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Auranofin, an antirheumatic drug, shows anticancer stem cell potential via suppression of the Stat3 signal

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dc.contributor.authorKo, Seung-Yeon-
dc.contributor.authorKim, Yuna-
dc.contributor.authorChung, Jin Sun-
dc.contributor.authorKim, Young Bin-
dc.contributor.authorKim, Su-Lim-
dc.contributor.authorLee, Dong-Sun-
dc.contributor.authorChun, Kyung-Hee-
dc.contributor.authorChoi, Hack Sun-
dc.date.accessioned2025-10-17T08:08:01Z-
dc.date.available2025-10-17T08:08:01Z-
dc.date.created2025-11-21-
dc.date.issued2025-07-
dc.identifier.issn1976-6696-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/207653-
dc.description.abstractAccumulating data have shown that targeting breast cancer stem cells (CSCs) is an auspicious way for anticancer therapies. This study demonstrated that the antirheumatic drug auranofin is a potent CSC inhibitor with anti-CSC action on breast cancer. This research focused on investigating the effect of auranofin on breast cancer and CSCs and its cellular mechanism. Mammosphere formation, colony formation, levels of CD44high/CD24low, and aldehyde dehydrogenase 1 expression in the cells were evaluated after auranofin treatment. The anti-CSC properties of auranofin were further examined by gel shift assay and cytokine detection. Auranofin suppressed cell growth, colony formation, migration, and mammosphere formation and triggered apoptosis in breast cancer. Auranofin decreased the CD44high/CD24low-and aldehyde dehydrogenaseexpressed subpopulations, as well as the Stat3-DNA interaction and phosphorylated Stat3 level. Auranofin also decreased the extracellular levels of interleukin-8 (IL-8) in the mammosphere media. Auranofin suppressed the Stat3/IL-8 signal and killed CSCs; therefore, it may be a potential target for CSCs. [BMB Reports 2025; 58(7): 293-299]-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.languageEnglish-
dc.publisherKorean Society for Biochemistry and Molecular Biology-
dc.relation.isPartOfBMB REPORTS-
dc.relation.isPartOfBMB REPORTS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAntineoplastic Agents / pharmacology-
dc.subject.MESHAntirheumatic Agents* / pharmacology-
dc.subject.MESHApoptosis / drug effects-
dc.subject.MESHAuranofin* / pharmacology-
dc.subject.MESHBreast Neoplasms / drug therapy-
dc.subject.MESHBreast Neoplasms / metabolism-
dc.subject.MESHBreast Neoplasms / pathology-
dc.subject.MESHCell Line, Tumor-
dc.subject.MESHCell Movement / drug effects-
dc.subject.MESHCell Proliferation / drug effects-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHInterleukin-8 / metabolism-
dc.subject.MESHMCF-7 Cells-
dc.subject.MESHNeoplastic Stem Cells* / drug effects-
dc.subject.MESHNeoplastic Stem Cells* / metabolism-
dc.subject.MESHSTAT3 Transcription Factor* / metabolism-
dc.subject.MESHSignal Transduction / drug effects-
dc.titleAuranofin, an antirheumatic drug, shows anticancer stem cell potential via suppression of the Stat3 signal-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Biochemistry and Molecular Biology (생화학-분자생물학교실)-
dc.contributor.googleauthorKo, Seung-Yeon-
dc.contributor.googleauthorKim, Yuna-
dc.contributor.googleauthorChung, Jin Sun-
dc.contributor.googleauthorKim, Young Bin-
dc.contributor.googleauthorKim, Su-Lim-
dc.contributor.googleauthorLee, Dong-Sun-
dc.contributor.googleauthorChun, Kyung-Hee-
dc.contributor.googleauthorChoi, Hack Sun-
dc.identifier.doi10.5483/BMBRep.2025-0037-
dc.relation.journalcodeJ00348-
dc.identifier.eissn1976-670X-
dc.identifier.pmid40495487-
dc.subject.keywordAuranofin-
dc.subject.keywordBreast cancer stem cells-
dc.subject.keywordIL-8-
dc.subject.keywordMammosphere-
dc.subject.keywordStat3-
dc.contributor.alternativeNameChun, Kyung Hee-
dc.contributor.affiliatedAuthorKo, Seung-Yeon-
dc.contributor.affiliatedAuthorKim, Yuna-
dc.contributor.affiliatedAuthorChung, Jin Sun-
dc.contributor.affiliatedAuthorKim, Young Bin-
dc.contributor.affiliatedAuthorChun, Kyung-Hee-
dc.contributor.affiliatedAuthorChoi, Hack Sun-
dc.identifier.scopusid2-s2.0-105012752379-
dc.identifier.wosid001578015800003-
dc.citation.volume58-
dc.citation.number7-
dc.citation.startPage293-
dc.citation.endPage299-
dc.identifier.bibliographicCitationBMB REPORTS, Vol.58(7) : 293-299, 2025-07-
dc.identifier.rimsid90209-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorAuranofin-
dc.subject.keywordAuthorBreast cancer stem cells-
dc.subject.keywordAuthorIL-8-
dc.subject.keywordAuthorMammosphere-
dc.subject.keywordAuthorStat3-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusCYTOKINE NETWORKS-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusEXPRESSION-
dc.type.docTypeArticle-
dc.identifier.kciidART003228633-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Biochemistry and Molecular Biology (생화학-분자생물학교실) > 1. Journal Papers

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