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Induction of apoptosis in the HepG2 cells by HY53, a novel natural compound isolated from Bauhinia forficata

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dc.contributor.authorLim, Haeyoung-
dc.contributor.authorLim, Yoongho-
dc.contributor.authorCho, Youl-Hee-
dc.contributor.authorLee, Chul-Hoon-
dc.date.accessioned2021-06-23T21:37:51Z-
dc.date.available2021-06-23T21:37:51Z-
dc.date.issued2006-08-
dc.identifier.issn1017-7825-
dc.identifier.issn1738-8872-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/44735-
dc.description.abstractIn the search for a novel cytotoxic substance from medicinal plants, HY53 (C17H32O2N2; molecular weight 296) was isolated from the leaves of Pata de Vaca (Bauhinia forficata). The growth of the HepG2 cells was inhibited in a dose-dependent manner when treated with 0.07 to 0.40 mM HY53 for 24 h (IC50: 0.13 mM). Furthermore, nuclear DAPI staining revealed the typical nuclear features of apoptosis in the HepG2 cells exposed to 0.27 mM HY53, whereas a flow cytometric analysis of the HepG2 cells using propidium iodide showed that the apoptotic cell population increased gradually from 8% at 0 mM to 23% at 0.14 mM and 45% at 0.40 mM after being exposed to each concentration of HY53 for 24 h. Moreover, a TUNEL assay also exhibited the apoptotic induction of the HepG2 cells treated with HY53. To obtain further information on the HY53-induced apoptosis, the expression level of certain apoptosis-associated proteins was examined using a Western blot analysis. Treatment of the HepG2 cells with HY53 resulted in the activation of caspase-3, and subsequent proteolytic cleavage of poly(ADP-ribose) polymerase (PARP). Consequently, the results confirmed that the apoptosis in the HepG2 cells was induced by HY53 and the involvement of caspase-3-mediated PARP cleavage in the apoptotic process.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisher한국미생물·생명공학회-
dc.titleInduction of apoptosis in the HepG2 cells by HY53, a novel natural compound isolated from Bauhinia forficata-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.scopusid2-s2.0-33748679748-
dc.identifier.wosid000240111200015-
dc.identifier.bibliographicCitationJournal of Microbiology and Biotechnology, v.16, no.8, pp 1262 - 1268-
dc.citation.titleJournal of Microbiology and Biotechnology-
dc.citation.volume16-
dc.citation.number8-
dc.citation.startPage1262-
dc.citation.endPage1268-
dc.type.docTypeArticle-
dc.identifier.kciidART001022871-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaMicrobiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.subject.keywordPlusPENICILLIUM-MINIOLUTEUM F558-
dc.subject.keywordPlusCYCLE PROGRESSION-
dc.subject.keywordPlusANTICANCER DRUGS-
dc.subject.keywordPlusHELA-CELLS-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusCHEMOTHERAPY-
dc.subject.keywordPlusINHIBITOR-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusFLAVONOIDS-
dc.subject.keywordPlusETOPOSIDE-
dc.subject.keywordAuthorHY53-
dc.subject.keywordAuthorBauhinia forficata-
dc.subject.keywordAuthorPata de Vaca-
dc.subject.keywordAuthorapoptosis-
dc.identifier.urlhttps://www.koreascience.or.kr/article/JAKO200634718411633.page-
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