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Novel suppressive effects of cardamonin on the activity and expression of transglutaminase-2 lead to blocking the migration and invasion of cancer cells

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dc.contributor.authorPark, Mi Kyung-
dc.contributor.authorJo, Seung Ho-
dc.contributor.authorLee, Hye Ja-
dc.contributor.authorKang, June Hee-
dc.contributor.authorKim, You Ri-
dc.contributor.authorKim, Hyun Ji-
dc.contributor.authorLee, Eun Ji-
dc.contributor.authorKoh, Jae Young-
dc.contributor.authorAhn, Kyung Ok-
dc.contributor.authorJung, Kyung Chae-
dc.contributor.authorOh, Seung Hyun-
dc.contributor.authorKim, Soo Youl-
dc.contributor.authorLee, Chang Hoon-
dc.date.available2020-02-29T00:44:07Z-
dc.date.created2020-02-06-
dc.date.issued2013-02-07-
dc.identifier.issn0024-3205-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/14742-
dc.description.abstractAims: Alpinia kaisumadai was recently found in our previous study to have anti-migratory and anti-invasion activities against HT-1080 cells. However, the study did not demonstrate the exact component of Alpinia katsumadai with anti-migratory and anti-invasive activities. We tested the effects and relevant mechanism of cardamonin (CDN) on the migration and invasion of cancer cells. Main methods: Migration and invasion of cancer cells were measured using multi-well chambers. Zymography and Western blots were used to examine the effects of CDN on the activities of matrix metalloproteinases (MMPs) and expression of transglutaminase-2 (Tgase-2). Key findings: CDN, but not alpinetin, dose-dependently suppressed the migration and 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced invasion of HT-1080 sarcoma cells. CDN suppressed the expression of Tgase-2, MMP-2, NF-kappa B and MMP-9 in HT-1080 cells, and suppressed MMP-2 and MMP-9 activities. Gene silencing of Tgase-2 suppressed the migration and invasion of HT-1080 cells and suppressed the activities of MMP-2 and MMP-9. Migration of various cancer cells having high levels of Tgase-2 were also inhibited by CDN. CDN and Alpinia katsumadai extracts also directly inhibited the activity of Tgase-2. Significance: CDN inhibits migration of several cancer cell lines expressing Tgase-2 via suppression of Tgase-2 expression and inhibition of Tgase-2 activity. The finding that CON has Tgase-2 inhibitory activity will give us a new scaffold or clue of pharmacophore for the development of more effective Tgase-2 inhibitors. (C) 2012 Elsevier Inc. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.relation.isPartOfLIFE SCIENCES-
dc.subjectNF-KAPPA-B-
dc.subjectTISSUE-TRANSGLUTAMINASE-
dc.subjectSIGNALING PATHWAY-
dc.subjectALPINIA-KATSUMADAI-
dc.subjectTUMOR-METASTASIS-
dc.subjectRETINOIC ACID-
dc.subjectBREAST-CANCER-
dc.subjectUP-REGULATION-
dc.subjectINHIBITION-
dc.subjectINFLAMMATION-
dc.titleNovel suppressive effects of cardamonin on the activity and expression of transglutaminase-2 lead to blocking the migration and invasion of cancer cells-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000314329800010-
dc.identifier.doi10.1016/j.lfs.2012.11.009-
dc.identifier.bibliographicCitationLIFE SCIENCES, v.92, no.2, pp.154 - 160-
dc.identifier.scopusid2-s2.0-84872356718-
dc.citation.endPage160-
dc.citation.startPage154-
dc.citation.titleLIFE SCIENCES-
dc.citation.volume92-
dc.citation.number2-
dc.contributor.affiliatedAuthorOh, Seung Hyun-
dc.type.docTypeArticle-
dc.subject.keywordAuthorCardamonin-
dc.subject.keywordAuthorTransglutaminase-2-
dc.subject.keywordAuthorMatrix metalloproteinases-
dc.subject.keywordAuthorNF-kappa B-
dc.subject.keywordAuthorMigration-
dc.subject.keywordAuthorInvasion-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusTISSUE-TRANSGLUTAMINASE-
dc.subject.keywordPlusSIGNALING PATHWAY-
dc.subject.keywordPlusALPINIA-KATSUMADAI-
dc.subject.keywordPlusTUMOR-METASTASIS-
dc.subject.keywordPlusRETINOIC ACID-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusUP-REGULATION-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusINFLAMMATION-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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