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dc.contributor.authorApraiz García, Aintzane ORCID
dc.contributor.authorBenedicto García, Aitor
dc.contributor.authorMárquez Clavijo, Joana ORCID
dc.contributor.authorAgüera Lorente, Andrea
dc.contributor.authorAsumendi Mallea, Aintzane ORCID
dc.contributor.authorOlaso Montero, Elvira
dc.contributor.authorArteta Ruiz, Beatriz ORCID
dc.date.accessioned2020-11-30T11:40:42Z
dc.date.available2020-11-30T11:40:42Z
dc.date.issued2020-10-29
dc.identifier.citationCancers 12(11) : (2020) // Article ID 3177es_ES
dc.identifier.issn2072-6694
dc.identifier.urihttp://hdl.handle.net/10810/48712
dc.description.abstractThe role of innate lymphoid cells (ILCs) in cancer progression has been uncovered in recent years. ILCs are classified as Type 1, Type 2, and Type 3 ILCs, which are characterized by the transcription factors necessary for their development and the cytokines and chemokines they produce. ILCs are a highly heterogeneous cell population, showing both anti– and protumoral properties and capable of adapting their phenotypes and functions depending on the signals they receive from their surrounding environment. ILCs are considered the innate counterparts of the adaptive immune cells during physiological and pathological processes, including cancer, and as such, ILC subsets reflect different types of T cells. In cancer, each ILC subset plays a crucial role, not only in innate immunity but also as regulators of the tumor microenvironment. ILCs’ interplay with other immune and stromal cells in the metastatic microenvironment further dictates and influences this dichotomy, further strengthening the seed-and-soil theory and supporting the formation of more suitable and organ-specific metastatic environments. Here, we review the present knowledge on the different ILC subsets, focusing on their interplay with components of the tumor environment during the development of primary melanoma as well as on metastatic progression to organs, such as the liver or lung.es_ES
dc.description.sponsorshipThis research was funded by University of Basque Country, grant number GIU17/66.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.subjectmelanomaes_ES
dc.subjecttumor microenvironmentes_ES
dc.subjectinnate lymphoid cellses_ES
dc.subjectextracellular vesicleses_ES
dc.titleInnate Lymphoid Cells in the Malignant Melanoma Microenvironmentes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2020-11-26T14:08:18Z
dc.rights.holder2020 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 (http://creativecommons.org/licenses/by/4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/2072-6694/12/11/3177/htmes_ES
dc.identifier.doi10.3390/cancers12113177
dc.departamentoesBiología celular e histología
dc.departamentoesBiología celular e histología
dc.departamentoeuZelulen biologia eta histologia


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2020 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 (http://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as 2020 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 (http://creativecommons.org/licenses/by/4.0/).