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Clusterin, a novel modulator of TGF-beta signaling, is involved in Smad2/3 stability

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dc.contributor.authorLee, Kwan-Bok-
dc.contributor.authorJeon, Jun-Ho-
dc.contributor.authorChoi, Inpyo-
dc.contributor.authorKwon, O-Yu-
dc.contributor.authorYu, Kweon-
dc.contributor.authorYou, Kwan-Hee-
dc.date.available2021-02-22T14:46:53Z-
dc.date.issued2008-02-22-
dc.identifier.issn0006-291X-
dc.identifier.issn1090-2104-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/14322-
dc.description.abstractClusterin (CLU) is known as a multifunctional protein involved in a variety of physiological processes including lipid transport, epithelial cell differentiation, tumorigenesis, and apoptosis. It is known that CLU interacts with TGF-beta type 11 receptor (T beta R11). However, the relationship of CLU and TGF-beta signaling is unclear. Here we present that CLU is a novel modulator of TGF-beta signaling by regulating Smad2/3 proteins. Overexpression of CLU enhanced TGF-beta-induced transcriptional activity and increased the amount of Smad2/3 proteins, while CLU siRNA repressed TGF-beta-induced transcriptional activity and decreased the amount of Smad2/3 proteins in Hep3B cells. We also found that CLU was involved in Smad2/3 stability at the protein level. These findings suggest that CLU regulates TGF-beta signaling pathway by modulating the stability of Smad2/3 proteins. (c) 2007 Elsevier Inc. All rights reserved.-
dc.format.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titleClusterin, a novel modulator of TGF-beta signaling, is involved in Smad2/3 stability-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.bbrc.2007.12.033-
dc.identifier.scopusid2-s2.0-37549041733-
dc.identifier.wosid000252512800007-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.366, no.4, pp 905 - 909-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume366-
dc.citation.number4-
dc.citation.startPage905-
dc.citation.endPage909-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusI-KAPPA-B-
dc.subject.keywordPlusUBIQUITIN-DEPENDENT DEGRADATION-
dc.subject.keywordPlusPROTEINS-
dc.subject.keywordPlusCHAPERONE-
dc.subject.keywordPlusTRANSCRIPTION-
dc.subject.keywordPlusHOMOLOG-
dc.subject.keywordPlusCOMPLEX-
dc.subject.keywordPlusSTRESS-
dc.subject.keywordPlusALPHA-
dc.subject.keywordPlusDEATH-
dc.subject.keywordAuthorclusterin-
dc.subject.keywordAuthorTGF-beta-
dc.subject.keywordAuthorSmad2-
dc.subject.keywordAuthorSmad3-
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