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Osthole interacts with an ER-mitochondria axis and facilitates tumor suppression in ovarian cancer

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dc.contributor.authorBae, Hyocheol-
dc.contributor.authorLee, Jin-Young-
dc.contributor.authorSong, Jisoo-
dc.contributor.authorSong, Gwonhwa-
dc.contributor.authorLim, Whasun-
dc.date.accessioned2021-08-30T03:28:54Z-
dc.date.available2021-08-30T03:28:54Z-
dc.date.created2021-06-19-
dc.date.issued2021-02-
dc.identifier.issn0021-9541-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/49663-
dc.description.abstractOsthole is a natural coumarin found in a variety of plants and has been reported to have diverse biological functions, including antimicrobial, antiviral, immunomodulatory, and anticancer effects. Here, we investigated the natural derivative osthole as a promising anticancer compound against ovarian cancer and evaluated its ability to suppress and abrogate tumor progression. In addition, we found the endoplasmic reticulum-mitochondrial axis-mediated anticancer mechanisms of osthole against ES2 and OV90 ovarian cancer cells and demonstrated its calcium-dependent pharmacological potential. Mechanistically, osthole was found to target the phosphatidylinositol 3-kinase/mitogen-activated protein kinase signaling pathway to facilitate tumor suppression in ovarian cancer. Furthermore, we identified the effects of osthole in a three-dimensional tumor-formation model using the zebrafish xenograft assay, providing convincing evidence of the pharmacological effects of osthole within the anchorage-independent tumor microenvironment. These findings suggest that osthole has strong potential as a pharmacological agent for targeting ovarian cancer.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-
dc.subjectCNIDIUM-MONNIERI-
dc.subjectDOWN-REGULATION-
dc.subjectGLIOMA-CELLS-
dc.subjectULK1-
dc.subjectAPOPTOSIS-
dc.subjectTUMORIGENESIS-
dc.subjectINHIBITION-
dc.subjectPI3K/AKT-
dc.subjectCALCIUM-
dc.subjectCOMPLEX-
dc.titleOsthole interacts with an ER-mitochondria axis and facilitates tumor suppression in ovarian cancer-
dc.typeArticle-
dc.contributor.affiliatedAuthorSong, Gwonhwa-
dc.identifier.doi10.1002/jcp.29913-
dc.identifier.scopusid2-s2.0-85088317267-
dc.identifier.wosid000550897400001-
dc.identifier.bibliographicCitationJOURNAL OF CELLULAR PHYSIOLOGY, v.236, no.2, pp.1025 - 1042-
dc.relation.isPartOfJOURNAL OF CELLULAR PHYSIOLOGY-
dc.citation.titleJOURNAL OF CELLULAR PHYSIOLOGY-
dc.citation.volume236-
dc.citation.number2-
dc.citation.startPage1025-
dc.citation.endPage1042-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaPhysiology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.relation.journalWebOfScienceCategoryPhysiology-
dc.subject.keywordPlusCNIDIUM-MONNIERI-
dc.subject.keywordPlusDOWN-REGULATION-
dc.subject.keywordPlusGLIOMA-CELLS-
dc.subject.keywordPlusULK1-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusTUMORIGENESIS-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusPI3K/AKT-
dc.subject.keywordPlusCALCIUM-
dc.subject.keywordPlusCOMPLEX-
dc.subject.keywordAuthorapoptosis-
dc.subject.keywordAuthorcalcium homeostasis-
dc.subject.keywordAuthorosthole-
dc.subject.keywordAuthorovarian cancer-
dc.subject.keywordAuthorzebrafish-
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