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The Role of Waixenicin A as Transient Receptor Potential Melastatin 7 Blocker

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dc.contributor.authorKim, Byung J.-
dc.contributor.authorNam, Joo H.-
dc.contributor.authorKwon, Young K.-
dc.contributor.authorSo, Insuk-
dc.contributor.authorKim, Seon J.-
dc.date.accessioned2021-08-02T18:58:02Z-
dc.date.available2021-08-02T18:58:02Z-
dc.date.issued2013-02-
dc.identifier.issn1742-7835-
dc.identifier.issn1742-7843-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/26780-
dc.description.abstractTransient receptor potential melastatin 7 (TRPM7) plays a role in a number of physiological and pharmacological functions in variety of cells. The aim of this study was to clarify the role for TRPM7 channels and the effect of waixenicin A on the pacemaking activity of interstitial cells of Cajal (ICCs) and on the cell viability of the human gastric and breast adenocarcinoma cell lines, AGS and MCF-7, respectively. Waixenicin A decreased the amplitude of pacemaker potentials in cultured ICC clusters and inhibited TRPM7 currents, but had no effect on Ca2+-activated Cl- conductance (ANO1). Furthermore, waixenicin A was found to inhibit the growth and survival of AGS and MCF-7 cells. These findings indicate that TRPM7 channel modulates intestinal motility and regulates the pathophysiology of human gastric and breast adenocarcinoma cells. These findings suggest that TRPM7 channel be considered a potential target for the treatment of gut motor disorders and gastric and breast cancer.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherNordic Pharmacological Society-
dc.titleThe Role of Waixenicin A as Transient Receptor Potential Melastatin 7 Blocker-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1111/j.1742-7843.2012.00929.x-
dc.identifier.scopusid2-s2.0-84872127066-
dc.identifier.wosid000313240600003-
dc.identifier.bibliographicCitationBasic and Clinical Pharmacology and Toxicology, v.112, no.2, pp 83 - 89-
dc.citation.titleBasic and Clinical Pharmacology and Toxicology-
dc.citation.volume112-
dc.citation.number2-
dc.citation.startPage83-
dc.citation.endPage89-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaToxicology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryToxicology-
dc.subject.keywordPlusINTERSTITIAL-CELLS-
dc.subject.keywordPlusELECTRICAL RHYTHMICITY-
dc.subject.keywordPlusGASTROINTESTINAL-TRACT-
dc.subject.keywordPlusTRPM7 CHANNELS-
dc.subject.keywordPlusION CHANNELS-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusCAJAL-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusMAGNESIUM-
dc.subject.keywordPlusCALCIUM-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1111/j.1742-7843.2012.00929.x-
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