Dihydroartemisinin mediating PKM2-caspase-8/3-GSDME axis for pyroptosis in esophageal squamous cell carcinoma

Chem Biol Interact. 2021 Dec 1;350:109704. doi: 10.1016/j.cbi.2021.109704. Epub 2021 Oct 13.

Abstract

Pyroptosis is a novel type of pro-inflammatory programmed cell death that has been strongly reported to be related to inflammation, immune, and cancer. Dihydroartemisinin (DHA) has good anti-tumor properties. However, the exact mechanism by which DHA induces pyroptosis to inhibit esophageal squamous cell carcinoma (ESCC) remains unclear. After applying DHA treatment to ESCC, we found that some dying cells exhibited the characteristic morphology of pyroptosis, such as blowing large bubbles from the cell membrane, accompanied by downregulation of pyruvate kinase isoform M2 (PKM2), activation of caspase-8/3, and production of GSDME-NT. Meanwhile, it was accompanied by an increased release of LDH and inflammatory factors (IL-18 and IL-1β). Both knockdown of GSDME and application of caspase-8/3 specific inhibitors (z-ITED-FMK/Ac-DEVD-CHO) significantly inhibited DHA-induced pyroptosis. However, the former did not affect the activation of caspase-3. In contrast, overexpression of PKM2 inhibited caspase-8/3 activation as well as GSDME-N production. Furthermore, both si-GSDME and OE-PKM2 inhibited DHA-induced pyroptosis in vivo and in vitro. Therefore, the results suggest that DHA can induce pyroptosis of ESCC cells via the PKM2-caspase-8/3-GSDME pathway. Implication: In this study, we identified new mechanism of DHA in inhibiting ESCC development and progression, and provide a potential therapeutic agent for the treatment of ESCC.

Keywords: Dihydroartemisinin; ESCC; Gasdermin E; Pyroptosis; Pyruvate kinase M2.

MeSH terms

  • Animals
  • Artemisinins / pharmacology*
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Caspase 3 / metabolism
  • Caspase 8 / metabolism
  • Caspase Inhibitors / pharmacology
  • Cell Line, Tumor
  • Esophageal Neoplasms / drug therapy*
  • Esophageal Neoplasms / metabolism
  • Esophageal Neoplasms / pathology
  • Esophageal Squamous Cell Carcinoma / drug therapy*
  • Esophageal Squamous Cell Carcinoma / metabolism
  • Esophageal Squamous Cell Carcinoma / pathology
  • Female
  • Gene Knockdown Techniques
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Models, Biological
  • Pyroptosis / drug effects*
  • Pyroptosis / physiology
  • Receptors, Estrogen / antagonists & inhibitors
  • Receptors, Estrogen / genetics
  • Receptors, Estrogen / metabolism
  • Signal Transduction / drug effects
  • Thyroid Hormones / genetics
  • Thyroid Hormones / metabolism
  • Up-Regulation
  • Xenograft Model Antitumor Assays

Substances

  • Artemisinins
  • Carrier Proteins
  • Caspase Inhibitors
  • GSDME protein, human
  • Membrane Proteins
  • Receptors, Estrogen
  • Thyroid Hormones
  • thyroid hormone-binding proteins
  • artenimol
  • CASP3 protein, human
  • CASP8 protein, human
  • Caspase 3
  • Caspase 8