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dc.contributor.author이지환-
dc.contributor.author이우정-
dc.contributor.author이승용-
dc.contributor.authorNoriko Yamabe-
dc.contributor.author김수남-
dc.contributor.author조은주-
dc.contributor.author김현영-
dc.contributor.author강기성-
dc.date.accessioned2024-01-20T14:31:27Z-
dc.date.available2024-01-20T14:31:27Z-
dc.date.created2021-09-06-
dc.date.issued2012-07-
dc.identifier.issn2288-3649-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/129083-
dc.description.abstractIn the present study, in vitro beneficial effects of tea catechins on gastrointestinal cancer as well as nephrotoxicity were explored. Antioxidant activities of 6 green tea catechins were evaluated by 1,1- diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity test. To evaluate the anticancer effect, the effect of (-)-epigallocatechin-3-gallate (EGCG) as a representative tea catechin was investigated in HCT-116 human colorectal cancer and AGS human gastric cancer cells. Protective effect of EGCG against oxidative renal cell damage was measured using radical generator, 2,2'-azobis (2-amidinopropane) dihydrochloride in LLC-PK1 cells. EGCG showed the strongest DPPH radical scavenging activity and completely decreased the gastrointestinal cancer cell viability at 10 μM. Moreover, EGCG protected renal epithelial LLC-PK1 cells from oxidative damage in the dose-dependent manner. Therefore, EGCG has beneficial effects on cancer therapy by its anticancer effect and by reducing oxidative stress-induced nephrotoxicity.-
dc.languageKorean-
dc.publisher대한암예방학회-
dc.title암치료 보조제로서 녹차 폴리페놀성 화합물의 가능성-
dc.title.alternativePossible Usage of Polyphenolic Compounds from Green Tea as Anticancer Supplement Agents-
dc.typeArticle-
dc.description.journalClass2-
dc.identifier.bibliographicCitation대한암예방학회지, v.17, no.2, pp.151 - 156-
dc.citation.title대한암예방학회지-
dc.citation.volume17-
dc.citation.number2-
dc.citation.startPage151-
dc.citation.endPage156-
dc.description.journalRegisteredClasskci-
dc.identifier.kciidART001711699-
dc.subject.keywordAuthorTea catechin-
dc.subject.keywordAuthorNephrotoxicity-
dc.subject.keywordAuthorOxidative stress-
dc.subject.keywordAuthorAnticancer effect-
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KIST Article > 2012
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