Down-regulation of Human Leukocyte Antigen class I heavy chain in tumors is associated with a poor prognosis in advanced esophageal cancer patients

Int J Oncol. 2012 Apr;40(4):965-74. doi: 10.3892/ijo.2011.1274. Epub 2011 Nov 30.

Abstract

The HLA class I antigen processing machinery (APM) plays a crucial role in the anticancer immune response. The aim of this study was to assess the clinical significance of APM components in esophageal cancer. A total of 11 esophageal cancer cell lines were evaluated by Western blot analysis for 13 HLA class I APM components. There was a different expression pattern among cancer cell lines for HLA class I heavy chain (HLA-HC), β2 microglobulin, Tapasin, TAP-1, TAP-2, LMP-7 and LMP-10. Immunohistochemical staining utilizing a tissue microarray method for HLA class I APM expression showing different expression patterns among cell lines was performed for 95 surgical specimens from patients with esophageal cancer. Prognostic factors were the down-regulation of HLA-HC, and the up-regulation of β2 microglobulin and TAP-1 in the cancer tissues. Multivariate analysis using a Cox regression model indicated that the down-regulation of HLA-HC, and up-regulation of TAP-1 in cancer tissues are independent, unfavorable prognostic factors (hazard ratio, 2.361 and 2.297; P=0.0141 and 0.0145, respectively). Although there was no significant difference in survival for selected p-stage I and II patients (n=54) in all APM components, only down-regulation of HLA-HC was an unfavorable prognostic factor by a Cox regression model for selected p-stage III and IV patients (n=41). In conclusion, the current results suggest that the down-regulation of HLA-HC in tumors is especially associated with a poor prognosis among advanced esophageal cancer patients.

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Down-Regulation
  • Esophageal Neoplasms / genetics
  • Esophageal Neoplasms / immunology*
  • Female
  • HLA Antigens / genetics
  • HLA Antigens / immunology*
  • Histocompatibility Antigens Class I / genetics
  • Histocompatibility Antigens Class I / immunology*
  • Humans
  • Immunohistochemistry
  • Mice
  • Mice, SCID
  • Microarray Analysis
  • Prognosis
  • Survival Rate
  • Transplantation, Heterologous
  • beta 2-Microglobulin / genetics
  • beta 2-Microglobulin / immunology

Substances

  • HLA Antigens
  • Histocompatibility Antigens Class I
  • beta 2-Microglobulin