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dc.contributor.authorAldareguía Fernández, Juncal
dc.contributor.authorOdriozola Larrañaga, Ainize
dc.contributor.authorMatheu Fernández, Ander
dc.contributor.authorGarcía Camino, Idoia
dc.date.accessioned2018-11-15T12:17:08Z
dc.date.available2018-11-15T12:17:08Z
dc.date.issued2018-07
dc.identifier.citationInternational Journal of Molecular Sciences 19(7) : (2018) // Article ID 1838es_ES
dc.identifier.issn1422-0067
dc.identifier.urihttp://hdl.handle.net/10810/29674
dc.description.abstractMechanistic target of rapamycin (mTOR) is a master signaling pathway that regulates organismal growth and homeostasis, because of its implication in protein and lipid synthesis, and in the control of the cell cycle and the cellular metabolism. Moreover, it is necessary in cerebellar development and stem cell pluripotency maintenance. Its deregulation has been implicated in the medulloblastoma and in medulloblastoma stem cells (MBSCs). Medulloblastoma is the most common malignant solid tumor in childhood. The current therapies have improved the overall survival but they carry serious side effects, such as permanent neurological sequelae and disability. Recent studies have given rise to a new molecular classification of the subgroups of medulloblastoma, specifying 12 different subtypes containing novel potential therapeutic targets. In this review we propose the targeting of mTOR, in combination with current therapies, as a promising novel therapeutic approach.es_ES
dc.description.sponsorshipJ.A. is recipient of a predoctoral fellowship from the Department of Education of the Basque Government. This work was supported by grants from the Department of Industry of the Basque Government (SAIO13-PC13BN011), and the European Regional Developmental Fund, Institute of Health Carlos III (ISCIII) (PI16/01730) to I.G.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.subjectmTORes_ES
dc.subjectmedulloblastomaes_ES
dc.subjectMBSCses_ES
dc.subjectrenal-cell carcinomaes_ES
dc.subjectembryonic stem-cellses_ES
dc.subjectcentral-nervous-systemes_ES
dc.subjectphase-iii triales_ES
dc.subjectsonic hedgehoges_ES
dc.subjectsignaling pathwayes_ES
dc.subjectneuroendocrine tumorses_ES
dc.subjectbreast-canceres_ES
dc.subjectbrain-tumorses_ES
dc.subjectdouble-blindes_ES
dc.titleTargeting mTOR as a Therapeutic Approach in Medulloblastomaes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2018 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.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://www.mdpi.com/1422-0067/19/7/1838es_ES
dc.identifier.doi10.3390/ijms19071838
dc.departamentoesFisiologíaes_ES
dc.departamentoeuFisiologiaes_ES


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© 2018 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 © 2018 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/).