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Age and sun exposure-related widespread genomic blocks of hypomethylation in nonmalignant skin
BACKGROUND: Aging and sun exposure are the leading causes of skin cancer. It has been shown that epigenetic changes, such as DNA methylation, are well established mechanisms for cancer, and also have emerging roles in aging and common disease. Here, we directly ask whether DNA methylation is altered...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4423110/ https://www.ncbi.nlm.nih.gov/pubmed/25886480 http://dx.doi.org/10.1186/s13059-015-0644-y |
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author | Vandiver, Amy R Irizarry, Rafael A Hansen, Kasper D Garza, Luis A Runarsson, Arni Li, Xin Chien, Anna L Wang, Timothy S Leung, Sherry G Kang, Sewon Feinberg, Andrew P |
author_facet | Vandiver, Amy R Irizarry, Rafael A Hansen, Kasper D Garza, Luis A Runarsson, Arni Li, Xin Chien, Anna L Wang, Timothy S Leung, Sherry G Kang, Sewon Feinberg, Andrew P |
author_sort | Vandiver, Amy R |
collection | PubMed |
description | BACKGROUND: Aging and sun exposure are the leading causes of skin cancer. It has been shown that epigenetic changes, such as DNA methylation, are well established mechanisms for cancer, and also have emerging roles in aging and common disease. Here, we directly ask whether DNA methylation is altered following skin aging and/or chronic sun exposure in humans. RESULTS: We compare epidermis and dermis of both sun-protected and sun-exposed skin derived from younger subjects (under 35 years old) and older subjects (over 60 years old), using the Infinium HumanMethylation450 array and whole genome bisulfite sequencing. We observe large blocks of the genome that are hypomethylated in older, sun-exposed epidermal samples, with the degree of hypomethylation associated with clinical measures of photo-aging. We replicate these findings using whole genome bisulfite sequencing, comparing epidermis from an additional set of younger and older subjects. These blocks largely overlap known hypomethylated blocks in colon cancer and we observe that these same regions are similarly hypomethylated in squamous cell carcinoma samples. CONCLUSIONS: These data implicate large scale epigenomic change in mediating the effects of environmental damage with photo-aging. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-015-0644-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4423110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44231102015-05-08 Age and sun exposure-related widespread genomic blocks of hypomethylation in nonmalignant skin Vandiver, Amy R Irizarry, Rafael A Hansen, Kasper D Garza, Luis A Runarsson, Arni Li, Xin Chien, Anna L Wang, Timothy S Leung, Sherry G Kang, Sewon Feinberg, Andrew P Genome Biol Research BACKGROUND: Aging and sun exposure are the leading causes of skin cancer. It has been shown that epigenetic changes, such as DNA methylation, are well established mechanisms for cancer, and also have emerging roles in aging and common disease. Here, we directly ask whether DNA methylation is altered following skin aging and/or chronic sun exposure in humans. RESULTS: We compare epidermis and dermis of both sun-protected and sun-exposed skin derived from younger subjects (under 35 years old) and older subjects (over 60 years old), using the Infinium HumanMethylation450 array and whole genome bisulfite sequencing. We observe large blocks of the genome that are hypomethylated in older, sun-exposed epidermal samples, with the degree of hypomethylation associated with clinical measures of photo-aging. We replicate these findings using whole genome bisulfite sequencing, comparing epidermis from an additional set of younger and older subjects. These blocks largely overlap known hypomethylated blocks in colon cancer and we observe that these same regions are similarly hypomethylated in squamous cell carcinoma samples. CONCLUSIONS: These data implicate large scale epigenomic change in mediating the effects of environmental damage with photo-aging. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-015-0644-y) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-16 2015 /pmc/articles/PMC4423110/ /pubmed/25886480 http://dx.doi.org/10.1186/s13059-015-0644-y Text en © Vandiver et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Vandiver, Amy R Irizarry, Rafael A Hansen, Kasper D Garza, Luis A Runarsson, Arni Li, Xin Chien, Anna L Wang, Timothy S Leung, Sherry G Kang, Sewon Feinberg, Andrew P Age and sun exposure-related widespread genomic blocks of hypomethylation in nonmalignant skin |
title | Age and sun exposure-related widespread genomic blocks of hypomethylation in nonmalignant skin |
title_full | Age and sun exposure-related widespread genomic blocks of hypomethylation in nonmalignant skin |
title_fullStr | Age and sun exposure-related widespread genomic blocks of hypomethylation in nonmalignant skin |
title_full_unstemmed | Age and sun exposure-related widespread genomic blocks of hypomethylation in nonmalignant skin |
title_short | Age and sun exposure-related widespread genomic blocks of hypomethylation in nonmalignant skin |
title_sort | age and sun exposure-related widespread genomic blocks of hypomethylation in nonmalignant skin |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4423110/ https://www.ncbi.nlm.nih.gov/pubmed/25886480 http://dx.doi.org/10.1186/s13059-015-0644-y |
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