Aging clock: the watchmaker's masterpiece

Cell Mol Life Sci. 2000 May;57(5):698-704. doi: 10.1007/s000180050034.

Abstract

The phenomenon of cellular senescence has been known for almost four decades. Yet, until very recently, the molecular mechanisms that lead to senescence have been poorly understood. However, substantial progress has been made in the last few years toward identifying the pathways executing senescence. This r view focuses on two major advances in this field, the telomere aging clock theory and the cell cycle regulatory mechanisms in senescent cells. These recent studies indicate that cellular senescence is a highly elaborate and active process, which presumably works as an anti-oncogenic mechanism.

Publication types

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

MeSH terms

  • Aging / genetics
  • Aging / physiology*
  • Animals
  • Biological Clocks / genetics
  • Biological Clocks / physiology*
  • Carrier Proteins / genetics
  • Carrier Proteins / physiology
  • Cellular Senescence / genetics
  • Cellular Senescence / physiology
  • Cyclin-Dependent Kinase Inhibitor p16
  • G1 Phase / genetics
  • G1 Phase / physiology
  • Humans
  • Phenotype
  • Proteins / genetics
  • Proteins / physiology
  • Retinoblastoma Protein / genetics
  • Retinoblastoma Protein / physiology
  • Telomerase / genetics
  • Telomerase / physiology
  • Telomere / genetics
  • Telomere / physiology
  • Tumor Suppressor Protein p14ARF
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / physiology

Substances

  • Carrier Proteins
  • Cyclin-Dependent Kinase Inhibitor p16
  • Proteins
  • Retinoblastoma Protein
  • Tumor Suppressor Protein p14ARF
  • Tumor Suppressor Protein p53
  • Telomerase