Literature DB >> 21334976

Prospects for the gene therapy of spinal muscular atrophy.

Marco A Passini1, Seng H Cheng.   

Abstract

Spinal muscular atrophy (SMA) is a neuromuscular disease caused by a deficiency of functional SMN protein because of mutations in SMN1. A decrease in SMN activity results in motor neuron cell loss in the spinal cord, leading to a weakness of the proximal muscles responsible for crawling, walking, head/neck control and swallowing as well as the involuntary muscles that control breathing and coughing. Thus, patients present with pulmonary manifestations, paralysis and a shortened lifespan. Gene therapy is emerging as a promising therapeutic strategy for SMA given that the molecular basis for this monogenic disorder is well established. Recent advances and findings from preclinical studies in animal models provide optimism that gene therapy might be an effective therapeutic strategy for treating SMA.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21334976     DOI: 10.1016/j.molmed.2011.01.002

Source DB:  PubMed          Journal:  Trends Mol Med        ISSN: 1471-4914            Impact factor:   11.951


  10 in total

1.  A role for SMN exon 7 splicing in the selective vulnerability of motor neurons in spinal muscular atrophy.

Authors:  Matteo Ruggiu; Vicki L McGovern; Francesco Lotti; Luciano Saieva; Darrick K Li; Shingo Kariya; Umrao R Monani; Arthur H M Burghes; Livio Pellizzoni
Journal:  Mol Cell Biol       Date:  2011-10-28       Impact factor: 4.272

2.  Intramuscular scAAV9-SMN injection mediates widespread gene delivery to the spinal cord and decreases disease severity in SMA mice.

Authors:  Sofia Benkhelifa-Ziyyat; Aurore Besse; Marianne Roda; Sandra Duque; Stéphanie Astord; Romain Carcenac; Thibaut Marais; Martine Barkats
Journal:  Mol Ther       Date:  2013-01-08       Impact factor: 11.454

3.  Astrocytes influence the severity of spinal muscular atrophy.

Authors:  Hansjörg Rindt; Zhihua Feng; Chiara Mazzasette; Jacqueline J Glascock; David Valdivia; Noah Pyles; Thomas O Crawford; Kathryn J Swoboda; Teresa N Patitucci; Allison D Ebert; Charlotte J Sumner; Chien-Ping Ko; Christian L Lorson
Journal:  Hum Mol Genet       Date:  2015-04-24       Impact factor: 6.150

Review 4.  Targeting RNA to treat neuromuscular disease.

Authors:  Francesco Muntoni; Matthew J A Wood
Journal:  Nat Rev Drug Discov       Date:  2011-08-01       Impact factor: 84.694

5.  Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophy.

Authors:  Melissa Bowerman; Lyndsay M Murray; Justin G Boyer; Carrie L Anderson; Rashmi Kothary
Journal:  BMC Med       Date:  2012-03-07       Impact factor: 8.775

Review 6.  Spinal muscular atrophy.

Authors:  Adele D'Amico; Eugenio Mercuri; Francesco D Tiziano; Enrico Bertini
Journal:  Orphanet J Rare Dis       Date:  2011-11-02       Impact factor: 4.123

Review 7.  Therapy development for spinal muscular atrophy in SMN independent targets.

Authors:  Li-Kai Tsai
Journal:  Neural Plast       Date:  2012-05-31       Impact factor: 3.599

Review 8.  Targeting Splicing in the Treatment of Human Disease.

Authors:  Marc Suñé-Pou; Silvia Prieto-Sánchez; Sofía Boyero-Corral; Cristina Moreno-Castro; Younes El Yousfi; Josep Mª Suñé-Negre; Cristina Hernández-Munain; Carlos Suñé
Journal:  Genes (Basel)       Date:  2017-02-24       Impact factor: 4.096

9.  A single intravenous AAV9 injection mediates bilateral gene transfer to the adult mouse retina.

Authors:  Alexis-Pierre Bemelmans; Sandra Duqué; Christel Rivière; Stéphanie Astord; Mélissa Desrosiers; Thibault Marais; José-Alain Sahel; Thomas Voit; Martine Barkats
Journal:  PLoS One       Date:  2013-04-15       Impact factor: 3.240

10.  A cell system for phenotypic screening of modifiers of SMN2 gene expression and function.

Authors:  Darrick K Li; Sarah Tisdale; Jorge Espinoza-Derout; Luciano Saieva; Francesco Lotti; Livio Pellizzoni
Journal:  PLoS One       Date:  2013-08-15       Impact factor: 3.240

  10 in total

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