Targeting Myotonic Dystrophy Type 1 with Metformin
dc.contributor.author | García Puga, Mikel | |
dc.contributor.author | Sáenz Antoñanzas, Ander | |
dc.contributor.author | Matheu Fernández, Ander | |
dc.contributor.author | López de Munain Arregui, Adolfo José | |
dc.date.accessioned | 2022-09-20T10:42:55Z | |
dc.date.available | 2022-09-20T10:42:55Z | |
dc.date.issued | 2022-03 | |
dc.identifier.citation | International Journal of Molecular Sciences 23(5) : (2022) // Article ID 2901 | es_ES |
dc.identifier.issn | 1422-0067 | |
dc.identifier.uri | http://hdl.handle.net/10810/57789 | |
dc.description.abstract | Myotonic 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.sponsorship | M.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.iso | eng | es_ES |
dc.publisher | MDPI | es_ES |
dc.rights | info:eu-repo/semantics/openAccess | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.subject | myotonic dystrophy | es_ES |
dc.subject | metformin | es_ES |
dc.subject | therapeutic strategies | es_ES |
dc.subject | aging | es_ES |
dc.subject | protein-kinase | es_ES |
dc.subject | skeletal-muscle | es_ES |
dc.subject | cancer-risk | es_ES |
dc.subject | trinucleotide repeat | es_ES |
dc.subject | cognitive function | es_ES |
dc.subject | molecular-basis | es_ES |
dc.subject | mouse model | es_ES |
dc.subject | CGT repeat | es_ES |
dc.subject | mortality | es_ES |
dc.subject | expansion | es_ES |
dc.title | Targeting Myotonic Dystrophy Type 1 with Metformin | es_ES |
dc.type | info:eu-repo/semantics/article | es_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.holder | Atribución 3.0 España | * |
dc.relation.publisherversion | https://www.mdpi.com/1422-0067/23/5/2901/htm | es_ES |
dc.identifier.doi | 10.3390/ijms23052901 | |
dc.departamentoes | Neurociencias | es_ES |
dc.departamentoeu | Neurozientziak | es_ES |
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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/).