Apoptosis induced by oxaliplatin in human colon cancer HCT15 cell line

Anticancer Res. 2004 Jan-Feb;24(1):219-26.

Abstract

Background: Oxaliplatin (L-OHP), active in a wide range of human and animal tumours, also CDDP-resistant, possesses unique molecular characteristics of action. However, the mechanisms by which the damage induced by L-OHP triggers a death signal are not yet fully defined.

Materials and methods: After L-OHP treatment of the HCT15 human colon cancer cell line, apoptosis was evaluated by DNA laddering detection and by flow cytometry; the effect on specific caspase-3, -8 and -9 inhibitors, mitochondrial membrane permeability transition, cytochrome C release and expression of CD95 and CD95L were also assessed.

Results: HCT15 cells underwent apoptosis when treated with all used drug concentrations (7-25 microM). Treatment of cells with L-OHP resulted in the activation of caspase-8, -9 and -3, in a mitochondrial membrane depolarisation, and in an increase of CD95 receptor and CD95 ligand levels.

Conclusion: The results correlated well with the ability of L-OHP to induce apoptosis and give further insights into the mechanisms underlying the L-OHP-induced apoptosis of tumor cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / drug therapy*
  • Adenocarcinoma / enzymology
  • Adenocarcinoma / pathology
  • Antineoplastic Agents / pharmacology*
  • Apoptosis / drug effects*
  • Apoptosis / physiology
  • Caspases / metabolism
  • Cell Line, Tumor
  • Colorectal Neoplasms / drug therapy*
  • Colorectal Neoplasms / enzymology
  • Colorectal Neoplasms / pathology
  • Cytochromes c / metabolism
  • Enzyme Activation / drug effects
  • Fas Ligand Protein
  • Humans
  • Intracellular Membranes / drug effects
  • Intracellular Membranes / physiology
  • Isoenzymes / metabolism
  • Membrane Glycoproteins / biosynthesis
  • Membrane Glycoproteins / physiology
  • Membrane Potentials / drug effects
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mitochondria / physiology
  • Organoplatinum Compounds / pharmacology*
  • Oxaliplatin
  • fas Receptor / physiology

Substances

  • Antineoplastic Agents
  • FASLG protein, human
  • Fas Ligand Protein
  • Isoenzymes
  • Membrane Glycoproteins
  • Organoplatinum Compounds
  • fas Receptor
  • Oxaliplatin
  • Cytochromes c
  • Caspases