Targeted protein degradation for the treatment of Parkinson’s disease: Advances and future perspective

Parkinson's disease (PD) is a progressive disorder that belongs to a class of neurodegenerative disorders (NDs) called Synucleinopathies. It has characterized by the misfolding and aggregation of a-synuclein. Our understanding of PD continues to evolve, and so does our approach to treatment. in...

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Published inBiomedicine & pharmacotherapy Vol. 166; p. 115408
Main Authors Amirian, Roshanak, Badrbani, Mehdi Azadi, Derakhshankhah, Hossein, Izadi, Zhila, Shahbazi, Mohammad-Ali
Format Journal Article
LanguageEnglish
Published Elsevier Masson SAS 01.10.2023
Elsevier
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Summary:Parkinson's disease (PD) is a progressive disorder that belongs to a class of neurodegenerative disorders (NDs) called Synucleinopathies. It has characterized by the misfolding and aggregation of a-synuclein. Our understanding of PD continues to evolve, and so does our approach to treatment. including therapies aimed at delaying pathology, quitting neuronal loss, and shortening the course of the disease by selectively targeting essential proteins suspected to play a role in PD pathogenesis. One emerging approach that is generating significant interest is Targeted Protein Degradation (TPD). TPD is an innovative method that allows us to specifically break down certain proteins using specially designed molecules or peptides, like PROteolysis-TArgeting-Chimera (PROTACs). This approach holds great promise, particularly in the context of NDs. In this review, we will briefly explain PD and its pathogenesis, followed by discussing protein degradation systems and TPD strategy in PD by reviewing synthesized small molecules and peptides. Finally, future perspectives and challenges in the field are discussed. •Targeted protein degradation is a promising technique for treating Neurodegenerative Diseases.•α-synuclein, LRRK2, and tau proteins are used for Targeted Protein Degradation.•Autophagy plays a key role in Parkinson's Disease through misfolding of proteins.
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ISSN:0753-3322
1950-6007
DOI:10.1016/j.biopha.2023.115408