Human melanoma cells with high susceptibility to cell-mediated lysis can be identified on the basis of ICAM-1 phenotype, VLA profile and invasive ability

Int J Cancer. 1990 Sep 15;46(3):508-15. doi: 10.1002/ijc.2910460330.

Abstract

Marked heterogeneity for susceptibility to lysis by autologous CTL clones and allogeneic IL-2-activated CD3- and CD3+ lymphocytes was found among 19 clones isolated from a human metastatic melanoma (Me665/2). A subset of 5 clones with the highest susceptibility to lysis had increased ICAM-1 antigen expression. Phenotype analysis for the presence of extracellular matrix receptors in the beta 1- and beta 3-integrin families revealed that the tumor clones with the highest susceptibility to lysis were also characterized by frequent expression or increased expression of multiple receptors in the beta 1 family including VLA-1, -2, -3, -4 and -6. The correlation between phenotypic markers and susceptibility to lysis, seen at the clonal level, was confirmed by selection experiments on the uncloned metastasis Me665/2. In fact, the neoplastic population surviving 3 cycles of immunoselection with IL-2-activated lymphocytes exhibited, in comparison to the unselected metastasis: (1) reduced susceptibility to lysis and (2) reduced expression of ICAM-1 and of VLA antigens. In contrast, enhanced susceptibility to lysis and up-regulation of ICAM-1, VLA-1 and VLA-3 antigens were observed on melanoma cells recovered after invading a reconstituted basement membrane. These data indicate that melanoma cells with enhanced susceptibility to cell-mediated lysis can be identified on the basis of phenotypic characteristics (ICAM-1 and VLA antigen profile) and functional features (invasive ability on reconstituted basement membranes).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal
  • Cell Adhesion Molecules / immunology
  • Cell Adhesion Molecules / metabolism*
  • Cell Survival
  • Clone Cells
  • Cytotoxicity, Immunologic
  • Flow Cytometry
  • Humans
  • Integrins / immunology
  • Integrins / metabolism
  • Intercellular Adhesion Molecule-1
  • Interleukin-2 / pharmacology
  • Lymphocyte Activation
  • Melanoma / immunology
  • Melanoma / metabolism*
  • Neoplasm Invasiveness / immunology
  • Phenotype
  • Receptors, Very Late Antigen / analysis*
  • T-Lymphocytes, Cytotoxic / drug effects
  • T-Lymphocytes, Cytotoxic / metabolism
  • Tumor Cells, Cultured

Substances

  • Antibodies, Monoclonal
  • Cell Adhesion Molecules
  • Integrins
  • Interleukin-2
  • Receptors, Very Late Antigen
  • Intercellular Adhesion Molecule-1