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Eupatilin inhibits proliferation of ras-transformed human breast epithelial (MCF-10A-ras) cells

DC Field Value Language
dc.contributor.authorKim, Do-Hee-
dc.contributor.authorNa, Hye-Kyung-
dc.contributor.authorOh, Tae Young-
dc.contributor.authorShin, Chang-Yell-
dc.contributor.authorSurh, Young-Joon-
dc.date.accessioned2021-01-31T10:16:58Z-
dc.date.available2021-01-31T10:16:58Z-
dc.date.created2017-11-16-
dc.date.issued2005-
dc.identifier.citationJournal of Environmental Pathology, Toxicology and Oncology, Vol.24 No.4, pp.251-259-
dc.identifier.issn0731-8898-
dc.identifier.other6288-
dc.identifier.urihttps://hdl.handle.net/10371/172784-
dc.description.abstractArtemisia asiatica Nakai has been used frequently in traditional Asian medicine for the treatment of inflammation and cancer. Eupatilin (5,7-dihydroxy-3',4', 6-trimethoxy-flavone) was shown to be a pharmacologically active ingredient of A asiatica. In the present study, we found that expression of cyclin D1, a key protein that regulates G(1)/S progression, was decreased in MCF-10A-ras cells treated with eupatilin. Downregulation of cyclin D1 expression by eupatifin was accompanied by a reduced expression of c-Jun and the DNA binding activity of the transcription factor AP-1. The expression of p21(waf1/Cip1) was also decreased by eupatilin treatment in both protein and the mRNA levels. We concluded that the inhibitory effect of eupatilin on p21(waf1/Cip1) expression is likely to be associated with the downregulation of cyclin D1 expression and AP-1 activation, which play an important role in the cell cycle arrest of ras-transformed breast epithelial cells.-
dc.language영어-
dc.publisherBegell House-
dc.titleEupatilin inhibits proliferation of ras-transformed human breast epithelial (MCF-10A-ras) cells-
dc.typeArticle-
dc.contributor.AlternativeAuthor서영준-
dc.identifier.doi10.1615/JEnvironPatholToxicolOncol.v24.i4.20-
dc.citation.journaltitleJournal of Environmental Pathology, Toxicology and Oncology-
dc.identifier.wosid000234089300002-
dc.identifier.scopusid2-s2.0-33644835136-
dc.citation.endpage259-
dc.citation.number4-
dc.citation.startpage251-
dc.citation.volume24-
dc.identifier.sci000234089300002-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorSurh, Young-Joon-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusFACTOR-KAPPA-B-
dc.subject.keywordPlusCYCLE PROGRESSION-
dc.subject.keywordPlusC-JUN-
dc.subject.keywordPlusARTEMISIA PLANTS-
dc.subject.keywordPlusDNA-DAMAGE-
dc.subject.keywordPlusP21 GENE-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusCURCUMIN-
dc.subject.keywordAuthorArtemisia asiatica-
dc.subject.keywordAuthoreupatilin-
dc.subject.keywordAuthorMCF-10A-ras cells-
dc.subject.keywordAuthorcell proliferation-
dc.subject.keywordAuthorcell cycle arrest-
dc.subject.keywordAuthorcyclin D1-
dc.subject.keywordAuthorAP-1-
dc.subject.keywordAuthorc-Jun-
dc.subject.keywordAuthorp21(waf1/Cip1)-
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  • College of Pharmacy
  • Department of Pharmacy
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