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Cited 31 time in webofscience Cited 31 time in scopus
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Novel anticancer activity of phloroglucinol against breast cancer stem-like cells

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dc.contributor.authorKim, Rae-Kwon-
dc.contributor.authorUddin, Nizam-
dc.contributor.authorHyun, Jin-Won-
dc.contributor.authorKim, Changil-
dc.contributor.authorSuh, Yongjoon-
dc.contributor.authorLee, Su-Jae-
dc.date.accessioned2021-08-02T17:54:52Z-
dc.date.available2021-08-02T17:54:52Z-
dc.date.issued2015-08-
dc.identifier.issn0041-008X-
dc.identifier.issn1096-0333-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/24905-
dc.description.abstractPoor prognosis of breast cancer patients is closely associated with metastasis and relapse. There is substantial evidence supporting that cancer stem-like cells (CSCs) are primarily responsible for relapse in breast cancer after anticancer treatment. However, there is a lack of suitable drugs that target breast cancer stem-like cells (BCSCs). Here, we report that phloroglucinol (PG), a natural phlorotannin component of brown algae, suppresses sphere formation, anchorage-independent colony formation and in vivo tumorigenicity. In line with these observations, treatment with PG also decreased CD44(+) cancer cell population as well as expression of CSC regulators such as Sox2, CD44, Oct4, Notch2 and beta-catenin. Also, treatment with PG sensitized breast cancer cells to anticancer drugs such as cisplatin, etoposide, and taxol as well as to ionizing radiation. Importantly, PG inhibited KRAS and its downstream PI3K/AKT and RAF-1/ERK signaling pathways that regulate the maintenance of CSCs. Taken together, our findings implicate PG as a good candidate to target BCSCs and to prevent the disease relapse. (C) 2015 Elsevier Inc. All rights reserved.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherAcademic Press-
dc.titleNovel anticancer activity of phloroglucinol against breast cancer stem-like cells-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.taap.2015.03.026-
dc.identifier.scopusid2-s2.0-84937966554-
dc.identifier.wosid000356398300001-
dc.identifier.bibliographicCitationToxicology and Applied Pharmacology, v.286, no.3, pp 143 - 150-
dc.citation.titleToxicology and Applied Pharmacology-
dc.citation.volume286-
dc.citation.number3-
dc.citation.startPage143-
dc.citation.endPage150-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaToxicology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryToxicology-
dc.subject.keywordPlusCISPLATIN RESISTANCE-
dc.subject.keywordPlusENDOCRINE THERAPY-
dc.subject.keywordPlusI N-VITRO-
dc.subject.keywordPlusCHEMOTHERAPY-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusPROGNOSIS-
dc.subject.keywordPlusPATHWAYS-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusDAMAGE-
dc.subject.keywordAuthorPhloroglucinol-
dc.subject.keywordAuthorBreast cancer stem-like cells-
dc.subject.keywordAuthorRelapse-
dc.subject.keywordAuthorResistance to anticancer treatment-
dc.subject.keywordAuthorKRAS-
dc.subject.keywordAuthorAnticancer activity-
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