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Therapeutic Targeting of Rab GTPases: Relevance for Alzheimer’s Disease

Rab GTPases (Rabs) are small proteins that play crucial roles in vesicle transport and membrane trafficking. Owing to their widespread functions in several steps of vesicle trafficking, Rabs have been implicated in the pathogenesis of several disorders, including cancer, diabetes, and multiple neuro...

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Autores principales: Jordan, Kate L., Koss, David J., Outeiro, Tiago F., Giorgini, Flaviano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9138223/
https://www.ncbi.nlm.nih.gov/pubmed/35625878
http://dx.doi.org/10.3390/biomedicines10051141
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author Jordan, Kate L.
Koss, David J.
Outeiro, Tiago F.
Giorgini, Flaviano
author_facet Jordan, Kate L.
Koss, David J.
Outeiro, Tiago F.
Giorgini, Flaviano
author_sort Jordan, Kate L.
collection PubMed
description Rab GTPases (Rabs) are small proteins that play crucial roles in vesicle transport and membrane trafficking. Owing to their widespread functions in several steps of vesicle trafficking, Rabs have been implicated in the pathogenesis of several disorders, including cancer, diabetes, and multiple neurodegenerative diseases. As treatments for neurodegenerative conditions are currently rather limited, the identification and validation of novel therapeutic targets, such as Rabs, is of great importance. This review summarises proof-of-concept studies, demonstrating that modulation of Rab GTPases in the context of Alzheimer’s disease (AD) can ameliorate disease-related phenotypes, and provides an overview of the current state of the art for the pharmacological targeting of Rabs. Finally, we also discuss the barriers and challenges of therapeutically targeting these small proteins in humans, especially in the context of AD.
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spelling pubmed-91382232022-05-28 Therapeutic Targeting of Rab GTPases: Relevance for Alzheimer’s Disease Jordan, Kate L. Koss, David J. Outeiro, Tiago F. Giorgini, Flaviano Biomedicines Review Rab GTPases (Rabs) are small proteins that play crucial roles in vesicle transport and membrane trafficking. Owing to their widespread functions in several steps of vesicle trafficking, Rabs have been implicated in the pathogenesis of several disorders, including cancer, diabetes, and multiple neurodegenerative diseases. As treatments for neurodegenerative conditions are currently rather limited, the identification and validation of novel therapeutic targets, such as Rabs, is of great importance. This review summarises proof-of-concept studies, demonstrating that modulation of Rab GTPases in the context of Alzheimer’s disease (AD) can ameliorate disease-related phenotypes, and provides an overview of the current state of the art for the pharmacological targeting of Rabs. Finally, we also discuss the barriers and challenges of therapeutically targeting these small proteins in humans, especially in the context of AD. MDPI 2022-05-16 /pmc/articles/PMC9138223/ /pubmed/35625878 http://dx.doi.org/10.3390/biomedicines10051141 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Jordan, Kate L.
Koss, David J.
Outeiro, Tiago F.
Giorgini, Flaviano
Therapeutic Targeting of Rab GTPases: Relevance for Alzheimer’s Disease
title Therapeutic Targeting of Rab GTPases: Relevance for Alzheimer’s Disease
title_full Therapeutic Targeting of Rab GTPases: Relevance for Alzheimer’s Disease
title_fullStr Therapeutic Targeting of Rab GTPases: Relevance for Alzheimer’s Disease
title_full_unstemmed Therapeutic Targeting of Rab GTPases: Relevance for Alzheimer’s Disease
title_short Therapeutic Targeting of Rab GTPases: Relevance for Alzheimer’s Disease
title_sort therapeutic targeting of rab gtpases: relevance for alzheimer’s disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9138223/
https://www.ncbi.nlm.nih.gov/pubmed/35625878
http://dx.doi.org/10.3390/biomedicines10051141
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