The combination of gamma-interferon and tumor necrosis factor causes a rapid and extensive differentiation of human neuroblastoma cells

Cancer Res. 1992 Feb 15;52(4):931-9.

Abstract

Neuroblastoma (NB), a tumor originating from the sympathetic nervous system, is the most common extracranial neurological tumor of childhood. Human NB cells may differentiate in vitro under treatment with biological agents, as gamma-interferon (IFN-gamma) and tumor necrosis factor (TNF). Unfortunately, NB cell lines resistant to the differentiation-inducing effects of both drugs have been observed. Here we demonstrate that a combination of IFN-gamma plus TNF causes extensive and generalized differentiation of NB cells toward a neuronal phenotype. Both IFN-gamma and TNF, given alone, moderately reduced cell growth and induced partial morphological maturation. Their combination further reduced cell proliferation. The combined treatment gave a synergistic rather than additive cytostatic effect, documented also by a dramatically enhanced differentiation toward a neuronal morphology. Membrane immunofluorescence showed a homologous and heterologous up-regulation of IFN-gamma receptor, as well as a marked induction of HLA Class I antigens and, to a lesser extent, of Class II antigens on NB cells induced to differentiate. Treatment of NB cell lines with IFN-gamma/TNF results in the induction of a differentiated phenotype, as indicated by the increased expression of the Mr 160,000 and 200,000 neurofilament proteins and that of microtubule-associated proteins. Evaluation of biochemical markers of neuronal differentiation confirmed the ability of the combined treatment to induce neuroblast maturation. These results suggest that the combination of IFN-gamma and TNF should be considered for experimental clinical trials in neuroblastoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholinesterase / metabolism
  • Antigens, Surface / analysis
  • Cell Differentiation / drug effects*
  • Cytoskeletal Proteins / analysis
  • Cytoskeletal Proteins / metabolism
  • DNA Replication / drug effects
  • Dihydroxyphenylalanine / metabolism
  • Dopamine / metabolism
  • Drug Synergism
  • Fluorescent Antibody Technique
  • Humans
  • Hydroxyindoleacetic Acid / metabolism
  • Interferon-gamma / pharmacology*
  • Kinetics
  • Neuroblastoma / metabolism
  • Neuroblastoma / pathology*
  • Norepinephrine / metabolism
  • Phosphopyruvate Hydratase / analysis
  • Recombinant Proteins / pharmacology
  • Serotonin / metabolism
  • Thymidine / metabolism
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Antigens, Surface
  • Cytoskeletal Proteins
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • Serotonin
  • Hydroxyindoleacetic Acid
  • Dihydroxyphenylalanine
  • Interferon-gamma
  • Acetylcholinesterase
  • Phosphopyruvate Hydratase
  • Thymidine
  • Dopamine
  • Norepinephrine