Blocking circ_UBR4 suppressed proliferation, migration, and cell cycle progression of human vascular smooth muscle cells in atherosclerosis

被引:14
作者
Zhang, Ying [1 ]
Zhang, Cheng [1 ]
Chen, Zongwei [1 ]
Wang, Meilan [1 ]
机构
[1] Dalian Univ, Zhongshan Affiliated Hosp, Dept Cardiol, 6 Zhonshan Rd, Dalian 116001, Liaoning, Peoples R China
关键词
circ_UBR4; miR-107; ROCK1; atherosclerosis; VSMCs; CIRCULAR RNAS; MOUSE MODEL; PATHWAY; GROWTH; INFLAMMATION; MIR-107;
D O I
10.1515/biol-2021-0044
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The circ_UBR4 (hsa_circ_0010283) is a novel abnormally overexpressed circRNA in oxidized low-density lipoprotein (ox-LDL)-induced model of atherosclerosis (AS) in human vascular smooth muscle cells (VSMCs). However, its role in the dysfunction of VSMCs remains to be further investigated. Here, we attempted to explore its role in ox-LDL-induced excessive proliferation and migration in VSMCs by regulating Rho/Rho-associated coiled-coil containing kinase 1 (ROCK1), a therapeutic target of AS. Expression of circ_UBR4 and ROCK1 was upregulated, whereas miR-107 was downregulated in human AS serum and ox-LDL-induced VSMCs. Depletion of circ_UBR4 arrested cell cycle, suppressed cell viability, colony-forming ability, and migration ability, and depressed expression of proliferating cell nuclear antigen and matrix metalloproteinase 2 in VSMCs in spite of the opposite effects of ox-LDL. Notably, ROCK1 upregulation mediated by plasmid transfection or miR-107 deletion could counteract the suppressive role of circ_UBR4 knockdown in ox-LDL-induced VSMCs proliferation, migration, and cell cycle progression. In mechanism, miR-107was identified as a target of circ_UBR4 to mediate the regulatory effect of circ_UBR4 on ROCK1. circ_UBR4might be a contributor in human AS partially by regulating VSMCs' cell proliferation, migration, and cell cycle progression via circ_UBR4/miR-107/ROCK1 pathway.
引用
收藏
页码:419 / 430
页数:12
相关论文
共 42 条
[1]   Circular RNA in cardiovascular disease [J].
Altesha, M-Ashraf ;
Ni, Tiffany ;
Khan, Afaan ;
Liu, Kexiang ;
Zheng, Xiufen .
JOURNAL OF CELLULAR PHYSIOLOGY, 2019, 234 (05) :5588-5600
[2]   Mathematical Modelling and Simulation of Atherosclerosis Formation and Progress: A Review [J].
Avgerinos, Nikolaos A. ;
Neofytou, Panagiotis .
ANNALS OF BIOMEDICAL ENGINEERING, 2019, 47 (08) :1764-1785
[3]  
Basatemur GL, 2019, NAT REV CARDIOL, V16, P727, DOI [10.1038/s41569-019-0227-9, 10.1161/CIRCRESAHA.115.306361]
[4]   Circular RNAs as Potential Theranostics in the Cardiovascular System [J].
Bei, Yihua ;
Yang, Tingting ;
Wang, Lijun ;
Holvoet, Paul ;
Das, Saumya ;
Sluijter, Joost P. G. ;
Monteiro, Marta Chagas ;
Liu, Yang ;
Zhou, Qiulian ;
Xiao, Junjie .
MOLECULAR THERAPY-NUCLEIC ACIDS, 2018, 13 :407-418
[5]   Activation of the ROCK1 Branch of the Transforming Growth Factor-β Pathway Contributes to RAGE-Dependent Acceleration of Atherosclerosis in Diabetic ApoE-Null Mice [J].
Bu, De-xiu ;
Rai, Vivek ;
Shen, Xiaoping ;
Rosario, Rosa ;
Lu, Yan ;
D'Agati, Vivette ;
Yan, Shi Fang ;
Friedman, Richard A. ;
Nuglozeh, Edem ;
Schmidt, Ann Marie .
CIRCULATION RESEARCH, 2010, 106 (06) :1040-U136
[6]   MicroRNA-107 may regulate lung cancer cell proliferation and apoptosis by targeting TP53 regulated inhibitor of apoptosis 1 [J].
Cai, Peng ;
Li, Jingjing ;
Chen, Guiming ;
Peng, Bing ;
Yu, Liuyang ;
Zhao, Bolin ;
Yu, Yi .
ONCOLOGY LETTERS, 2020, 19 (03) :1958-1966
[7]   Circular RNAs in the pathogenesis of atherosclerosis [J].
Cao, Qidong ;
Guo, Ziyuan ;
Du, Shuangshuang ;
Ling, Hao ;
Song, Chunli .
LIFE SCIENCES, 2020, 255
[8]   MicroRNA-145 alleviates high glucose-induced proliferation and migration of vascular smooth muscle cells through targeting ROCK1 [J].
Chen, Mantian ;
Zhang, Yi ;
Li, Wei ;
Yang, Jieying .
BIOMEDICINE & PHARMACOTHERAPY, 2018, 99 :81-86
[9]  
Chen SY, 2019, INT J CLIN EXP PATHO, V12, P1599
[10]   MicroRNA-125b Affects Vascular Smooth Muscle Cell Function by Targeting Serum Response Factor [J].
Chen, Zhibo ;
Wang, Mian ;
Huang, Kai ;
He, Qiong ;
Li, Honghao ;
Chang, Guangqi .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2018, 46 (04) :1566-1580