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Cited 90 time in webofscience Cited 92 time in scopus
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dc.contributor.authorKim, WJ-
dc.contributor.authorKim, JH-
dc.contributor.authorJang, SK-
dc.date.accessioned2016-04-01T01:29:20Z-
dc.date.available2016-04-01T01:29:20Z-
dc.date.created2009-08-19-
dc.date.issued2007-12-12-
dc.identifier.issn0261-4189-
dc.identifier.other2008-OAK-0000007354-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/23042-
dc.description.abstractThe signaling lipid molecule 15-deoxy-delta 12,14-prostaglandin J2 (15d-PGJ2) has multiple cellular functions, including anti-inflammatory and antineoplastic activities. Here, we report that 15d-PGJ2 blocks translation through inactivation of translational initiation factor eIF4A. Binding of 15d-PGJ2 to eIF4A blocks the interaction between eIF4A and eIF4G that is essential for translation of many mRNAs. Cysteine 264 in eIF4A is the target site of 15d-PGJ2. The antineoplastic activity of 15d-PGJ2 is likely attributed to inhibition of translation. Moreover, inhibition of translation by 15d-PGJ2 results in stress granule (SG) formation, into which TRAF2 is sequestered. The sequestration of TRAF2 contributes to the anti-inflammatory activity of 15d-PGJ2. These findings reveal a novel crosstalk between translation and inflammatory response, and offer new approaches to develop anticancer and anti-inflammatory drugs that target translation factors including eIF4A.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherNATURE PUBLISHING GROUP-
dc.relation.isPartOfEMBO JOURNAL-
dc.subjecteIF4A-
dc.subject15d-PGJ2-
dc.subjectinflammation-
dc.subjectproliferation-
dc.subjecttranslation-
dc.subjectTRANSFORMATION SUPPRESSOR PDCD4-
dc.subjectSTRESS GRANULE FORMATION-
dc.subjectPRODUCT PATEAMINE-A-
dc.subjectKAPPA-B ACTIVATION-
dc.subjectRNA HELICASE EIF4A-
dc.subjectHEPATITIS-C VIRUS-
dc.subject15-DEOXY-DELTA(12,14)-PROSTAGLANDIN J(2)-
dc.subjectINITIATION CODON-
dc.subjectBINDING-PROTEIN-
dc.subjectPATHWAY-
dc.titleAnti-inflammatory lipid mediator 15d-PGJ2 inhibits translation through inactivation of eIF4A-
dc.typeArticle-
dc.contributor.college생명과학과-
dc.identifier.doi10.1038/sj.emboj.7601920-
dc.author.googleKim, WJ-
dc.author.googleKim, JH-
dc.author.googleJang, SK-
dc.relation.volume26-
dc.relation.issue24-
dc.relation.startpage5020-
dc.relation.lastpage5032-
dc.contributor.id10088382-
dc.relation.journalEMBO JOURNAL-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationEMBO JOURNAL, v.26, no.24, pp.5020 - 5032-
dc.identifier.wosid000251613900009-
dc.date.tcdate2019-01-01-
dc.citation.endPage5032-
dc.citation.number24-
dc.citation.startPage5020-
dc.citation.titleEMBO JOURNAL-
dc.citation.volume26-
dc.contributor.affiliatedAuthorJang, SK-
dc.identifier.scopusid2-s2.0-37149023303-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc60-
dc.type.docTypeArticle-
dc.subject.keywordPlusTRANSFORMATION SUPPRESSOR PDCD4-
dc.subject.keywordPlusSTRESS GRANULE FORMATION-
dc.subject.keywordPlusPRODUCT PATEAMINE-A-
dc.subject.keywordPlusKAPPA-B ACTIVATION-
dc.subject.keywordPlusRNA HELICASE EIF4A-
dc.subject.keywordPlusHEPATITIS-C VIRUS-
dc.subject.keywordPlus15-DEOXY-DELTA(12,14)-PROSTAGLANDIN J(2)-
dc.subject.keywordPlusINITIATION CODON-
dc.subject.keywordPlusBINDING-PROTEIN-
dc.subject.keywordPlusPATHWAY-
dc.subject.keywordAuthoreIF4A-
dc.subject.keywordAuthor15d-PGJ2-
dc.subject.keywordAuthorinflammation-
dc.subject.keywordAuthorproliferation-
dc.subject.keywordAuthortranslation-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaCell Biology-

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Dept of Life Sciences
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