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Developmental windows of breast cancer risk provide opportunities for targeted chemoprevention
The magnitude of the breast cancer problem implores researchers to aggressively investigate prevention strategies. However, several barriers currently reduce the feasibility of breast cancer prevention. These barriers include the inability to accurately predict future breast cancer diagnosis at the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3980135/ https://www.ncbi.nlm.nih.gov/pubmed/23664839 http://dx.doi.org/10.1016/j.yexcr.2013.04.018 |
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author | Martinson, Holly A. Lyons, Traci R. Giles, Erin D. Borges, Virginia F. Schedin, Pepper |
author_facet | Martinson, Holly A. Lyons, Traci R. Giles, Erin D. Borges, Virginia F. Schedin, Pepper |
author_sort | Martinson, Holly A. |
collection | PubMed |
description | The magnitude of the breast cancer problem implores researchers to aggressively investigate prevention strategies. However, several barriers currently reduce the feasibility of breast cancer prevention. These barriers include the inability to accurately predict future breast cancer diagnosis at the individual level, the need for improved understanding of when to implement interventions, uncertainty with respect to optimal duration of treatment, and negative side effects associated with currently approved chemoprevention therapies. None-the-less, the unique biology of the mammary gland, with its postnatal development and conditional terminal differentiation, may permit the resolution of many of these barriers. Specifically, lifecycle-specific windows of breast cancer risk have been identified that may be amenable to risk-reducing strategies. Here, we argue for prevention research focused on two of these lifecycle windows of risk: postpartum mammary gland involution and peri-menopause. We provide evidence that these windows are highly amenable to targeted, limited duration treatments. Such approaches could result in the prevention of postpartum and postmenopausal breast cancers, correspondingly. |
format | Online Article Text |
id | pubmed-3980135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-39801352014-09-15 Developmental windows of breast cancer risk provide opportunities for targeted chemoprevention Martinson, Holly A. Lyons, Traci R. Giles, Erin D. Borges, Virginia F. Schedin, Pepper Exp Cell Res Article The magnitude of the breast cancer problem implores researchers to aggressively investigate prevention strategies. However, several barriers currently reduce the feasibility of breast cancer prevention. These barriers include the inability to accurately predict future breast cancer diagnosis at the individual level, the need for improved understanding of when to implement interventions, uncertainty with respect to optimal duration of treatment, and negative side effects associated with currently approved chemoprevention therapies. None-the-less, the unique biology of the mammary gland, with its postnatal development and conditional terminal differentiation, may permit the resolution of many of these barriers. Specifically, lifecycle-specific windows of breast cancer risk have been identified that may be amenable to risk-reducing strategies. Here, we argue for prevention research focused on two of these lifecycle windows of risk: postpartum mammary gland involution and peri-menopause. We provide evidence that these windows are highly amenable to targeted, limited duration treatments. Such approaches could result in the prevention of postpartum and postmenopausal breast cancers, correspondingly. 2013-05-09 2013-07-01 /pmc/articles/PMC3980135/ /pubmed/23664839 http://dx.doi.org/10.1016/j.yexcr.2013.04.018 Text en © 2013 The Authors. Published by Elsevier Inc. All rights reserved. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Article Martinson, Holly A. Lyons, Traci R. Giles, Erin D. Borges, Virginia F. Schedin, Pepper Developmental windows of breast cancer risk provide opportunities for targeted chemoprevention |
title | Developmental windows of breast cancer risk provide opportunities for targeted chemoprevention |
title_full | Developmental windows of breast cancer risk provide opportunities for targeted chemoprevention |
title_fullStr | Developmental windows of breast cancer risk provide opportunities for targeted chemoprevention |
title_full_unstemmed | Developmental windows of breast cancer risk provide opportunities for targeted chemoprevention |
title_short | Developmental windows of breast cancer risk provide opportunities for targeted chemoprevention |
title_sort | developmental windows of breast cancer risk provide opportunities for targeted chemoprevention |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3980135/ https://www.ncbi.nlm.nih.gov/pubmed/23664839 http://dx.doi.org/10.1016/j.yexcr.2013.04.018 |
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