Antitumoral effect of IL-12 gene transfected via liposomes into B16F0 cells

Acta Biochim Pol. 2009;56(2):249-53. Epub 2009 May 7.

Abstract

Murine melanoma B16F0 cells were transfected with SA:DPPC:DOPE (2:1:1 molar ratio) liposomes associated with a plasmid encoding murine IL-12. Stearylamine, a cationic lipid, showed a greater transfection efficiency compared to DOTAP-containing liposomes. The lipid:DNA ratio was 2:1 (w/w). Control groups were mock transfected or transfected with an empty plasmid (pNeo). pNeo or IL-12 transfected cells and controls were inoculated intradermically into the dorsal region of the foot or the lateral flank of C57BL6 mice. Results showed that IL-12 expression had a marked effect on in vivo growth of B16 melanoma tumors developed in both anatomic sites, significantly retarding their growth and prolonging host survival.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amines
  • Analysis of Variance
  • Animals
  • Cell Line, Tumor
  • Cell Survival
  • Disease Progression
  • Fatty Acids, Monounsaturated
  • Genes, Reporter
  • Interleukin-12 / genetics*
  • Interleukin-12 / metabolism
  • Liposomes
  • Melanoma, Experimental / metabolism
  • Melanoma, Experimental / mortality
  • Melanoma, Experimental / pathology
  • Melanoma, Experimental / therapy*
  • Mice
  • Mice, Inbred C57BL
  • Neoplasm Transplantation
  • Quaternary Ammonium Compounds
  • Transfection / methods*
  • Tumor Burden

Substances

  • Amines
  • Fatty Acids, Monounsaturated
  • Liposomes
  • Quaternary Ammonium Compounds
  • Interleukin-12
  • stearylamine
  • 1,2-dioleoyloxy-3-(trimethylammonium)propane