New potential modulators of CYP4F2 enzyme activity in angina pectoris: hsa-miR-24-3p and hsa-miR-34a-5p.
Dovydas GecysVacis TatarunasAudrone VeikutieneVaiva LesauskaitePublished in: Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals (2019)
Purpose: To find an association of relative expression of hsa-miR-24-3p and hsa-miR-34a-5p molecules and CYP4F2 enzyme activity in blood plasma of stable angina pectoris (AP) patients'.Materials and Methods: MiRNA gene expression analysis was performed on total RNA extracted from blood plasma, using quantitative real-time polymerase chain reaction. CYP4F2 enzyme levels were determined using commercial ELISA kit. In total, 32 AP and 15 control samples were examined.Results: The relative expression of hsa-miR-24-3p and hsa-miR-34a-5p was upregulated by 4.4 (p = 0.0001) and 3.8 (p = 0.005) -fold in AP patient's blood plasma compared to control subjects. CYP4F2 enzyme level in blood plasma were 2.1 (p = 0.001) times lower in AP patients. Circulating hsa-miR-24-3p was negatively associated with CYP4F2 enzyme level (Spearman correlation coefficient rank r= -0.32; p = 0.03). Moreover, patients that were taking atorvastatin, had 1.5 (p = 0.04) times higher hsa-miR-24-3p expression in blood plasma.Conclusions. Our data suggest that hsa-miR-24-3p might have an effect on CYP4F2 activity during atherosclerosis.
Keyphrases
- end stage renal disease
- newly diagnosed
- poor prognosis
- chronic kidney disease
- transcription factor
- cardiovascular disease
- coronary artery disease
- prognostic factors
- magnetic resonance imaging
- type diabetes
- risk assessment
- small molecule
- coronary artery
- long non coding rna
- gene expression
- acute coronary syndrome
- percutaneous coronary intervention
- dna methylation
- atrial fibrillation
- big data
- deep learning