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Regulation of voltage-gated potassium channels attenuates resistance of side-population cells to gefitinib in the human lung cancer cell line NCI-H460

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dc.contributor.authorChoi, Seon Young-
dc.contributor.authorKim, Hang-Rae-
dc.contributor.authorRyu, Pan Dong-
dc.contributor.authorLee, So Yeong-
dc.date.accessioned2024-05-16T01:31:00Z-
dc.date.available2024-05-16T01:31:00Z-
dc.date.created2018-08-08-
dc.date.created2018-08-08-
dc.date.created2018-08-08-
dc.date.created2018-08-08-
dc.date.issued2017-02-
dc.identifier.citationBMC pharmacology & toxicology, Vol.18, p. 14-
dc.identifier.issn2050-6511-
dc.identifier.urihttps://hdl.handle.net/10371/202608-
dc.description.abstractBackground: Side-population (SP) cells that exclude anti-cancer drugs have been found in various tumor cell lines. Moreover, SP cells have a higher proliferative potential and drug resistance than main population cells (Non-SP cells). Also, several ion channels are responsible for the drug resistance and proliferation of SP cells in cancer. Methods: To confirm the expression and function of voltage-gated potassium (Kv) channels of SP cells, these cells, as well as highly expressed ATP-binding cassette (ABC) transporters and stemness genes, were isolated from a gefitinib-resistant human lung adenocarcinoma cell line (NCI-H460), using Hoechst 33342 efflux. Results: In the present study, we found that mRNA expression of Kv channels in SP cells was different compared to Non-SP cells, and the resistance of SP cells to gefitinib was weakened with a combination treatment of gefitinib and Kv channel blockers or a Kv7 opener, compared to single-treatment gefitinib, through inhibition of the Ras-Raf signaling pathway. Conclusions: The findings indicate that Kv channels in SP cells could be new targets for reducing the resistance to gefitinib.-
dc.language영어-
dc.publisherBioMed Central-
dc.titleRegulation of voltage-gated potassium channels attenuates resistance of side-population cells to gefitinib in the human lung cancer cell line NCI-H460-
dc.typeArticle-
dc.identifier.doi10.1186/s40360-017-0118-9-
dc.citation.journaltitleBMC pharmacology & toxicology-
dc.identifier.wosid000397893700001-
dc.identifier.scopusid2-s2.0-85013287859-
dc.citation.startpage14-
dc.citation.volume18-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorKim, Hang-Rae-
dc.contributor.affiliatedAuthorRyu, Pan Dong-
dc.contributor.affiliatedAuthorLee, So Yeong-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusTYROSINE KINASE INHIBITORS-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusTHERAPEUTIC IMPLICATIONS-
dc.subject.keywordPlusSIGNALING PATHWAYS-
dc.subject.keywordPlusK+ CHANNEL-
dc.subject.keywordPlusABCG2-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusGLIOMA-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordAuthorLung cancer cell-
dc.subject.keywordAuthorDrug resistance-
dc.subject.keywordAuthorSide population-
dc.subject.keywordAuthorVoltage-gated potassium channel-
dc.subject.keywordAuthorCombination therapy-
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