Circulating miR-200c is up-regulated in paediatric patients with familial hypercholesterolaemia and correlates with miR-33a/b levels: implication of a ZEB1-dependent mechanism

Clin Sci (Lond). 2017 Sep 8;131(18):2397-2408. doi: 10.1042/CS20171121. Print 2017 Sep 15.

Abstract

Hypercholesterolaemia provokes reactive oxygen species (ROS) increase and is a major risk factor for cardiovascular disease (CVD) development. We previously showed that circulating miR-33a/b expression levels were up-regulated in children with familial hypercholesterolaemia (FH). miR-33a/b control cholesterol homoeostasis and recently miR-33b has been demonstrated to directly target the transcription factor zinc finger E-box-binding homeobox 1 (ZEB1). The latter acts in a negative feedback loop with the miR-200 family. Our previous studies showed that the ROS-dependent miR-200c up-regulation induces endothelial dysfunction and provokes a ZEB1-dependent apoptosis and senescence. In the present study, we aimed to verify whether circulating miR-200c was induced in FH children, and whether a correlation existed with miR-33a/b Total RNA was extracted from plasma of 28 FH children and 25 age-matched healthy subjects (HS) and miR-200c levels were measured. We found that miR-200c was up-regulated in FH compared with HS (4.00 ± 0.48-fold increase, P<0.05) and exhibited a positive correlation with miR-33a/b. miR-200c did not correlate with plasma lipids, but correlated with C-reactive protein (CRP) plasma levels and glycaemia (GLI). Ordinary least squares (OLS) regression analysis revealed that miR-200c was significantly affected by GLI and by miR-33a (P<0.01; P<0.001 respectively). Moreover, we found that miR-33 overexpression, in different cell lines, decreased ZEB1 expression and up-regulated both the intracellular and the extracellular miR-200c expression levels. In conclusion, circulating miR-200c is up-regulated in FH, probably due to oxidative stress and inflammation and via a miR-33a/b-ZEB1-dependent mechanism. The present study could provide the first evidence to point to the use of miR-33a/b and miR-200c, as early biomarkers of CVD, in paediatric FH.

Keywords: Zinc Finger E-box-Binding Homeobox 1; cardiovascular disease; hypercholesterolaemia; miR-200c; miR-33; microRNA; oxidative stress; paediatrics.

MeSH terms

  • Adolescent
  • Blood Glucose / analysis
  • C-Reactive Protein / analysis
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Female
  • Humans
  • Hyperlipoproteinemia Type II / genetics
  • Hyperlipoproteinemia Type II / metabolism*
  • Male
  • MicroRNAs / blood
  • MicroRNAs / metabolism*
  • Reactive Oxygen Species / metabolism
  • Up-Regulation
  • Zinc Finger E-box-Binding Homeobox 1 / physiology*

Substances

  • Blood Glucose
  • MIRN200 microRNA, human
  • MIRN33a microRNA, human
  • MicroRNAs
  • Reactive Oxygen Species
  • ZEB1 protein, human
  • Zinc Finger E-box-Binding Homeobox 1
  • C-Reactive Protein