Identification of the miRNA-target gene regulatory network in intracranial aneurysm based on microarray expression data

被引:8
作者
Wang, Kezhen [1 ]
Wang, Xinmin [1 ]
Lv, Hongzhu [1 ]
Cui, Chengzhi [1 ]
Leng, Jiyong [1 ]
Xu, Kai [2 ]
Yu, Guosong [2 ]
Chen, Jianwei [2 ]
Cong, Peiyu [1 ]
机构
[1] Dalian Med Univ, Dalian Municipal Cent Hosp, Dept Neurosurg, 826 Xinan Rd, Dalian 116033, Liaoning, Peoples R China
[2] Dalian Med Univ, Dalian Med Univ Grad Sch, Dalian 116044, Liaoning, Peoples R China
关键词
mRNA expression data; miRNA expression data; intracranial aneurysms; regulatory network; miRNA target genes; COFFIN-LOWRY SYNDROME; SUBARACHNOID HEMORRHAGE; PROFILES; MICRORNAS; GLIOBLASTOMA; GENOMICS; PATHOGENESIS; DISCOVERY; CARCINOMA; BIOLOGY;
D O I
10.3892/etm.2017.4378
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Intracranial aneurysm (IA) remains one of the most devastating neurological conditions. However, the pathophysiology of IA formation and rupture still remains unclear. The purpose of the present study was to identify the crucial microRNA (miRNA/miR) and genes involved in IAs and elucidate the mechanisms underlying the development of IAs. In the present study, novel miRNA regulation activities in IAs were investigated through the integration of public gene expression data of miRNA and mRNA using the Gene Expression Omnibus database, combined with bioinformatics prediction. A total of 15 differentially expressed miRNA and 1,447differentially expressed mRNA between IAs and controls were identified. A number of miRNA-target gene pairs (770), whose expression levels were inversely correlated, were used to construct a regulatory network of miRNA-target genes in IAs. The biological functions and pathways of these target genes were revealed to be associated with IAs. Specific miRNA and genes, such as hsa-let-7f, hsa-let-7d, hsa-miR-7, RPS6KA3, TSC1 and IGF1 may possess key roles in the development of IAs. The integrated analysis in the present study may provide insights into the understanding of underlying molecular mechanisms of IAs and novel therapeutic targets.
引用
收藏
页码:3239 / 3248
页数:10
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