Advances in tau-focused drug discovery for Alzheimer's disease and related tauopathies

被引:375
作者
Brunden, Kurt R. [1 ]
Trojanowski, John Q.
Lee, Virginia M. -Y.
机构
[1] Univ Penn, Sch Med, Inst Aging, Ctr Neurodegenerat Dis Res, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
GLYCOGEN-SYNTHASE KINASE-3; PAIRED HELICAL FILAMENTS; AMYLOID PRECURSOR PROTEIN; CYCLIN-DEPENDENT KINASE-5; CHRONIC LITHIUM TREATMENT; NEUROFIBRILLARY TANGLES; IN-VITRO; MICROTUBULE-BINDING; MOUSE MODEL; PHOSPHORYLATED-TAU;
D O I
10.1038/nrd2959
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Neuronal inclusions comprised of the microtubule-associated protein tau are found in numerous neurodegenerative diseases, commonly known as tauopathies. In Alzheimer's disease-the most prevalent tauopathy-misfolded tau is probably a key pathological agent. The recent failure of amyloid-beta-targeted therapeutics in Phase III clinical trials suggests that it is timely and prudent to consider alternative drug discovery strategies for Alzheimer's disease. Here, we focus on strategies directed at reducing misfolded tau and compensating for the loss of normal tau function.
引用
收藏
页码:783 / 793
页数:11
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