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Epigenetic Changes in Individuals with Arsenicosis
[Image: see text] Inorganic arsenic (iAs) is an environmental toxicant currently poisoning millions of people worldwide, and chronically exposed individuals are susceptible to arsenicosis or arsenic poisoning. Using a state-of-the-art technique to map the methylomes of our study subjects, we identif...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042796/ https://www.ncbi.nlm.nih.gov/pubmed/21291286 http://dx.doi.org/10.1021/tx1004419 |
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author | Smeester, Lisa Rager, Julia E. Bailey, Kathryn A. Guan, Xiaojun Smith, Nikia García-Vargas, Gonzalo Del Razo, Luz-Maria Drobná, Zuzana Kelkar, Hemant Stýblo, Miroslav Fry, Rebecca C. |
author_facet | Smeester, Lisa Rager, Julia E. Bailey, Kathryn A. Guan, Xiaojun Smith, Nikia García-Vargas, Gonzalo Del Razo, Luz-Maria Drobná, Zuzana Kelkar, Hemant Stýblo, Miroslav Fry, Rebecca C. |
author_sort | Smeester, Lisa |
collection | PubMed |
description | [Image: see text] Inorganic arsenic (iAs) is an environmental toxicant currently poisoning millions of people worldwide, and chronically exposed individuals are susceptible to arsenicosis or arsenic poisoning. Using a state-of-the-art technique to map the methylomes of our study subjects, we identified a large interactome of hypermethylated genes that are enriched for their involvement in arsenic-associated diseases, such as cancer, heart disease, and diabetes. Notably, we have uncovered an arsenic-induced tumor suppressorome, a complex of 17 tumor suppressors known to be silenced in human cancers. This finding represents a pivotal clue in unraveling a possible epigenetic mode of arsenic-induced disease. |
format | Text |
id | pubmed-3042796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-30427962011-02-22 Epigenetic Changes in Individuals with Arsenicosis Smeester, Lisa Rager, Julia E. Bailey, Kathryn A. Guan, Xiaojun Smith, Nikia García-Vargas, Gonzalo Del Razo, Luz-Maria Drobná, Zuzana Kelkar, Hemant Stýblo, Miroslav Fry, Rebecca C. Chem Res Toxicol [Image: see text] Inorganic arsenic (iAs) is an environmental toxicant currently poisoning millions of people worldwide, and chronically exposed individuals are susceptible to arsenicosis or arsenic poisoning. Using a state-of-the-art technique to map the methylomes of our study subjects, we identified a large interactome of hypermethylated genes that are enriched for their involvement in arsenic-associated diseases, such as cancer, heart disease, and diabetes. Notably, we have uncovered an arsenic-induced tumor suppressorome, a complex of 17 tumor suppressors known to be silenced in human cancers. This finding represents a pivotal clue in unraveling a possible epigenetic mode of arsenic-induced disease. American Chemical Society 2011-02-04 2011-02-18 /pmc/articles/PMC3042796/ /pubmed/21291286 http://dx.doi.org/10.1021/tx1004419 Text en Copyright © 2011 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. |
spellingShingle | Smeester, Lisa Rager, Julia E. Bailey, Kathryn A. Guan, Xiaojun Smith, Nikia García-Vargas, Gonzalo Del Razo, Luz-Maria Drobná, Zuzana Kelkar, Hemant Stýblo, Miroslav Fry, Rebecca C. Epigenetic Changes in Individuals with Arsenicosis |
title | Epigenetic Changes in Individuals with Arsenicosis |
title_full | Epigenetic Changes in Individuals with Arsenicosis |
title_fullStr | Epigenetic Changes in Individuals with Arsenicosis |
title_full_unstemmed | Epigenetic Changes in Individuals with Arsenicosis |
title_short | Epigenetic Changes in Individuals with Arsenicosis |
title_sort | epigenetic changes in individuals with arsenicosis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042796/ https://www.ncbi.nlm.nih.gov/pubmed/21291286 http://dx.doi.org/10.1021/tx1004419 |
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