Koji Mold-derived Lipids Disrupt the Intracellular Redox State by Decreasing the GPx4 and Intracellular Glutathione Levels, Promoting Membrane Lipid Peroxidation, and Inducing Ferroptosis in HL-60 Cells

J Oleo Sci. 2024;73(7):991-999. doi: 10.5650/jos.ess24043.

Abstract

In this study, we evaluated the cancer cell killing activity of koji mold-derived extracts using several solvents. The koji mold lipid extract (KML) exhibited potent cytotoxicity against a human leukemia cell line. Fractionation of the KML via silica gel chromatography revealed the presence of active components in fraction (Fr.) 6. Cytotoxic effects of Fr. 6 were inhibited by the ferroptosis inhibitors, ferrostatin-1 and SRS11-92, and the iron chelator, deferoxamine. Interestingly, ferroptosis inhibitors failed to prevent the KML-induced cell death. Fr. 6 decreased the expression of glutathione peroxidase 4 (GPx4) and increased the level of peroxidized plasma membrane lipids. Furthermore, Fr. 6 decreased the intracellular glutathione levels. Overall, our results suggest that Fr. 6 included in KML induces ferroptosis in HL-60 cells.

Keywords: GPx4; cancer cell; ferroptosis; koji mold; lipid.

MeSH terms

  • Cyclohexylamines / pharmacology
  • Deferoxamine / pharmacology
  • Ferroptosis* / drug effects
  • Glutathione* / metabolism
  • HL-60 Cells
  • Humans
  • Iron Chelating Agents / pharmacology
  • Lipid Peroxidation* / drug effects
  • Lipids
  • Membrane Lipids / metabolism
  • Oxidation-Reduction* / drug effects
  • Phenylenediamines / pharmacology
  • Phospholipid Hydroperoxide Glutathione Peroxidase* / metabolism

Substances

  • Phospholipid Hydroperoxide Glutathione Peroxidase
  • Glutathione
  • ferrostatin-1
  • Deferoxamine
  • Cyclohexylamines
  • Lipids
  • Phenylenediamines
  • Membrane Lipids
  • Iron Chelating Agents