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Salinomycin possesses anti-tumor activity and inhibits breast cancer stem-like cells via an apoptosis-independent pathway

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dc.contributor.authorAn, Hyunsook-
dc.contributor.authorKim, Ji Young-
dc.contributor.authorLee, Nahyun-
dc.contributor.authorCho, Youngkwan-
dc.contributor.authorOh, Eunhye-
dc.contributor.authorSeo, Jae Hong-
dc.date.accessioned2021-09-04T11:16:32Z-
dc.date.available2021-09-04T11:16:32Z-
dc.date.created2021-06-10-
dc.date.issued2015-10-30-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/92151-
dc.description.abstractCancer stem cells (CSCs) play important roles in the formation, growth and recurrence of tumors, particularly following therapeutic intervention. Salinomycin has received recent attention for its ability to target breast cancer stem cells (BCSCs), but the mechanisms of action involved are not fully understood. In the present study, we sought to investigate the mechanisms responsible for salinomycin's selective targeting of BCSCs and its anti-tumor activity. Salinomycin suppressed cell viability, concomitant with the downregulation of cyclin D1 and increased p27(kip1) nuclear accumulation. Mammosphere formation assays revealed that salinomycin suppresses self-renewal of ALDH1-positive BCSCs and down-regulates the transcription factors Nanog, Oct4 and Sox2. TUNEL analysis of MDA-MB-231-derived xenografts revealed that salinomycin administration elicited a significant reduction in tumor growth with a marked downregulation of ALDH1 and CD44 levels, but seemingly without the induction of apoptosis. Our findings shed further light on the mechanisms responsible for salinomycin's effects on BCSCs. (C) 2015 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectMARKER-
dc.subjectSOX2-
dc.titleSalinomycin possesses anti-tumor activity and inhibits breast cancer stem-like cells via an apoptosis-independent pathway-
dc.typeArticle-
dc.contributor.affiliatedAuthorSeo, Jae Hong-
dc.identifier.doi10.1016/j.bbrc.2015.09.108-
dc.identifier.scopusid2-s2.0-84943233240-
dc.identifier.wosid000363601600014-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.466, no.4, pp.696 - 703-
dc.relation.isPartOfBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume466-
dc.citation.number4-
dc.citation.startPage696-
dc.citation.endPage703-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusMARKER-
dc.subject.keywordPlusSOX2-
dc.subject.keywordAuthorSalinomycin-
dc.subject.keywordAuthorBreast cancer stem cells-
dc.subject.keywordAuthorMammosphere-
dc.subject.keywordAuthorALDH1-
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