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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
15
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pubmed:dateCreated |
2006-6-20
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pubmed:abstractText |
Inhibition of histone deacetylases (HDACs) is emerging as a new strategy in human cancer therapy. Novel 2-aminophenyl benzamides and acrylamides, that can inhibit human HDAC enzymes and induce hyperacetylation of histones in human cancer cells, have been designed and synthesized. These compounds selectively inhibit proliferation and cause cell cycle arrest in various human cancer cells but not in normal cells. The growth inhibition of 2-aminophenyl benzamides and acrylamides against human cancer cells in vitro is reversible and is dependent on the induction of histone acetylation. Compounds of this class can significantly reduce tumor growth in human tumor xenograft models.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0960-894X
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pubmed:author |
pubmed-author:BestermanJeffrey MJM,
pubmed-author:BouchainGilianeG,
pubmed-author:DelormeDanielD,
pubmed-author:FournelMarielleM,
pubmed-author:FréchetteSylvieS,
pubmed-author:GaudetteFrédéricF,
pubmed-author:KalitaAnnA,
pubmed-author:LeitSilvanaS,
pubmed-author:LiZuomeiZ,
pubmed-author:LiuJianhongJ,
pubmed-author:LuAihuaA,
pubmed-author:MacLeodA RobertAR,
pubmed-author:MoradeiOscarO,
pubmed-author:PaquinIsabelleI,
pubmed-author:RaeppelStéphaneS,
pubmed-author:RahilJubrailJ,
pubmed-author:SeinHH,
pubmed-author:Trachy-BourgetMarie-ClaudeMC,
pubmed-author:VaisburgArkadiiA,
pubmed-author:WooSoon HSH,
pubmed-author:ZhouNancyN
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pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4048-52
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
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pubmed:year |
2006
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pubmed:articleTitle |
Substituted N-(2-aminophenyl)-benzamides, (E)-N-(2-aminophenyl)-acrylamides and their analogues: novel classes of histone deacetylase inhibitors.
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pubmed:affiliation |
MethylGene Inc., Department of Medicinal Chemistry, 7220 Frederick-Banting, Montréal, QC, Canada H4S 2A1. moradeio@methylgene.com
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pubmed:publicationType |
Journal Article
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