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Silencing of Kv4.1 potassium channels inhibits cell proliferation of tumorigenic human mammary epithelial cells

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dc.contributor.authorJang, Soo Hwa-
dc.contributor.authorChoi, Changsun-
dc.contributor.authorHong, Seong-Geun-
dc.contributor.authorYarishkin, Oleg V.-
dc.contributor.authorBae, Young Min-
dc.contributor.authorKim, Jae Gon-
dc.contributor.authorO'Grady, Scott M.-
dc.contributor.authorYoon, Kyong-Ah-
dc.contributor.authorKang, Kyung-Sun-
dc.contributor.authorRyu, Pan Dong-
dc.contributor.authorLee, So Yeong-
dc.date.accessioned2022-12-27T05:10:56Z-
dc.date.available2022-12-27T05:10:56Z-
dc.date.issued2009-06-26-
dc.identifier.issn0006-291X-
dc.identifier.issn1090-2104-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/26274-
dc.description.abstractPotassium channel activity has been shown to facilitate cell proliferation in cancer cells. In the present study, the role of Kv4.1 channels in immortal and tumorigenic human mammary epithelia] cells was investigated. Kv4.1 protein expression was positively correlated with tumorigenicity. Moreover, transfection with siRNAs targeting Kv4.1 mRNA suppressed proliferation of tumorigenic mammary epithelial cells. Experiments using mRNA isolated from human breast cancer tissues revealed that the level of Kv4.1 mRNA expression varied depending on the stage of the tumor. Kv4.1 protein expression increased during stages T2 and T3 compared to normal tissue. These results demonstrated that Kv4.1 plays a role in proliferation of tumorigenic human mammary epithelial cells. In addition, elevated Kv4.1 expression may be useful as a diagnostic marker for staging mammary tumors and selective blockers of Kv4.1 may serve to suppress tumor cell proliferation. (C) 2009 Elsevier Inc. All rights reserved.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titleSilencing of Kv4.1 potassium channels inhibits cell proliferation of tumorigenic human mammary epithelial cells-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.bbrc.2009.04.108-
dc.identifier.scopusid2-s2.0-65549137217-
dc.identifier.wosid000266462500009-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.384, no.2, pp 180 - 186-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume384-
dc.citation.number2-
dc.citation.startPage180-
dc.citation.endPage186-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusHUMAN PROSTATE-CANCER-
dc.subject.keywordPlusGATED K+ CHANNELS-
dc.subject.keywordPlusION CHANNELS-
dc.subject.keywordPlusCARCINOMA-CELLS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusINVOLVEMENT-
dc.subject.keywordPlusMARKER-
dc.subject.keywordAuthorVoltage-gated K+ channels-
dc.subject.keywordAuthorBreast cancer-
dc.subject.keywordAuthorCell growth-
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