miR-21 induces endothelial progenitor cells proliferation and angiogenesis via targeting FASLG and is a potential prognostic marker in deep venous thrombosis

J Transl Med. 2019 Aug 15;17(1):270. doi: 10.1186/s12967-019-2015-z.

Abstract

Background: Deep venous thrombosis (DVT) of lower extremities is a common thrombotic disease, occurring either in isolation or as a complication of other diseases or procedures. MiR-21 is one of important microRNAs which play critical role in various cellular function. This study aim to determine the effect of miR-21 on endothelial progenitor cells (EPCs) and its role in predicting prognosis of DVT.

Methods: EPCs was isolated from DVT models and control subjects. miR-21 expression was confirmed by RT-PCR. Potential target mRNA was predicted by bioinformatics analysis. EPCs biological functions were examined by CCK-8 and tube formation assay. Besides, miR-21 expression was determined in DVT patients to investigate the correlation between miR-21 expression and prognosis of DVT. Cox proportional hazard regression analyses were also performed to reveal the risk factors associated with prognosis.

Results: Here, we found miR-21 was downregulated in EPCs of DVT model rats. Increased miR-21 expression promoted proliferation and angiogenesis of EPCs. Moreover, we demonstrated that FASLG was a target of miR-21 and revealed that FASLG knockdown inhibited function of EPCs. Upregulation of miR-21 led to thrombus resolution in a rat model of venous thrombosis. In addition, lower expression level of miR-21 in DVT patients was associated with an increase of recurrent DVT and post thrombotic syndrome (PTS). Furthermore, Cox proportional hazard regression analyses demonstrated miR-21 expression level as an independent predictor of recurrence of DVT.

Conclusions: Our data revealed a role of miR-21 in regulating biological function of EPCs and could be a predictor for recurrent DVT or PTS.

Keywords: Angiogenesis; Endothelial progenitor cells; Prognosis; Proliferation; Venous thrombosis; miR-21.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Base Sequence
  • Binding Sites
  • Biomarkers / metabolism
  • Cell Proliferation / genetics
  • Endothelial Progenitor Cells / metabolism*
  • Endothelial Progenitor Cells / pathology*
  • Fas Ligand Protein / metabolism*
  • Female
  • Gene Expression Regulation
  • Humans
  • Male
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Multivariate Analysis
  • Neovascularization, Physiologic / genetics*
  • Prognosis
  • Proportional Hazards Models
  • Rats, Sprague-Dawley
  • Recurrence
  • Venous Thrombosis / genetics*

Substances

  • Biomarkers
  • Fas Ligand Protein
  • MIRN21 microRNA, human
  • MicroRNAs
  • mirn21 microRNA, rat