Roles of NAD+ and Its Metabolites Regulated Calcium Channels in Cancer

Molecules. 2020 Oct 20;25(20):4826. doi: 10.3390/molecules25204826.

Abstract

Nicotinamide adenine dinucleotide (NAD+) is an essential cofactor for redox enzymes, but also moonlights as a regulator for ion channels, the same as its metabolites. Ca2+ homeostasis is dysregulated in cancer cells and affects processes such as tumorigenesis, angiogenesis, autophagy, progression, and metastasis. Herein, we summarize the regulation of the most common calcium channels (TRPM2, TPCs, RyRs, and TRPML1) by NAD+ and its metabolites, with a particular focus on their roles in cancers. Although the mechanisms of NAD+ metabolites in these pathological processes are yet to be clearly elucidated, these ion channels are emerging as potential candidates of alternative targets for anticancer therapy.

Keywords: NAD+; calcium channels; cancer; metabolites.

Publication types

  • Review

MeSH terms

  • Calcium / metabolism*
  • Calcium Channels / genetics*
  • Calcium Channels / metabolism
  • Calcium Signaling / genetics
  • Carcinogenesis / genetics
  • Humans
  • NAD / metabolism*
  • Neoplasms / metabolism*
  • Neoplasms / pathology
  • Neovascularization, Pathologic / genetics
  • Neovascularization, Pathologic / metabolism
  • TRPM Cation Channels / genetics
  • Transient Receptor Potential Channels / genetics

Substances

  • Calcium Channels
  • MCOLN1 protein, human
  • TRPM Cation Channels
  • TRPM2 protein, human
  • Transient Receptor Potential Channels
  • NAD
  • Calcium