Literature DB >> 22482025

Protein misfolding and clearance in demyelinating peripheral neuropathies: Therapeutic implications.

Samuel M Lee1, Lih-Shen Chin, Lian Li.   

Abstract

Peripheral neuropathies such as Charcot-Marie-Tooth disease (CMT) are a group of neurological disorders that affect the peripheral nervous system. Although demyelinating CMT is the most prevalent hereditary peripheral neuropathy, there are currently no effective treatments for patients suffering from this disease. Recent studies by our group and others have provided a link between protein misfolding and demyelinating CMT and indicate that impairment of the proteasome and aggresome-autophagy pathways may contribute to CMT pathogenesis. These studies suggest that targeting protein quality control systems involved in cytoprotection against CMT-associated misfolded proteins could have therapeutic benefits for treating demyelinating CMT.

Entities:  

Keywords:  Charcot-Marie-Tooth disease; Peripheral neuropathy; Proteasome; Schwann cells; aggresome; autophagy; demyelination; misfolded protein

Year:  2012        PMID: 22482025      PMCID: PMC3291304          DOI: 10.4161/cib.18638

Source DB:  PubMed          Journal:  Commun Integr Biol        ISSN: 1942-0889


  30 in total

Review 1.  Functional aspects of cellular microcompartmentation in the development of neurodegeneration: mutation induced aberrant protein-protein associations.

Authors:  Judit Ovádi; Ferenc Orosz; Susan Hollán
Journal:  Mol Cell Biochem       Date:  2004 Jan-Feb       Impact factor: 3.396

2.  Opening a new DOR to autophagy.

Authors:  Jaeline Spowart; Julian J Lum
Journal:  EMBO Rep       Date:  2010-01       Impact factor: 8.807

3.  Mutations associated with Charcot-Marie-Tooth disease cause SIMPLE protein mislocalization and degradation by the proteasome and aggresome-autophagy pathways.

Authors:  Samuel M Lee; James A Olzmann; Lih-Shen Chin; Lian Li
Journal:  J Cell Sci       Date:  2011-09-06       Impact factor: 5.285

4.  The Chediak-Higashi syndrome: electrophysiological and electron microscopic observations on the peripheral neuropathy.

Authors:  L A Lockman; W R Kennedy; J G White
Journal:  J Pediatr       Date:  1967-06       Impact factor: 4.406

Review 5.  Update on Charcot-Marie-Tooth disease.

Authors:  Agnes Patzkó; Michael E Shy
Journal:  Curr Neurol Neurosci Rep       Date:  2011-02       Impact factor: 5.081

6.  Impaired proteasome activity and accumulation of ubiquitinated substrates in a hereditary neuropathy model.

Authors:  Jenny Fortun; Jie Li; Jocelyn Go; Ali Fenstermaker; Bradley S Fletcher; Lucia Notterpek
Journal:  J Neurochem       Date:  2005-03       Impact factor: 5.372

7.  Aggresome formation in neuropathy models based on peripheral myelin protein 22 mutations.

Authors:  Mary C Ryan; Eric M Shooter; Lucia Notterpek
Journal:  Neurobiol Dis       Date:  2002-07       Impact factor: 5.996

8.  Emerging role for autophagy in the removal of aggresomes in Schwann cells.

Authors:  Jenny Fortun; William A Dunn; Shale Joy; Jie Li; Lucia Notterpek
Journal:  J Neurosci       Date:  2003-11-19       Impact factor: 6.167

9.  Phenotypic differences between peripheral myelin protein-22 (PMP22) and myelin protein zero (P0) mutations associated with Charcot-Marie-Tooth-related diseases.

Authors:  Igor Shames; Andrew Fraser; Joshua Colby; Wayel Orfali; G Jackson Snipes
Journal:  J Neuropathol Exp Neurol       Date:  2003-07       Impact factor: 3.685

10.  Enhancement of proteasome activity by a small-molecule inhibitor of USP14.

Authors:  Byung-Hoon Lee; Min Jae Lee; Soyeon Park; Dong-Chan Oh; Suzanne Elsasser; Ping-Chung Chen; Carlos Gartner; Nevena Dimova; John Hanna; Steven P Gygi; Scott M Wilson; Randall W King; Daniel Finley
Journal:  Nature       Date:  2010-09-09       Impact factor: 49.962

View more
  8 in total

1.  Stimulation of heat shock protein 90 chaperone function through binding of a novobiocin analog KU-32.

Authors:  Bhaskar K Chatterjee; Abhilash Jayaraj; Vinay Kumar; Brian Blagg; Rachel E Davis; B Jayaram; Shashank Deep; Tapan K Chaudhuri
Journal:  J Biol Chem       Date:  2019-02-21       Impact factor: 5.157

2.  Alpha-1 Antitrypsin Reduces Disease Progression in a Mouse Model of Charcot-Marie-Tooth Type 1A: A Role for Decreased Inflammation and ADAM-17 Inhibition.

Authors:  Nikolay Zhukovsky; Marianna Silvano; Thierry Filloux; Sergio Gonzalez; Karl-Heinz Krause
Journal:  Int J Mol Sci       Date:  2022-07-03       Impact factor: 6.208

3.  Therapeutic implications of protein homeostasis in demyelinating peripheral neuropathies.

Authors:  Samuel M Lee; Lih-Shen Chin; Lian Li
Journal:  Expert Rev Neurother       Date:  2012-09       Impact factor: 4.618

Review 4.  Dysregulation of ErbB Receptor Trafficking and Signaling in Demyelinating Charcot-Marie-Tooth Disease.

Authors:  Samuel M Lee; Lih-Shen Chin; Lian Li
Journal:  Mol Neurobiol       Date:  2016-01-05       Impact factor: 5.590

5.  Motor and sensory neuropathy due to myelin infolding and paranodal damage in a transgenic mouse model of Charcot-Marie-Tooth disease type 1C.

Authors:  Samuel M Lee; Di Sha; Anum A Mohammed; Seneshaw Asress; Jonathan D Glass; Lih-Shen Chin; Lian Li
Journal:  Hum Mol Genet       Date:  2013-01-28       Impact factor: 6.150

6.  Recommendations to enable drug development for inherited neuropathies: Charcot-Marie-Tooth and Giant Axonal Neuropathy.

Authors:  Lori Sames; Allison Moore; Renee Arnold; Sean Ekins
Journal:  F1000Res       Date:  2014-04-03

7.  SIMPLE: A new regulator of endosomal trafficking and signaling in health and disease.

Authors:  Lih-Shen Chin; Samuel M Lee; Lian Li
Journal:  Commun Integr Biol       Date:  2013-04-09

Review 8.  Key Developments in the Potential of Curcumin for the Treatment of Peripheral Neuropathies.

Authors:  Martial Caillaud; Yu Par Aung Myo; Bryan D McKiver; Urszula Osinska Warncke; Danielle Thompson; Jared Mann; Egidio Del Fabbro; Alexis Desmoulière; Fabrice Billet; M Imad Damaj
Journal:  Antioxidants (Basel)       Date:  2020-10-02
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.