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Differential susceptibility to endocrine disruptor-induced epimutagenesis
There is now considerable evidence indicating the potential for endocrine disrupting chemicals to alter the epigenome and for subsets of these epigenomic changes or “epimutations” to be heritably transmitted to offspring in subsequent generations. While there have been many studies indicating how ex...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722801/ https://www.ncbi.nlm.nih.gov/pubmed/33324495 http://dx.doi.org/10.1093/eep/dvaa016 |
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author | Lehle, Jake D McCarrey, John R |
author_facet | Lehle, Jake D McCarrey, John R |
author_sort | Lehle, Jake D |
collection | PubMed |
description | There is now considerable evidence indicating the potential for endocrine disrupting chemicals to alter the epigenome and for subsets of these epigenomic changes or “epimutations” to be heritably transmitted to offspring in subsequent generations. While there have been many studies indicating how exposure to endocrine disrupting chemicals can disrupt various organs associated with the body’s endocrine systems, there is relatively limited information regarding the relative susceptibility of different specific organs, tissues, or cell types to endocrine disrupting chemical-induced epimutagenesis. Here we review available information about different organs, tissues, cell types, and/or cell lines which have been shown to be susceptible to specific endocrine disrupting chemical-induced epimutations. In addition, we discuss possible mechanisms that may be involved, or impacted by this tissue- or cell type-specific, differential susceptibility to different endocrine disrupting chemicals. Finally, we summarize available information indicating that certain periods of development display elevated susceptibility to endocrine disrupting chemical exposure and we describe how this may affect the extent to which germline epimutations can be transmitted inter- or transgenerationally. We conclude that cell type-specific differential susceptibility to endocrine disrupting chemical-induced epimutagenesis is likely to directly impact the extent to, or manner in, which endocrine disrupting chemical exposure initially induces epigenetic changes to DNA methylation and/or histone modifications, and how these endocrine disrupting chemical-induced epimutations can then subsequently impact gene expression, potentially leading to the development of heritable disease states. |
format | Online Article Text |
id | pubmed-7722801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-77228012020-12-14 Differential susceptibility to endocrine disruptor-induced epimutagenesis Lehle, Jake D McCarrey, John R Environ Epigenet Review Article There is now considerable evidence indicating the potential for endocrine disrupting chemicals to alter the epigenome and for subsets of these epigenomic changes or “epimutations” to be heritably transmitted to offspring in subsequent generations. While there have been many studies indicating how exposure to endocrine disrupting chemicals can disrupt various organs associated with the body’s endocrine systems, there is relatively limited information regarding the relative susceptibility of different specific organs, tissues, or cell types to endocrine disrupting chemical-induced epimutagenesis. Here we review available information about different organs, tissues, cell types, and/or cell lines which have been shown to be susceptible to specific endocrine disrupting chemical-induced epimutations. In addition, we discuss possible mechanisms that may be involved, or impacted by this tissue- or cell type-specific, differential susceptibility to different endocrine disrupting chemicals. Finally, we summarize available information indicating that certain periods of development display elevated susceptibility to endocrine disrupting chemical exposure and we describe how this may affect the extent to which germline epimutations can be transmitted inter- or transgenerationally. We conclude that cell type-specific differential susceptibility to endocrine disrupting chemical-induced epimutagenesis is likely to directly impact the extent to, or manner in, which endocrine disrupting chemical exposure initially induces epigenetic changes to DNA methylation and/or histone modifications, and how these endocrine disrupting chemical-induced epimutations can then subsequently impact gene expression, potentially leading to the development of heritable disease states. Oxford University Press 2020-12-08 /pmc/articles/PMC7722801/ /pubmed/33324495 http://dx.doi.org/10.1093/eep/dvaa016 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Review Article Lehle, Jake D McCarrey, John R Differential susceptibility to endocrine disruptor-induced epimutagenesis |
title | Differential susceptibility to endocrine disruptor-induced epimutagenesis |
title_full | Differential susceptibility to endocrine disruptor-induced epimutagenesis |
title_fullStr | Differential susceptibility to endocrine disruptor-induced epimutagenesis |
title_full_unstemmed | Differential susceptibility to endocrine disruptor-induced epimutagenesis |
title_short | Differential susceptibility to endocrine disruptor-induced epimutagenesis |
title_sort | differential susceptibility to endocrine disruptor-induced epimutagenesis |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7722801/ https://www.ncbi.nlm.nih.gov/pubmed/33324495 http://dx.doi.org/10.1093/eep/dvaa016 |
work_keys_str_mv | AT lehlejaked differentialsusceptibilitytoendocrinedisruptorinducedepimutagenesis AT mccarreyjohnr differentialsusceptibilitytoendocrinedisruptorinducedepimutagenesis |