p53-dependent Chk1 phosphorylation is required for maintenance of prolonged G2 Arrest

Radiat Res. 2007 Dec;168(6):706-15. doi: 10.1667/RR1075.1.

Abstract

Targeting checkpoint kinases has been shown to have a potential chemosensitizing effect in cancer treatment. However, inhibitors of such kinases preferentially abrogate the DNA damage-induced G2 checkpoint in p53-/- as opposed to p53+/+ cells. The mechanisms by which p53 (TP53) can prevent abrogation of the G2 checkpoint are unclear. Using normal human diploid p53+/+ and p53-/- fibroblasts as model systems, we have compared the effects of three checkpoint inhibitors, caffeine, staurosporine and UCN-01, on gamma-radiation-induced G2 arrest. The G2 arrest in p53+/+ cells was abrogated by caffeine, but not by staurosporine and UCN-01, whereas the G2 arrest in p53-/- cells was sensitive to all three inhibitors. Chk2 (CHEK1) phosphorylation was maintained in the presence of all three inhibitors in both p53+/+ and p53-/- cells. Chk1 phosphorylation was maintained only in the presence of staurosporine and UCN-01 in p53+/+ cells. In the presence of caffeine Chk1 phosphorylation was inhibited regardless of p53 status. The pathway of Chk1 phosphorylation --> Cdc25A degradation --> inhibition of cyclin B1/Cdk1 activity --> G2 arrest is accordingly resistant to staurosporine and UCN-01 in p53+/+ cells. Moreover, sustained phosphorylation of Chk1 in the presence of staurosporine and UCN-01 is strongly related to phosphorylation of p53. The present study suggests the unique role of Chk1 in preventing abrogation of the G2 checkpoint in p53+/+ cells.

Publication types

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

MeSH terms

  • Caffeine / pharmacology
  • Cell Line
  • Checkpoint Kinase 1
  • Checkpoint Kinase 2
  • Down-Regulation / radiation effects
  • G2 Phase* / drug effects
  • G2 Phase* / radiation effects
  • Humans
  • Phosphorylation / drug effects
  • Phosphorylation / radiation effects
  • Protein Kinases / metabolism*
  • Protein Serine-Threonine Kinases / metabolism
  • Staurosporine / analogs & derivatives
  • Staurosporine / pharmacology
  • Tumor Suppressor Protein p53 / deficiency
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism*
  • cdc25 Phosphatases / metabolism

Substances

  • Tumor Suppressor Protein p53
  • Caffeine
  • 7-hydroxystaurosporine
  • Protein Kinases
  • Checkpoint Kinase 2
  • CHEK1 protein, human
  • CHEK2 protein, human
  • Checkpoint Kinase 1
  • Protein Serine-Threonine Kinases
  • CDC25A protein, human
  • cdc25 Phosphatases
  • Staurosporine