Group UK 2023-05-09 /pmc/articles/PMC10170133/ /pubmed/37160903 http://dx.doi.org/10.1038/s41523-023-00539-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Holmes, Julia Gaber, Mohamed Jenks, Mónica Z. Wilson, Adam Loy, Tucker Lepetit, Cassandra Vitolins, Mara Z. Herbert, Brittney-Shea Cook, Katherine L. Vidi, Pierre-Alexandre Reversion of breast epithelial polarity alterations caused by obesity |
title | Reversion of breast epithelial polarity alterations caused by obesity |
title_full | Reversion of breast epithelial polarity alterations caused by obesity |
title_fullStr | Reversion of breast epithelial polarity alterations caused by obesity |
title_full_unstemmed | Reversion of breast epithelial polarity alterations caused by obesity |
title_short | Reversion of breast epithelial polarity alterations caused by obesity |
title_sort | reversion of breast epithelial polarity alterations caused by obesity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10170133/ https://www.ncbi.nlm.nih.gov/pubmed/37160903 http://dx.doi.org/10.1038/s41523-023-00539-w |
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