Prevalence of HLA-DRB1 genotype and altered Fas/Fas ligand expression in adrenocortical carcinoma

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Gernot W. Wolkersdörfer - , Department of internal Medicine I (Author)
  • Christian Marx - , Department of internal Medicine I (Author)
  • John Brown - , Department of Veterans Affairs (Author)
  • Sabine Schröder - , Leipzig University (Author)
  • Monika Füssel - , Institute for Immunology (Author)
  • E. Peter Rieber - , Institute for Immunology (Author)
  • Eberhard Kuhlisch - , Institute for Medical Informatics and Biometry (Author)
  • Gerhard Ehninger - , Department of internal Medicine I (Author)
  • Stefan R. Bornstein - , Department of Internal Medicine III (Author)

Abstract

A distinctive feature of malignant adrenocortical neoplasms is decreased major histocompatibility complex (MHC) class II molecule expression. However, it is unknown whether there exists a restriction to certain MHC genotypes and whether this involves alterations of the Fas/Fas ligand system and thereby affects tissue homeostasis. Therefore, MHC class II phenotype and genotype and expression patterns of the Fas/Fas ligand system were investigated in 24 adrenocortical tumors (nAdenomas = 14, nCarcinomas = 10) and an adrenal cancer cell line (NCI-H295). No MHC class II antigen expression was detected in carcinomas. The DRB1*01 genotype was found in 54.5% of patients with carcinoma (P = 0.046). No prevalence of any genotype could be detected in patients with adenomas, which exhibited varying levels of antigen expression. Fas receptor expression was 75.0% in adenomas compared with 20.0% in carcinomas (P = 0.0196), whereas ligand expression was 37.7% in adenomas and reached almost 100% in the carcinomas investigated in this study (P = 0.0033). In summary, the DRB1*01 genotype may be correlated to a higher risk for malignancy. Additional studies on MHC class II genotype and phenotype and the altered Fas/Fas ligand system in adrenal neoplasms may help to identify mechanisms of immune escape and suggest new diagnostic approaches.

Details

Original languageEnglish
Pages (from-to)1768-1774
Number of pages7
JournalJournal of Clinical Endocrinology and Metabolism
Volume90
Issue number3
Publication statusPublished - Mar 2005
Peer-reviewedYes

External IDs

PubMed 15585555