Cited 25 time in
The Role of Waixenicin A as Transient Receptor Potential Melastatin 7 Blocker
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kim, Byung J. | - |
| dc.contributor.author | Nam, Joo H. | - |
| dc.contributor.author | Kwon, Young K. | - |
| dc.contributor.author | So, Insuk | - |
| dc.contributor.author | Kim, Seon J. | - |
| dc.date.accessioned | 2021-08-02T18:58:02Z | - |
| dc.date.available | 2021-08-02T18:58:02Z | - |
| dc.date.issued | 2013-02 | - |
| dc.identifier.issn | 1742-7835 | - |
| dc.identifier.issn | 1742-7843 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/26780 | - |
| dc.description.abstract | Transient 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.extent | 7 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | Nordic Pharmacological Society | - |
| dc.title | The Role of Waixenicin A as Transient Receptor Potential Melastatin 7 Blocker | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1111/j.1742-7843.2012.00929.x | - |
| dc.identifier.scopusid | 2-s2.0-84872127066 | - |
| dc.identifier.wosid | 000313240600003 | - |
| dc.identifier.bibliographicCitation | Basic and Clinical Pharmacology and Toxicology, v.112, no.2, pp 83 - 89 | - |
| dc.citation.title | Basic and Clinical Pharmacology and Toxicology | - |
| dc.citation.volume | 112 | - |
| dc.citation.number | 2 | - |
| dc.citation.startPage | 83 | - |
| dc.citation.endPage | 89 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
| dc.relation.journalResearchArea | Toxicology | - |
| dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
| dc.relation.journalWebOfScienceCategory | Toxicology | - |
| dc.subject.keywordPlus | INTERSTITIAL-CELLS | - |
| dc.subject.keywordPlus | ELECTRICAL RHYTHMICITY | - |
| dc.subject.keywordPlus | GASTROINTESTINAL-TRACT | - |
| dc.subject.keywordPlus | TRPM7 CHANNELS | - |
| dc.subject.keywordPlus | ION CHANNELS | - |
| dc.subject.keywordPlus | CANCER | - |
| dc.subject.keywordPlus | CAJAL | - |
| dc.subject.keywordPlus | PROLIFERATION | - |
| dc.subject.keywordPlus | MAGNESIUM | - |
| dc.subject.keywordPlus | CALCIUM | - |
| dc.identifier.url | https://onlinelibrary.wiley.com/doi/10.1111/j.1742-7843.2012.00929.x | - |
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