激酶
p38丝裂原活化蛋白激酶
神经科学
τ蛋白
磷酸化
疾病
细胞周期蛋白依赖激酶5
发病机制
蛋白激酶A
阿尔茨海默病
细胞外
MAPK/ERK通路
细胞内
人口
神经退行性变
化学
细胞生物学
医学
生物
病理
细胞周期蛋白依赖激酶2
环境卫生
作者
Zhijia Li,Bo Yin,Shuangqian Zhang,Zhigang Lan,Lan Zhang
标识
DOI:10.1016/j.ejmech.2023.115817
摘要
Alzheimer's disease (AD) is a serious neurodegenerative disease characterized by memory impairment, mental retardation, impaired motor balance, loss of self-care and even death. Among the complex and diverse pathological changes in AD, protein kinases are deeply involved in abnormal phosphorylation of Tau proteins to form intracellular neuronal fiber tangles, neuronal loss, extracellular β-amyloid (Aβ) deposits to form amyloid plaques, and synaptic disturbances. As a disease of the elderly, the growing geriatric population is directly driving the market demand for AD therapeutics, and protein kinases are potential targets for the future fight against AD. This perspective provides an in-depth look at the role of the major protein kinases (GSK-3β, CDK5, p38 MAPK, ERK1/2, and JNK3) in the pathogenesis of AD. At the same time, the development of different protein kinase inhibitors and the current state of clinical advancement are also outlined.
科研通智能强力驱动
Strongly Powered by AbleSci AI