Geranylgeraniol potently induces caspase-3-like activity during apoptosis in human leukemia U937 cells

Biochem Biophys Res Commun. 1997 May 29;234(3):641-5. doi: 10.1006/bbrc.1997.6690.

Abstract

In a previous study, we showed that geranylgeraniol (GGO) is a potent inducer of apoptosis in human leukemia cells. The present study describes the effects of GGO on the activity of cysteine-dependent aspartate-directed proteases (caspases) in human leukemia U937 cells. The caspase-3 (CPP32) activity was increased in a time-dependent manner by treatment with 50 microM GGO, whereas no activation of caspase-1 (interleukin-1beta converting enzyme (ICE)) was observed in any time period under the same experimental conditions. Other isoprenyl compounds such as geraniol, geranylgerany-lacetone, and vitamin K2 had no measurable effects on the activities of either caspase-3 or caspase-1. A inhibitor that preferentially inhibits the caspase-3 related caspases, Z-DEVD-FMK, strongly blocked the GGO-induced DNA fragmentation. These results suggest the involvement of caspase-3 in GGO-induced apoptosis in U937 human leukemia cells.

MeSH terms

  • Apoptosis*
  • Caspase 3
  • Caspases*
  • Cysteine Endopeptidases / biosynthesis*
  • Diterpenes / pharmacology*
  • Enzyme Induction
  • Humans
  • Leukemia / enzymology
  • Leukemia / pathology*
  • Tetradecanoylphorbol Acetate / pharmacology
  • Tumor Cells, Cultured

Substances

  • Diterpenes
  • geranylgeraniol
  • CASP3 protein, human
  • Caspase 3
  • Caspases
  • Cysteine Endopeptidases
  • Tetradecanoylphorbol Acetate