TAMing immunity through an unexpected source

Cancer Cell. 2025 Jun 9;43(6):1002-1004. doi: 10.1016/j.ccell.2025.04.004. Epub 2025 May 1.

Abstract

Arginine availability and metabolism critically shape tumor-immune interactions. In this issue of Cancer Cell, Zhu et al. demonstrate that breast cancer-cell-derived arginine synthesized via ASS1 fuels macrophage polyamine synthesis, reinforcing immunosuppressive tumor-associated macrophages (TAMs). Mechanistically, this occurs through TDG/p53-dependent DNA demethylation and activation of PPARG.

MeSH terms

  • Animals
  • Arginine* / metabolism
  • Breast Neoplasms* / immunology
  • Breast Neoplasms* / metabolism
  • Female
  • Humans
  • Macrophages* / immunology
  • Macrophages* / metabolism
  • Tumor Suppressor Protein p53 / metabolism
  • Tumor-Associated Macrophages* / immunology
  • Tumor-Associated Macrophages* / metabolism

Substances

  • Arginine
  • Tumor Suppressor Protein p53