Caloric restriction: is mammalian life extension linked to p53?

Aging (Albany NY). 2012 Aug;4(8):525-34. doi: 10.18632/aging.100481.

Abstract

Caloric restriction, that is limiting food intake, is recognized in mammals as the best characterized and most reproducible strategy for extending lifespan, retarding physiological aging and delaying the onset of age-associated diseases. The aim of this mini review is to argue that p53 is the connection in the abilities of both the Sirt-1 pathway and the TOR pathway to impact on longevity of cells and organisms. This novel, lifespan regulating function of p53 may be evolutionarily more ancient than its relatively recent role in apoptosis and tumour suppression, and is likely to provide many new insights into lifespan modulation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Aging / metabolism*
  • Animals
  • Caloric Restriction*
  • Cell Cycle / physiology
  • Cell Death / physiology
  • Humans
  • Insulin-Like Growth Factor I / metabolism
  • Longevity / physiology*
  • Mammals / metabolism*
  • Metabolic Networks and Pathways / physiology
  • Sirtuin 1 / metabolism*
  • TOR Serine-Threonine Kinases / metabolism*
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • Tumor Suppressor Protein p53
  • Insulin-Like Growth Factor I
  • TOR Serine-Threonine Kinases
  • Sirtuin 1