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Cited 15 time in webofscience Cited 15 time in scopus
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dc.contributor.authorLee, YN-
dc.contributor.authorLee, HY-
dc.contributor.authorKim, JS-
dc.contributor.authorPark, C-
dc.contributor.authorChoi, YH-
dc.contributor.authorLee, TG-
dc.contributor.authorRyu, SH-
dc.contributor.authorKwak, JY-
dc.contributor.authorBae, YS-
dc.date.accessioned2016-04-01T02:10:28Z-
dc.date.available2016-04-01T02:10:28Z-
dc.date.created2009-08-13-
dc.date.issued2005-05-26-
dc.identifier.issn0304-3835-
dc.identifier.other2005-OAK-0000005137-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/24583-
dc.description.abstractWe investigated the effect of the novel phospholipase C activator, m-3M3FBS, on the apoptosis of leukemic cells. m-3M3FBS inhibited the growth of the leukemic cell lines U937 and THP-1, but not primary monocytes. m-3M3FBS induced the apoptosis of U937 cells, which was accompanied by chromatin condensation and DNA fragmentation. Moreover, m-3M3FBS-induced apoptosis appeared to involve the down-regulation of anti-apoptotic Bcl-2, the up-regulation of proapoptotic Bax, the release of cytochrome c, and caspase activation. m-3M3FBS-induced apoptosis of U937 cells was also partly inhibited by BAPTA-AM and EGTA, indicating the involvement of intracellular calcium signaling on the apoptosis in U937 cells. The results of our study suggest that m-3M3FBS can be developed as a novel anti-leukemic agent. (c) 2004 Elsevier Ireland Ltd. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherELSEVIER IRELAND LTD-
dc.relation.isPartOfCANCER LETTERS-
dc.subjectm-3M3FBS-
dc.subjectapoptosis-
dc.subjectU937-
dc.subjectCa2+-
dc.subjectBcl-2-
dc.subjectcaspase-
dc.subjectOXIDATIVE STRESS-
dc.subjectINTRACELLULAR CA2+-
dc.subjectHYDROGEN-PEROXIDE-
dc.subjectN-ACETYLCYSTEINE-
dc.subjectCYTOCHROME-C-
dc.subjectU937 CELLS-
dc.subjectCALCIUM-
dc.subjectDEATH-
dc.subjectIDENTIFICATION-
dc.subjectSUPEROXIDE-
dc.titleThe novel phospholipase C activator, m-3M3FBS, induces monocytic leukemia cell apoptosis-
dc.typeArticle-
dc.contributor.college생명과학과-
dc.identifier.doi10.1016/j.canlet.2004.09.017-
dc.author.googleLee, YN-
dc.author.googleLee, HY-
dc.author.googleKim, JS-
dc.author.googlePark, C-
dc.author.googleChoi, YH-
dc.author.googleLee, TG-
dc.author.googleRyu, SH-
dc.author.googleKwak, JY-
dc.author.googleBae, YS-
dc.relation.volume222-
dc.relation.issue2-
dc.relation.startpage227-
dc.relation.lastpage235-
dc.contributor.id10069853-
dc.relation.journalCANCER LETTERS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationCANCER LETTERS, v.222, no.2, pp.227 - 235-
dc.identifier.wosid000229351800012-
dc.date.tcdate2019-02-01-
dc.citation.endPage235-
dc.citation.number2-
dc.citation.startPage227-
dc.citation.titleCANCER LETTERS-
dc.citation.volume222-
dc.contributor.affiliatedAuthorRyu, SH-
dc.identifier.scopusid2-s2.0-18044381911-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc13-
dc.type.docTypeArticle-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusINTRACELLULAR CA2+-
dc.subject.keywordPlusHYDROGEN-PEROXIDE-
dc.subject.keywordPlusN-ACETYLCYSTEINE-
dc.subject.keywordPlusCYTOCHROME-C-
dc.subject.keywordPlusU937 CELLS-
dc.subject.keywordPlusCALCIUM-
dc.subject.keywordPlusDEATH-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusSUPEROXIDE-
dc.subject.keywordAuthorm-3M3FBS-
dc.subject.keywordAuthorapoptosis-
dc.subject.keywordAuthorU937-
dc.subject.keywordAuthorCa2+-
dc.subject.keywordAuthorBcl-2-
dc.subject.keywordAuthorcaspase-
dc.relation.journalWebOfScienceCategoryOncology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-

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Dept of Life Sciences
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