Interleukin-6 increases carcinoembryonic antigen and histocompatibility leukocyte antigen expression on the surface of human colorectal carcinoma cells

J Immunother (1991). 1992 Nov;12(4):231-41. doi: 10.1097/00002371-199211000-00003.

Abstract

Human colorectal carcinoma cells that were treated in vitro with interleukin-6 (IL-6) expressed increased levels of carcinoembryonic antigen (CEA) and normal histocompatibility leukocyte antigen (HLA) class I on their cell surface. The IL-6 mediated increase of CEA expression on the surface of a moderately differentiated colon carcinoma cell line (WiDr) was time- and dose-dependent. A 5-day treatment of the WiDr cells with 100 U IL-6/ml increased the percentage of cells that expressed CEA from 29 to > 80% and enhanced the level of HLA class I expression. The increase in CEA expression as a result of IL-6 treatment was also observed using SDS-PAGE/Western blot analyses, and subsequent Northern blot analyses revealed concomitant increases in CEA-related mRNA transcripts. A comparison of the increases in CEA expression after IL-6, interferon-beta, and interferon-gamma on a nanomolar basis revealed that IL-6 was more potent than either of the interferons. Of 11 different human colorectal tumor cell lines that were treated with IL-6, CEA and/or HLA class I expression were increased in five. Thus, IL-6 can act directly on human colon carcinoma cells and selectively increase the expression of CEA and HLA class I antigens, which may provide some insight into the mechanisms involved in the ability of IL-6 to suppress in vivo tumor growth.

Publication types

  • Comparative Study

MeSH terms

  • Antigens, Neoplasm / biosynthesis*
  • Carcinoembryonic Antigen / biosynthesis*
  • Colorectal Neoplasms / immunology*
  • Colorectal Neoplasms / pathology
  • Gene Expression Regulation, Neoplastic / drug effects*
  • Histocompatibility Antigens Class I / biosynthesis*
  • Humans
  • Interferon-beta / pharmacology
  • Interferon-gamma / pharmacology
  • Interleukin-6 / pharmacology*
  • Neoplasm Proteins / biosynthesis*
  • Receptors, Immunologic / analysis
  • Receptors, Interleukin-6
  • Recombinant Proteins / pharmacology
  • Tumor Cells, Cultured / drug effects

Substances

  • Antigens, Neoplasm
  • Carcinoembryonic Antigen
  • Histocompatibility Antigens Class I
  • Interleukin-6
  • Neoplasm Proteins
  • Receptors, Immunologic
  • Receptors, Interleukin-6
  • Recombinant Proteins
  • Interferon-beta
  • Interferon-gamma