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Cited 4 time in webofscience Cited 4 time in scopus
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dc.contributor.authorYUN, EUN JIN-
dc.contributor.authorSeo, Kang-Sik-
dc.contributor.authorKim, Hoon-
dc.contributor.authorHong, Tae-Hwa-
dc.contributor.authorKim, Jong-Seok-
dc.contributor.authorSong, Kyoung-Sub-
dc.contributor.authorPark, Ji-Hoon-
dc.contributor.authorJung, Young-Hoon-
dc.contributor.authorPark, Jong-Il-
dc.contributor.authorKweon, Gi Ryang-
dc.contributor.authorYoon, Wan-Hee-
dc.contributor.authorLim, Kyu-
dc.contributor.authorHwang, Byung-Doo-
dc.date.accessioned2018-01-09T09:03:47Z-
dc.date.available2018-01-09T09:03:47Z-
dc.date.created2017-11-13-
dc.date.issued2013-05-10-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/40838-
dc.description.abstractApicularen A is a novel antitumor agent and strongly induces death in tumor cells. In this study, we synthesized apicularen A acetate, an acetyl derivative of apicularen A, and investigated its antitumor effect and mechanism in HM7 colon cancer cells. Apicularen A acetate induced apoptotic cell death and caspase-3 activation; however, the pan-caspase inhibitor Z-VAD-fmk could not prevent this cell death. Apicularen A acetate induced the loss of mitochondrial membrane potential and the translocation of apoptosis-inducing factor (AIF) from mitochondria. In addition, apicularen A acetate significantly decreased tubulin mRNA and protein levels and induced disruption of microtubule networks. Taken together, these results indicate that the mechanism of apicularen A acetate involves caspase-independent apoptotic cell death and disruption of microtubule architecture. (C) 2013 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER-
dc.relation.isPartOfBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.subjectINDUCED APOPTOSIS-
dc.subjectRAW-264.7 CELLS-
dc.subjectINDUCTION-
dc.subjectLINE-
dc.subjectFAS-
dc.subjectCASPASE-3-
dc.titleApicularen A acetate induced cell death via AIF translocation and disrupts the microtubule network by down-regulating tubulin in HM7 human colon cancer cells-
dc.typeArticle-
dc.identifier.doi10.1016/j.bbrc.2013.03.133-
dc.type.rimsART-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.434, no.3, pp.634 - 640-
dc.identifier.wosid000319481500039-
dc.date.tcdate2019-02-01-
dc.citation.endPage640-
dc.citation.number3-
dc.citation.startPage634-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume434-
dc.contributor.affiliatedAuthorYUN, EUN JIN-
dc.identifier.scopusid2-s2.0-84880482712-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc2-
dc.type.docTypeArticle-
dc.subject.keywordPlusINDUCED APOPTOSIS-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordPlusLINE-
dc.subject.keywordPlusFAS-
dc.subject.keywordPlusCASPASE-3-
dc.subject.keywordAuthorApicularen A acetate-
dc.subject.keywordAuthorCaspase-independent apoptosis-
dc.subject.keywordAuthorApoptosis-inducing factor-
dc.subject.keywordAuthorMicrotubule disruption-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-

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