{"@context":{"@vocab":"https://cir.nii.ac.jp/schema/1.0/","rdfs":"http://www.w3.org/2000/01/rdf-schema#","dc":"http://purl.org/dc/elements/1.1/","dcterms":"http://purl.org/dc/terms/","foaf":"http://xmlns.com/foaf/0.1/","prism":"http://prismstandard.org/namespaces/basic/2.0/","cinii":"http://ci.nii.ac.jp/ns/1.0/","datacite":"https://schema.datacite.org/meta/kernel-4/","ndl":"http://ndl.go.jp/dcndl/terms/","jpcoar":"https://github.com/JPCOAR/schema/blob/master/2.0/"},"@id":"https://cir.nii.ac.jp/crid/1361699993754801536.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.3390/molecules21070965"}},{"identifier":{"@type":"URI","@value":"https://www.mdpi.com/1420-3049/21/7/965/pdf"}}],"dc:title":[{"@value":"Targeting Epithelial–Mesenchymal Transition (EMT) to Overcome Drug Resistance in Cancer"}],"description":[{"type":"abstract","notation":[{"@value":"<jats:p>Epithelial–mesenchymal transition (EMT) is known to play an important role in cancer progression, metastasis and drug resistance. Although there are controversies surrounding the causal relationship between EMT and cancer metastasis, the role of EMT in cancer drug resistance has been increasingly recognized. Numerous EMT-related signaling pathways are involved in drug resistance in cancer cells. Cells undergoing EMT show a feature similar to cancer stem cells (CSCs), such as an increase in drug efflux pumps and anti-apoptotic effects. Therefore, targeting EMT has been considered a novel opportunity to overcome cancer drug resistance. This review describes the mechanism by which EMT contributes to drug resistance in cancer cells and summarizes new advances in research in EMT-associated drug resistance.</jats:p>"}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1381699993754801536","@type":"Researcher","foaf:name":[{"@value":"Bowen Du"}],"jpcoar:affiliationName":[{"@value":"Faculty of Health Sciences, University of Macau, Avenida da Universidade, Taipa, Macau SAR 999078, China"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699993754801537","@type":"Researcher","foaf:name":[{"@value":"Joong Shim"}],"jpcoar:affiliationName":[{"@value":"Faculty of Health Sciences, University of Macau, Avenida da Universidade, Taipa, Macau SAR 999078, China"}]}],"publication":{"publicationIdentifier":[{"@type":"EISSN","@value":"14203049"}],"prism:publicationName":[{"@value":"Molecules"}],"dc:publisher":[{"@value":"MDPI AG"}],"prism:publicationDate":"2016-07-22","prism:volume":"21","prism:number":"7","prism:startingPage":"965"},"reviewed":"false","dc:rights":["https://creativecommons.org/licenses/by/4.0/"],"url":[{"@id":"https://www.mdpi.com/1420-3049/21/7/965/pdf"}],"createdAt":"2016-07-22","modifiedAt":"2025-10-11","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1050577895541786240","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Growth and Migration Blocking Effect of Nanaomycin K, a Compound Produced by Streptomyces sp., on Prostate Cancer Cell Lines In Vitro and In Vivo"}]},{"@id":"https://cir.nii.ac.jp/crid/1360017280643911680","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Establishment of an experimental model of normal dog bladder organoid using a three-dimensional culture 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