Mechanisms of loss of HLA class I expression on colorectal tumor cells

Tissue Antigens. 1996 May;47(5):364-71. doi: 10.1111/j.1399-0039.1996.tb02571.x.

Abstract

For several years this laboratory has studied the expression of HLA class I on established colorectal tumor cell lines and on fresh tumors. We review here the mechanisms by which colorectal tumor cells may lose surface expression of HLA class I molecules. Several independent mechanisms have been identified, including loss or mutations in beta 2-microglobulin genes, loss of HLA heavy chain genes, selective lack of expression of HLA alleles, and regulatory defects in HLA expression including loss of expression of the peptide transporters associated with antigen processing (TAP). The data suggest that colorectal tumor cells may evade tumor specific, HLA restricted immune attack by loss of HLA class I expression through a number of mechanisms.

Publication types

  • Comparative Study

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 2
  • ATP-Binding Cassette Transporters / physiology
  • Antigens, Neoplasm / biosynthesis*
  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / immunology
  • Colorectal Neoplasms / genetics
  • Colorectal Neoplasms / immunology*
  • Colorectal Neoplasms / pathology
  • Enzyme-Linked Immunosorbent Assay
  • Flow Cytometry
  • Gene Deletion
  • Gene Expression Regulation, Neoplastic
  • HLA Antigens / biosynthesis*
  • HLA Antigens / genetics
  • HLA Antigens / immunology
  • Humans
  • Immunophenotyping
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • Tumor Cells, Cultured / immunology
  • beta 2-Microglobulin / biosynthesis
  • beta 2-Microglobulin / genetics

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 2
  • ATP-Binding Cassette Transporters
  • Antigens, Neoplasm
  • HLA Antigens
  • TAP1 protein, human
  • beta 2-Microglobulin