| Literature DB >> 27751442 |
Mansi R Khanna1, Jane Kovalevich1, Virginia M-Y Lee1, John Q Trojanowski1, Kurt R Brunden2.
Abstract
A group of neurodegenerative diseases referred to as tauopathies are characterized by the presence of brain cells harboring inclusions of pathological species of the tau protein. These disorders include Alzheimer's disease and frontotemporal lobar degeneration due to tau pathology, including progressive supranuclear palsy, corticobasal degeneration, and Pick's disease. Tau is normally a microtubule (MT)-associated protein that appears to play an important role in ensuring proper axonal transport, but in tauopathies tau becomes hyperphosphorylated and disengages from MTs, with consequent misfolding and deposition into inclusions that mainly affect neurons but also glia. A body of experimental evidence suggests that the development of tau inclusions leads to the neurodegeneration observed in tauopathies, and there is a growing interest in developing tau-directed therapeutic agents. The following review provides a summary of strategies under investigation for the potential treatment of tauopathies, highlighting both the promises and challenges associated with these various therapeutic approaches.Entities:
Keywords: Alzheimer's disease; Amyloid; Drugs; Fibrils; Microtubules; Neurons; Tau; Tauopathy; Therapeutics
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Year: 2016 PMID: 27751442 PMCID: PMC5116305 DOI: 10.1016/j.jalz.2016.06.006
Source DB: PubMed Journal: Alzheimers Dement ISSN: 1552-5260 Impact factor: 21.566