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Reduction in promotor methylation utilizing EGCG (epigallocatechin-3-gallate) restores RXRα expression in human colon cancer cells

Silencing of regulatory genes through hypermethylation of CpG islands is an important mechanism in tumorigenesis. In colon cancer, RXRα, an important dimerization partner with other nuclear transcription factors, is silenced through this mechanism. We previously found that colon tumors in Apc(Min/+)...

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Autores principales: Morris, Jay, Moseley, Vondina R., Cabang, April B., Coleman, Katie, Wei, Wei, Garrett-Mayer, Elizabeth, Wargovich, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5085231/
https://www.ncbi.nlm.nih.gov/pubmed/27167203
http://dx.doi.org/10.18632/oncotarget.9204
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author Morris, Jay
Moseley, Vondina R.
Cabang, April B.
Coleman, Katie
Wei, Wei
Garrett-Mayer, Elizabeth
Wargovich, Michael J.
author_facet Morris, Jay
Moseley, Vondina R.
Cabang, April B.
Coleman, Katie
Wei, Wei
Garrett-Mayer, Elizabeth
Wargovich, Michael J.
author_sort Morris, Jay
collection PubMed
description Silencing of regulatory genes through hypermethylation of CpG islands is an important mechanism in tumorigenesis. In colon cancer, RXRα, an important dimerization partner with other nuclear transcription factors, is silenced through this mechanism. We previously found that colon tumors in Apc(Min/+) mice had diminished levels of RXRα protein and expression levels of this gene were restored by treatment with a green tea intervention, due to reduced promoter methylation of RXRα. We hypothesized that CIMP+ cell lines, which epigenetically silence key regulatory genes would also evidence silencing of RXRα and EGCG treatment would restore its expression. We indeed found EGCG to restore RXRα activity levels in the human cell lines, in a dose dependent manner and reduced RXRα promoter methylation. EGCG induced methylation changes in several other colon cancer related genes but did not cause a decrease in global methylation. Numerous epidemiological reports have shown the benefits of green tea consumption in reducing colon cancer risk but to date no studies have shown that the risk reduction may be related to the epigenetic restoration by tea polyphenols. Our results show that EGCG modulates the reversal of gene silencing involved in colon carcinogenesis providing a possible avenue for colon cancer prevention and treatment.
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spelling pubmed-50852312016-10-31 Reduction in promotor methylation utilizing EGCG (epigallocatechin-3-gallate) restores RXRα expression in human colon cancer cells Morris, Jay Moseley, Vondina R. Cabang, April B. Coleman, Katie Wei, Wei Garrett-Mayer, Elizabeth Wargovich, Michael J. Oncotarget Research Paper Silencing of regulatory genes through hypermethylation of CpG islands is an important mechanism in tumorigenesis. In colon cancer, RXRα, an important dimerization partner with other nuclear transcription factors, is silenced through this mechanism. We previously found that colon tumors in Apc(Min/+) mice had diminished levels of RXRα protein and expression levels of this gene were restored by treatment with a green tea intervention, due to reduced promoter methylation of RXRα. We hypothesized that CIMP+ cell lines, which epigenetically silence key regulatory genes would also evidence silencing of RXRα and EGCG treatment would restore its expression. We indeed found EGCG to restore RXRα activity levels in the human cell lines, in a dose dependent manner and reduced RXRα promoter methylation. EGCG induced methylation changes in several other colon cancer related genes but did not cause a decrease in global methylation. Numerous epidemiological reports have shown the benefits of green tea consumption in reducing colon cancer risk but to date no studies have shown that the risk reduction may be related to the epigenetic restoration by tea polyphenols. Our results show that EGCG modulates the reversal of gene silencing involved in colon carcinogenesis providing a possible avenue for colon cancer prevention and treatment. Impact Journals LLC 2016-05-06 /pmc/articles/PMC5085231/ /pubmed/27167203 http://dx.doi.org/10.18632/oncotarget.9204 Text en Copyright: © 2016 Morris et al. 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 Research Paper
Morris, Jay
Moseley, Vondina R.
Cabang, April B.
Coleman, Katie
Wei, Wei
Garrett-Mayer, Elizabeth
Wargovich, Michael J.
Reduction in promotor methylation utilizing EGCG (epigallocatechin-3-gallate) restores RXRα expression in human colon cancer cells
title Reduction in promotor methylation utilizing EGCG (epigallocatechin-3-gallate) restores RXRα expression in human colon cancer cells
title_full Reduction in promotor methylation utilizing EGCG (epigallocatechin-3-gallate) restores RXRα expression in human colon cancer cells
title_fullStr Reduction in promotor methylation utilizing EGCG (epigallocatechin-3-gallate) restores RXRα expression in human colon cancer cells
title_full_unstemmed Reduction in promotor methylation utilizing EGCG (epigallocatechin-3-gallate) restores RXRα expression in human colon cancer cells
title_short Reduction in promotor methylation utilizing EGCG (epigallocatechin-3-gallate) restores RXRα expression in human colon cancer cells
title_sort reduction in promotor methylation utilizing egcg (epigallocatechin-3-gallate) restores rxrα expression in human colon cancer cells
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5085231/
https://www.ncbi.nlm.nih.gov/pubmed/27167203
http://dx.doi.org/10.18632/oncotarget.9204
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