The Clinical Significance of Abnormal Tim-3 Expression on NK Cells from Patients with Gastric Cancer

Immunol Invest. 2015;44(6):578-89. doi: 10.3109/08820139.2015.1052145. Epub 2015 Jul 27.

Abstract

Aim: To investigate the clinical significance of Tim-3 (T-cell immunoglobulin- and mucin-domain-containing molecule 3) expression in natural killer (NK) cells from patients with gastric cancer.

Materials and methods: Sixty-two patients with gastric cancer and 32 healthy controls were recruited for this study. Tim-3 expression in peripheral blood samples was analyzed using flow cytometry. The expression pattern of Tim-3 on NK cells was also confirmed using a gastric cancer-bearing mouse model. To further investigate the mechanisms that regulate Tim-3 expression, T-bet(-/-), Eomes(-/-), and Eomes/T-bet double knockout mice were utilized. Additionally, we statistically analyzed the clinical significance of Tim-3 expression on NK cells.

Results: We found that the levels of Tim-3 in NK cells obtained from patients with gastric cancer were significantly higher than the levels in healthy controls. Clinical analyses showed that Tim-3 levels on NK cells were associated with advanced tumor stage. In a tumor-bearing mouse model, Tim-3 levels in NK cells increased with tumor growth, indicating that tumor progression could induce Tim-3 expression in NK cells. Finally, we report that T-bet is a key factor involved in regulating Tim-3 expression.

Conclusion: Our data indicate that Tim-3 expression on NK cells is regulated by T-bet, and that Tim-3 levels correlate with advanced stages of gastric cancer.

Keywords: T-bet; Tim-3; gastric cancer; natural killer cells; tumor progression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Female
  • Hepatitis A Virus Cellular Receptor 2
  • Humans
  • Killer Cells, Natural / immunology*
  • Male
  • Membrane Proteins / immunology*
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Middle Aged
  • Receptors, Virus / immunology*
  • Stomach Neoplasms / immunology*
  • T-Box Domain Proteins / genetics
  • T-Box Domain Proteins / immunology*

Substances

  • HAVCR2 protein, human
  • Havcr2 protein, mouse
  • Hepatitis A Virus Cellular Receptor 2
  • Membrane Proteins
  • Receptors, Virus
  • T-Box Domain Proteins
  • T-box transcription factor TBX21