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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)\u2010associated 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\u2010directed 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.<\/jats:p><\/jats:sec>","DOI":"10.1016\/j.jalz.2016.06.006","type":"journal-article","created":{"date-parts":[[2016,10,15]],"date-time":"2016-10-15T10:53:45Z","timestamp":1476528825000},"page":"1051-1065","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":109,"title":["Therapeutic strategies for the treatment of tauopathies: Hopes and challenges"],"prefix":"10.1002","volume":"12","author":[{"given":"Mansi R.","family":"Khanna","sequence":"first","affiliation":[{"name":"Department of Pathology and Laboratory Medicine, Center for Neurodegenerative Disease Research, Institute on Aging University of Pennsylvania  Philadelphia PA 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