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Spinal and bulbar muscular atrophy (SBMA) is a currently untreatable adult-onset neuromuscular disease caused by expansion of a polyglutamine repeat in the androgen receptor (AR). In SBMA, as in other polyglutamine diseases, a toxic gain of function in the mutant protein is an important factor in the disease mechanism; therefore, reducing the mutant protein holds promise as an effective treatment strategy. In this work, we evaluated a microRNA (miRNA) to reduce AR expression. From a list of predicted miRNAs that target human AR, we selected microRNA-298 (miR-298) for its ability to downregulate AR mRNA and protein levels when transfected in cells overexpressing wild-type and mutant AR and in SBMA patient-derived fibroblasts. We showed that miR-298 directly binds to the 3'-untranslated region of the human AR transcript, and counteracts AR toxicity in vitro. Intravenous delivery of miR-298 with adeno-associated virus serotype 9 vector resulted in efficient transduction of muscle and spinal cord and amelioration of the disease phenotype in SBMA mice. Our findings support the development of miRNAs as a therapeutic strategy for SBMA and other neurodegenerative disorders caused by toxic proteins.

Original publication

DOI

10.1038/mt.2016.13

Type

Journal article

Journal

Mol Ther

Publication Date

05/2016

Volume

24

Pages

937 - 945

Keywords

3' Untranslated Regions, Administration, Intravenous, Animals, Cell Line, Dependovirus, Disease Models, Animal, Down-Regulation, Genetic Therapy, Genetic Vectors, Humans, MCF-7 Cells, Mice, MicroRNAs, Muscular Atrophy, Spinal, Receptors, Androgen