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Exosomes derived from microRNA-584 transfected mesenchymal stem cells: novel alternative therapeutic vehicles for cancer therapy

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dc.contributor.authorKim, Ran-
dc.contributor.authorLee, Seokyeon-
dc.contributor.authorLee, Jihyun-
dc.contributor.authorKim, Minji-
dc.contributor.authorKim, Won Jung-
dc.contributor.authorLee, Hee Won-
dc.contributor.authorLee, Min Young-
dc.contributor.authorKim, Jongmin-
dc.contributor.authorChang, Woochul-
dc.date.available2021-02-22T08:46:02Z-
dc.date.issued2018-08-
dc.identifier.issn1976-6696-
dc.identifier.issn1976-670X-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/4378-
dc.description.abstractExosomes are small membranous vesicles which contain abundant RNA molecules, and are transferred from releasing cells to uptaking cells. MicroRNA (miRNA) is one of the transferred molecules affecting the adopted cells, including glioma cells. We hypothesized that mesenchymal stem cells (MSCs) can secrete exosomes loading miRNA and have important effects on the progress of gliomas. To determine these effects by treating exosomal miRNA in culture media of miRNA mimic transfected MSCs, we assessed the in vitro cell proliferation and invasion capabilities, and the expression level of relative proteins associated with cell apoptosis, growth and migration. For animal studies, the mice injected with U87 cells were exposed to exosomes derived from miRNA-584-5p transfected MSCs, to confirrn the influence of exosomal miRNA on the progress of glioma. Based on our results, we propose a new targeted cancer therapy wherein exosomes derived from miRNA transfected MSCs could be used to modulate tumor progress as the anticancer vehicles.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherKOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY-
dc.titleExosomes derived from microRNA-584 transfected mesenchymal stem cells: novel alternative therapeutic vehicles for cancer therapy-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.5483/BMBRep.2018.51.8.105-
dc.identifier.scopusid2-s2.0-85055071593-
dc.identifier.wosid000452141700008-
dc.identifier.bibliographicCitationBMB REPORTS, v.51, no.8, pp 406 - 411-
dc.citation.titleBMB REPORTS-
dc.citation.volume51-
dc.citation.number8-
dc.citation.startPage406-
dc.citation.endPage411-
dc.type.docTypeArticle-
dc.identifier.kciidART002377219-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.subject.keywordPlusMIGRATION-
dc.subject.keywordPlusGLIOMA-
dc.subject.keywordPlusPROMOTES-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusINHIBIT-
dc.subject.keywordAuthorCancer therapy-
dc.subject.keywordAuthorExosomes-
dc.subject.keywordAuthorGlioma-
dc.subject.keywordAuthorMesenchymal stem cells-
dc.subject.keywordAuthorMicroRNA-
dc.identifier.urlhttp://www.bmbreports.org/journal/view.html?doi=10.5483/BMBRep.2018.51.8.105-
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