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Cited 23 time in webofscience Cited 26 time in scopus
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dc.contributor.authorLee, D-
dc.contributor.authorKwon, JH-
dc.contributor.authorKim, EH-
dc.contributor.authorKim, ES-
dc.contributor.authorChoi, KY-
dc.date.accessioned2016-04-01T02:33:23Z-
dc.date.available2016-04-01T02:33:23Z-
dc.date.created2010-12-06-
dc.date.issued2010-06-01-
dc.identifier.issn0304-3835-
dc.identifier.other2010-OAK-0000022343-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/25348-
dc.description.abstractWe investigated the effect of HMGB2 on the stability of p53 protein in HeLa cells. Overexpression of HMGB2 led to accumulation of the p53 protein, whereas HMGB2 knockdown with siRNA resulted in a substantial decrease in the p53 protein level. The HMGB2-dependent increase of p53 stability was specific for HPV-positive HeLa cells as HCT116 and MCF7 cell lines did not demonstrate this response. Co-expression of HMGB2 and HPV E6 prevented HPV E6 protein-mediated ubiquitination and degradation of p53. FACS analysis exhibited that HeLa cells transfected with HMGB2 displayed decreased cell proliferation, with a concomitant increase of the p53 protein and arrest of the cell cycle, predominantly in Cl phase. Our findings collectively suggest that HMGB2 could stabilize p53 by interfering with E6/E6AP-mediated p53 degradation in HPV-positive HeLa cells. (C) 2009 Elsevier Ireland Ltd. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherELSEVIER IRELAND LTD-
dc.relation.isPartOfCANCER LETTERS-
dc.subjectHigh mobility group B2-
dc.subjectp53 degradation-
dc.subjectHPV E6-
dc.subjectHeLa cells-
dc.subjectTYPE-18 E6-
dc.subjectPROTEIN-
dc.subjectBINDING-
dc.subjectDNA-
dc.subjectUBIQUITINATION-
dc.titleHMGB2 stabilizes p53 by interfering with E6/E6AP-mediated p53 degradation in human papillomavirus-positive HeLa cells-
dc.typeArticle-
dc.contributor.college생명과학과-
dc.identifier.doi10.1016/J.CANLET.2009.11.015-
dc.author.googleLee, D-
dc.author.googleKwon, JH-
dc.author.googleKim, EH-
dc.author.googleKim, ES-
dc.author.googleChoi, KY-
dc.relation.volume292-
dc.relation.issue1-
dc.relation.startpage125-
dc.relation.lastpage132-
dc.contributor.id10052985-
dc.relation.journalCANCER LETTERS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationCANCER LETTERS, v.292, no.1, pp.125 - 132-
dc.identifier.wosid000277744800016-
dc.date.tcdate2019-02-01-
dc.citation.endPage132-
dc.citation.number1-
dc.citation.startPage125-
dc.citation.titleCANCER LETTERS-
dc.citation.volume292-
dc.contributor.affiliatedAuthorChoi, KY-
dc.identifier.scopusid2-s2.0-77951212834-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc20-
dc.description.scptc21*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusTYPE-18 E6-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusBINDING-
dc.subject.keywordPlusDNA-
dc.subject.keywordPlusUBIQUITINATION-
dc.subject.keywordAuthorHigh mobility group B2-
dc.subject.keywordAuthorp53 degradation-
dc.subject.keywordAuthorHPV E6-
dc.subject.keywordAuthorHeLa cells-
dc.relation.journalWebOfScienceCategoryOncology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-

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최관용CHOI, KWAN YONG
Div of Integrative Biosci & Biotech
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