MicroRNA and their target mRNAs change expression in whole blood of patients after intracerebral hemorrhage

被引:48
作者
Cheng, Xiyuan [1 ,2 ]
Ander, Bradley P. [1 ]
Jickling, Glen C. [1 ]
Zhan, Xinhua [1 ]
Hull, Heather [1 ]
Sharp, Frank R. [1 ,2 ]
Stamova, Boryana [1 ]
机构
[1] Univ Calif Davis, Dept Neurol, 2805 50th St, Sacramento, CA 95817 USA
[2] Univ Calif Davis, Toxicol & Pharmacol Grad Program, Davis, CA 95616 USA
基金
美国国家卫生研究院;
关键词
microRNA; mRNA; intracerebral hemorrhage; blood; human; inflammation; CIRCULATING MICRORNAS; CEREBROSPINAL-FLUID; ISCHEMIC-STROKE; SUBARACHNOID HEMORRHAGE; MIR-17-92; CLUSTER; INHIBITION; CELLS; INJURY; PROLIFERATION; INFLAMMATION;
D O I
10.1177/0271678X19839501
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Previous studies showed changes in mRNA levels in whole blood of rats and humans, and in miRNA in whole blood of rats following intracerebral hemorrhage (ICH). Thus, this study assessed miRNA and their putative mRNA targets in whole blood of humans following ICH. Whole transcriptome profiling identified altered miRNA and mRNA levels in ICH patients compared to matched controls. Target mRNAs of the differentially expressed miRNAs were identified, and functional analysis of the miRNA-mRNA targets was performed. Twenty-nine miRNAs (22 down, 7 up) and 250 target mRNAs (136 up, 114 down), and 7 small nucleolar RNA changed expression after ICH compared to controls (FDR < 0.05, and fold change >= |1.2|). These included Let7i, miR-146a-5p, miR210-5p, miR-93-5p, miR-221, miR-874, miR-17-3p, miR-378a-5p, miR-532-5p, mir-4707, miR-4450, mir-1183, Let-7d-3p, miR-3937, miR-4288, miR-4741, miR-92a-1-3p, miR-4514, mir-4658, mir-3689d-1, miR-4760-3p, and mir-3183. Pathway analysis showed regulated miRNAs/mRNAs were associated with toll-like receptor, natural killer cell, focal adhesion, TGF-beta, phagosome, JAK-STAT, cytokine-cytokine receptor, chemokine, apoptosis, vascular smooth muscle, and RNA degradation signaling. Many of these pathways have been implicated in ICH. The differentially expressed miRNA and their putative mRNA targets and associated pathways may provide diagnostic biomarkers as well as point to therapeutic targets for ICH treatments in humans.
引用
收藏
页码:775 / 786
页数:12
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