Different mechanisms can lead to the same altered HLA class I phenotype in tumors

Tissue Antigens. 2007 Apr:69 Suppl 1:259-63. doi: 10.1111/j.1399-0039.2006.00776.x.

Abstract

Human leukocyte antigen (HLA) class I plays an important role in tumor recognition and rejection. Total or selective losses of HLA class I antigens (classified into seven HLA class I altered phenotypes) represent one of the main routes of tumor escape from immune surveillance. Abnormal expression of HLA class I has been reported in different human tumor samples with distinct underlying mechanisms. Notably, different molecular mechanisms can generate the same altered HLA class I phenotype. Here, we describe various molecular mechanisms that can lead to HLA total loss or downregulation (phenotype I) in melanoma, colorectal carcinoma and bladder cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 2
  • ATP Binding Cassette Transporter, Subfamily B, Member 3
  • ATP-Binding Cassette Transporters / genetics
  • Chromosomes, Human, Pair 15 / genetics
  • Colorectal Neoplasms / genetics*
  • Colorectal Neoplasms / immunology
  • Down-Regulation*
  • Histocompatibility Antigens Class I / genetics*
  • Humans
  • Loss of Heterozygosity*
  • Melanoma / genetics*
  • Melanoma / immunology
  • Microsatellite Repeats
  • Phenotype
  • Urinary Bladder Neoplasms / genetics*
  • Urinary Bladder Neoplasms / immunology

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 2
  • ATP Binding Cassette Transporter, Subfamily B, Member 3
  • ATP-Binding Cassette Transporters
  • Histocompatibility Antigens Class I
  • TAP1 protein, human
  • TAP2 protein, human