Loading…
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...
Saved in:
Published in: | International journal of cancer 2003-01, Vol.103 (2), p.177-184 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c3869-b1a337b5794cc633b2b943c90b6a5f3b7169cae29eb9850e9a7e98f2b80034133 |
---|---|
cites | cdi_FETCH-LOGICAL-c3869-b1a337b5794cc633b2b943c90b6a5f3b7169cae29eb9850e9a7e98f2b80034133 |
container_end_page | 184 |
container_issue | 2 |
container_start_page | 177 |
container_title | International journal of cancer |
container_volume | 103 |
creator | Primeau, Mélanie Gagnon, Jacynthe 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. |
doi_str_mv | 10.1002/ijc.10789 |
format | article |
fullrecord | <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_ijc_10789</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>IJC10789</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3869-b1a337b5794cc633b2b943c90b6a5f3b7169cae29eb9850e9a7e98f2b80034133</originalsourceid><addsrcrecordid>eNp1kLtO5DAUhq3VomW4FPsCKzdbUATsOE7icjTchaAAGprIdk52jHKTnRGk4xF4ECoeiSfhQEZiGwrbx_bn71g_Ib852-eMxQfu3mKR5eoHmXGmsojFXP4kM7xjUcZFukm2QrhnjHPJkl9kk8eJlEzwGXm5Hlvw_1wYnKW6HVwLXV_raWsH17W0q-jh5Zw2MCzHWn8euXbpjBs6T-Xb0_P8bo5z_Pb0iksJ3eNox8GVqEJjSZco77AuQVsYUBHgP0EJfXA99PgAKKqXq0a31HjAP1CrvXVt12hqoa7DDtmodB1gd71uk9vjo5vFaXRxdXK2mF9EVuSpigzXQmRGZiqxNhXCxEYlwipmUi0rYTKeKqshVmBULhkonYHKq9jkjImEC7FN9iav9V0IHqqi967Rfiw4Kz4SLzDx4jNxZP9MbL8yDZRf5DpiBP6uAR2sriuvW-vCF5ckEkeK3MHEPbgaxu87Fmfni6n1O7EEny8</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synergistic antineoplastic action of DNA methylation inhibitor 5‐AZA‐2′‐deoxycytidine and histone deacetylase inhibitor depsipeptide on human breast carcinoma cells</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Primeau, Mélanie ; Gagnon, Jacynthe ; Momparler, Richard L.</creator><creatorcontrib>Primeau, Mélanie ; Gagnon, Jacynthe ; Momparler, Richard L.</creatorcontrib><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.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.10789</identifier><identifier>PMID: 12455031</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>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</subject><ispartof>International journal of cancer, 2003-01, Vol.103 (2), p.177-184</ispartof><rights>Copyright © 2003 Wiley‐Liss, Inc.</rights><rights>2003 INIST-CNRS</rights><rights>Copyright 2002 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3869-b1a337b5794cc633b2b943c90b6a5f3b7169cae29eb9850e9a7e98f2b80034133</citedby><cites>FETCH-LOGICAL-c3869-b1a337b5794cc633b2b943c90b6a5f3b7169cae29eb9850e9a7e98f2b80034133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14451446$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12455031$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Primeau, Mélanie</creatorcontrib><creatorcontrib>Gagnon, Jacynthe</creatorcontrib><creatorcontrib>Momparler, Richard L.</creatorcontrib><title>Synergistic antineoplastic action of DNA methylation inhibitor 5‐AZA‐2′‐deoxycytidine and histone deacetylase inhibitor depsipeptide on human breast carcinoma cells</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><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.</description><subject>5‐aza‐2′‐deoxycytydine</subject><subject>Antimetabolites, Antineoplastic - pharmacology</subject><subject>Antineoplastic agents</subject><subject>Azacitidine - analogs & derivatives</subject><subject>Azacitidine - pharmacology</subject><subject>Biological and medical sciences</subject><subject>breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - enzymology</subject><subject>Breast Neoplasms - genetics</subject><subject>depsipeptide</subject><subject>DNA methylation</subject><subject>DNA Methylation - drug effects</subject><subject>DNA Primers - chemistry</subject><subject>Drug Combinations</subject><subject>Drug Synergism</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Female</subject><subject>gelsolin</subject><subject>Gelsolin - genetics</subject><subject>Gelsolin - metabolism</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Gene Silencing</subject><subject>General aspects</subject><subject>Genes, Tumor Suppressor</subject><subject>Histone Deacetylase