Jordan Kate L, Koss David J, Outeiro Tiago F, Giorgini Flaviano
Department of Genetics and Genome Biology, University of Leicester, University Road, Leicester LE1 7RH, UK.
Faculty of Medical Sciences, Translational and Clinical Research Institute, Newcastle University, Newcastle Upon Tyne NE2 4HH, UK.
Biomedicines. 2022 May 16;10(5):1141. doi: 10.3390/biomedicines10051141.
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.
Rab 鸟苷三磷酸酶(Rabs)是一类小蛋白,在囊泡运输和膜 trafficking 中发挥关键作用。由于它们在囊泡运输的多个步骤中具有广泛功能,Rabs 已被认为与包括癌症、糖尿病和多种神经退行性疾病在内的几种疾病的发病机制有关。鉴于目前神经退行性疾病的治疗方法相当有限,鉴定和验证诸如 Rabs 等新型治疗靶点至关重要。本综述总结了概念验证研究,表明在阿尔茨海默病(AD)背景下调节 Rab 鸟苷三磷酸酶可改善疾病相关表型,并概述了针对 Rabs 进行药物靶向治疗的当前技术水平。最后,我们还讨论了在人类中对这些小蛋白进行治疗性靶向的障碍和挑战,特别是在 AD 的背景下。