MicroRNA Dysregulation in Alzheimer's Disease

被引:41
|
作者
Putteeraj, Manish [1 ]
Fairuz, Yahaya Mohamad [2 ]
Teoh, Seong Lin [2 ]
机构
[1] Univ Technol Mauritius, Sch Hlth Sci, Pointe Aux Sables, Mauritius
[2] Univ Kebangsaan Malaysia, Med Ctr, Dept Anat, Kuala Lumpur, Malaysia
关键词
Alzheimer disease; microRNA; beta-amyloid; Tauopathy; biomarker; treatment; TRANSGENIC MOUSE MODEL; EARLY-ONSET; AMYLOID-BETA; PRECURSOR PROTEIN; TAU-PHOSPHORYLATION; APOLIPOPROTEIN-E; CHOLINESTERASE-INHIBITORS; EXPRESSION PROFILES; SENILE PLAQUES; WHITE-MATTER;
D O I
10.2174/1871527316666170807142311
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background and Objective: Alzheimer's disease (AD) is arguably the largest healthcare issue of our time. AD is thought to be principally the result of an inter-play between the beta-amyloid peptide and Tau, and it is driven by several genetic and environmental risk factors. Recent studies have shown that small non-protein-coding microRNA (miRNA) and the associated post-transcriptional gene regulation are important regulators of many neurodegenerative diseases, including AD. We reviewed recent studies identifying various miRNA dysregulated in AD. These miRNAs could play a significant role in the pathophysiology of AD, in both beta-amyloid peptide and Tau toxicity. Conclusion: The identification of dysregulated miRNAs pattern can serve as specific AD biomarkers which may provide the basis for new and effective diagnostic approach. In addition, these miRNAs may represent new targets for pharmaceutical development.
引用
收藏
页码:1000 / 1009
页数:10
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