Mangosenone F, A furanoxanthone from Garciana mangostana, induces reactive oxygen species-mediated apoptosis in lung cancer cells and decreases xenograft tumor growth

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dc.contributor.authorK H Seo-
dc.contributor.authorHyung Won Ryu-
dc.contributor.authorM J Park-
dc.contributor.authorK H Park-
dc.contributor.authorJ H Kim-
dc.contributor.authorM J Lee-
dc.contributor.authorH J Kang-
dc.contributor.authorS L Kim-
dc.contributor.authorJ H Lee-
dc.contributor.authorW D Seo-
dc.date.accessioned2017-04-19T10:14:01Z-
dc.date.available2017-04-19T10:14:01Z-
dc.date.issued2015-
dc.identifier.issn0951418X-
dc.identifier.uri10.1002/ptr.5428ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/12967-
dc.description.abstractMangosenone F (MSF), a natural xanthone, was isolated form Carcinia mangotana, and a few studies have reported its glycosidase inhibitor effect. In this study we investigated the anti lung cancer effect of MSF both in vitro and in vivo. MSF inhibited cancer cell cytotoxicity and induced and induced apoptosis via reactive oxygen species (ROS) generation in NCI-H460. MSF treatment also showed in pronounced release of apoptogenic cytochrome c from the mitochondria to the cytosol, downregulation of Bcl-2 and Bcl-xL, and upregulation of Bax, suggesting that caspase-mediated pathways were involved in MSF-induced apoptosis. ROS activation of the mitogen-activated protein kinase signaling pathway was shown to play a predominant role in the apoptosis mechanism of MSF. Compared with cisplatin treatment, MSF treatment showed significantly increased inhibition of the growth of NCI-H460 cells xenografted in nude mice. Together, these results indicate the potential of MSF as a candidate natural anticancer drug by promoting ROS production.-
dc.publisherWiley-
dc.titleMangosenone F, A furanoxanthone from Garciana mangostana, induces reactive oxygen species-mediated apoptosis in lung cancer cells and decreases xenograft tumor growth-
dc.title.alternativeMangosenone F, A furanoxanthone from Garciana mangostana, induces reactive oxygen species-mediated apoptosis in lung cancer cells and decreases xenograft tumor growth-
dc.typeArticle-
dc.citation.titlePhytotherapy Research-
dc.citation.number11-
dc.citation.endPage1760-
dc.citation.startPage1753-
dc.citation.volume29-
dc.contributor.affiliatedAuthorHyung Won Ryu-
dc.contributor.alternativeName서경혜-
dc.contributor.alternativeName류형원-
dc.contributor.alternativeName박미진-
dc.contributor.alternativeName박기훈-
dc.contributor.alternativeName김진효-
dc.contributor.alternativeName이미자-
dc.contributor.alternativeName강현정-
dc.contributor.alternativeName김선림-
dc.contributor.alternativeName이진환-
dc.contributor.alternativeName서우덕-
dc.identifier.bibliographicCitationPhytotherapy Research, vol. 29, no. 11, pp. 1753-1760-
dc.identifier.doi10.1002/ptr.5428-
dc.subject.keywordapoptosis-
dc.subject.keywordcaspase-
dc.subject.keywordlung cancer cell-
dc.subject.keywordmangosenone F-
dc.subject.keywordROS-
dc.subject.keywordxenografted nude mice-
dc.subject.localapoptosis-
dc.subject.localApoptosis-
dc.subject.localcaspase-
dc.subject.localCaspase-
dc.subject.locallung cancer cell-
dc.subject.localmangosenone F-
dc.subject.localROS-
dc.subject.localxenografted nude mice-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Natural Medicine Research Center > 1. Journal Articles
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