Inhibitors</subject><subject>histone deacetylation</subject><subject>Humans</subject><subject>In Vitro Techniques</subject><subject>maspin</subject><subject>Medical sciences</subject><subject>Pharmacology. Drug treatments</subject><subject>Proteins - genetics</subject><subject>Proteins - metabolism</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - metabolism</subject><subject>Serpins - genetics</subject><subject>Serpins - metabolism</subject><subject>Tumor Cells, Cultured - drug effects</subject><subject>Tumor Cells, Cultured - metabolism</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNp1kLtO5DAUhq3VomW4FPsCKzdbUATsOE7icjTchaAAGprIdk52jHKTnRGk4xF4ECoeiSfhQEZiGwrbx_bn71g_Ib852-eMxQfu3mKR5eoHmXGmsojFXP4kM7xjUcZFukm2QrhnjHPJkl9kk8eJlEzwGXm5Hlvw_1wYnKW6HVwLXV_raWsH17W0q-jh5Zw2MCzHWn8euXbpjBs6T-Xb0_P8bo5z_Pb0iksJ3eNox8GVqEJjSZco77AuQVsYUBHgP0EJfXA99PgAKKqXq0a31HjAP1CrvXVt12hqoa7DDtmodB1gd71uk9vjo5vFaXRxdXK2mF9EVuSpigzXQmRGZiqxNhXCxEYlwipmUi0rYTKeKqshVmBULhkonYHKq9jkjImEC7FN9iav9V0IHqqi967Rfiw4Kz4SLzDx4jNxZP9MbL8yDZRf5DpiBP6uAR2sriuvW-vCF5ckEkeK3MHEPbgaxu87Fmfni6n1O7EEny8</recordid><startdate>20030110</startdate><enddate>20030110</enddate><creator>Primeau, Mélanie</creator><creator>Gagnon, Jacynthe</creator><creator>Momparler, Richard L.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20030110</creationdate><title>Synergistic antineoplastic action of DNA methylation inhibitor 5‐AZA‐2′‐deoxycytidine and histone deacetylase inhibitor depsipeptide on human breast carcinoma cells</title><author>Primeau, Mélanie ; Gagnon, Jacynthe ; Momparler, Richard L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3869-b1a337b5794cc633b2b943c90b6a5f3b7169cae29eb9850e9a7e98f2b80034133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>5‐aza‐2′‐deoxycytydine</topic><topic>Antimetabolites, Antineoplastic - pharmacology</topic><topic>Antineoplastic agents</topic><topic>Azacitidine - analogs & derivatives</topic><topic>Azacitidine - pharmacology</topic><topic>Biological and medical sciences</topic><topic>breast cancer</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - enzymology</topic><topic>Breast Neoplasms - genetics</topic><topic>depsipeptide</topic><topic>DNA methylation</topic><topic>DNA Methylation - drug effects</topic><topic>DNA Primers - chemistry</topic><topic>Drug Combinations</topic><topic>Drug Synergism</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Female</topic><topic>gelsolin</topic><topic>Gelsolin - genetics</topic><topic>Gelsolin - metabolism</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Gene Silencing</topic><topic>General aspects</topic><topic>Genes, Tumor Suppressor</topic><topic>Histone Deacetylase Inhibitors</topic><topic>histone deacetylation</topic><topic>Humans</topic><topic>In Vitro Techniques</topic><topic>maspin</topic><topic>Medical sciences</topic><topic>Pharmacology. 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. 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.</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> |
fulltext | fulltext |
identifier | ISSN: 0020-7136 |
ispartof | International journal of cancer, 2003-01, Vol.103 (2), p.177-184 |
issn | 0020-7136 1097-0215 |
language | eng |
recordid | cdi_crossref_primary_10_1002_ijc_10789 |
source | Wiley-Blackwell Read & Publish Collection |
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 |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T23%3A11%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synergistic%20antineoplastic%20action%20of%20DNA%20methylation%20inhibitor%205%E2%80%90AZA%E2%80%902%E2%80%B2%E2%80%90deoxycytidine%20and%20histone%20deacetylase%20inhibitor%20depsipeptide%20on%20human%20breast%20carcinoma%20cells&rft.jtitle=International%20journal%20of%20cancer&rft.au=Primeau,%20M%C3%A9lanie&rft.date=2003-01-10&rft.volume=103&rft.issue=2&rft.spage=177&rft.epage=184&rft.pages=177-184&rft.issn=0020-7136&rft.eissn=1097-0215&rft.coden=IJCNAW&rft_id=info:doi/10.1002/ijc.10789&rft_dat=%3Cwiley_cross%3EIJC10789%3C/wiley_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3869-b1a337b5794cc633b2b943c90b6a5f3b7169cae29eb9850e9a7e98f2b80034133%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/12455031&rfr_iscdi=true |