Targeting Tau Hyperphosphorylation via Kinase Inhibition: Strategy to Address Alzheimer's Disease

Author(s): Ahmad Abu Turab Naqvi, Gulam Mustafa Hasan, Md. Imtaiyaz Hassan*.

Journal Name: Current Topics in Medicinal Chemistry

Volume 20 , Issue 12 , 2020

Become EABM
Become Reviewer

Graphical Abstract:


Microtubule-associated protein tau is involved in the tubulin binding leading to microtubule stabilization in neuronal cells which is essential for stabilization of neuron cytoskeleton. The regulation of tau activity is accommodated by several kinases which phosphorylate tau protein on specific sites. In pathological conditions, abnormal activity of tau kinases such as glycogen synthase kinase-3 β (GSK3β), cyclin-dependent kinase 5 (CDK5), c-Jun N-terminal kinases (JNKs), extracellular signal-regulated kinase 1 and 2 (ERK1/2) and microtubule affinity regulating kinase (MARK) lead to tau hyperphosphorylation. Hyperphosphorylation of tau protein leads to aggregation of tau into paired helical filaments like structures which are major constituents of neurofibrillary tangles, a hallmark of Alzheimer’s disease. In this review, we discuss various tau protein kinases and their association with tau hyperphosphorylation. We also discuss various strategies and the advancements made in the area of Alzheimer's disease drug development by designing effective and specific inhibitors for such kinases using traditional in vitro/in vivo methods and state of the art in silico techniques.

Keywords: Alzheimer's disease, Neurodegenerative diseases, Tau hyperphosphorylation, Tau kinases, Kinase Inhibitors, Drug discovery.

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2020
Page: [1059 - 1073]
Pages: 15
DOI: 10.2174/1568026620666200106125910
Price: $65

Article Metrics

PDF: 13