Literature DB >> 11405346

Inhibition of substrate synthesis as a strategy for glycolipid lysosomal storage disease therapy.

F M Platt1, M Jeyakumar, U Andersson, D A Priestman, R A Dwek, T D Butters, T M Cox, R H Lachmann, C Hollak, J M Aerts, S Van Weely, M Hrebícek, C Moyses, I Gow, D Elstein, A Zimran.   

Abstract

The glycosphingolipid (GSL) lysosomal storage diseases are caused by mutations in the genes encoding the glycohydrolases that catabolize GSLs within lysosomes. In these diseases the substrate for the defective enzyme accumulates in the lysosome and the stored GSL leads to cellular dysfunction and disease. The diseases frequently have a progressive neurodegenerative course. The therapeutic options for treating these diseases are relatively limited, and for the majority there are no effective therapies. The problem is further compounded by difficulties in delivering therapeutic agents to the brain. Most research effort to date has focused on strategies for augmenting enzyme levels to compensate for the underlying defect. These include bone marrow transplantation (BMT), enzyme replacement and gene therapy. An alternative strategy that we have been exploring is substrate deprivation. This approach aims to balance the rate of GSL synthesis with the impaired rate of GSL breakdown. The imino sugar N-butyldeoxynojirimycin (NB-DNJ) inhibits the first step in GSL biosynthesis and has been used to evaluate this approach. Studies in an asymptomatic mouse model of Tay-Sachs disease have shown that substrate deprivation prevents GSL storage in the CNS. In a severe neurodegenerative mouse model of Sandhoff disease, substrate deprivation delayed the onset of symptoms and disease progression and significantly increased life expectancy. Combining NB-DNJ and BMT was found to be synergistic in the Sandhoff mouse model. A clinical trial in type I Gaucher disease has been undertaken and has shown beneficial effects. Efficacy was demonstrated on the basis of significant decreases in liver and spleen volumes, gradual but significant improvement in haematological parameters and disease activity markers, together with diminished GSL biosynthesis and storage as determined by independent biochemical assays. Further trials in type I Gaucher disease are in progress; studies are planned in patients with GSL storage in the CNS.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11405346     DOI: 10.1023/a:1010335505357

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  43 in total

1.  Gene therapy at a crossroads.

Authors:  R SoRelle
Journal:  Circulation       Date:  2000-02-15       Impact factor: 29.690

2.  Novel oral treatment of Gaucher's disease with N-butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis.

Authors:  T Cox; R Lachmann; C Hollak; J Aerts; S van Weely; M Hrebícek; F Platt; T Butters; R Dwek; C Moyses; I Gow; D Elstein; A Zimran
Journal:  Lancet       Date:  2000-04-29       Impact factor: 79.321

3.  Bone marrow transplantation prolongs life span and ameliorates neurologic manifestations in Sandhoff disease mice.

Authors:  F Norflus; C J Tifft; M P McDonald; G Goldstein; J N Crawley; A Hoffmann; K Sandhoff; K Suzuki; R L Proia
Journal:  J Clin Invest       Date:  1998-05-01       Impact factor: 14.808

4.  Enzyme therapy for pompe disease with recombinant human alpha-glucosidase from rabbit milk.

Authors:  J M Van den Hout; A J Reuser; J B de Klerk; W F Arts; J A Smeitink; A T Van der Ploeg
Journal:  J Inherit Metab Dis       Date:  2001-04       Impact factor: 4.982

5.  Extensive glycosphingolipid depletion in the liver and lymphoid organs of mice treated with N-butyldeoxynojirimycin.

Authors:  F M Platt; G Reinkensmeier; R A Dwek; T D Butters
Journal:  J Biol Chem       Date:  1997-08-01       Impact factor: 5.157

6.  Enhanced survival in Sandhoff disease mice receiving a combination of substrate deprivation therapy and bone marrow transplantation.

Authors:  M Jeyakumar; F Norflus; C J Tifft; M Cortina-Borja; T D Butters; R L Proia; V H Perry; R A Dwek; F M Platt
Journal:  Blood       Date:  2001-01-01       Impact factor: 22.113

7.  Clinical and biochemical outcome of marrow transplantation for Gaucher disease of the Norrbottnian type.

Authors:  A Erikson; C G Groth; J E Månsson; A Percy; O Ringdén; L Svennerholm
Journal:  Acta Paediatr Scand       Date:  1990 Jun-Jul

8.  Neuropathology of mice with targeted disruption of Hexa gene, a model of Tay-Sachs disease.

Authors:  M Taniike; S Yamanaka; R L Proia; C Langaman; T Bone-Turrentine; K Suzuki
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

9.  Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases.

