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DC FieldValueLanguage
dc.contributor.author김선정-
dc.date.accessioned2018-03-25T07:07:19Z-
dc.date.available2018-03-25T07:07:19Z-
dc.date.issued2013-02-
dc.identifier.citationBasic & Clinical Pharmacology & Toxicology, Feb 2013, 112(2), P.83-89en_US
dc.identifier.issn1742-7835-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/abs/10.1111/j.1742-7843.2012.00929.x-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/51948-
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.en_US
dc.language.isoenen_US
dc.publisherWiley-Blackwellen_US
dc.subjectINTERSTITIAL-CELLSen_US
dc.subjectELECTRICAL RHYTHMICITYen_US
dc.subjectGASTROINTESTINAL-TRACTen_US
dc.subjectTRPM7 CHANNELSen_US
dc.subjectION CHANNELSen_US
dc.subjectCANCERen_US
dc.subjectCAJALen_US
dc.subjectPROLIFERATIONen_US
dc.subjectMAGNESIUMen_US
dc.subjectCALCIUMen_US
dc.titleThe Role of Waixenicin A as Transient Receptor Potential Melastatin 7 Blockeren_US
dc.typeArticleen_US
dc.relation.no2-
dc.relation.volume112-
dc.identifier.doi10.1111/j.1742-7843.2012.00929.x-
dc.relation.page83-89-
dc.relation.journalBASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY-
dc.contributor.googleauthorKim, B. J.-
dc.contributor.googleauthorNam, J. H.-
dc.contributor.googleauthorKwon, Y. K.-
dc.contributor.googleauthorSo, I.-
dc.contributor.googleauthorKim, S. J.-
dc.relation.code2013009084-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF ENGINEERING[S]-
dc.sector.departmentDIVISION OF ELECTRICAL AND BIOMEDICAL ENGINEERING-
dc.identifier.pidsjk-


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