Gengnianchun Against H2O2-Induced Oxidative Damage in KGN Cells via miR-548m/FOXO3 Signaling

J Cell Biochem. 2025 Jan;126(1):e30701. doi: 10.1002/jcb.30701.

Abstract

Gengnianchun (GNC) is a traditional remedy used for diminished ovarian reserve, but its underlying mechanisms remain unclear. This study aimed to explore these mechanisms in human granulosa-like cancer (KGN) cells pretreated with medicated rat serum (MRS) before H2O2 exposure. MRS pretreatment significantly alleviated H2O2-induced cell damage, including improvements in cell viability, superoxide dismutase and GSH-Px activities, and Bcl-2 expression. Conversely, H2O2 treatment increased apoptosis, autophagosomes, IL-1β, TNF-α, reactive oxygen species, malondialdehyde levels, and the expression of LC-II/LC3-I, Bax, and Beclin-1. GEO database analysis revealed significant differential expression of several miRNAs, including miR-548m. qPCR confirmed that MRS upregulated miR-548m expression, which was downregulated by H2O2 in a dose-dependent manner. Preincubation with MRS prevented the decline in miR-548m expression and mitigated H2O2-induced damage, including improvements in cell viability, apoptosis, autophagy, and oxidative stress. miR-548m suppressed FOXO3 3'-UTR luciferase activity, and anti-miR-548m enhanced it. Transfection with miR-548m reduced FOXO3 mRNA and protein levels, while anti-miR-548m increased them. These findings suggest that GNC protects against H2O2-induced ovarian damage by modulating the miR-548m/FOXO3 axis, triggering autophagy and apoptosis.

Keywords: FOXO3; Gengnianchun; autophagy; diminished ovarian reserve; miR‐548m; oxidative stress.

MeSH terms

  • Animals
  • Apoptosis* / drug effects
  • Autophagy / drug effects
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Female
  • Forkhead Box Protein O3* / genetics
  • Forkhead Box Protein O3* / metabolism
  • Humans
  • Hydrogen Peroxide* / pharmacology
  • Hydrogen Peroxide* / toxicity
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Oxidative Stress* / drug effects
  • Rats
  • Signal Transduction* / drug effects

Substances

  • Forkhead Box Protein O3
  • MicroRNAs
  • Hydrogen Peroxide
  • FOXO3 protein, human
  • FOXO3 protein, rat