MicroRNA Networks in Cognition and Dementia

被引:23
作者
Blount, Grace S. [1 ]
Coursey, Layton [1 ]
Kocerha, Jannet [1 ]
机构
[1] Georgia Southern Univ, Dept Chem, Statesboro, GA 30460 USA
关键词
miRNA; COVID-19; Alzheimer's; FTD; vascular; dementia; noncoding; therapeutics; biomarkers; STEM-CELL PROLIFERATION; ALZHEIMERS-DISEASE; FRONTOTEMPORAL DEMENTIA; MOUSE MODEL; EXPRESSION; DIFFERENTIATION; IDENTIFICATION; THERAPEUTICS; PROGRESSION; IMPAIRMENT;
D O I
10.3390/cells11121882
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The change from viewing noncoding RNA as "junk" in the genome to seeing it as a critical epigenetic regulator in almost every human condition or disease has forced a paradigm shift in biomedical and clinical research. Small and long noncoding RNA transcripts are now routinely evaluated as putative diagnostic or therapeutic agents. A prominent role for noncoding microRNAs in the central nervous system has uncovered promising new clinical candidates for dementia-related disorders, treatments for which currently remain elusive even as the percentage of diagnosed patients increases significantly. Cognitive decline is a core neurodegenerative process in Alzheimer's Disease, Frontotemporal Dementia, Lewy body dementia, vascular dementia, Huntington's Disease, Creutzfeldt-Jakob disease, and a significant portion of Parkinson's Disease patients. This review will discuss the microRNA-associated networks which influence these pathologies, including inflammatory and viral-mediated pathways (such as the novel SARS-CoV-2 virus implicated in COVID-19), and their current status in clinical trials.
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页数:18
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