4.6 Review

Mechanisms and Therapeutic Implications of GSK-3 in Treating Neurodegeneration

期刊

CELLS
卷 10, 期 2, 页码 -

出版社

MDPI
DOI: 10.3390/cells10020262

关键词

GSK-3; neurodegeneration; microtubules; mTOR; autophagy; lysosome; mitochondria; GSK-3 inhibitors

向作者/读者索取更多资源

Neurodegenerative disorders pose a significant threat to public health globally, with a lack of effective treatment options. Research indicates that GSK-3 plays a crucial role in regulating mood behavior, cognitive functions, and neuron viability, potentially serving as a common target for therapeutic interventions in these disorders.
Neurodegenerative disorders are spreading worldwide and are one of the greatest threats to public health. There is currently no adequate therapy for these disorders, and therefore there is an urgent need to accelerate the discovery and development of effective treatments. Although neurodegenerative disorders are broad ranging and highly complex, they may share overlapping mechanisms, and thus potentially manifest common targets for therapeutic interventions. Glycogen synthase kinase-3 (GSK-3) is now acknowledged to be a central player in regulating mood behavior, cognitive functions, and neuron viability. Indeed, many targets controlled by GSK-3 are critically involved in progressing neuron deterioration and disease pathogenesis. In this review, we focus on three pathways that represent prominent mechanisms linking GSK-3 with neurodegenerative disorders: cytoskeleton organization, the mammalian target of rapamycin (mTOR)/autophagy axis, and mitochondria. We also consider the challenges and opportunities in the development of GSK-3 inhibitors for treating neurodegeneration.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据