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Epigenetic Regulation and Dietary Control of Triple Negative Breast Cancer
Triple negative breast cancer (TNBC) represents a highly heterogeneous group of breast cancers, lacking expression of the estrogen (ER) and progesterone (PR) receptors, and human epidermal growth factor receptor 2 (HER2). TNBC are characterized by a high level of mutation and metastasis, poor clinic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7506147/ https://www.ncbi.nlm.nih.gov/pubmed/33015128 http://dx.doi.org/10.3389/fnut.2020.00159 |
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author | Selmin, Ornella I. Donovan, Micah G. Stillwater, Barbara J. Neumayer, Leigh Romagnolo, Donato F. |
author_facet | Selmin, Ornella I. Donovan, Micah G. Stillwater, Barbara J. Neumayer, Leigh Romagnolo, Donato F. |
author_sort | Selmin, Ornella I. |
collection | PubMed |
description | Triple negative breast cancer (TNBC) represents a highly heterogeneous group of breast cancers, lacking expression of the estrogen (ER) and progesterone (PR) receptors, and human epidermal growth factor receptor 2 (HER2). TNBC are characterized by a high level of mutation and metastasis, poor clinical outcomes and overall survival. Here, we review the epigenetic mechanisms of regulation involved in cell pathways disrupted in TNBC, with particular emphasis on dietary food components that may be exploited for the development of effective strategies for management of TNBC. |
format | Online Article Text |
id | pubmed-7506147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75061472020-10-02 Epigenetic Regulation and Dietary Control of Triple Negative Breast Cancer Selmin, Ornella I. Donovan, Micah G. Stillwater, Barbara J. Neumayer, Leigh Romagnolo, Donato F. Front Nutr Nutrition Triple negative breast cancer (TNBC) represents a highly heterogeneous group of breast cancers, lacking expression of the estrogen (ER) and progesterone (PR) receptors, and human epidermal growth factor receptor 2 (HER2). TNBC are characterized by a high level of mutation and metastasis, poor clinical outcomes and overall survival. Here, we review the epigenetic mechanisms of regulation involved in cell pathways disrupted in TNBC, with particular emphasis on dietary food components that may be exploited for the development of effective strategies for management of TNBC. Frontiers Media S.A. 2020-09-08 /pmc/articles/PMC7506147/ /pubmed/33015128 http://dx.doi.org/10.3389/fnut.2020.00159 Text en Copyright © 2020 Selmin, Donovan, Stillwater, Neumayer and Romagnolo. 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) and the copyright owner(s) 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 | Nutrition Selmin, Ornella I. Donovan, Micah G. Stillwater, Barbara J. Neumayer, Leigh Romagnolo, Donato F. Epigenetic Regulation and Dietary Control of Triple Negative Breast Cancer |
title | Epigenetic Regulation and Dietary Control of Triple Negative Breast Cancer |
title_full | Epigenetic Regulation and Dietary Control of Triple Negative Breast Cancer |
title_fullStr | Epigenetic Regulation and Dietary Control of Triple Negative Breast Cancer |
title_full_unstemmed | Epigenetic Regulation and Dietary Control of Triple Negative Breast Cancer |
title_short | Epigenetic Regulation and Dietary Control of Triple Negative Breast Cancer |
title_sort | epigenetic regulation and dietary control of triple negative breast cancer |
topic | Nutrition |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7506147/ https://www.ncbi.nlm.nih.gov/pubmed/33015128 http://dx.doi.org/10.3389/fnut.2020.00159 |
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