Dietary phytochemicals, HDAC inhibition, and DNA damage/repair defects in cancer cells

<p>Abstract</p> <p>Genomic instability is a common feature of cancer etiology. This provides an avenue for therapeutic intervention, since cancer cells are more susceptible than normal cells to DNA damaging agents. However, there is growing evidence that the epigenetic mechanisms t...

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Main Authors: Rajendran Praveen, Ho Emily, Williams David E, Dashwood Roderick H
Format: Article
Language:English
Published: BMC 2011-10-01
Series:Clinical Epigenetics
Subjects:
Online Access:http://www.clinicalepigeneticsjournal.com/content/3/1/4
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author Rajendran Praveen
Ho Emily
Williams David E
Dashwood Roderick H
author_facet Rajendran Praveen
Ho Emily
Williams David E
Dashwood Roderick H
author_sort Rajendran Praveen
collection DOAJ
description <p>Abstract</p> <p>Genomic instability is a common feature of cancer etiology. This provides an avenue for therapeutic intervention, since cancer cells are more susceptible than normal cells to DNA damaging agents. However, there is growing evidence that the epigenetic mechanisms that impact DNA methylation and histone status also contribute to genomic instability. The DNA damage response, for example, is modulated by the acetylation status of histone and non-histone proteins, and by the opposing activities of histone acetyltransferase and histone deacetylase (HDAC) enzymes. Many HDACs overexpressed in cancer cells have been implicated in protecting such cells from genotoxic insults. Thus, HDAC inhibitors, in addition to unsilencing tumor suppressor genes, also can silence DNA repair pathways, inactivate non-histone proteins that are required for DNA stability, and induce reactive oxygen species and DNA double-strand breaks. This review summarizes how dietary phytochemicals that affect the epigenome also can trigger DNA damage and repair mechanisms. Where such data is available, examples are cited from studies <it>in vitro </it>and <it>in vivo </it>of polyphenols, organosulfur/organoselenium compounds, indoles, sesquiterpene lactones, and miscellaneous agents such as anacardic acid. Finally, by virtue of their genetic and epigenetic mechanisms, cancer chemopreventive agents are being redefined as chemo- or radio-sensitizers. A sustained DNA damage response coupled with insufficient repair may be a pivotal mechanism for apoptosis induction in cancer cells exposed to dietary phytochemicals. Future research, including appropriate clinical investigation, should clarify these emerging concepts in the context of both genetic and epigenetic mechanisms dysregulated in cancer, and the pros and cons of specific dietary intervention strategies.</p>
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spelling doaj.art-9989c94664f7481eba3845df75fe1f572022-12-22T02:48:21ZengBMCClinical Epigenetics1868-70832011-10-0131410.1186/1868-7083-3-4Dietary phytochemicals, HDAC inhibition, and DNA damage/repair defects in cancer cellsRajendran PraveenHo EmilyWilliams David EDashwood Roderick H<p>Abstract</p> <p>Genomic instability is a common feature of cancer etiology. This provides an avenue for therapeutic intervention, since cancer cells are more susceptible than normal cells to DNA damaging agents. However, there is growing evidence that the epigenetic mechanisms that impact DNA methylation and histone status also contribute to genomic instability. The DNA damage response, for example, is modulated by the acetylation status of histone and non-histone proteins, and by the opposing activities of histone acetyltransferase and histone deacetylase (HDAC) enzymes. Many HDACs overexpressed in cancer cells have been implicated in protecting such cells from genotoxic insults. Thus, HDAC inhibitors, in addition to unsilencing tumor suppressor genes, also can silence DNA repair pathways, inactivate non-histone proteins that are required for DNA stability, and induce reactive oxygen species and DNA double-strand breaks. This review summarizes how dietary phytochemicals that affect the epigenome also can trigger DNA damage and repair mechanisms. Where such data is available, examples are cited from studies <it>in vitro </it>and <it>in vivo </it>of polyphenols, organosulfur/organoselenium compounds, indoles, sesquiterpene lactones, and miscellaneous agents such as anacardic acid. Finally, by virtue of their genetic and epigenetic mechanisms, cancer chemopreventive agents are being redefined as chemo- or radio-sensitizers. A sustained DNA damage response coupled with insufficient repair may be a pivotal mechanism for apoptosis induction in cancer cells exposed to dietary phytochemicals. Future research, including appropriate clinical investigation, should clarify these emerging concepts in the context of both genetic and epigenetic mechanisms dysregulated in cancer, and the pros and cons of specific dietary intervention strategies.</p>http://www.clinicalepigeneticsjournal.com/content/3/1/4EpigeneticshistoneHDACDNA damageDNA repairphytochemicalcancer
spellingShingle Rajendran Praveen
Ho Emily
Williams David E
Dashwood Roderick H
Dietary phytochemicals, HDAC inhibition, and DNA damage/repair defects in cancer cells
Clinical Epigenetics
Epigenetics
histone
HDAC
DNA damage
DNA repair
phytochemical
cancer
title Dietary phytochemicals, HDAC inhibition, and DNA damage/repair defects in cancer cells
title_full Dietary phytochemicals, HDAC inhibition, and DNA damage/repair defects in cancer cells
title_fullStr Dietary phytochemicals, HDAC inhibition, and DNA damage/repair defects in cancer cells
title_full_unstemmed Dietary phytochemicals, HDAC inhibition, and DNA damage/repair defects in cancer cells
title_short Dietary phytochemicals, HDAC inhibition, and DNA damage/repair defects in cancer cells
title_sort dietary phytochemicals hdac inhibition and dna damage repair defects in cancer cells
topic Epigenetics
histone
HDAC
DNA damage
DNA repair
phytochemical
cancer
url http://www.clinicalepigeneticsjournal.com/content/3/1/4
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AT hoemily dietaryphytochemicalshdacinhibitionanddnadamagerepairdefectsincancercells
AT williamsdavide dietaryphytochemicalshdacinhibitionanddnadamagerepairdefectsincancercells
AT dashwoodroderickh dietaryphytochemicalshdacinhibitionanddnadamagerepairdefectsincancercells