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An Ethacrynic Acid-Brominated BODIPY Photosensitizer (EA-BPS) Construct Enhances the Lethality of Reactive Oxygen Species in Hypoxic Tumor-Targeted Photodynamic Therapy

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dc.contributor.authorWon, Miae-
dc.contributor.authorKoo, Seyoung-
dc.contributor.authorLi, Hao-
dc.contributor.authorSessler, Jonathan L.-
dc.contributor.authorLee, Jin Yong-
dc.contributor.authorSharma, Amit-
dc.contributor.authorKim, Jong Seung-
dc.date.accessioned2024-09-24T06:31:05Z-
dc.date.available2024-09-24T06:31:05Z-
dc.date.issued2021-02-
dc.identifier.issn1433-7851-
dc.identifier.issn1521-3773-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/120612-
dc.description.abstractDespite being a clinically approved intervention for cancer, photodynamic therapy (PDT) still suffers from limitations. Prime among these is a therapeutic response that is mostly oxygen dependent. This limits the utility of PDT in treating hypoxic tumors since lower levels of cytotoxic reactive oxygen species (ROS) are generated in regions of low oxygen tension. Glutathione-pi (GST-pi) is a key enzyme that militates against ROS-mediated apoptosis. We report herein a new construct, EA-BPS, that contains both a brominated BODIPY photosensitizer (BPS) and an ethacrynic acid (EA) GST-pi inhibitor. Photoirradiation of EA-BPS induces a synergistic antitumor effect that results from the combination of ROS production and GST-pi inhibition. Relative to BPS alone, an enhanced cell-killing effect is seen under hypoxic conditions both in vitro and in vivo. We conclude that by making better use of the available oxygen in tumor environments, improved therapeutic PDT outcomes should be achievable even under hypoxic conditions. © 2020 Wiley-VCH GmbH-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherJohn Wiley & Sons Ltd.-
dc.titleAn Ethacrynic Acid-Brominated BODIPY Photosensitizer (EA-BPS) Construct Enhances the Lethality of Reactive Oxygen Species in Hypoxic Tumor-Targeted Photodynamic Therapy-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.1002/anie.202012687-
dc.identifier.scopusid2-s2.0-85097600581-
dc.identifier.wosid000599067600001-
dc.identifier.bibliographicCitationAngewandte Chemie International Edition, v.60, no.6, pp 3196 - 3204-
dc.citation.titleAngewandte Chemie International Edition-
dc.citation.volume60-
dc.citation.number6-
dc.citation.startPage3196-
dc.citation.endPage3204-
dc.type.docType정기학술지(Article(Perspective Article포함))-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusAnimals-
dc.subject.keywordPlusApoptosis-
dc.subject.keywordPlusBoron Compounds-
dc.subject.keywordPlusCell Hypoxia-
dc.subject.keywordPlusCell Line, Tumor-
dc.subject.keywordPlusCell Survival-
dc.subject.keywordPlusEthacrynic Acid-
dc.subject.keywordPlusGlutathione S-Transferase pi-
dc.subject.keywordPlusHalogenation-
dc.subject.keywordPlusHumans-
dc.subject.keywordPlusLight-
dc.subject.keywordPlusMice-
dc.subject.keywordPlusNeoplasms-
dc.subject.keywordPlusPhotochemotherapy-
dc.subject.keywordPlusPhotosensitizing Agents-
dc.subject.keywordPlusReactive Oxygen Species-
dc.subject.keywordPlusTransplantation, Heterologous-
dc.subject.keywordAuthorBODIPY-
dc.subject.keywordAuthorethacrynic acid-
dc.subject.keywordAuthorglutathione S-transferase-pi-
dc.subject.keywordAuthorHypoxia-
dc.subject.keywordAuthorphotodynamic therapy-
dc.identifier.urlhttps://www.scopus.com/record/display.uri?eid=2-s2.0-85097600581&origin=inward&txGid=fb13650413a34cef171471fc593d8adb-
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ERICA 공학대학 (ERICA 에너지바이오학과)
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