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dc.contributor.authorGarcía Puga, Mikel
dc.contributor.authorSáenz Antoñanzas, Ander
dc.contributor.authorMatheu Fernández, Ander
dc.contributor.authorLópez de Munain Arregui, Adolfo José
dc.date.accessioned2022-09-20T10:42:55Z
dc.date.available2022-09-20T10:42:55Z
dc.date.issued2022-03
dc.identifier.citationInternational Journal of Molecular Sciences 23(5) : (2022) // Article ID 2901es_ES
dc.identifier.issn1422-0067
dc.identifier.urihttp://hdl.handle.net/10810/57789
dc.description.abstractMyotonic dystrophy type 1 (DM1) is a multisystemic disorder of genetic origin. Progressive muscular weakness, atrophy and myotonia are its most prominent neuromuscular features, while additional clinical manifestations in multiple organs are also common. Overall, DM1 features resemble accelerated aging. There is currently no cure or specific treatment for myotonic dystrophy patients. However, in recent years a great effort has been made to identify potential new therapeutic strategies for DM1 patients. Metformin is a biguanide antidiabetic drug, with potential to delay aging at cellular and organismal levels. In DM1, different studies revealed that metformin rescues multiple phenotypes of the disease. This review provides an overview of recent findings describing metformin as a novel therapy to combat DM1 and their link with aging.es_ES
dc.description.sponsorshipM.G.-P. and A.S.-A. are recipient of predoctoral fellowships from the University of the Basque Country (PIF 15/245) and Carlos III Institute (FI17/00250), respectively. This work is supported by grants from the Carlos III Institute and FEDER funds (PI17/01841, DTS18/00181, PI19/01355, PI21/00557), Health Department from Basque Country (2017222021, 2018222021, 2020333008) and CIBERNED funds.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.subjectmyotonic dystrophyes_ES
dc.subjectmetformines_ES
dc.subjecttherapeutic strategieses_ES
dc.subjectaginges_ES
dc.subjectprotein-kinasees_ES
dc.subjectskeletal-musclees_ES
dc.subjectcancer-riskes_ES
dc.subjecttrinucleotide repeates_ES
dc.subjectcognitive functiones_ES
dc.subjectmolecular-basises_ES
dc.subjectmouse modeles_ES
dc.subjectCGT repeates_ES
dc.subjectmortalityes_ES
dc.subjectexpansiones_ES
dc.titleTargeting Myotonic Dystrophy Type 1 with Metformines_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 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 (https://creativecommons.org/licenses/by/4.0/).es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://www.mdpi.com/1422-0067/23/5/2901/htmes_ES
dc.identifier.doi10.3390/ijms23052901
dc.departamentoesNeurocienciases_ES
dc.departamentoeuNeurozientziakes_ES


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