The effect of radiation on the expression of intercellular adhesion molecule-1 of human adenocarcinoma cells

Int J Radiat Oncol Biol Phys. 1998 Feb 1;40(3):691-6. doi: 10.1016/s0360-3016(97)00860-2.

Abstract

Purpose: To investigate the changes in antigenic expression of intercellular adhesion molecule-1 (ICAM-1) caused by ionizing radiation of cultured human adenocarcinoma cells.

Methods and materials: Human colonic BM314 and gastric MKN45 adenocarcinoma cells were irradiated to investigate the expression of ICAM-1 on the cell membrane and in the supernatant. In addition, the ICAM-1 gene expression (mRNA) was analyzed using a ICAM-1 cDNA as a probe.

Results: The expression of ICAM-1 on the membrane was found to increase by irradiation. This effect was also observed in the supernatant. In addition, the irradiated cell population showed slight, but clear increases in ICAM-1 mRNA expression.

Conclusions: These results show that the enhancement of expression of ICAM-1 by radiation takes place at the ICAM-1 gene expression (mRNA) level. The results suggest that the low dose radiation may be useful for accumulating LFA-1 positive cytotoxic T lymphocytes (CTL) at the local tumor tissue, by which tumor cells may be attacked.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / immunology
  • Antigens, Neoplasm / drug effects
  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / metabolism
  • Antigens, Neoplasm / radiation effects*
  • Antineoplastic Agents / pharmacology
  • Flow Cytometry
  • Humans
  • Intercellular Adhesion Molecule-1 / drug effects
  • Intercellular Adhesion Molecule-1 / genetics
  • Intercellular Adhesion Molecule-1 / metabolism
  • Intercellular Adhesion Molecule-1 / radiation effects*
  • Interferons / pharmacology
  • RNA, Messenger / drug effects
  • RNA, Messenger / metabolism
  • RNA, Messenger / radiation effects
  • Radiation Dosage
  • Stomach Neoplasms / immunology
  • Tumor Cells, Cultured / drug effects
  • Tumor Cells, Cultured / radiation effects

Substances

  • Antigens, Neoplasm
  • Antineoplastic Agents
  • RNA, Messenger
  • Intercellular Adhesion Molecule-1
  • Interferons