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Ethacrynic Acid: A Promising Candidate for Drug Repurposing as an Anticancer Agent

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dc.contributor.authorYu, Lu-
dc.contributor.authorLee, Ho-
dc.contributor.authorRho, Seung Bae-
dc.contributor.authorPark, Mi Kyung-
dc.contributor.authorLee, Chang Hoon-
dc.date.accessioned2024-08-08T08:31:10Z-
dc.date.available2024-08-08T08:31:10Z-
dc.date.issued2023-04-
dc.identifier.issn1661-6596-
dc.identifier.issn1422-0067-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/20523-
dc.description.abstractEthacrynic acid (ECA) is a diuretic that inhibits Na-K-2Cl cotransporter (NKCC2) present in the thick ascending loop of Henle and muculo dens and is clinically used for the treatment of edema caused by excessive body fluid. However, its clinical use is limited due to its low bioavailability and side effects, such as liver damage and hearing loss at high doses. Despite this, ECA has recently emerged as a potential anticancer agent through the approach of drug repositioning, with a novel mechanism of action. ECA has been shown to regulate cancer hallmark processes such as proliferation, apoptosis, migration and invasion, angiogenesis, inflammation, energy metabolism, and the increase of inhibitory growth factors through various mechanisms. Additionally, ECA has been used as a scaffold for synthesizing a new material, and various derivatives have been synthesized. This review explores the potential of ECA and its derivatives as anticancer agents, both alone and in combination with adjuvants, by examining their effects on ten hallmarks of cancer and neuronal contribution to cancer. Furthermore, we investigated the trend of synthesis research of a series of ECA derivatives to improve the bioavailability of ECA. This review highlights the importance of ECA research and its potential to provide a cost-effective alternative to new drug discovery and development for cancer treatment. © 2023 by the authors.-
dc.format.extent27-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI-
dc.titleEthacrynic Acid: A Promising Candidate for Drug Repurposing as an Anticancer Agent-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/ijms24076712-
dc.identifier.scopusid2-s2.0-85152354005-
dc.identifier.wosid001096625300001-
dc.identifier.bibliographicCitationInternational Journal of Molecular Sciences, v.24, no.7, pp 1 - 27-
dc.citation.titleInternational Journal of Molecular Sciences-
dc.citation.volume24-
dc.citation.number7-
dc.citation.startPage1-
dc.citation.endPage27-
dc.type.docTypeReview-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusGLUTATHIONE-S-TRANSFERASE-
dc.subject.keywordPlusWNT/BETA-CATENIN PATHWAY-
dc.subject.keywordPlusIN-VIVO EFFICACY-
dc.subject.keywordPlusSIGNALING PATHWAY-
dc.subject.keywordPlusCANCER CELLS-
dc.subject.keywordPlusCOLON-CANCER-
dc.subject.keywordPlusC-FOS-
dc.subject.keywordPlusTELOMERASE ACTIVITY-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusECONOMIC BURDEN-
dc.subject.keywordAuthorcancer hallmarks-
dc.subject.keywordAuthorethacrynic acid-
dc.subject.keywordAuthorglutathione-
dc.subject.keywordAuthorion channel-
dc.subject.keywordAuthorlung cancer-
dc.subject.keywordAuthorWnt signaling-
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