Helicobacter pylori CagA promotes gastric cancer immune escape by upregulating SQLE

Cell Death Dis. 2025 Jan 14;16(1):17. doi: 10.1038/s41419-024-07318-w.

Abstract

Helicobacter pylori (H. pylori) infection is a well-established risk factor for gastric cancer, primarily due to its virulence factor, cytotoxin-associated gene A (CagA). Although PD-L1/PD-1-mediated immune evasion is critical in cancer development, the impact of CagA on PD-L1 regulation remains unclear. This study revealed that H. pylori CagA upregulated squalene epoxidase (SQLE) expression, a key enzyme in the cholesterol biosynthesis pathway. Elevated SQLE activity increased cellular palmitoyl-CoA levels, enhancing PD-L1 palmitoylation while decreasing its ubiquitination. This ultimately increases PD-L1 stability, suppressing T cell activity and facilitating immune evasion in gastric cancer. In summary, our findings highlight the crucial role of the CagA-SQLE-PD-L1 axis in gastric cancer progression, suggesting potential therapeutic strategies for targeting CagA-positive gastric cancer.

MeSH terms

  • Animals
  • Antigens, Bacterial* / immunology
  • Antigens, Bacterial* / metabolism
  • B7-H1 Antigen / metabolism
  • Bacterial Proteins* / metabolism
  • Cell Line, Tumor
  • Helicobacter Infections / immunology
  • Helicobacter Infections / microbiology
  • Helicobacter Infections / pathology
  • Helicobacter pylori* / pathogenicity
  • Humans
  • Mice
  • Squalene Monooxygenase / genetics
  • Squalene Monooxygenase / metabolism
  • Stomach Neoplasms* / immunology
  • Stomach Neoplasms* / microbiology
  • Stomach Neoplasms* / pathology
  • Tumor Escape
  • Up-Regulation*

Substances

  • Antigens, Bacterial
  • cagA protein, Helicobacter pylori
  • Bacterial Proteins
  • Squalene Monooxygenase
  • B7-H1 Antigen