Urinary MicroRNA biomarkers of nephrotoxicity in Macaca fascicularis

Regul Toxicol Pharmacol. 2024 Aug:151:105668. doi: 10.1016/j.yrtph.2024.105668. Epub 2024 Jun 25.

Abstract

Drug-induced kidney injury (DIKI) refers to kidney damage resulting from the administration of medications. The aim of this project was to identify reliable urinary microRNA (miRNAs) biomarkers that can be used as potential predictors of DIKI before disease diagnosis. This study quantified a panel of six miRNAs (miRs-210-3p, 423-5p, 143-3p, 130b-3p, 486-5p, 193a-3p) across multiple time points using urinary samples from a previous investigation evaluating effects of a nephrotoxicant in cynomolgus monkeys. Exosome-associated miRNA exhibited distinctive trends when compared to miRNAs quantified in whole urine, which may reflect a different urinary excretion mechanism of miRNAs than those released passively into the urine. Although further research and mechanistic studies are required to elucidate how these miRNAs regulate signaling in disease pathways, we present, for the first time, data that several miRNAs displayed strong correlations with histopathology scores, thus indicating their potential use as biomarkers to predict the development of DIKI in preclinical studies and clinical trials. Also, these findings can potentially be translated into other non-clinical species or human for the detection of DIKI.

Keywords: Extracellular vesicles; Nephrotoxicity; Urine biomarkers; microRNAs.

MeSH terms

  • Animals
  • Biomarkers* / urine
  • Exosomes / genetics
  • Kidney / drug effects
  • Kidney / metabolism
  • Kidney / pathology
  • Macaca fascicularis*
  • Male
  • MicroRNAs* / genetics
  • MicroRNAs* / urine

Substances

  • MicroRNAs
  • Biomarkers