Literature DB >> 21804598

Targeting RNA to treat neuromuscular disease.

Francesco Muntoni1, Matthew J A Wood.   

Abstract

The development of effective therapies for neuromuscular disorders such as Duchenne muscular dystrophy (DMD) is hampered by considerable challenges: skeletal muscle is the most abundant tissue in the body, and many neuromuscular disorders are multisystemic conditions. However, despite these barriers there has recently been substantial progress in the search for novel treatments. In particular, the use of antisense oligonucleotides, which are designed to target RNA and modulate pre-mRNA splicing to restore functional protein isoforms or directly inhibit the toxic effects of pathogenic RNAs, offers great promise and these approaches are now being tested in the clinic. Here, we review recent advances in the development of such antisense oligonucleotides and other promising novel approaches, including the induction of readthrough nonsense mutations.

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Year:  2011        PMID: 21804598     DOI: 10.1038/nrd3459

Source DB:  PubMed          Journal:  Nat Rev Drug Discov        ISSN: 1474-1776            Impact factor:   84.694


  149 in total

1.  Chemical reversal of the RNA gain of function in myotonic dystrophy.

Authors:  Thomas A Cooper
Journal:  Proc Natl Acad Sci U S A       Date:  2009-10-28       Impact factor: 11.205

2.  Gentamicin fails to increase dystrophin expression in dystrophin-deficient muscle.

Authors:  Patrick Dunant; Maggie C Walter; George Karpati; Hanns Lochmüller
Journal:  Muscle Nerve       Date:  2003-05       Impact factor: 3.217

3.  Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum.

Authors:  J W Day; K Ricker; J F Jacobsen; L J Rasmussen; K A Dick; W Kress; C Schneider; M C Koch; G J Beilman; A R Harrison; J C Dalton; L P W Ranum
Journal:  Neurology       Date:  2003-02-25       Impact factor: 9.910

Review 4.  Pathogenic mechanisms of myotonic dystrophy.

Authors:  Johanna E Lee; Thomas A Cooper
Journal:  Biochem Soc Trans       Date:  2009-12       Impact factor: 5.407

5.  Myotonic dystrophy type 2: human founder haplotype and evolutionary conservation of the repeat tract.

Authors:  Christina L Liquori; Yoshio Ikeda; Marcy Weatherspoon; Kenneth Ricker; Benedikt G H Schoser; Joline C Dalton; John W Day; Laura P W Ranum
Journal:  Am J Hum Genet       Date:  2003-09-22       Impact factor: 11.025

Review 6.  Antisense technologies. Improvement through novel chemical modifications.

Authors:  Jens Kurreck
Journal:  Eur J Biochem       Date:  2003-04

7.  Effective exon skipping and restoration of dystrophin expression by peptide nucleic acid antisense oligonucleotides in mdx mice.

Authors:  Haifang Yin; Qilong Lu; Matthew Wood
Journal:  Mol Ther       Date:  2007-10-30       Impact factor: 11.454

8.  Sustained dystrophin expression induced by peptide-conjugated morpholino oligomers in the muscles of mdx mice.

Authors:  Natee Jearawiriyapaisarn; Hong M Moulton; Brian Buckley; Jennifer Roberts; Peter Sazani; Suthat Fucharoen; Patrick L Iversen; Ryszard Kole
Journal:  Mol Ther       Date:  2008-06-10       Impact factor: 11.454

9.  RNAi-mediated knockdown of dystrophin expression in adult mice does not lead to overt muscular dystrophy pathology.

Authors:  Mohammad M Ghahramani Seno; Ian R Graham; Takis Athanasopoulos; Capucine Trollet; Marita Pohlschmidt; Mark R Crompton; George Dickson
Journal:  Hum Mol Genet       Date:  2008-05-28       Impact factor: 6.150

Review 10.  Myotonic dystrophy: RNA pathogenesis comes into focus.

Authors:  Laura P W Ranum; John W Day
Journal:  Am J Hum Genet       Date:  2004-04-02       Impact factor: 11.025

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  63 in total

1.  [Computer experience and further developments in the respiratory function laboratory (author's transl)].

Authors:  R Schindl; K Mayer; K Aigner
Journal:  Med Klin       Date:  1975-11-07

2.  Muscular dystrophy: A hidden ancestral legacy trumped.

Authors:  Masayuki Nakamori; Charles Thornton
Journal:  Nature       Date:  2011-10-05       Impact factor: 49.962

Review 3.  Allele-selective inhibition of trinucleotide repeat genes.

Authors:  Masayuki Matsui; David R Corey
Journal:  Drug Discov Today       Date:  2012-01-18       Impact factor: 7.851

4.  Synthesis, Characterization, and Function of an RNA-Based Transfection Reagent.

Authors:  Harsh V Jain; Jessica F Boehler; Kanneboyina Nagaraju; Serge L Beaucage
Journal:  Curr Protoc Nucleic Acid Chem       Date:  2018-03

5.  Antisense therapeutics: Nuclear RNA more susceptible to knockdown.

Authors:  Man Tsuey Tse
Journal:  Nat Rev Drug Discov       Date:  2012-08-20       Impact factor: 84.694

6.  Exosome-mediated delivery of siRNA in vitro and in vivo.

Authors:  Samir El-Andaloussi; Yi Lee; Samira Lakhal-Littleton; Jinghuan Li; Yiqi Seow; Chris Gardiner; Lydia Alvarez-Erviti; Ian L Sargent; Matthew J A Wood
Journal:  Nat Protoc       Date:  2012-11-15       Impact factor: 13.491

Review 7.  Gene therapy for the nervous system: challenges and new strategies.

Authors:  Casey A Maguire; Servio H Ramirez; Steven F Merkel; Miguel Sena-Esteves; Xandra O Breakefield
Journal:  Neurotherapeutics       Date:  2014-10       Impact factor: 7.620

Review 8.  Mechanistic principles of antisense targets for the treatment of spinal muscular atrophy.

Authors:  Natalia N Singh; Brian M Lee; Christine J DiDonato; Ravindra N Singh
Journal:  Future Med Chem       Date:  2015-09-18       Impact factor: 3.808

Review 9.  Targeting RNA in mammalian systems with small molecules.

Authors:  Anita Donlic; Amanda E Hargrove
Journal:  Wiley Interdiscip Rev RNA       Date:  2018-05-03       Impact factor: 9.957

Review 10.  Antisense oligonucleotides: rising stars in eliminating RNA toxicity in myotonic dystrophy.

Authors:  Zhihua Gao; Thomas A Cooper
Journal:  Hum Gene Ther       Date:  2013-01-30       Impact factor: 5.695

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