Ecto-nucleotide pyrophosphatase/phosphodiesterase 1 inhibitors: Research progress and prospects

Eur J Med Chem. 2024 Mar 5:267:116211. doi: 10.1016/j.ejmech.2024.116211. Epub 2024 Feb 10.

Abstract

The cancer immunotherapies involved in cGAS-STING pathway have been made great progress in recent years. STING agonists exhibit broad-spectrum anti-tumor effects with strong immune response. As a negative regulator of the cGAS-STING pathway, ecto-nucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) can hydrolyze extracellular 2', 3'-cGAMP and reduce extracellular 2', 3'-cGAMP concentration. ENPP1 has been validated to play important roles in diabetes, cancers, and cardiovascular disease and now become a promising target for tumor immunotherapy. Several ENPP1 inhibitors under development have shown good anti-tumor effects alone or in combination with other agents in clinical and preclinical researches. In this review, the biological profiles of ENPP1 were described, and the structures and the structure-activity relationships (SAR) of the known ENPP1 inhibitors were summarized. This review also provided the prospects and challenges in the development of ENPP1 inhibitors.

Keywords: 2′,3′-cGAMP; ENPP1 inhibitors; Tumor immunotherapy; cGAS-STING pathway.

Publication types

  • Review

MeSH terms

  • Humans
  • Immunotherapy
  • Neoplasms*
  • Nucleotidyltransferases / metabolism
  • Phosphoric Diester Hydrolases* / metabolism
  • Pyrophosphatases*

Substances

  • nucleotide pyrophosphatase
  • Phosphoric Diester Hydrolases
  • Nucleotidyltransferases
  • Pyrophosphatases