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Cited 35 time in webofscience Cited 40 time in scopus
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Non-thermal plasma with 2-deoxy-D-glucose synergistically induces cell death by targeting glycolysis in blood cancer cells

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dc.contributor.authorKaushik, Neha-
dc.contributor.authorLee, Su Jae-
dc.contributor.authorChoi, Tae Gyu-
dc.contributor.authorBaik, Ku Youn-
dc.contributor.authorUhm, Han Sup-
dc.contributor.authorKim, Chung Hyeok-
dc.contributor.authorKaushik, Nagendra Kumar-
dc.contributor.authorChoi, Eun Ha-
dc.date.accessioned2021-08-02T18:26:36Z-
dc.date.available2021-08-02T18:26:36Z-
dc.date.created2021-05-12-
dc.date.issued2015-03-
dc.identifier.issn2045-2322-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/25635-
dc.description.abstractIn this study, we show the selective and efficient anti-cancer effects of plasma (at a low dose) when cell metabolic modifiers are also included. 2-deoxy-D-glucose (2-DG), a glycolytic inhibitor, was used with effective doses of non-thermal plasma, synergistically attenuating cell metabolic viability and inducing caspase-dependent and independent cell death. The combination treatment decreased the intracellular ATP and lactate production in various types of blood cancer cells in vitro. Taken together, our findings suggest that 2-DG enhances the efficacy and selectivity of plasma and induces the synergistic inhibition of cancer cell growth by targeting glycolysis and apoptosis. Specifically, this treatment strategy demonstrated an enhanced growth inhibitory effect of plasma in the presence of a metabolic modifier that was selective against cancer cells, not non-malignant cells. This is the first study to report the advantage of combining plasma with 2-DG to eradicate blood cancer cells. Finally, we conclude that 2-DG with non-thermal plasma may be used as a combination treatment against blood cancer cells.-
dc.language영어-
dc.language.isoen-
dc.publisherNATURE PUBLISHING GROUP-
dc.titleNon-thermal plasma with 2-deoxy-D-glucose synergistically induces cell death by targeting glycolysis in blood cancer cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Su Jae-
dc.identifier.doi10.1038/srep08726-
dc.identifier.scopusid2-s2.0-84924170554-
dc.identifier.wosid000350375000006-
dc.identifier.bibliographicCitationSCIENTIFIC REPORTS, v.5-
dc.relation.isPartOfSCIENTIFIC REPORTS-
dc.citation.titleSCIENTIFIC REPORTS-
dc.citation.volume5-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusMETABOLISM-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusMITOCHONDRIA-
dc.subject.keywordPlusCYTOTOXICITY-
dc.subject.keywordPlusPROTEINS-
dc.subject.keywordPlusPATHWAYS-
dc.subject.keywordPlusSTRESS-
dc.subject.keywordPlusCYCLE-
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서울 자연과학대학 > 서울 생명과학과 > 1. Journal Articles

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