Literature DB >> 18538324

Can overexpression of parkin provide a novel strategy for neuroprotection in Parkinson's disease?

Ayse Ulusoy1, Deniz Kirik.   

Abstract

Parkinson's disease (PD) is a progressive neurodegenerative disorder caused by selective degeneration of the dopamine producing neurons in the substantia nigra. There is currently no clinically applicable therapy for treating or preventing Parkinsonian neurodegeneration. Great effort is put behind the development of novel therapeutic approaches that aim to alter the natural progression of the disease. For example, a disease-modifying strategy based on the use of glial cell line-derived neurotrophic factor family of ligands have yielded successful results in animal models and later in initial clinical trials. More recently, identification of the gene mutations underlying the familial forms of the disease opened new frontiers in tackling the underlying neuropathological changes seen in PD brains. Overexpression of parkin, in particular, emerged as a powerful approach with complementary effects to those described with use of neurotrophic factors. In light of the fact that the mechanism of disease in the affected patient population might be significantly variable, the ability to intervene the disease process at multiple levels should be seen as a key point in devising effective treatments.

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Year:  2008        PMID: 18538324     DOI: 10.1016/j.expneurol.2008.04.026

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  13 in total

Review 1.  Lentiviral vector-mediated gene transfer and RNA silencing technology in neuronal dysfunctions.

Authors:  Jean-Luc Dreyer
Journal:  Mol Biotechnol       Date:  2011-02       Impact factor: 2.695

Review 2.  Parkin and PINK1 functions in oxidative stress and neurodegeneration.

Authors:  Sandeep K Barodia; Rose B Creed; Matthew S Goldberg
Journal:  Brain Res Bull       Date:  2016-12-23       Impact factor: 4.077

Review 3.  Role of the ubiquitin-proteasome system in nervous system function and disease: using C. elegans as a dissecting tool.

Authors:  Márcio S Baptista; Carlos B Duarte; Patrícia Maciel
Journal:  Cell Mol Life Sci       Date:  2012-03-03       Impact factor: 9.261

4.  Regulation of parkin and PINK1 by neddylation.

Authors:  Yeun Su Choo; Georg Vogler; Danling Wang; Sreehari Kalvakuri; Anton Iliuk; W Andy Tao; Rolf Bodmer; Zhuohua Zhang
Journal:  Hum Mol Genet       Date:  2012-03-02       Impact factor: 6.150

Review 5.  A New Hope for a Devastating Disease: Hydrogen Sulfide in Parkinson's Disease.

Authors:  Xu Cao; Lei Cao; Lei Ding; Jin-Song Bian
Journal:  Mol Neurobiol       Date:  2017-05-23       Impact factor: 5.590

6.  Surprising behavioral and neurochemical enhancements in mice with combined mutations linked to Parkinson's disease.

Authors:  Meghan R Hennis; Marian A Marvin; Charles M Taylor; Matthew S Goldberg
Journal:  Neurobiol Dis       Date:  2013-09-26       Impact factor: 5.996

7.  Considerations regarding the etiology and future treatment of autosomal recessive versus idiopathic Parkinson disease.

Authors:  Tohru Kitada; Julianna J Tomlinson; Hei Sio Ao; David A Grimes; Michael G Schlossmacher
Journal:  Curr Treat Options Neurol       Date:  2012-06       Impact factor: 3.598

8.  KF-1 Ubiquitin Ligase: An Anxiety Suppressor.

Authors:  Tamotsu Hashimoto-Gotoh; Naoyuki Iwabe; Atsushi Tsujimura; Keizo Takao; Tsuyoshi Miyakawa
Journal:  Front Neurosci       Date:  2009-05-01       Impact factor: 4.677

9.  Parkin promotes degradation of the mitochondrial pro-apoptotic ARTS protein.

Authors:  Stav Kemeny; Dikla Dery; Yelena Loboda; Marshall Rovner; Tali Lev; Dotan Zuri; John P M Finberg; Sarit Larisch
Journal:  PLoS One       Date:  2012-07-09       Impact factor: 3.240

10.  Overexpression of parkin ameliorates dopaminergic neurodegeneration induced by 1- methyl-4-phenyl-1,2,3,6-tetrahydropyridine in mice.

Authors:  Minjuan Bian; Jie Liu; Xiaoqi Hong; Mei Yu; Yufang Huang; Zhejin Sheng; Jian Fei; Fang Huang
Journal:  PLoS One       Date:  2012-06-29       Impact factor: 3.240

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