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dc.contributor.authorMorante Ezquerra, Martaes_ES
dc.contributor.authorPandiella, Atanasioes_ES
dc.contributor.authorCrespo Baraja, Piero es_ES
dc.contributor.authorHerrero Mier, Anaes_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2023-01-17T15:53:28Z
dc.date.available2023-01-17T15:53:28Z
dc.date.issued2022es_ES
dc.identifier.issn2218-273Xes_ES
dc.identifier.otherPID2021-126288OB-I00es_ES
dc.identifier.otherPID2020-115605RB-I00es_ES
dc.identifier.urihttps://hdl.handle.net/10902/27267
dc.description.abstractMetastatic melanoma is a highly immunogenic tumor with very poor survival rates due to immune system escape-mechanisms. Immune checkpoint inhibitors (ICIs) targeting the cytotoxic T-lymphocyte-associated protein 4 (CTLA4) and the programmed death-1 (PD1) receptors, are being used to impede immune evasion. This immunotherapy entails an increment in the overall survival rates. However, melanoma cells respond with evasive molecular mechanisms. ERK cascade inhibitors are also used in metastatic melanoma treatment, with the RAF activity blockade being the main therapeutic approach for such purpose, and in combination with MEK inhibitors improves many parameters of clinical efficacy. Despite their efficacy in inhibiting ERK signaling, the rewiring of the melanoma cell-signaling results in disease relapse, constituting the reinstatement of ERK activation, which is a common cause of some resistance mechanisms. Recent studies revealed that the combination of RAS-ERK pathway inhibitors and ICI therapy present promising advantages for metastatic melanoma treatment. Here, we present a recompilation of the combined therapies clinically evaluated in patients.es_ES
dc.description.sponsorshipFunding: PC lab is supported by grant PID2021-126288OB-I00 from the Spanish Ministry of Science (MICIU/AEI/FEDER, UE); PIE 202220E003 from Agencia Estatal Consejo Superior de Investigaciones Científicas; and CIBERONC from the Instituto de Salud Carlos III (ISCIII). AP: Spanish Ministry of Science (PID2020-115605RB-I00), CIBERONC, Junta de Castilla y León (CSI146P20), and the CRIS Cancer Foundation. Our labs receive support from the European Union Regional Development Funding Program (FEDER).es_ES
dc.format.extent21 p.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsAttribution 4.0 International*
dc.rights© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceBiomolecules 2022, 12(11), 1562es_ES
dc.subject.otherRAS–ERKes_ES
dc.subject.otherMelanomaes_ES
dc.subject.otherInhibitorses_ES
dc.subject.otherImmunotherapyes_ES
dc.titleImmune Checkpoint Inhibitors and RAS–ERK Pathway-Targeted Drugs as Combined Therapy for the Treatment of Melanomaes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.3390/ biom12111562es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.3390/biom12111562es_ES
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International