The antiproliferative effect of beta-carotene requires p21waf1/cip1 in normal human fibroblasts

Eur J Biochem. 2000 Apr;267(8):2290-6. doi: 10.1046/j.1432-1327.2000.01236.x.

Abstract

In normal human fibroblasts, beta-carotene induces a cell-cycle delay in the G1 phase independent of its provitamin A activity via a mechanism not yet elucidated. In this study we provide biochemical evidence showing that delayed progression through the G1 phase occurs concomitantly with: an increase in both nuclear-bound and total p21waf1/cip1 protein levels; an increase in the amount of p21waf1/cip1 associated with cdk4; the inhibition of cyclin D1-associated cdk4 kinase activity; and a reduction in the levels of hyperphosphorylated forms of retinoblastoma protein, and particularly, in phosphorylated Ser780. The role of p21waf1/cip1 in the antiproliferative effect of the carotenoid was further supported by genetic evidence that neither changes in cell-cycle progression nor in the phosphorylation status of retinoblastoma protein were observed in p21waf1/cip1-deficient human fibroblasts treated with beta-carotene. These results clearly demonstrate that p21waf1/cip1 is involved directly in the molecular pathway by which beta-carotene inhibits cell-cycle progression.

MeSH terms

  • Cell Cycle / drug effects
  • Cell Division / drug effects
  • Cyclin-Dependent Kinase 4
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclin-Dependent Kinases / metabolism
  • Cyclins / metabolism*
  • Fibroblasts
  • Fluorescent Antibody Technique
  • G1 Phase / drug effects
  • Humans
  • Liposomes / metabolism
  • Phosphorylation
  • Precipitin Tests
  • Protein Kinases / metabolism
  • Proto-Oncogene Proteins*
  • Retinoblastoma Protein / metabolism
  • beta Carotene / pharmacology*

Substances

  • CDKN1A protein, human
  • Cyclin-Dependent Kinase Inhibitor p21
  • Cyclins
  • Liposomes
  • Proto-Oncogene Proteins
  • Retinoblastoma Protein
  • beta Carotene
  • Protein Kinases
  • histone H1 kinase
  • CDK4 protein, human
  • Cyclin-Dependent Kinase 4
  • Cyclin-Dependent Kinases