Literature DB >> 19167250

Promising results of the chaperone effect caused by imino sugars and aminocyclitol derivatives on mutant glucocerebrosidases causing Gaucher disease.

Gessamí Sánchez-Ollé1, Joana Duque, Meritxell Egido-Gabás, Josefina Casas, Montserrat Lluch, Amparo Chabás, Daniel Grinberg, Lluïsa Vilageliu.   

Abstract

Gaucher disease is an autosomal recessive disorder. It is characterized by the accumulation of glucosylceramide in lysosomes of mononuclear phagocyte system, attributable to acid beta-glucosidase deficiency. The main consequences of this disease are hepatosplenomegaly, skeletal lesions and, sometimes, neurological manifestations. At sub-inhibitory concentrations, several competitive inhibitors act as chemical chaperones by inducing protein stabilization and increasing enzymatic activity. Here we tested two iminosugars (NB-DNJ and NN-DNJ) and four aminocyclitols with distinct degrees of lipophilicity as pharmacological chaperones for glucocerebrosidase (GBA). We report an increase in the activity of GBA using NN-DNJ, NB-DNJ and aminocyclitol 1 in stably transfected cell lines, and an increment with NN-DNJ and aminocyclitol 4 in patient fibroblasts. These results on specific mutations validate the use of chemical chaperones as a therapeutic approach for Gaucher disease. However, the development and analysis of new compounds is required in order to find more effective therapeutic agents that are active on a broader range of mutations.

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Year:  2009        PMID: 19167250     DOI: 10.1016/j.bcmd.2008.11.002

Source DB:  PubMed          Journal:  Blood Cells Mol Dis        ISSN: 1079-9796            Impact factor:   3.039


  12 in total

1.  Binding of 3,4,5,6-tetrahydroxyazepanes to the acid-β-glucosidase active site: implications for pharmacological chaperone design for Gaucher disease.

Authors:  Susan D Orwig; Yun Lei Tan; Neil P Grimster; Zhanqian Yu; Evan T Powers; Jeffery W Kelly; Raquel L Lieberman
Journal:  Biochemistry       Date:  2011-11-14       Impact factor: 3.162

2.  Enzyme enhancers for the treatment of Fabry and Pompe disease.

Authors:  Jan Lukas; Anne-Marie Pockrandt; Susanne Seemann; Muhammad Sharif; Franziska Runge; Susann Pohlers; Chaonan Zheng; Anne Gläser; Matthias Beller; Arndt Rolfs; Anne-Katrin Giese
Journal:  Mol Ther       Date:  2014-11-20       Impact factor: 11.454

Review 3.  Identification and characterization of pharmacological chaperones to correct enzyme deficiencies in lysosomal storage disorders.

Authors:  Kenneth J Valenzano; Richie Khanna; Allan C Powe; Robert Boyd; Gary Lee; John J Flanagan; Elfrida R Benjamin
Journal:  Assay Drug Dev Technol       Date:  2011-06       Impact factor: 1.738

4.  Synthesis of lipophilic 1-deoxygalactonojirimycin derivatives as D-galactosidase inhibitors.

Authors:  Georg Schitter; Elisabeth Scheucher; Andreas J Steiner; Arnold E Stütz; Martin Thonhofer; Chris A Tarling; Stephen G Withers; Jacqueline Wicki; Katrin Fantur; Eduard Paschke; Don J Mahuran; Brigitte A Rigat; Michael Tropak; Tanja M Wrodnigg
Journal:  Beilstein J Org Chem       Date:  2010-03-01       Impact factor: 2.883

5.  Structural snapshots illustrate the catalytic cycle of β-galactocerebrosidase, the defective enzyme in Krabbe disease.

Authors:  Chris H Hill; Stephen C Graham; Randy J Read; Janet E Deane
Journal:  Proc Natl Acad Sci U S A       Date:  2013-12-02       Impact factor: 11.205

Review 6.  Progress and potential of non-inhibitory small molecule chaperones for the treatment of Gaucher disease and its implications for Parkinson disease.

Authors:  Olive Jung; Samarjit Patnaik; Juan Marugan; Ellen Sidransky; Wendy Westbroek
Journal:  Expert Rev Proteomics       Date:  2016-04-21       Impact factor: 3.940

7.  ELIGLUSTAT TARTRATE: Glucosylceramide Synthase Inhibitor Treatment of Type 1 Gaucher Disease.

Authors:  J A Shayman
Journal:  Drugs Future       Date:  2010-08-01       Impact factor: 0.148

8.  Azasugar inhibitors as pharmacological chaperones for Krabbe disease.

Authors:  Chris H Hill; Agnete H Viuff; Samantha J Spratley; Stéphane Salamone; Stig H Christensen; Randy J Read; Nigel W Moriarty; Henrik H Jensen; Janet E Deane
Journal:  Chem Sci       Date:  2015-03-30       Impact factor: 9.825

Review 9.  Less Is More: Substrate Reduction Therapy for Lysosomal Storage Disorders.

Authors:  Maria Francisca Coutinho; Juliana Inês Santos; Sandra Alves
Journal:  Int J Mol Sci       Date:  2016-07-04       Impact factor: 5.923

10.  Insights into Hunter syndrome from the structure of iduronate-2-sulfatase.

Authors:  Mykhaylo Demydchuk; Chris H Hill; Aiwu Zhou; Gábor Bunkóczi; Penelope E Stein; Denis Marchesan; Janet E Deane; Randy J Read
Journal:  Nat Commun       Date:  2017-06-08       Impact factor: 14.919

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