Sulfur metabolism and its contribution to malignancy

Int Rev Cell Mol Biol. 2019:347:39-103. doi: 10.1016/bs.ircmb.2019.05.001. Epub 2019 Jun 17.

Abstract

Metabolic dysregulation is an appreciated hallmark of cancer and a target for therapeutic intervention. Cellular metabolism involves a series of oxidation/reduction (redox) reactions that yield the energy and biomass required for tumor growth. Cells require diverse molecular species with constituent sulfur atoms to facilitate these processes. For humans, this sulfur is derived from the dietary consumption of the proteinogenic amino acids cysteine and methionine, as only lower organisms (e.g., bacteria, fungi, and plants) can synthesize them de novo. In addition to providing the sulfur required to sustain redox chemistry, the metabolism of these sulfur-containing amino acids yield intermediate metabolites that constitute the cellular antioxidant system, mediate inter- and intracellular signaling, and facilitate the epigenetic regulation of gene expression, all of which contribute to tumorigenesis.

Keywords: Cancer metabolism; Cysteine; Glutathione; Hydrogen sulfide; Methionine; S-Adenosylmethionine; Sulfur.

Publication types

  • Review

MeSH terms

  • Animals
  • Carcinogenesis
  • Chelating Agents
  • Cysteine / metabolism*
  • Humans
  • Metallothionein / metabolism
  • Methionine / metabolism*
  • Mitogen-Activated Protein Kinase Kinases / metabolism
  • Neoplasms / metabolism*
  • Neoplasms / pathology
  • Oxidation-Reduction
  • Oxidative Stress
  • Sulfhydryl Compounds / chemistry
  • Sulfhydryl Compounds / metabolism
  • Sulfur / chemistry
  • Sulfur / metabolism*

Substances

  • Chelating Agents
  • Sulfhydryl Compounds
  • Sulfur
  • Metallothionein
  • Methionine
  • Mitogen-Activated Protein Kinase Kinases
  • Cysteine