lncRNA PCA3 Suppressed Carotid Artery Stenosis and Vascular Smooth Muscle Cell Function via Negatively Modulating the miR-124-3p/ITGB1 Axis

被引:1
|
作者
Li, Guosheng [1 ]
Chen, Qiang [2 ]
机构
[1] Yangzhou Univ, Affiliated Taizhou Peoples Hosp 2, Taizhou, Peoples R China
[2] Xuzhou Med Univ, Dept Neurol, Huaian Hosp, Huaian, Peoples R China
关键词
atherosclerosis; plaque stability; ceRNA; vascular smooth muscle cell; NONCODING RNA PCA3; ISCHEMIC-STROKE; PLAQUE; SENESCENCE; AUTOPHAGY;
D O I
10.1177/10760296231190383
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background & objectives: Due to the hidden pathogen, carotid artery stenosis (CAS) always occurred at an advanced stage leading to serious sequelae and even deaths. The significance of long noncoding RNA (lncRNA) prostate cancer antigen 3 (PCA3) in CAS incidence and progression were evaluated aiming to explore a potential target for its therapy. Materials and methods: Serum samples were collected from 83 asymptomatic CAS patients and 52 healthy individuals and PCA3 was compared using polymerase chain reaction (PCR). The PCA3 levels were compared between stable and unstable plaque in CAS patients. The effect of PCA3 on vascular smooth muscle cells (VSMCs) proliferation and motility was assessed by CCK8 and transwell assay. Results: PCA3 was downregulated in CAS patients and their unstable plaque tissues compared with healthy individuals and stable plaque, respectively. Reduced PCA3 could discriminate CAS patients with relatively high sensitivity and specificity and were associated with higher total cholesterol level and stenosis degree, unstable plaque, and complications. PCA3 downregulation predicted the adverse outcomes of CAS patients. In VSMCs, overexpressing PCA3 significantly suppressed cell proliferation, migration, and invasion, which was alleviated by miR-124-3p/ITGB1 axis. Conclusion: PCA3 served as a biomarker of CAS and regulates the function of VSMCs through sponging miR-124-3p/ITGB1 and indirectly influence the stability of plaque.
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页数:8
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