International journal of molecular sciences · 2021
Allosteric Modulation of GSK-3β as a New Therapeutic Approach in Limb Girdle Muscular Dystrophy R1 Calpain 3-Related.
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Rico Anabel, Guembelzu Garazi, Palomo Valle, Martínez Ana, Aiastui Ana, Casas-Fraile Leire, Valls Andrea, López de Munain Adolfo, Sáenz Amets
Аннотация
Limb-girdle muscular dystrophy R1 calpain 3-related (LGMDR1) is an autosomal recessive muscular dystrophy produced by mutations in the CAPN3 gene. It is a rare disease and there is no cure or treatment for the disease while the pathophysiological mechanism by which the absence of calpain 3 provokes the dystrophy in muscles is not clear. However, key proteins implicated in Wnt and mTOR signaling pathways, which regulate muscle homeostasis, showed a considerable reduction in their expression and in their phosphorylation in LGMDR1 patients' muscles. Finally, the administration of tideglusib and VP0.7, ATP non-competitive inhibitors of glycogen synthase kinase 3β (GSK-3β), restore the expression and phosphorylation of these proteins in LGMDR1 cells, opening the possibility of their use as therapeutic options.
Предметные рубрики MeSH
Adenosine TriphosphateAllosteric SiteCD56 AntigenCalpainFibroblastsGene Expression RegulationGlycogen Synthase Kinase 3 betaHumansHydrazinesIntracellular Signaling Peptides and ProteinsMuscle Fibers, SkeletalMuscle ProteinsMuscular Dystrophies, Limb-GirdleNerve Tissue ProteinsPhosphorylationProtein Processing, Post-TranslationalProto-Oncogene Proteins c-aktQuinolonesSignal TransductionTOR Serine-Threonine KinasesThiadiazolesWnt Signaling Pathway