Targeting NAD+ metabolism: dual roles in cancer treatment

Front Immunol. 2023 Dec 5:14:1269896. doi: 10.3389/fimmu.2023.1269896. eCollection 2023.

Abstract

Nicotinamide adenine dinucleotide (NAD+) is indispensable for various oxidation-reduction reactions in mammalian cells, particularly during energy production. Malignant cells increase the expression levels of NAD+ biosynthesis enzymes for rapid proliferation and biomass production. Furthermore, mounting proof has indicated that NAD-degrading enzymes (NADases) play a role in creating the immunosuppressive tumor microenvironment (TME). Interestingly, both inhibiting NAD+ synthesis and targeting NADase have positive implications for cancer treatment. Here we summarize the detrimental outcomes of increased NAD+ production, the functions of NAD+ metabolic enzymes in creating an immunosuppressive TME, and discuss the progress and clinical translational potential of inhibitors for NAD+ synthesis and therapies targeting NADase.

Keywords: CD38; NAD+ metabolism; NAMPT inhibitor; cancer immunotherapy; cancer treatment; tumor microenvironment.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Mammals / metabolism
  • NAD* / metabolism
  • NAD+ Nucleosidase
  • Neoplasms* / drug therapy
  • Neoplasms* / pathology

Substances

  • NAD
  • NAD+ Nucleosidase

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The National Natural Science Foundation of China (82072612, 81930065, 82173128) and the CAMS Innovation Fund for Medical Sciences (CIFMS) (2019-I2M-5-036) provide funding for this article.