Hydrogen peroxide induces apoptosis in human hepatoma cells and alters cell redox status.

Abstract

Direct exposure of human hepatoma cell line SMMC-7721 to hydrogen peroxide (H2O2) can induce apoptosis. Apoptosis induced by H2O2 was inhibited by cycloheximide, actinomycin D, 3-aminobenzamide, EGTA or Zn2+. H2O2 can increase the level of intracellular Ca2+, downregulate GSH levels, slightly induce lipid peroxidation, and lead to change in the ratio of reduced ion components to oxidized ion components of cells. Analysis of flow cytometry indicates that H2O2 decreases the level of Bcl-2. The data indicate that H2O2-induced apoptosis requires new mRNA and protein syntheses; H2O2 can activate Ca2+/Mg2+-dependent endonuclease leading to internucleosomal DNA fragmentation and activation of poly (ADP-ribose) polymerase interfering with the energy metabolism of the cell. The H2O2 downregulation of GSH may be more important for apoptosis than H2O2 induction of lipid peroxidation, and the H2O2 induced changes in redox status of the cell may be among the original events which lead up to other biochemical changes.

• Authors: J Li, C Y Huang, R L Zheng, K R Cui, J F Li
• Journal: Cell biology international (Cell Biol Int) Vol. 24 Issue 1 Pg. 9-23 ( 2000) ISSN: 1065-6995 [Print] England
• PMID: 10826769 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Enzyme Inhibitors
• Nucleic Acid Synthesis Inhibitors
• Poly(ADP-ribose) Polymerase Inhibitors
• Protein Synthesis Inhibitors
• Proto-Oncogene Proteins c-bcl-2
• Hydrogen Peroxide
• Glutathione
• Calcium

Topics

• Apoptosis (physiology)
• Calcium (metabolism)
• Carcinoma, Hepatocellular
• Cell Division (drug effects)
• Cell Survival
• DNA Fragmentation
• Down-Regulation
• Enzyme Inhibitors (pharmacology)
• Flow Cytometry
• Glutathione (antagonists & inhibitors)
• Humans
• Hydrogen Peroxide (pharmacology)
• Lipid Peroxidation
• Microscopy, Fluorescence
• Nucleic Acid Synthesis Inhibitors (pharmacology)
• Oxidation-Reduction
• Oxidative Stress
• Poly(ADP-ribose) Polymerase Inhibitors
• Protein Synthesis Inhibitors (pharmacology)
• Proto-Oncogene Proteins c-bcl-2 (metabolism)
• Tumor Cells, Cultured