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The activation of ERK1/2 via a tyrosine kinase pathway attenuates trail- induced apoptosis in HeLa cells

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dc.contributor.authorLee, Myoung Woo-
dc.contributor.authorBach, Jae Hyung-
dc.contributor.authorLee, Hyun Jung-
dc.contributor.authorLee, Do Yeon-
dc.contributor.authorJoo, Wan Seok-
dc.contributor.authorKim, Yong Sik-
dc.contributor.authorPark, Soon Cheol-
dc.contributor.authorKim, Kyung Yong-
dc.contributor.authorLee, Won Bok-
dc.contributor.authorKim, Sung Su-
dc.date.available2019-05-30T08:33:39Z-
dc.date.issued2005-
dc.identifier.issn0735-7907-
dc.identifier.issn1532-4192-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/24700-
dc.description.abstractTumor necrosis factor-related apoptosis-inducing ligand ( TRAIL) serves as an extracellular signal that triggers apoptosis in tumor cells. To characterize the molecular events involved in TRAIL-induced apoptotic signaling, we investigated the role of extracellular signal-regulated kinase 1/2 (ERK1/2) in HeLa cell death. Here we show that TRAIL-activated ERK1/2 through a tyrosine kinase-dependent pathway, subsequently elevated antiapoptotic Bcl-2 protein levels. ERK1/2 inhibition with PD98059 promoted apoptotic cell death through the downregulation of ERK1/2 activity and Bcl-2 protein levels. Moreover, tyrosine kinase inhibition with Genistein in TRAIL-induced apoptosis effectively attenuated ERK1/2 activity and enhanced apoptotic cell death. Taken together, our results indicate that ERK1/2 activation via tyrosine kinase pathway plays a protective role as the cellular defense mechanism through the upregulation of Bcl-2 protein levels in TRAIL-induced apoptosis.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherTAYLOR & FRANCIS INC-
dc.titleThe activation of ERK1/2 via a tyrosine kinase pathway attenuates trail- induced apoptosis in HeLa cells-
dc.typeArticle-
dc.identifier.doi10.1080/07357900500283036-
dc.identifier.bibliographicCitationCANCER INVESTIGATION, v.23, no.7, pp 586 - 592-
dc.description.isOpenAccessN-
dc.identifier.wosid000234072600004-
dc.identifier.scopusid2-s2.0-33344476441-
dc.citation.endPage592-
dc.citation.number7-
dc.citation.startPage586-
dc.citation.titleCANCER INVESTIGATION-
dc.citation.volume23-
dc.type.docTypeArticle-
dc.publisher.location영국-
dc.subject.keywordAuthorTRAIL-
dc.subject.keywordAuthorERK1/2-
dc.subject.keywordAuthortyrosine kinase-
dc.subject.keywordAuthorBcl-2 protein-
dc.subject.keywordAuthorapoptosis-
dc.subject.keywordPlusPROTEIN-COUPLED RECEPTORS-
dc.subject.keywordPlusCYTOTOXIC LIGAND TRAIL-
dc.subject.keywordPlusMAP KINASE-
dc.subject.keywordPlusPROMOTES SURVIVAL-
dc.subject.keywordPlusDEPENDENT PATHWAY-
dc.subject.keywordPlusCANCER CELLS-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusBCL-2-
dc.subject.keywordPlusPHOSPHORYLATION-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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