Cargando…

Impact of Natural Compounds on DNA Methylation Levels of the Tumor Suppressor Gene RASSF1A in Cancer

Epigenetic inactivation of tumor suppressor genes (TSG) is a fundamental event in the pathogenesis of human cancer. This silencing is accomplished by aberrant chromatin modifications including DNA hypermethylation of the gene promoter. One of the most frequently hypermethylated TSG in human cancer i...

Descripción completa

Detalles Bibliográficos
Autores principales: Dammann, Reinhard H., Richter, Antje M., Jiménez, Adriana P., Woods, Michelle, Küster, Miriam, Witharana, Chamindri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666841/
https://www.ncbi.nlm.nih.gov/pubmed/29039788
http://dx.doi.org/10.3390/ijms18102160
_version_ 1783275385365987328
author Dammann, Reinhard H.
Richter, Antje M.
Jiménez, Adriana P.
Woods, Michelle
Küster, Miriam
Witharana, Chamindri
author_facet Dammann, Reinhard H.
Richter, Antje M.
Jiménez, Adriana P.
Woods, Michelle
Küster, Miriam
Witharana, Chamindri
author_sort Dammann, Reinhard H.
collection PubMed
description Epigenetic inactivation of tumor suppressor genes (TSG) is a fundamental event in the pathogenesis of human cancer. This silencing is accomplished by aberrant chromatin modifications including DNA hypermethylation of the gene promoter. One of the most frequently hypermethylated TSG in human cancer is the Ras Association Domain Family 1A (RASSF1A) gene. Aberrant methylation of RASSF1A has been reported in melanoma, sarcoma and carcinoma of different tissues. RASSF1A hypermethylation has been correlated with tumor progression and poor prognosis. Reactivation of epigenetically silenced TSG has been suggested as a therapy in cancer treatment. In particular, natural compounds isolated from herbal extracts have been tested for their capacity to induce RASSF1A in cancer cells, through demethylation. Here, we review the treatment of cancer cells with natural supplements (e.g., methyl donors, vitamins and polyphenols) that have been utilized to revert or prevent the epigenetic silencing of RASSF1A. Moreover, we specify pathways that were involved in RASSF1A reactivation. Several of these compounds (e.g., reseveratol and curcumin) act by inhibiting the activity or expression of DNA methyltransferases and reactive RASSF1A in cancer. Thus natural compounds could serve as important agents in tumor prevention or cancer therapy. However, the exact epigenetic reactivation mechanism is still under investigation.
format Online
Article
Text
id pubmed-5666841
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-56668412017-11-09 Impact of Natural Compounds on DNA Methylation Levels of the Tumor Suppressor Gene RASSF1A in Cancer Dammann, Reinhard H. Richter, Antje M. Jiménez, Adriana P. Woods, Michelle Küster, Miriam Witharana, Chamindri Int J Mol Sci Review Epigenetic inactivation of tumor suppressor genes (TSG) is a fundamental event in the pathogenesis of human cancer. This silencing is accomplished by aberrant chromatin modifications including DNA hypermethylation of the gene promoter. One of the most frequently hypermethylated TSG in human cancer is the Ras Association Domain Family 1A (RASSF1A) gene. Aberrant methylation of RASSF1A has been reported in melanoma, sarcoma and carcinoma of different tissues. RASSF1A hypermethylation has been correlated with tumor progression and poor prognosis. Reactivation of epigenetically silenced TSG has been suggested as a therapy in cancer treatment. In particular, natural compounds isolated from herbal extracts have been tested for their capacity to induce RASSF1A in cancer cells, through demethylation. Here, we review the treatment of cancer cells with natural supplements (e.g., methyl donors, vitamins and polyphenols) that have been utilized to revert or prevent the epigenetic silencing of RASSF1A. Moreover, we specify pathways that were involved in RASSF1A reactivation. Several of these compounds (e.g., reseveratol and curcumin) act by inhibiting the activity or expression of DNA methyltransferases and reactive RASSF1A in cancer. Thus natural compounds could serve as important agents in tumor prevention or cancer therapy. However, the exact epigenetic reactivation mechanism is still under investigation. MDPI 2017-10-17 /pmc/articles/PMC5666841/ /pubmed/29039788 http://dx.doi.org/10.3390/ijms18102160 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Dammann, Reinhard H.
Richter, Antje M.
Jiménez, Adriana P.
Woods, Michelle
Küster, Miriam
Witharana, Chamindri
Impact of Natural Compounds on DNA Methylation Levels of the Tumor Suppressor Gene RASSF1A in Cancer
title Impact of Natural Compounds on DNA Methylation Levels of the Tumor Suppressor Gene RASSF1A in Cancer
title_full Impact of Natural Compounds on DNA Methylation Levels of the Tumor Suppressor Gene RASSF1A in Cancer
title_fullStr Impact of Natural Compounds on DNA Methylation Levels of the Tumor Suppressor Gene RASSF1A in Cancer
title_full_unstemmed Impact of Natural Compounds on DNA Methylation Levels of the Tumor Suppressor Gene RASSF1A in Cancer
title_short Impact of Natural Compounds on DNA Methylation Levels of the Tumor Suppressor Gene RASSF1A in Cancer
title_sort impact of natural compounds on dna methylation levels of the tumor suppressor gene rassf1a in cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666841/
https://www.ncbi.nlm.nih.gov/pubmed/29039788
http://dx.doi.org/10.3390/ijms18102160
work_keys_str_mv AT dammannreinhardh impactofnaturalcompoundsondnamethylationlevelsofthetumorsuppressorgenerassf1aincancer
AT richterantjem impactofnaturalcompoundsondnamethylationlevelsofthetumorsuppressorgenerassf1aincancer
AT jimenezadrianap impactofnaturalcompoundsondnamethylationlevelsofthetumorsuppressorgenerassf1aincancer
AT woodsmichelle impactofnaturalcompoundsondnamethylationlevelsofthetumorsuppressorgenerassf1aincancer
AT kustermiriam impactofnaturalcompoundsondnamethylationlevelsofthetumorsuppressorgenerassf1aincancer
AT witharanachamindri impactofnaturalcompoundsondnamethylationlevelsofthetumorsuppressorgenerassf1aincancer