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Synergistic antineoplastic action of DNA methylation inhibitor 5‐AZA‐2′‐deoxycytidine and histone deacetylase inhibitor depsipeptide on human breast carcinoma cells

During tumorigenesis, cancer‐related genes can be silenced by aberrant DNA methylation and by changes in chromatin structure. It has been reported that 5‐aza‐2′‐deoxycytidine, a potent inhibitor of DNA methylation, in combination with histone deacetylase inhibitors, can produce a synergistic reactiv...

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Published in:International journal of cancer 2003-01, Vol.103 (2), p.177-184
Main Authors: Primeau, Mélanie, Gagnon, Jacynthe, Momparler, Richard L.
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Momparler, Richard L.
description During tumorigenesis, cancer‐related genes can be silenced by aberrant DNA methylation and by changes in chromatin structure. It has been reported that 5‐aza‐2′‐deoxycytidine, a potent inhibitor of DNA methylation, in combination with histone deacetylase inhibitors, can produce a synergistic reactivation of these genes. The aim of our study was to investigate the in vitro antineoplastic activity of 5‐aza‐2′‐deoxycytidine in combination with depsipeptide, a potent histone deacetylase inhibitor, against MDA‐MB‐231 and MDA‐MB‐435 human breast carcinoma cell lines. We observed that the combination of 5‐aza‐2′‐deoxycytidine and depsipeptide produced a synergistic antineoplastic effect against these tumor cells as compared to either agent administered alone. We also investigated the effect of this drug combination on the activation of maspin and gelsolin expression. These 2 genes whose function is to suppress tumor metastasis have been reported to be silenced by epigenetic events in breast cancer. Using semi‐quantitative RT‐PCR, we observed that 5‐aza‐2′‐deoxycytidine in combination with depsipeptide produced a greater reactivation of both maspin and gelsolin as compared to each agent alone. The synergistic interaction between 5‐aza‐2′‐deoxycytidine and depsipeptide on breast carcinoma cell lines provides a rationale to investigate this interesting drug combination in future clinical trials on patients with advanced breast cancer. © 2002 Wiley‐Liss, Inc.
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Using semi‐quantitative RT‐PCR, we observed that 5‐aza‐2′‐deoxycytidine in combination with depsipeptide produced a greater reactivation of both maspin and gelsolin as compared to each agent alone. 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Drug treatments</topic><topic>Proteins - genetics</topic><topic>Proteins - metabolism</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - metabolism</topic><topic>Serpins - genetics</topic><topic>Serpins - metabolism</topic><topic>Tumor Cells, Cultured - drug effects</topic><topic>Tumor Cells, Cultured - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Primeau, Mélanie</creatorcontrib><creatorcontrib>Gagnon, Jacynthe</creatorcontrib><creatorcontrib>Momparler, Richard L.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Primeau, Mélanie</au><au>Gagnon, Jacynthe</au><au>Momparler, Richard L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synergistic antineoplastic action of DNA methylation inhibitor 5‐AZA‐2′‐deoxycytidine and histone deacetylase inhibitor depsipeptide on human breast carcinoma cells</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2003-01-10</date><risdate>2003</risdate><volume>103</volume><issue>2</issue><spage>177</spage><epage>184</epage><pages>177-184</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>During tumorigenesis, cancer‐related genes can be silenced by aberrant DNA methylation and by changes in chromatin structure. 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Using semi‐quantitative RT‐PCR, we observed that 5‐aza‐2′‐deoxycytidine in combination with depsipeptide produced a greater reactivation of both maspin and gelsolin as compared to each agent alone. The synergistic interaction between 5‐aza‐2′‐deoxycytidine and depsipeptide on breast carcinoma cell lines provides a rationale to investigate this interesting drug combination in future clinical trials on patients with advanced breast cancer. © 2002 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>12455031</pmid><doi>10.1002/ijc.10789</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects 5‐aza‐2′‐deoxycytydine
Antimetabolites, Antineoplastic - pharmacology
Antineoplastic agents
Azacitidine - analogs & derivatives
Azacitidine - pharmacology
Biological and medical sciences
breast cancer
Breast Neoplasms - drug therapy
Breast Neoplasms - enzymology
Breast Neoplasms - genetics
depsipeptide
DNA methylation
DNA Methylation - drug effects
DNA Primers - chemistry
Drug Combinations
Drug Synergism
Enzyme Inhibitors - pharmacology
Female
gelsolin
Gelsolin - genetics
Gelsolin - metabolism
Gene Expression Regulation, Neoplastic
Gene Silencing
General aspects
Genes, Tumor Suppressor
Histone Deacetylase Inhibitors
histone deacetylation
Humans
In Vitro Techniques
maspin
Medical sciences
Pharmacology. Drug treatments
Proteins - genetics
Proteins - metabolism
Reverse Transcriptase Polymerase Chain Reaction
RNA, Messenger - metabolism
Serpins - genetics
Serpins - metabolism
Tumor Cells, Cultured - drug effects
Tumor Cells, Cultured - metabolism
title Synergistic antineoplastic action of DNA methylation inhibitor 5‐AZA‐2′‐deoxycytidine and histone deacetylase inhibitor depsipeptide on human breast carcinoma cells
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