Role of multifaceted regulators in cancer glucose metabolism and their clinical significance

Oncotarget. 2016 May 24;7(21):31572-85. doi: 10.18632/oncotarget.7765.

Abstract

Aberrant glucose metabolism, "aerobic glycolysis" or "Warburg effect", is a hallmark of human cancers. There is a cluster of "multifaceted regulators", which plays a pivotal role in the regulation of glucose metabolism. They can not only modulate the activities of specific enzymes, but also act as transcriptional activators to regulate the expression of metabolism related genes. Additionally, they can crosstalk with other key factors involved in glucose metabolism and work together to initiate multiple oncogenic processes. These "multifaceted regulators", especially p53, HIF-1, TIGAR and microRNA, will be focused in this review. And we will comprehensively illustrate their regulatory effects on cancer glucose metabolism, and further elaborate on their clinical significance. In-depth elucidation the role of "multifaceted regulators" in cancer glucose metabolism will provide us novel insights in cancer research field and offer promising therapeutic targets for anti-cancer therapies.

Keywords: HIF-1; TIGAR; glucose metabolism; multifaceted regulators; p53.

Publication types

  • Review

MeSH terms

  • Apoptosis Regulatory Proteins
  • Gene Expression Regulation, Neoplastic
  • Glucose / metabolism*
  • Glycolysis / genetics*
  • Humans
  • Hypoxia-Inducible Factor 1 / genetics
  • Hypoxia-Inducible Factor 1 / metabolism
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism
  • MicroRNAs / genetics
  • Models, Genetic
  • Neoplasms / genetics*
  • Neoplasms / metabolism*
  • Neoplasms / pathology
  • Phosphoric Monoester Hydrolases
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Apoptosis Regulatory Proteins
  • Hypoxia-Inducible Factor 1
  • Intracellular Signaling Peptides and Proteins
  • MicroRNAs
  • Tumor Suppressor Protein p53
  • Phosphoric Monoester Hydrolases
  • TIGAR protein, human
  • Glucose