Cationic liposomes with plasmid DNA influence cancer metastatic capability

Anticancer Res. 2002 Nov-Dec;22(6C):4049-52.

Abstract

Background: Cancer gene therapy is now being developing to provide new strategies for the treatment of human tumors. Cationic lipids represent one of the powerful mediators for DNA delivery. The liposome-plasmid DNA complex itself is known to inhibit tumor cell growth, but other effects on cancer cell behaviors have not been reported so far.

Materials and methods: Six commercially available cationic liposomes complexed with plasmid DNA were applied to cancer cells and their metastatic potentials were measured.

Results: The liposome-plasmid DNA complexes affected metastatic capability in three different ways: TM-TPS:DOPE and DOTAP:DOPE had no effect on metastatic capability; a suppressive effect was observed in DOSPA:DOPE and DMRIE:cholesterol; while an augmentative effect was observed in DOTMA:DOPE and Effectene. These effects are likely to be DNA sequence independent, because different plasmids have the same effects.

Conclusion: Liposome-plasmid DNA complexes influence cancer metastasis capability, dependent upon the cationic liposome formulations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Animals
  • Carcinoma, Lewis Lung / secondary
  • Carcinoma, Lewis Lung / therapy
  • Cation Exchange Resins / administration & dosage
  • Cation Exchange Resins / pharmacology
  • Cations
  • Cell Line, Transformed
  • DNA / administration & dosage*
  • DNA / genetics
  • Genetic Therapy / methods*
  • Lipids / administration & dosage
  • Lipids / pharmacology
  • Liposomes / administration & dosage
  • Liposomes / pharmacology*
  • Male
  • Melanoma, Experimental / secondary
  • Melanoma, Experimental / therapy
  • Mice
  • Mice, Inbred BALB C
  • Phosphatidylethanolamines / administration & dosage
  • Phosphatidylethanolamines / pharmacology
  • Plasmids / administration & dosage*
  • Plasmids / genetics
  • Tumor Cells, Cultured

Substances

  • Cation Exchange Resins
  • Cations
  • Lipids
  • Lipofectamine
  • Liposomes
  • Phosphatidylethanolamines
  • 1,2-dielaidoylphosphatidylethanolamine
  • DNA