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Combination Effect of Equol and TRAIL against Human Cervical Cancer Cells

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dc.contributor.authorKim, Eun Young-
dc.contributor.authorKim, An Keun-
dc.date.available2021-02-22T12:16:43Z-
dc.date.issued2013-03-
dc.identifier.issn0250-7005-
dc.identifier.issn1791-7530-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/11331-
dc.description.abstractBackground/Aim: Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is a promising candidate for cancer therapy due to its selective ability to induce apoptosis of cancer cells. However, some cancer dells are resistant to TRAIL. Here, we demonstrated that treatment with TRAIL, in combination with equol, sensitizes TRAIL-mediated apoptosis of HeLa cells. Materials and Methods: Cell viability was evaluated by the colorimetric cell viability assay (MTT). Apoptotic cell death was analyzed by flow cytometry and microscopy. Western blotting was performed to examine protein expression and cell surface expression was evaluated by flow cytometry. Enzymatic activity of caspases was measured by the colorimetric assay. Results: Equol enhanced TRAIL-induced apoptosis through activation of caspase-3, -8, -9, and cleavage of BID. Furthermore, DR4/Fc chimera protein and DR5/Fc chimera protein efficiently reduced the activation of caspases and BID cleavage, as well as apoptotic cell death induced by co-treatment with equol and TRAIL. Conclusion: Equol enhances TRAIL-induced apoptosis of HeLa cells through a death receptor-mediated caspase pathway.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherINT INST ANTICANCER RESEARCH-
dc.titleCombination Effect of Equol and TRAIL against Human Cervical Cancer Cells-
dc.typeArticle-
dc.publisher.location그리이스-
dc.identifier.scopusid2-s2.0-84875876070-
dc.identifier.wosid000316770400020-
dc.identifier.bibliographicCitationANTICANCER RESEARCH, v.33, no.3, pp 903 - 912-
dc.citation.titleANTICANCER RESEARCH-
dc.citation.volume33-
dc.citation.number3-
dc.citation.startPage903-
dc.citation.endPage912-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.subject.keywordPlusMALIGNANT GLIOMA-CELLS-
dc.subject.keywordPlusMEDIATED APOPTOSIS-
dc.subject.keywordPlusDEATH RECEPTORS-
dc.subject.keywordPlusMOLECULAR-MECHANISMS-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusGENISTEIN-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordPlusPATHWAY-
dc.subject.keywordPlusLIGAND-
dc.subject.keywordPlusISOFLAVONES-
dc.subject.keywordAuthorTRAIL-
dc.subject.keywordAuthorcervical cancer cells-
dc.subject.keywordAuthorequol-
dc.subject.keywordAuthorcaspases-
dc.subject.keywordAuthordeath receptors-
dc.subject.keywordAuthorapoptosis-
dc.identifier.urlhttps://ar.iiarjournals.org/content/33/3/903.long-
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