Regulation of tumor metabolism by post translational modifications on metabolic enzymes

Cancer Gene Ther. 2023 Apr;30(4):548-558. doi: 10.1038/s41417-022-00521-x. Epub 2022 Aug 23.

Abstract

Metabolic reprogramming is a hallmark of cancer development, progression, and metastasis. Several metabolic pathways such as glycolysis, tricarboxylic acid (TCA) cycle, lipid metabolism, and glutamine catabolism are frequently altered to support cancer growth. Importantly, the activity of the rate-limiting metabolic enzymes in these pathways are specifically modulated in cancer cells. This is achieved by transcriptional, translational, and post translational regulations that enhance the expression, activity, stability, and substrate sensitivity of the rate-limiting enzymes. These mechanisms allow the enzymes to retain increased activity supporting the metabolic needs of rapidly growing tumors, sustain their survival in the hostile tumor microenvironments and in the metastatic lesions. In this review, we primarily focused on the post translational modifications of the rate-limiting enzymes in the glucose and glutamine metabolism, TCA cycle, and fatty acid metabolism promoting tumor progression and metastasis.

Publication types

  • Review
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Citric Acid Cycle
  • Glutamine* / metabolism
  • Glycolysis
  • Humans
  • Neoplasms* / pathology
  • Protein Processing, Post-Translational
  • Tumor Microenvironment

Substances

  • Glutamine