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Circadian disruption and breast cancer: An epigenetic link?

Breast cancer is already the most common malignancy affecting women worldwide, and evidence is mounting that breast cancer induced by circadian disruption (CD) is a warranted concern. Numerous studies have investigated various aspects of the circadian clock in relation to breast cancer, and evidence...

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Detalles Bibliográficos
Autores principales: Kochan, David Z., Kovalchuk, Olga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627279/
https://www.ncbi.nlm.nih.gov/pubmed/26220712
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author Kochan, David Z.
Kovalchuk, Olga
author_facet Kochan, David Z.
Kovalchuk, Olga
author_sort Kochan, David Z.
collection PubMed
description Breast cancer is already the most common malignancy affecting women worldwide, and evidence is mounting that breast cancer induced by circadian disruption (CD) is a warranted concern. Numerous studies have investigated various aspects of the circadian clock in relation to breast cancer, and evidence from these studies indicates that melatonin and the core clock genes can play a crucial role in breast cancer development. Even though epigenetics has been increasingly recognized as a key player in the etiology of breast cancer and linked to circadian rhythms, and there is evidence of overlap between epigenetic deregulation and breast cancer induced by circadian disruption, only a handful of studies have directly investigated the role of epigenetics in CD-induced breast cancer. This review explores the circadian clock and breast cancer, and the growing role of epigenetics in breast cancer development and circadian rhythms. We also summarize the current knowledge and next steps for the investigation of the epigenetic link in CD-induced breast cancer.
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spelling pubmed-46272792015-12-02 Circadian disruption and breast cancer: An epigenetic link? Kochan, David Z. Kovalchuk, Olga Oncotarget Review Breast cancer is already the most common malignancy affecting women worldwide, and evidence is mounting that breast cancer induced by circadian disruption (CD) is a warranted concern. Numerous studies have investigated various aspects of the circadian clock in relation to breast cancer, and evidence from these studies indicates that melatonin and the core clock genes can play a crucial role in breast cancer development. Even though epigenetics has been increasingly recognized as a key player in the etiology of breast cancer and linked to circadian rhythms, and there is evidence of overlap between epigenetic deregulation and breast cancer induced by circadian disruption, only a handful of studies have directly investigated the role of epigenetics in CD-induced breast cancer. This review explores the circadian clock and breast cancer, and the growing role of epigenetics in breast cancer development and circadian rhythms. We also summarize the current knowledge and next steps for the investigation of the epigenetic link in CD-induced breast cancer. Impact Journals LLC 2015-07-09 /pmc/articles/PMC4627279/ /pubmed/26220712 Text en Copyright: © 2015 Kochan and Kovalchuk http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
Kochan, David Z.
Kovalchuk, Olga
Circadian disruption and breast cancer: An epigenetic link?
title Circadian disruption and breast cancer: An epigenetic link?
title_full Circadian disruption and breast cancer: An epigenetic link?
title_fullStr Circadian disruption and breast cancer: An epigenetic link?
title_full_unstemmed Circadian disruption and breast cancer: An epigenetic link?
title_short Circadian disruption and breast cancer: An epigenetic link?
title_sort circadian disruption and breast cancer: an epigenetic link?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627279/
https://www.ncbi.nlm.nih.gov/pubmed/26220712
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