G6PC3, ALDOA and CS induction accompanies mir-122 down-regulation in the mechanical asphyxia and can serve as hypoxia biomarkers

Oncotarget. 2016 Oct 26;7(46):74526-74536. doi: 10.18632/oncotarget.12931.

Abstract

Hypoxia influences different cellular biological processes. To reveal the dynamics of hypoxia's effects on miRNA regulation in vivo, we examined the expression levels of all miRNAs in human brain and heart specimens from cases of mechanical asphyxia compared with those from cases of craniocerebral injury and hemorrhagic shock. We further validated differently expressed miRNAs in another 84 human specimens and rat models. We found that mir-122 was significantly down-regulated and that its putative targets G6PC3, ALDOA and CS were increased in the brain and cardiac tissues in cases of mechanical asphyxia compared with craniocerebral injury and hemorrhagic shock. Our data indicate that mir-122 and its targets G6PC3, ALDOA and CS play roles in the hypoxia responses that regulate glucose and energy metabolism and can serve as hypoxia biomarkers.

Keywords: ALDOA; G6PC3; Gerotarget; hypoxia; mechanical asphyxia; mir-122.

MeSH terms

  • Animals
  • Asphyxia / metabolism*
  • Biomarkers / analysis
  • Brain / metabolism
  • Cell Hypoxia
  • Citrate (si)-Synthase / genetics*
  • Down-Regulation
  • Female
  • Fructose-Bisphosphate Aldolase / genetics*
  • Glucose / metabolism
  • Glucose-6-Phosphatase / genetics*
  • Humans
  • Male
  • MicroRNAs / physiology*
  • Myocardium / metabolism
  • RNA, Messenger / analysis
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Biomarkers
  • MIRN122 microRNA, human
  • MicroRNAs
  • RNA, Messenger
  • Citrate (si)-Synthase
  • Glucose-6-Phosphatase
  • G6PC3 protein, human
  • ALDOA protein, human
  • Fructose-Bisphosphate Aldolase
  • Glucose