Sensitization of tumor necrosis factor alpha-resistant human melanoma by tumor-specific in vivo transfer of the gene encoding endothelial monocyte-activating polypeptide II using recombinant vaccinia virus

Cancer Res. 1999 Sep 15;59(18):4668-74.

Abstract

Tumor necrosis factor alpha (TNF-alpha) is a proinflammatory cytokine with potent experimental antitumor activity. Its clinical use in cancer treatment is severely limited by its considerable toxicity after systemic administration, and it is currently confined to isolated limb and organ perfusion settings. In this report, we introduce a novel concept of TNF-alpha-based gene therapy using the TNF-sensitizing properties of endothelial cell monocyte-activating polypeptide II (EMAP-II). We hypothesized that transfer of the EMAP-II gene into established TNF-resistant human melanomas would render these tumors sensitive to subsequent systemic TNF-alpha treatment. To achieve tumor selective gene delivery, we constructed a recombinant vaccinia virus encoding the human EMAP-II gene (vvEMAP). In vitro transfection of human melanoma cells led to the production of EMAP-II by these cells. Supernatants of vvEMAP-transfected tumor cells mediated the induction of tissue factor in endothelial cells. We characterized the pattern of gene expression after systemic administration of a recombinant vaccinia virus encoding a reporter gene in a murine in vivo model of s.c. human melanoma. Gene expression in tumor tissue was increased 100-fold as compared with normal tissue, providing evidence for tumor-selective gene delivery. Finally, human melanomas in nude mice were sensitized in vivo by transferring the EMAP-II gene using vvEMAP. Subsequent systemic administration of TNF-alpha led to tumor regression and growth inhibition of these previously TNF-resistant tumors (P < 0.05). This approach using gene therapy to sensitize primarily unresponsive tumors toward TNF-alpha may enhance the usefulness of TNF-alpha in clinical treatment strategies by increasing the window for the therapeutic application of the cytokine, thus reducing the dose necessary for antitumor responses and subsequently reduce toxicity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cells, Cultured
  • Culture Media, Conditioned
  • Cytokines*
  • Drug Resistance, Neoplasm*
  • Endothelium, Vascular / physiology
  • Female
  • Genes, Reporter
  • Genetic Therapy*
  • Growth Inhibitors / genetics
  • Growth Inhibitors / physiology
  • Humans
  • Luciferases / genetics
  • Melanoma / pathology
  • Melanoma / therapy*
  • Mice
  • Mice, Nude
  • Neoplasm Proteins / genetics*
  • Neoplasm Proteins / physiology*
  • RNA-Binding Proteins / genetics*
  • RNA-Binding Proteins / physiology*
  • Recombinant Proteins / metabolism
  • Skin Neoplasms / therapy*
  • Thromboplastin / genetics
  • Transfection
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / toxicity*
  • Vaccinia virus

Substances

  • Culture Media, Conditioned
  • Cytokines
  • Growth Inhibitors
  • Neoplasm Proteins
  • RNA-Binding Proteins
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • small inducible cytokine subfamily E, member 1
  • Thromboplastin
  • Luciferases