Modulation of the antigenic phenotype of human melanoma cells by differentiation-inducing and growth-suppressing agents

Pigment Cell Res. 1992:Suppl 2:123-31. doi: 10.1111/j.1600-0749.1990.tb00361.x.

Abstract

Tumor cells often display alterations in their normal program of cellular differentiation. A promising approach for the treatment of cancer involves the induction of terminal differentiation and a loss of proliferative capacity in cancer cells. In human melanoma cells, the combination of mezerein (MEZ) and fibroblast interferon (IFN-beta), results in a rapid and irreversible suppression of cell growth with a concomitant increase in the synthesis of melanin. The induction of terminal differentiation is associated with alterations in the expression of several cellular genes, including fibronectin, ISG-15 and ISG-54, and changes in the expression of specific cell surface antigens, including intercellular adhesion molecule-1 (ICAM-1) and HLA Class I antigens. In the HO-1 human melanoma cell line, induction of terminal differentiation by MEZ plus IFN-beta results in an induction and/or increased expression of ICAM-1, HLA Class I antigens and HLA Class II antigens. IFN-beta and MEZ alone can modulate expression of these antigens to a lower extent than does the combination of compounds. Induction of terminal differentiation and the irreversible suppression of cell growth is not a prerequisite for antigenic modulation in HO-1 cells. This is indicated by the inability of immune interferon (IFN-gamma), a strong inducer of ICAM-1, HLA Class I antigens and HLA Class II antigens synthesis, or the combination of IFN-beta plus IFN-gamma which synergistically but reversibly suppresses HO-1 growth, to induce melanin synthesis or terminal differentiation in HO-1 cells.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

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

MeSH terms

  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
  • Antigens, Neoplasm / biosynthesis*
  • Antigens, Neoplasm / genetics
  • Cell Adhesion Molecules / biosynthesis*
  • Cell Adhesion Molecules / genetics
  • Cell Differentiation / drug effects
  • Cell Division / drug effects
  • Diterpenes*
  • Drug Synergism
  • Enzyme Activation / drug effects
  • Gene Expression Regulation, Neoplastic / drug effects
  • HLA Antigens / biosynthesis*
  • HLA Antigens / genetics
  • Humans
  • Intercellular Adhesion Molecule-1
  • Interferon-beta / pharmacology*
  • Interferon-gamma / pharmacology*
  • Isoquinolines / pharmacology*
  • Melanins / biosynthesis
  • Melanoma / genetics
  • Melanoma / immunology*
  • Melanoma / pathology
  • Neoplasm Proteins / biosynthesis
  • Neoplasm Proteins / genetics
  • Piperazines / pharmacology*
  • Protein Kinase C / antagonists & inhibitors
  • Terpenes / pharmacology*
  • Tumor Cells, Cultured / drug effects
  • Tumor Cells, Cultured / immunology
  • Tumor Cells, Cultured / metabolism

Substances

  • Antigens, Neoplasm
  • Cell Adhesion Molecules
  • Diterpenes
  • HLA Antigens
  • Isoquinolines
  • Melanins
  • Neoplasm Proteins
  • Piperazines
  • Terpenes
  • Intercellular Adhesion Molecule-1
  • mezerein
  • Interferon-beta
  • Interferon-gamma
  • 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine
  • Protein Kinase C