Literature DB >> 16798086

Stop-codon read-through for patients affected by a lysosomal storage disorder.

Doug A Brooks1, Viv J Muller, John J Hopwood.   

Abstract

Lysosomal storage disorders are a group of inherited diseases that can result in severe and progressive pathology due to a specific lysosomal dysfunction. Current treatment strategies include bone-marrow transplantation, substrate reduction, chemical-chaperone and enzyme-replacement therapy. However, each of these treatments has its limitations. Enhanced stop-codon read-through is a potential alternative or adjunct therapeutic strategy for treating lysosomal-storage-disorder patients. Premature stop-codon mutations have been identified in a large cohort of patients with a lysosomal storage disorder, making stop-codon read-through a possible treatment for this disease. In lysosomal-storage-disorder cells (mucopolysaccharidosis type I, alpha-L-iduronidase deficient), preclinical studies have shown that gentamicin induced the read-through of premature stop codons, resulting in enzyme activity that reduced substrate storage.

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Year:  2006        PMID: 16798086     DOI: 10.1016/j.molmed.2006.06.001

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


  34 in total

1.  Therapeutic approaches for lysosomal storage diseases.

Authors:  Gregory M Pastores
Journal:  Ther Adv Endocrinol Metab       Date:  2010-08       Impact factor: 3.565

2.  Long-term nonsense suppression therapy moderates MPS I-H disease progression.

Authors:  Gwen Gunn; Yanying Dai; Ming Du; Valery Belakhov; Jeyakumar Kandasamy; Trenton R Schoeb; Timor Baasov; David M Bedwell; Kim M Keeling
Journal:  Mol Genet Metab       Date:  2013-12-17       Impact factor: 4.797

Review 3.  Small molecules as therapeutic agents for inborn errors of metabolism.

Authors:  Leslie Matalonga; Laura Gort; Antonia Ribes
Journal:  J Inherit Metab Dis       Date:  2016-12-13       Impact factor: 4.982

Review 4.  Substrate deprivation therapy: a new hope for patients suffering from neuronopathic forms of inherited lysosomal storage diseases.

Authors:  Joanna Jakóbkiewicz-Banecka; Alicja Wegrzyn; Grzegorz Wegrzyn
Journal:  J Appl Genet       Date:  2007       Impact factor: 3.240

Review 5.  Nonsense-mediated decay in genetic disease: friend or foe?

Authors:  Jake N Miller; David A Pearce
Journal:  Mutat Res Rev Mutat Res       Date:  2014-05-28       Impact factor: 5.657

6.  Storage correction in cells of patients suffering from mucopolysaccharidoses types IIIA and VII after treatment with genistein and other isoflavones.

Authors:  Audrey Arfi; Magali Richard; Christelle Gandolphe; Daniel Scherman
Journal:  J Inherit Metab Dis       Date:  2010-02       Impact factor: 4.982

7.  The role of nonsense-mediated decay in neuronal ceroid lipofuscinosis.

Authors:  Jake N Miller; Chun-Hung Chan; David A Pearce
Journal:  Hum Mol Genet       Date:  2013-03-28       Impact factor: 6.150

8.  The effect of gentamicin-induced readthrough on a novel premature termination codon of CD18 leukocyte adhesion deficiency patients.

Authors:  Amos J Simon; Atar Lev; Baruch Wolach; Ronit Gavrieli; Ninette Amariglio; Ester Rosenthal; Ephraim Gazit; Eran Eyal; Gideon Rechavi; Raz Somech
Journal:  PLoS One       Date:  2010-11-16       Impact factor: 3.240

9.  Aminoglycoside-Induced Premature Stop Codon Read-Through of Mucopolysaccharidosis Type I Patient Q70X and W402X Mutations in Cultured Cells.

Authors:  Makoto Kamei; Karissa Kasperski; Maria Fuller; Emma J Parkinson-Lawrence; Litsa Karageorgos; Valery Belakhov; Timor Baasov; John J Hopwood; Doug A Brooks
Journal:  JIMD Rep       Date:  2013-11-06

10.  Reawakening retrocyclins: ancestral human defensins active against HIV-1.

Authors:  Nitya Venkataraman; Amy L Cole; Piotr Ruchala; Alan J Waring; Robert I Lehrer; Olga Stuchlik; Jan Pohl; Alexander M Cole
Journal:  PLoS Biol       Date:  2009-04-28       Impact factor: 8.029

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