Thyroid cancers express CD-40 and CD-40 ligand: cancers that express CD-40 ligand may have a greater risk of recurrence in young patients

Thyroid. 2005 Feb;15(2):105-13. doi: 10.1089/thy.2005.15.105.

Abstract

The immune response might suppress thyroid cancer recurrence. Although the factors that control this are unknown, CD-40 and CD-40 ligand might be important. To test this, we stained 36 papillary (PTC) and four follicular (FTC) thyroid carcinomas for CD-40 (n = 37) and CD-40 ligand (n = 36) and graded staining from absent (grade 0) to intense (grade 3). Follicular cells of the majority of thyroid tumors expressed CD-40 (30/37, 81%) and CD-40 ligand (15/24, 69%). Cancers from young patients (< or =21 years of age) that expressed CD-40 contained more numerous lymphocytes/high-power field (36 +/- 11) than cancers that failed to express CD-40 (4 +/- 3, p = 0.01), but there was no correlation with clinical outcome. Among young patients, CD-40 ligand expression was more intense in multifocal (1.1 +/- 0.2 vs. 0.45 +/- 0.2, p = 0.037), aggressive (1.14 +/- 0.14 vs. 0.65 +/- 0.2, p = 0.05) and recurrent tumors (1.2 +/- 0.2 vs. 0.65 +/- 0.2, p = 0.05) and associated with reduced disease-free survival (p = 0.03). We conclude that the majority of thyroid cancers express CD-40 and CD-40 ligand. In patients < or =21 years of age, tumors with intense expression of CD-40 ligand are more often multifocal, aggressive, and recurrent.

MeSH terms

  • Adenocarcinoma, Follicular / epidemiology
  • Adenocarcinoma, Follicular / immunology
  • Adenocarcinoma, Follicular / metabolism
  • Adolescent
  • Adult
  • Age Distribution
  • CD40 Antigens / genetics
  • CD40 Antigens / metabolism*
  • CD40 Ligand / genetics
  • CD40 Ligand / metabolism*
  • Carcinoma, Papillary / epidemiology
  • Carcinoma, Papillary / immunology
  • Carcinoma, Papillary / metabolism*
  • Child
  • Disease-Free Survival
  • Female
  • Gene Expression Regulation, Neoplastic / immunology
  • Humans
  • Immunohistochemistry
  • Male
  • Neoplasm Recurrence, Local / epidemiology
  • Neoplasm Recurrence, Local / immunology
  • Neoplasm Recurrence, Local / metabolism*
  • RNA, Messenger / analysis
  • Reverse Transcriptase Polymerase Chain Reaction
  • Risk Factors
  • Thyroid Neoplasms / epidemiology
  • Thyroid Neoplasms / immunology
  • Thyroid Neoplasms / metabolism*

Substances

  • CD40 Antigens
  • RNA, Messenger
  • CD40 Ligand