Authors:  D Phaneuf; N Wakamatsu; J Q Huang; A Borowski; A C Peterson; S R Fortunato; G Ritter; S A Igdoura; C R Morales; G Benoit; B R Akerman; D Leclerc; N Hanai; J D Marth; J M Trasler; R A Gravel
Journal:  Hum Mol Genet       Date:  1996-01       Impact factor: 6.150

Review 10.  Microglia: the effector cell for reconstitution of the central nervous system following bone marrow transplantation for lysosomal and peroxisomal storage diseases.

Authors:  W Krivit; J H Sung; E G Shapiro; L A Lockman
Journal:  Cell Transplant       Date:  1995 Jul-Aug       Impact factor: 4.139

View more
  33 in total

1.  CCL18: a urinary marker of Gaucher cell burden in Gaucher patients.

Authors:  Rolf G Boot; Marri Verhoek; Mirjam Langeveld; G Herma Renkema; Carla E M Hollak; Jan J Weening; Wilma E Donker-Koopman; Johanna E Groener; Johannes M F G Aerts
Journal:  J Inherit Metab Dis       Date:  2006-05-30       Impact factor: 4.982

2.  Therapeutic effects of stem cells and substrate reduction in juvenile Sandhoff mice.

Authors:  J R Arthur; J P Lee; E Y Snyder; T N Seyfried
Journal:  Neurochem Res       Date:  2012-02-25       Impact factor: 3.996

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.  Selective action of the iminosugar isofagomine, a pharmacological chaperone for mutant forms of acid-beta-glucosidase.

Authors:  Richard Steet; Stephen Chung; Wang-Sik Lee; Corey W Pine; Hung Do; Stuart Kornfeld
Journal:  Biochem Pharmacol       Date:  2006-12-15       Impact factor: 5.858

Review 5.  Enzyme replacement and beyond.

Authors:  R J Desnick
Journal:  J Inherit Metab Dis       Date:  2001-04       Impact factor: 4.982

6.  Elevated plasma glucosylsphingosine in Gaucher disease: relation to phenotype, storage cell markers, and therapeutic response.

Authors:  Nick Dekker; Laura van Dussen; Carla E M Hollak; Herman Overkleeft; Saskia Scheij; Karen Ghauharali; Mariëlle J van Breemen; Maria J Ferraz; Johanna E M Groener; Mario Maas; Frits A Wijburg; Dave Speijer; Anna Tylki-Szymanska; Pramod K Mistry; Rolf G Boot; Johannes M Aerts
Journal:  Blood       Date:  2011-08-25       Impact factor: 22.113

7.  Distinguishing the differences in β-glycosylceramidase folds, dynamics, and actions informs therapeutic uses.

Authors:  Fredj Ben Bdira; Marta Artola; Herman S Overkleeft; Marcellus Ubbink; Johannes M F G Aerts
Journal:  J Lipid Res       Date:  2018-10-02       Impact factor: 5.922

8.  Real-world clinical experience with long-term miglustat maintenance therapy in type 1 Gaucher disease: the ZAGAL project.

Authors:  Pilar Giraldo; Pilar Alfonso; Koldo Atutxa; María A Fernández-Galán; Abelardo Barez; Rafael Franco; Dora Alonso; Alejandro Martin; Paz Latre; Miguel Pocovi
Journal:  Haematologica       Date:  2009-07-16       Impact factor: 9.941

9.  Dysregulated sphingolipid metabolism in endometriosis.

Authors:  Yie Hou Lee; Chin Wen Tan; Abhishek Venkatratnam; Chuen Seng Tan; Liang Cui; Seong Feei Loh; Linda Griffith; Steven R Tannenbaum; Jerry Kok Yen Chan
Journal:  J Clin Endocrinol Metab       Date:  2014-06-24       Impact factor: 5.958

10.  Role of β-glucosidase 2 in aberrant glycosphingolipid metabolism: model of glucocerebrosidase deficiency in zebrafish.

Authors:  Lindsey T Lelieveld; Mina Mirzaian; Chi-Lin Kuo; Marta Artola; Maria J Ferraz; Remco E A Peter; Hisako Akiyama; Peter Greimel; Richard J B H N van den Berg; Herman S Overkleeft; Rolf G Boot; Annemarie H Meijer; Johannes M F G Aerts
Journal:  J Lipid Res       Date:  2019-09-27       Impact factor: 5.922

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.