Emerging roles of long non-coding RNAs in the pathogenesis of Alzheimer's disease

被引:55
作者
Cortini, Francesca [1 ,2 ]
Roma, Francesca [3 ]
Villa, Chiara [3 ]
机构
[1] Univ Milan, IRCCS Ca Granda Fdn, Dept Clin Sci & Community Hlth, Milan, Italy
[2] IRCCS Ca Granda Fdn Osped Maggiore Policlin, Dept Med Prevent Serv, UOC Occupat Med, Milan, Italy
[3] Univ Milano Bicocca, Sch Med & Surg, Via Cadore 48, I-20900 Monza, Italy
关键词
Long non-coding RNAs; Alzheimer's disease; Post-trascriptional regulation; AMYLOID PRECURSOR PROTEIN; DENDRITIC BC1 RNA; CHROMOSOME; 9P21.3; NEURONAL BC1; BC200; RNA; BRAIN; GENE; EXPRESSION; ASSOCIATION; EVOLUTION;
D O I
10.1016/j.arr.2019.01.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Alzheimer's disease (AD) is a heterogeneous neurodegenerative disorder and represents the most common form of senile dementia. The pathogenesis of AD is not yet completely understood and no curative treatment is currently available. With the recent advancement in transcriptome-wide profiling approach, several non-coding RNAs (ncRNAs) have been identified. Among them, long non-coding RNAs (lncRNAs), which are long transcripts without apparent protein-coding capacity, have received increasing interest for their involvement in a wide range of biological processes as regulatory molecules. Recent studies have suggested that IncRNAs play a role in AD pathogenesis, although their specific influences in the disorder remain to be largely unknown. Herein, we will summarize the biology and mechanisms of action of the best characterized dysregulated IncRNAs in AD, focusing the attention on their potential role in the disease pathogenesis. A deeper understanding of the molecular mechanisms and the complex network of interactions in which they are implicated should open the doors to new research considering IncRNAs as novel therapeutic targets and prognostic/diagnostic biomarkers.
引用
收藏
页码:19 / 26
页数:8
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