Lack of effect of different cytokines on expression of membrane-bound regulators of complement activity on human uveal melanoma cells

J Interferon Cytokine Res. 1997 Nov;17(11):695-700. doi: 10.1089/jir.1997.17.695.

Abstract

Tumor cells are protected from antibody-dependent complement-mediated lysis by membrane-bound regulators of complement activation (m-RCA). m-RCA are expressed on uveal melanoma cells. We determined whether cytokine treatment affects expression of m-RCA on these cells in vitro. m-RCA expression on uveal melanoma cell lines was studied by flow cytometry, using monoclonal antibodies directed against CD46, CD55, and CD59. Cytokines studied were interferon-alpha (IFN-alpha), IFN-gamma, interleukin-1B (IL-1B), IL-12, and tumor necrosis factor-alpha (TNF-alpha). All three m-RCA were expressed on the uveal melanoma cell lines (CD59>>CD46>CD55), although in variable amounts. With a few exceptions, the cytokines had no effect on m-RCA expression. CD55 expression was not influenced by any of the cytokines. IFN-gamma downregulated expression of CD46 on one cell line (p < 0.01). TNF-alpha upregulated CD59 expression on two of the five cell lines (p < 0.012 and p < 0.001, respectively), which effect was dose dependent. IFN-alpha, IFN-gamma, IL1-beta, IL12, and TNF-alpha had limited effects on m-RCA expression on uveal melanoma cells in vitro.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • Complement System Proteins / metabolism*
  • Cytokines / therapeutic use*
  • Drug Screening Assays, Antitumor
  • Humans
  • Interferons / therapeutic use
  • Interleukins / therapeutic use
  • Melanoma / drug therapy*
  • Melanoma / metabolism
  • Membrane Proteins / metabolism*
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / therapeutic use
  • Uveal Neoplasms / drug therapy*
  • Uveal Neoplasms / metabolism

Substances

  • Antineoplastic Agents
  • Cytokines
  • Interleukins
  • Membrane Proteins
  • Tumor Necrosis Factor-alpha
  • Complement System Proteins
  • Interferons