Caerin 1.1 and 1.9 peptides induce acute caspase 3/GSDME-mediated pyroptosis in epithelial cancer cells

Sci Rep. 2025 Apr 18;15(1):13377. doi: 10.1038/s41598-025-96438-0.

Abstract

Caerin peptides exhibit a dual role in cancer treatment by directly killing cancer cells and modulating the tumour microenvironment to enhance anti-tumour immunity. This study investigates the mechanisms underlying caerin 1.1/1.9-induced acute cell death in epithelial cancer cells and explores their therapeutic potential. HeLa, A549, and Huh-7 cancer cell lines were treated with caerin 1.1/1.9 peptides. Morphological observations, flow cytometry, lactate dehydrogenase (LDH) release, and IL-18 secretion assays revealed the occurrence of pyroptosis following treatment. Specifically, a 1-h treatment with caerin 1.1/1.9 induced pyroptosis in HeLa, A549, and Huh-7 cells, characterised by cell swelling, membrane bubbling, and the release of IL-18 and LDH. Western blotting confirmed the upregulation of pyroptosis markers, including caspase-3, cleaved caspase-3, and GSDME-N fragments. These findings highlight the significant role of caerin peptides in inducing acute pyroptosis, a form of programmed cell death that enhances the immunogenicity of dying cancer cells, thus potentially improving the effectiveness of immunotherapies. This research underscores the therapeutic potential of caerin 1.1/1.9 peptides in cancer treatment, providing a foundation for developing new anti-cancer strategies that leverage both direct cytotoxic effects and immune modulation to achieve more effective and sustained anti-tumour responses.

Keywords: Caerin peptide; Caspase 3/GSDME signalling pathway; IL-18; Lactate dehydrogenase; Pyroptosis.

MeSH terms

  • Caspase 3* / metabolism
  • Cell Line, Tumor
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Gasdermins
  • HeLa Cells
  • Humans
  • Interleukin-18 / metabolism
  • Peptides* / pharmacology
  • Phosphate-Binding Proteins / metabolism
  • Pyroptosis* / drug effects

Substances

  • GSDME protein, human
  • Caspase 3
  • Peptides
  • Interleukin-18
  • CASP3 protein, human
  • Phosphate-Binding Proteins
  • Gasdermins