Caspase-1 cleaves PPARγ for potentiating the pro-tumor action of TAMs

Nat Commun. 2017 Oct 3;8(1):766. doi: 10.1038/s41467-017-00523-6.

Abstract

Tumor-associated macrophages are increasingly viewed as a target of great relevance in the tumor microenvironment, because of their important role in cancer progression and metastasis. However, the endogenous regulatory mechanisms underlying tumor-associated macrophage differentiation remain largely unknown. Here, we report that caspase-1 promotes tumor-associated macrophage differentiation by cleaving peroxisome proliferator-activated receptor gamma (PPARγ) at Asp64, thus generating a 41 kDa fragment. This truncated PPARγ translocates to mitochondria, where it directly interacts with medium-chain acyl-CoA dehydrogenase (MCAD). This binding event attenuates MCAD activity and inhibits fatty acid oxidation, thereby leading to the accumulation of lipid droplets and promoting tumor-associated macrophage differentiation. Furthermore, the administration of caspase-1 inhibitors or the infusion of bone marrow-derived macrophages genetically engineered to overexpress murine MCAD markedly suppresses tumor growth. Therefore, targeting the caspase-1/PPARγ/MCAD pathway might be a promising therapeutic approach to prevent tumor progression.Tumor associated macrophages (TAMs) promote cancer progression. Here, the author show that caspase-1 promotes TAMs differentiation by attenuating medium-chain acyl-CoA dehydrogenase activity and that inhibition of this axis results in suppression of tumour growth in a transgenic mouse model of breast cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyl-CoA Dehydrogenase / genetics
  • Acyl-CoA Dehydrogenase / metabolism
  • Animals
  • Caspase 1 / metabolism*
  • Caspase Inhibitors / pharmacology
  • Cell Differentiation / immunology*
  • Energy Metabolism
  • Fatty Acids / metabolism
  • Female
  • Humans
  • Lipid Metabolism
  • MCF-7 Cells
  • Macrophages / drug effects
  • Macrophages / immunology*
  • Mice
  • Mice, Nude
  • Mitochondria / metabolism*
  • Neoplasms / immunology
  • Neoplasms / metabolism*
  • PPAR gamma / metabolism*
  • THP-1 Cells
  • Tumor Microenvironment / immunology*

Substances

  • Caspase Inhibitors
  • Fatty Acids
  • PPAR gamma
  • Acyl-CoA Dehydrogenase
  • Caspase 1