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Flexible ligated ruthenium(II) self-assemblies sensitizes glioma tumor initiating cells in vitro

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dc.contributor.authorElumalai, Palani-
dc.contributor.authorKaushik, Neha-
dc.contributor.authorKim, Dong Hwan-
dc.contributor.authorKim, Hyunuk-
dc.contributor.authorLee, Su Jae-
dc.contributor.authorChoi, Eun Ha-
dc.contributor.authorChi, Ki-Whan-
dc.contributor.authorKaushik, Nagendra Kumar-
dc.date.accessioned2021-08-02T14:51:05Z-
dc.date.available2021-08-02T14:51:05Z-
dc.date.created2021-05-12-
dc.date.issued2017-09-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/19418-
dc.description.abstractThe tumorigenic potentials of residual cancer stem-like cells within tumors represent limitations of current cancer therapies. Here, the authors describe the effects of synthesized flexible, ligated, supramolecular self-assembled chair type tetranuclear ruthenium (II) metallacycles (2-5) on glioblastoma and glioma stem like cells. These self-assemblies were observed to be selectively toxic to glioma cells and CD133-positive glioma stem like cells population. Of the self-assembled compounds tested, metallacycle 4 more efficiently induced glioma stem like cells death within a brain cancer cell population and simultaneously inhibited the formation of free-floating gliospheres by reducing the sphere size. Detailed cell death studies revealed that treatment with metallacycle 4 reduced mitochondrial membrane potentials (an indicator of apoptosis) of glioma stem like cells. These results shows the elimination of cancer stem-like cells using an appropriate ligand binding adaptor offers a potential means of developing metal-based compounds for the treatment of chemo-resistant tumors.-
dc.language영어-
dc.language.isoen-
dc.publisherIMPACT JOURNALS LLC-
dc.titleFlexible ligated ruthenium(II) self-assemblies sensitizes glioma tumor initiating cells in vitro-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Su Jae-
dc.identifier.doi10.18632/oncotarget.19028-
dc.identifier.scopusid2-s2.0-85030479542-
dc.identifier.wosid000408944300014-
dc.identifier.bibliographicCitationONCOTARGET, v.8, no.36, pp.60188 - 60200-
dc.relation.isPartOfONCOTARGET-
dc.citation.titleONCOTARGET-
dc.citation.volume8-
dc.citation.number36-
dc.citation.startPage60188-
dc.citation.endPage60200-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusSELECTIVE SYNTHESIS-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusPLASMA-
dc.subject.keywordPlusDRUG-
dc.subject.keywordPlusSOLVENT-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusMETALLACAGES-
dc.subject.keywordPlusMEDICINE-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordAuthorself-assembly-
dc.subject.keywordAuthorflexible ligand-
dc.subject.keywordAuthorarene-ruthenium-
dc.subject.keywordAuthormetallacycle-
dc.subject.keywordAuthorsolid cancer-
dc.identifier.urlhttps://www.oncotarget.com/article/19028/text/-
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서울 자연과학대학 > 서울 생명과학과 > 1. Journal Articles

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