Circular RNA circCHFR Facilitates the Proliferation and Migration of Vascular Smooth Muscle via miR-370/FOXO1/Cyclin D1 Pathway

被引:115
|
作者
Yang, Lei [1 ,3 ]
Yang, Fan [2 ]
Zhao, Haikang [3 ]
Wang, Maode [4 ]
Zhang, Yuelin [5 ]
机构
[1] Xi An Jiao Tong Univ, Xian 710061, Shaanxi, Peoples R China
[2] Xian Med Coll, Affiliated Hosp 2, Xian 710038, Shaanxi, Peoples R China
[3] Xian Med Coll, Affiliated Hosp 2, Dept Neurosurg, Xian 710038, Shaanxi, Peoples R China
[4] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Neurosurg, Xian 710061, Shaanxi, Peoples R China
[5] Xian Med Coll, Dept Neurosurg, Xian 710021, Shaanxi, Peoples R China
来源
关键词
CELLS PROLIFERATION; GROWTH; GLUCONEOGENESIS; EXPRESSION;
D O I
10.1016/j.omtn.2019.02.028
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
Circular RNA (circRNA) is a novel subgroup of noncoding RNA in the human transcriptome playing a vital role in the atherosclerosis of cerebrovascular disease. However, the in-depth mechanism by which circRNA regulates the vascular smooth muscle proliferation and migration is still elusive. Here, a novel identified circRNA, circCHFR, was validated to be aberrantly overexpressed in the ox-LDL-induced vascular smooth muscle cell (VSMCs). Functionally, the circCHFR silencing by oligonucleotide transfection suppressed the proliferation and migration ability of VSMCs. Mechanically, bioinformatics tools and luciferase reporter assay state that circCHFR acts as a sponge of miR-370, and miR-370 targets the 3' UTR of FOXO1. Furthermore, the transcription factor FOXO1 could bind with the promoter region of CCND1 mRNA and promote Cyclin D1 expression. In summary, this finding states the vital role of the circCHFR/miR-370/FOXO1/Cyclin D1 axis and provides a profound understanding about the circRNA in smooth muscle cells and atherosclerosis.
引用
收藏
页码:434 / 441
页数:8
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