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Cu(ii)-BODIPY photosensitizer for CAIX overexpressed cancer stem cell therapy

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dc.contributor.authorJung, Hyo Sung-
dc.contributor.authorKoo, Seyoung-
dc.contributor.authorWon, Miae-
dc.contributor.authorAn, Seeun-
dc.contributor.authorPark, Haebeen-
dc.contributor.authorSessler, Jonathan L.-
dc.contributor.authorHan, Jiyou-
dc.contributor.authorKim, Jong Seung-
dc.date.accessioned2024-04-09T03:02:18Z-
dc.date.available2024-04-09T03:02:18Z-
dc.date.issued2023-02-
dc.identifier.issn2041-6520-
dc.identifier.issn2041-6539-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/118595-
dc.description.abstractChemoresistance originating from cancer stem cells (CSCs) is a major cause of cancer treatment failure and highlights the need to develop CSC-targeting therapies. Although enormous progress in both photodynamic therapy (PDT) and chemodynamic therapy (CDT) has been made in recent decades, the efficacy of these modalities against CSC remains limited. Here, we report a new generation photosensitizer, CA9-BPS-Cu(ii), a system that combines three subunits within a single molecule, namely a copper catalyst for CDT, a boron dipyrromethene photosensitizer for PDT, and acetazolamide for CSC targeting via carbonic anhydrase-9 (CA9) binding. A therapeutic effect in MDA-MB-231 cells was observed that is ascribed to elevated oxidative stress mediated by a combined CDT/PDT effect, as well as through copper-catalysed glutathione oxidation. The CSC targeting ability of CA9-BPS-Cu(ii) was evident from the enhanced affinity of CA9-BPS-Cu(ii) towards CD133-positive MDA-MB-231 cells where CA9 is overexpressed vs. CD133-negative cells. Moreover, the efficacy of CA9-BPS-Cu(ii) was successfully demonstrated in a xenograft mouse tumour model. © 2023 The Royal Society of Chemistry.-
dc.format.extent12-
dc.language영어-
dc.language.isoENG-
dc.publisherRoyal Society of Chemistry-
dc.titleCu(ii)-BODIPY photosensitizer for CAIX overexpressed cancer stem cell therapy-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1039/d2sc03945a-
dc.identifier.scopusid2-s2.0-85147353302-
dc.identifier.wosid000922648900001-
dc.identifier.bibliographicCitationChemical Science, v.14, no.7, pp 1808 - 1819-
dc.citation.titleChemical Science-
dc.citation.volume14-
dc.citation.number7-
dc.citation.startPage1808-
dc.citation.endPage1819-
dc.type.docType정기학술지(Article(Perspective Article포함))-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusCARBONIC-ANHYDRASE-IX-
dc.subject.keywordPlusPHOTODYNAMIC-THERAPY-
dc.subject.keywordPlusSINGLET-OXYGEN-
dc.subject.keywordPlusSOLID TUMORS-
dc.subject.keywordPlusGLUTATHIONE-
dc.subject.keywordPlusCOPPER-
dc.subject.keywordPlusGENERATION-
dc.subject.keywordPlusHYPOXIA-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusINHIBITION-
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2023/sc/d2sc03945a-
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ERICA 공학대학 (ERICA 에너지바이오학과)
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