高磷酸化
τ蛋白
药物发现
疾病
神经科学
Tau病理学
药物靶点
陶氏病
药品
医学
痴呆
临床试验
机制(生物学)
药物开发
生物信息学
阿尔茨海默病
神经退行性变
心理学
生物
药理学
病理
磷酸化
哲学
认识论
生物化学
作者
Khalid Iqbal,Fei Liu,Gong Chen
标识
DOI:10.1080/17460441.2018.1445084
摘要
Alzheimer's disease (AD), which accounts for three fourth of all cases of dementia, is a major public health problem in modern society and, yet, there is no effective treatment available that can prevent or inhibit this chronic progressive neurodegenerative disease. A major current drug target is intraneuronal abnormally hyperphosphorylated microtubule-associated protein tau which is a histopathological hallmark of this disease and of a family of neurodegenerative diseases called tauopathies. Areas covered: In this review, the authors discuss a growing number of studies that describe the nature and mechanism of tau pathology and various drug discovery options and most recent developments in tau-based therapeutics. PubMed was used to obtain relevant literature while clinicaltrials.gov site and Google search were employed to obtain the latest information on tau based AD clinical trials. Expert opinion: In authors' opinion, loss of neuronal connectivity leads to the hyperphosphorylation of tau and is thus a key therapeutic target. Rescue of neuronal connectivity loss and hyperphosphorylation of tau are most promising approaches. Consequently, tau immunotherapy has a high therapeutic potential.
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