Cellular and Molecular Mechanisms Underlying Glioblastoma and Zebrafish Models for the Discovery of New Treatments

dc.contributor.affiliationUniversidade de Santiago de Compostela. Centro de Investigación en Medicina Molecular e Enfermidades Crónicasgl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Zooloxía, Xenética e Antropoloxía Físicagl
dc.contributor.authorReimunde Figueira, Pedro Marcos
dc.contributor.authorPensado López, Alba
dc.contributor.authorCarreira Crende, Martín
dc.contributor.authorLombao Iglesias, Vanesa
dc.contributor.authorSánchez Piñón, Laura
dc.contributor.authorTorrecilla Parra, Marta
dc.contributor.authorRamírez, Cristina M.
dc.contributor.authorAnfray, Clément
dc.contributor.authorTorres Andón, Fernando
dc.date.accessioned2021-03-12T13:36:57Z
dc.date.available2021-03-12T13:36:57Z
dc.date.issued2021
dc.description.abstractGlioblastoma (GBM) is the most common of all brain malignant tumors; it displays a median survival of 14.6 months with current complete standard treatment. High heterogeneity, aggressive and invasive behavior, the impossibility of completing tumor resection, limitations for drug administration and therapeutic resistance to current treatments are the main problems presented by this pathology. In recent years, our knowledge of GBM physiopathology has advanced significantly, generating relevant information on the cellular heterogeneity of GBM tumors, including cancer and immune cells such as macrophages/microglia, genetic, epigenetic and metabolic alterations, comprising changes in miRNA expression. In this scenario, the zebrafish has arisen as a promising animal model to progress further due to its unique characteristics, such as transparency, ease of genetic manipulation, ethical and economic advantages and also conservation of the major brain regions and blood–brain–barrier (BBB) which are similar to a human structure. A few papers described in this review, using genetic and xenotransplantation zebrafish models have been used to study GBM as well as to test the anti-tumoral efficacy of new drugs, their ability to interact with target cells, modulate the tumor microenvironment, cross the BBB and/or their toxicity. Prospective studies following these lines of research may lead to a better diagnosis, prognosis and treatment of patients with GBMgl
dc.description.peerreviewedSIgl
dc.description.sponsorshipF.T.A. has been supported by the AECC (“Asociación Española Contra el Cáncer”, Spain). We would also like to thank the following: the Talento Program from Madrid Government, Spain (2017-T1/BMD-5333); Convocatoria 2018 de proyectos de I+D+i «RETOS INVESTIGACIÓN» (RTI2018-095061-B-I00) (to C.M.R.); “Convocatoria de ayudas para la contratación de ayudantes de investigación” (PEJ-2018-AI/BMD-9724) (to M.T.-P.); the Xunta de Galicia Pre-doctoral Fellowship (ED481A-2018/095) (to A.P.L.)gl
dc.identifier.citationCancers 2021, 13(5), 1087; https://doi.org/10.3390/cancers13051087gl
dc.identifier.doi10.3390/cancers13051087
dc.identifier.essn2072-6694
dc.identifier.urihttp://hdl.handle.net/10347/24730
dc.language.isoenggl
dc.publisherMDPIgl
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RTI2018-095061-B-I00/ES/NUEVOS REGULADORES POSTRANSCRIPCIONALES COMO VINCULO MOLECULAR ENTRE DIABETES, OBESIDAD Y ALZHEIMER
dc.relation.publisherversionhttps://doi.org/10.3390/cancers13051087gl
dc.rights© 2021 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/)gl
dc.rightsAtribución 4.0 Internacional
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectGlioblastomagl
dc.subjectCancergl
dc.subjectTumor microenvironmentgl
dc.subjectGlioma-associated microglia/macrophagesgl
dc.subjectGeneticsgl
dc.subjectMetabolismgl
dc.subjectmiRNAgl
dc.subjectZebrafishgl
dc.subjectDrug discoverygl
dc.titleCellular and Molecular Mechanisms Underlying Glioblastoma and Zebrafish Models for the Discovery of New Treatmentsgl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
relation.isAuthorOfPublication017b2725-d3de-40d7-8859-18c50f038d1d
relation.isAuthorOfPublication.latestForDiscovery017b2725-d3de-40d7-8859-18c50f038d1d

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