Role of the tumor suppressor RASSF2 in regulation of MST1 kinase activity

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dc.contributor.authorSong, Hoo-Geunko
dc.contributor.authorOh, Sang-Philko
dc.contributor.authorOh, Hyun-Jungko
dc.contributor.authorLim, Dae-Sikko
dc.date.accessioned2013-03-09T21:00:12Z-
dc.date.available2013-03-09T21:00:12Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2010-01-
dc.identifier.citationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.391, no.1, pp.969 - 973-
dc.identifier.issn0006-291X-
dc.identifier.urihttp://hdl.handle.net/10203/97446-
dc.description.abstractThe tumor suppressor, RASSF2 (Ras association domain family 2), is frequently downregulated in a number of cancers Although exogenously expressed RASSF2 induces apoptotic cell death, the precise roles of RASSF2 under pro-apoptotic conditions remain largely unknown Here. we demonstrate that MST1 (mammalian sterile 20-like kinase 1) regulates RASSF2 protein stability Knockdown of MST1 in cancer cells markedly destabilizes RASSF2, and Mst1-deficient mice show reduced Rassf2 protein levels in several organs. Conversely. RASSF2 activates MsT1 kinase activity through formation of a RASSF2-MST1 complex, which inhibits the MST-FOXO3 signaling pathway RASSF2 also engages the JNK pathway and induces apoptosis in an MST1-independent manner. Collectively, these findings indicate that MST1 is a major determinant of RASSF2 protein stability. and suggest that RASSF2 acts in a complex manner that extends beyond simple protein-protein association to play an important role in MST1 regulation (C) 2009 Published by Elsevier Inc-
dc.languageEnglish-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectEPIGENETIC INACTIVATION-
dc.subjectPROMOTER METHYLATION-
dc.subjectSIGNALING PATHWAY-
dc.subjectGASTRIC-CANCER-
dc.subjectHIPPO PATHWAY-
dc.subjectAPOPTOSIS-
dc.subjectEFFECTOR-
dc.subjectTRANSCRIPTION-
dc.subjectACTIVATION-
dc.subjectGENE-
dc.titleRole of the tumor suppressor RASSF2 in regulation of MST1 kinase activity-
dc.typeArticle-
dc.identifier.wosid000273624500171-
dc.identifier.scopusid2-s2.0-72949094426-
dc.type.rimsART-
dc.citation.volume391-
dc.citation.issue1-
dc.citation.beginningpage969-
dc.citation.endingpage973-
dc.citation.publicationnameBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.identifier.doi10.1016/j.bbrc.2009.11.175-
dc.contributor.localauthorLim, Dae-Sik-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorRASSF2-
dc.subject.keywordAuthorMST1-
dc.subject.keywordAuthorJNK-
dc.subject.keywordAuthorApoptosis-
dc.subject.keywordPlusEPIGENETIC INACTIVATION-
dc.subject.keywordPlusPROMOTER METHYLATION-
dc.subject.keywordPlusSIGNALING PATHWAY-
dc.subject.keywordPlusGASTRIC-CANCER-
dc.subject.keywordPlusHIPPO PATHWAY-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusEFFECTOR-
dc.subject.keywordPlusTRANSCRIPTION-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusGENE-
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