Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/109149
DC FieldValueLanguage
dc.contributor.authorBezu, Lucillia-
dc.contributor.authorSilva, Lígia C. Gomes da-
dc.contributor.authorDewitte, Heleen-
dc.contributor.authorBreckpot, Karine-
dc.contributor.authorFucikova, Jitka-
dc.contributor.authorSpisek, Radek-
dc.contributor.authorGalluzzi, Lorenzo-
dc.contributor.authorKepp, Oliver-
dc.contributor.authorKroemer, Guido-
dc.date.accessioned2023-09-29T08:14:38Z-
dc.date.available2023-09-29T08:14:38Z-
dc.date.issued2015-
dc.identifier.issn1664-3224pt
dc.identifier.urihttps://hdl.handle.net/10316/109149-
dc.description.abstractThe term "immunogenic cell death" (ICD) is commonly employed to indicate a peculiar instance of regulated cell death (RCD) that engages the adaptive arm of the immune system. The inoculation of cancer cells undergoing ICD into immunocompetent animals elicits a specific immune response associated with the establishment of immunological memory. Only a few agents are intrinsically endowed with the ability to trigger ICD. These include a few chemotherapeutics that are routinely employed in the clinic, like doxorubicin, mitoxantrone, oxaliplatin, and cyclophosphamide, as well as some agents that have not yet been approved for use in humans. Accumulating clinical data indicate that the activation of adaptive immune responses against dying cancer cells is associated with improved disease outcome in patients affected by various neoplasms. Thus, novel therapeutic regimens that trigger ICD are urgently awaited. Here, we discuss current combinatorial approaches to convert otherwise non-immunogenic instances of RCD into bona fide ICD.pt
dc.description.sponsorshipGK issupportedbytheLiguecontreleCancer(équipelabelisée); AgenceNationaldelaRecherche(ANR);Associationpour larecherchesurlecancer(ARC);CancéropôleIle-de-France; InstitutNationalduCancer(INCa);FondationBettencourt- Schueller;FondationdeFrance;FondationpourlaRecherche Médicale(FRM);theEuropeanCommission(ArtForce);the EuropeanResearchCouncil(ERC);theLabExImmuno- Oncology;theSIRICStratifiedOncologyCellDNARepair andTumorImmuneElimination(SOCRATE);theSIRIC CancerResearchandPersonalizedMedicine(CARPEM); andtheParisAllianceofCancerResearchInstitutes (PACRI).pt
dc.language.isoengpt
dc.publisherFrontiers Media S.A.pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subjectATPpt
dc.subjectautophagypt
dc.subjectcalreticulinpt
dc.subjectendoplasmic reticulum stresspt
dc.subjectHMGB1pt
dc.subjecttype I interferonpt
dc.titleCombinatorial strategies for the induction of immunogenic cell deathpt
dc.typearticle-
degois.publication.firstPage187pt
degois.publication.issueAPRpt
degois.publication.titleFrontiers in Immunologypt
dc.peerreviewedyespt
dc.identifier.doi10.3389/fimmu.2015.00187pt
degois.publication.volume6pt
dc.date.embargo2015-01-01*
uc.date.periodoEmbargo0pt
item.openairetypearticle-
item.fulltextCom Texto completo-
item.languageiso639-1en-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0003-0624-8819-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
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