Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/103390
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dc.contributor.authorLeonardo-Sousa, Carlota-
dc.contributor.authorCarvalho, Andreia Neves-
dc.contributor.authorGuedes, Romina A.-
dc.contributor.authorFernandes, Pedro M. P.-
dc.contributor.authorAniceto, Natália-
dc.contributor.authorSalvador, Jorge A. R.-
dc.contributor.authorGama, Maria João-
dc.contributor.authorGuedes, Rita C.-
dc.date.accessioned2022-11-10T11:55:16Z-
dc.date.available2022-11-10T11:55:16Z-
dc.date.issued2022-03-28-
dc.identifier.issn1420-3049pt
dc.identifier.urihttps://hdl.handle.net/10316/103390-
dc.description.abstractProteasome inhibitors have shown relevant clinical activity in several hematological malignancies, namely in multiple myeloma and mantle cell lymphoma, improving patient outcomes such as survival and quality of life, when compared with other therapies. However, initial response to the therapy is a challenge as most patients show an innate resistance to proteasome inhibitors, and those that respond to the therapy usually develop late relapses suggesting the development of acquired resistance. The mechanisms of resistance to proteasome inhibition are still controversial and scarce in the literature. In this review, we discuss the development of proteasome inhibitors and the mechanisms of innate and acquired resistance to their activity-a major challenge in preclinical and clinical therapeutics. An improved understanding of these mechanisms is crucial to guiding the design of new and more effective drugs to tackle these devastating diseases. In addition, we provide a comprehensive overview of proteasome inhibitors used in combination with other chemotherapeutic agents, as this is a key strategy to combat resistance.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationPD/BD/145161/2019pt
dc.relationPD/BD/143158/2019pt
dc.relationPTDC/QEQ-MED/7042/2014pt
dc.relationUIDB/04138/2020pt
dc.relationUIDP/04138/2020pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectubiquitin–proteasome pathwaypt
dc.subjectproteasome inhibitorspt
dc.subjectmechanisms of resistancept
dc.subjectinnate resistancept
dc.subjectacquired resistancept
dc.subjectmultiple myelomapt
dc.subjectcancerpt
dc.subject.meshAdultpt
dc.subject.meshBortezomibpt
dc.subject.meshHumanspt
dc.subject.meshProteasome Endopeptidase Complexpt
dc.subject.meshProteasome Inhibitorspt
dc.subject.meshQuality of Lifept
dc.subject.meshAntineoplastic Agentspt
dc.subject.meshMultiple Myelomapt
dc.subject.meshNeoplasmspt
dc.titleRevisiting Proteasome Inhibitors: Molecular Underpinnings of Their Development, Mechanisms of Resistance and Strategies to Overcome Anti-Cancer Drug Resistancept
dc.typearticle-
degois.publication.firstPage2201pt
degois.publication.issue7pt
degois.publication.titleMoleculespt
dc.peerreviewedyespt
dc.identifier.doi10.3390/molecules27072201pt
degois.publication.volume27pt
dc.date.embargo2022-03-28*
uc.date.periodoEmbargo0pt
item.fulltextCom Texto completo-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextopen-
crisitem.project.grantnoResearch Institute for Medicines - iMed.ULisboa-
crisitem.project.grantnoResearch Institute for Medicines - iMed-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0002-2202-4383-
crisitem.author.orcid0000-0003-0779-6083-
Appears in Collections:I&D CNC - Artigos em Revistas Internacionais
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This item is licensed under a Creative Commons License Creative Commons