Heat shock and cytokines modulate the expression of adhesion molecules on different human gastric-cancer cell lines

Int J Cancer. 1996 Sep 4;67(5):690-4. doi: 10.1002/(SICI)1097-0215(19960904)67:5<690::AID-IJC17>3.0.CO;2-9.

Abstract

In order to understand the expression and modulation of adhesion molecules (AMs) on the surface of different gastric cancers, we studied 4 gastric-cancer cell lines including SC-M1, KATO-III, AGS and AZ-521. The expression of E-cadherin, integrins (beta1, beta2 and beta3), ICAMs (1 and 2), and CD11 (a, b and c) on the cells was detected by flow cytometry. We found that E-cadherin was only expressed on SC-M1 and KATO-III. CD29 (beta1 integrin) could be found in cells of all 4 lines. CD54 (ICAM- 1) could not be detected in AZ-521. In contrast, CD18 (beta2 integrin), CD61 (beta3 integrin), ICAM-2, CD11a, CD11b and CD11c were all absent from these cells. Heat-shock treatment (42.5 degrees C, 60 min) enhanced the expression of E-cadherin, CD29 and CD54 on SC-M1, and of CD29 on AGS. In addition, TNF-alpha (50U/ml) and IL-1beta (10U/ml) modulated the expression of these AMs, like heat-shock treatment. The increment of these adhesion molecules caused by heat shock, TNF-alpha and IL-1beta stimulation on SC-M1 was also confirmed by Western blot analysis. Functionally, these treatments increased the binding between normal human mononuclear cells and SC-Ml cells. The heat-shock treatment could induce a significant amount of TNF-alpha and IL-1beta release from SC-M1 and KATO-III, but seemed irrelevant to the expression of AMs. These results suggest that limited adhesion molecules were expressed on the surface of different gastric cancer cells. Heat shock, IL-1beta and TNF-alpha may selectively modulate the expression of these 3 molecules on some of the cells, and this is probably related to their antitumor effect.

MeSH terms

  • Antigens, CD / metabolism
  • Blotting, Western
  • CD11 Antigens / metabolism
  • Cadherins / metabolism
  • Cell Adhesion Molecules / metabolism*
  • Cytokines / pharmacology*
  • Flow Cytometry
  • Hot Temperature*
  • Humans
  • Integrins / metabolism
  • Intercellular Adhesion Molecule-1 / metabolism
  • Interleukin-1 / pharmacology
  • Stomach Neoplasms / metabolism*
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Antigens, CD
  • CD11 Antigens
  • Cadherins
  • Cell Adhesion Molecules
  • Cytokines
  • ICAM2 protein, human
  • Integrins
  • Interleukin-1
  • Tumor Necrosis Factor-alpha
  • Intercellular Adhesion Molecule-1