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pubmed-article:20006609pubmed:abstractTextDNA damage checkpoints are essential for maintenance of genome integrity. We report here that inducible overexpression of the transcription factor Sharp-1 results in an S and G2/M cell cycle arrest, concomitant with the upregulation of Brca1 and GADD45alpha expression. In addition, we show that endogenous Sharp-1 mRNA is increased by DNA-damaging agents. Consistently, Sharp-1 overexpressing cells exhibit reduced apoptosis in response to chemotherapeutic drugs along with lower p53 expression and activity. Our studies identify a novel function for Sharp-1 in cell cycle arrest and DNA damage-induced apoptosis. Inappropriate Sharp-1 expression may therefore be associated with tumorigenesis.lld:pubmed
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pubmed-article:20006609pubmed:authorpubmed-author:LiuJian-JunJJlld:pubmed
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pubmed-article:20006609pubmed:authorpubmed-author:ChungTeng-Kai...lld:pubmed
pubmed-article:20006609pubmed:copyrightInfo2009 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.lld:pubmed
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pubmed-article:20006609pubmed:articleTitleSharp-1 modulates the cellular response to DNA damage.lld:pubmed
pubmed-article:20006609pubmed:affiliationDepartment of Physiology, National University of Singapore, Singapore, Singapore.lld:pubmed
pubmed-article:20006609pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:20006609pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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