Gene co-expression network for analysis of plasma exosomal miRNAs in the elderly as markers of aging and cognitive decline

被引:15
|
作者
Ye, Zheng [1 ]
Sun, Bo [1 ]
Mi, Xue [1 ]
Xiao, Zhongdang [1 ]
机构
[1] Southeast Univ, Sch Biol Sci & Med Engn, State Key Lab Bioelect, Nanjing, Jiangsu, Peoples R China
来源
PEERJ | 2020年 / 8卷
基金
中国国家自然科学基金;
关键词
WGCNA; Plasma; Exsome; miRNA; Eldly; Aging; Cognitive decline; MoCA score; Biomarker; ALZHEIMERS-DISEASE; EXTRACELLULAR VESICLES; CEREBROSPINAL-FLUID; CANCER-CELLS; EXPRESSION; MICRORNAS; BRAIN; BIOMARKERS; AGE; MECHANISMS;
D O I
10.7717/peerj.8318
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Evidence has shown that microRNA (miRNAs) are involved in molecular pathways responsible for aging and age-related cognitive decline. However, there is a lack of research linked plasma exosome-derived miRNAs changes with cognitive function in older people and aging, which might prove a new insight on the transformation of miRNAs on clinical applications for cognitive decline for older people. Methods: We applied weighted gene co-expression network analysis to investigated miRNAs within plasma exosomes of older people for a better understanding of the relationship of exosome-derived miRNAs with cognitive decline in elderly adults. We identified network modules of co-expressed miRNAs in the elderly exosomal miRNAs dataset. In each module, we selected vital miRNAs and carried out functional enrichment analyses of their experimentally known target genes and their function. Results: We found that plasma exosomal miRNAs hsa-mir-376a-3p, miR-10a-5p, miR-125-5p, miR-15a-5p have critical regulatory roles in the development of aging and cognitive dysfunction in the elderly and may serve as biomarkers and putative novel therapeutic targets for aging and cognitive decline.
引用
收藏
页数:21
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