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Cited 23 time in webofscience Cited 27 time in scopus
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dc.contributor.authorYang, SH-
dc.contributor.authorLee, CG-
dc.contributor.authorLee, CW-
dc.contributor.authorChoi, EJ-
dc.contributor.authorYoon, SK-
dc.contributor.authorAhn, KS-
dc.contributor.authorSung, YC-
dc.date.accessioned2016-03-31T13:04:27Z-
dc.date.available2016-03-31T13:04:27Z-
dc.date.created2009-02-28-
dc.date.issued2002-06-30-
dc.identifier.issn1016-8478-
dc.identifier.other2002-OAK-0000002742-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/19010-
dc.description.abstractThe p38 mitogen activated kinase (MAPK) signaling pathway plays an essential role in regulating many cellular processes, including inflammation, cell differentiation, and cell death. Here, we report that the hepatitis C virus (HCV) core inhibits the Fas-mediated p38 signaling pathway. The Fas-mediated p38 activation is suppressed in core-expressing HepG2 cell lines, as well as in the hepatocytes of transgenic mice. In addition, core protein blocked the Fas-mediated activation of apoptosis signal-regulating kinase 1 (ASK1), a major upstream MAPKKK of p38. Treatment of a specific p38 inhibitor (SB203580) or overexpression of a kinase-defective mutant, ASK1 (K709R), promoted Fas-mediated cell death in HepG2 cells. This suggests that the p38 and ASK1 activation is required for cell survival against Fas-mediated cell death. In addition, we observed that the HCV core protein enhances Fas-mediated liver injury and lethality in transgenic mice. Collectively, our findings suggest that the HCV core inhibits the Fas-mediated p38 signaling pathway, which results in accelerated Fas-mediated cell death.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherSPRINGER-VERLAG SINGAPORE PTE LTD-
dc.relation.isPartOfMOLECULES AND CELLS-
dc.subjectASK1-
dc.subjectcore-
dc.subjectFas-
dc.subjecthepatitis C virus-
dc.subjectp38-
dc.subjectNECROSIS-FACTOR-ALPHA-
dc.subjectICE/CED-3 FAMILY PROTEASES-
dc.subjectPROTEIN-KINASE-
dc.subjectMAP KINASE-
dc.subjectTRANSDUCTION PATHWAY-
dc.subjectCELL-DEATH-
dc.subjectT-CELLS-
dc.subjectAPOPTOSIS-
dc.subjectLIVER-
dc.subjectSURVIVAL-
dc.titleHepatitis C virus core inhibits the fas-mediated p38 mitogen activated kinase signaling pathway in hepatocytes-
dc.typeArticle-
dc.contributor.college생명과학과-
dc.author.googleYang, SH-
dc.author.googleLee, CG-
dc.author.googleLee, CW-
dc.author.googleChoi, EJ-
dc.author.googleYoon, SK-
dc.author.googleAhn, KS-
dc.author.googleSung, YC-
dc.relation.volume13-
dc.relation.issue3-
dc.relation.startpage452-
dc.relation.lastpage462-
dc.contributor.id10053752-
dc.relation.journalMOLECULES AND CELLS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationMOLECULES AND CELLS, v.13, no.3, pp.452 - 462-
dc.identifier.wosid000176557400014-
dc.date.tcdate2019-01-01-
dc.citation.endPage462-
dc.citation.number3-
dc.citation.startPage452-
dc.citation.titleMOLECULES AND CELLS-
dc.citation.volume13-
dc.contributor.affiliatedAuthorSung, YC-
dc.identifier.scopusid2-s2.0-0013254477-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc22-
dc.type.docTypeArticle-
dc.subject.keywordPlusNECROSIS-FACTOR-ALPHA-
dc.subject.keywordPlusICE/CED-3 FAMILY PROTEASES-
dc.subject.keywordPlusPROTEIN-KINASE-
dc.subject.keywordPlusMAP KINASE-
dc.subject.keywordPlusTRANSDUCTION PATHWAY-
dc.subject.keywordPlusCELL-DEATH-
dc.subject.keywordPlusT-CELLS-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusLIVER-
dc.subject.keywordPlusSURVIVAL-
dc.subject.keywordAuthorASK1-
dc.subject.keywordAuthorcore-
dc.subject.keywordAuthorFas-
dc.subject.keywordAuthorhepatitis C virus-
dc.subject.keywordAuthorp38-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaCell Biology-

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성영철SUNG, YOUNG CHUL
Dept of Life Sciences
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