IFN-gamma-dependent delay of in vivo tumor progression by Fas overexpression on murine renal cancer cells

J Immunol. 2000 Jan 1;164(1):231-9. doi: 10.4049/jimmunol.164.1.231.

Abstract

The role of Fas in the regulation of solid tumor growth was investigated. Murine renal carcinoma (Renca) cells were constitutively resistant to Fas-mediated killing in vitro, but exhibited increased expression of Fas and sensitivity to Fas-mediated killing after exposure to IFN-gamma and TNF. Transfected Renca cells overexpressing Fas were efficiently killed in vitro upon exposure to anti-Fas Ab (Jo2). When Fas-overexpressing Renca cells were injected into syngenic BALB/c mice, there was a consistent and significant delay in tumor progression, reduced metastasis, and prolonged survival that was not observed for Renca cells that overexpressed a truncated nonfunctional Fas receptor. The delay of in vivo tumor growth induced by Fas overexpression was not observed in IFN-gamma-/- mice, indicating that IFN-gamma is required for the delay of in vivo tumor growth. However, there was a significant increase of infiltrated T cells and in vivo apoptosis in Fas-overexpressing Renca tumors, and Fas-overexpressing Renca cells were also efficiently killed in vitro by T cells. In addition, a strong therapeutic effect was observed on Fas-overexpressing tumor cells by in vivo administration of anti-Fas Ab, confirming that overexpressed Fas provides a functional target in vivo for Fas-specific ligands. Therefore, our findings demonstrate that Fas overexpression on solid tumor cells can delay tumor growth and provides a rationale for therapeutic manipulation of Fas expression as a means of inducing tumor regression in vivo.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenocarcinoma / genetics
  • Adenocarcinoma / immunology*
  • Adenocarcinoma / pathology
  • Adenocarcinoma / prevention & control*
  • Animals
  • Apoptosis / immunology
  • Cell Division / genetics
  • Cell Division / immunology
  • Drug Synergism
  • Immune Sera / administration & dosage
  • Immunity, Innate
  • Injections, Intralesional
  • Interferon-gamma / physiology*
  • Kidney Neoplasms / genetics
  • Kidney Neoplasms / immunology*
  • Kidney Neoplasms / pathology
  • Kidney Neoplasms / prevention & control*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • Recombinant Proteins / biosynthesis
  • Sequence Deletion
  • T-Lymphocytes / immunology
  • Time Factors
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / physiology
  • Up-Regulation / immunology
  • fas Receptor / biosynthesis*
  • fas Receptor / genetics
  • fas Receptor / immunology
  • fas Receptor / physiology

Substances

  • Immune Sera
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • fas Receptor
  • Interferon-gamma