The role of p53 in cell metabolism

Xing Ding Zhang, Zheng Hong Qin, Jin Wang

Research output: Contribution to journalReview articlepeer-review

90 Scopus citations

Abstract

The p53 tumor suppressor gene has recently been shown to mediate metabolic changes in cells under physiological and pathological conditions. It has been revealed that p53 regulates energy metabolism, oxidative stress, and amino acid metabolism through balancing glycolysis and oxidative phosphorylation (OXPHOS) as well as the autophagy pathway. p53 is activated by metabolic stress through AMP-activated protein kinase (AMPK) and the mammalian target of rapamycin (mTOR) signaling pathways. p53 regulates OXPHOS through the transcriptional regulation of fructose-2,6-bisphosophatase, TP53-induced glycolysis regulator (TIGAR) and synthesis of cytochrome c oxidase (SCO2) subunit of complex IV of the electron transport chain. p53 also indirectly influences the energy metabolism through regulating glucose transporter (GLUT) expression, glutaminase 2 (GLS2) and fatty acid synthase (FAS). In addition, p53 regulates autophagy to provide cell metabolites for surviving through damage regulated autophagy modulator (DRAM1). Here we review the recent findings to elucidate the important role of p53 in cell metabolism.

Original languageEnglish (US)
Pages (from-to)1208-1212
Number of pages5
JournalActa Pharmacologica Sinica
Volume31
Issue number9
DOIs
StatePublished - Sep 2010

Keywords

  • TP53-induced glycolysis regulator
  • damage-regulated autophagy modulator
  • glycolysis
  • oxidative phosphorylation
  • tumor suppressor 53

ASJC Scopus subject areas

  • Pharmacology
  • Pharmacology (medical)

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