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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...

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Autores principales: 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.
Formato: Texto
Lenguaje:English
Publicado: American Chemical Society 2011
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.
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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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