Expression of CD105 but not of E-cadherin is associated with malignancy recurrence and disease-free interval in laryngeal cancer in men

Folia Histochem Cytobiol. 2023;61(3):183-192. doi: 10.5603/fhc.97035. Epub 2023 Oct 3.

Abstract

Introduction: In this study we analyzed CD105 (endoglin) and E-cadherin expression in laryngeal squamous cell carcinoma (LSCC) to evaluate their clinicopathologic significance.

Material and methods: Expression of CD105 and E-cadherin was examined immunohistochemically using paraffin-embedded archival tissues of 72 (35 glottic and 37 supraglottic) previously untreated LSCC male patients. The mean value of the positively-stained microvessels for CD105 counted in four hot spots for each case was used as the final intratumoralmicrovessel density (MVD). A staining score of E-cadherin was calculated based on the percentage of cells stained (0-100%).

Results: MVD was significantly higher in patients with advanced TNM stage (P = 0.004) and younger than 65 (P = 0.008). Nodal metastases were more frequent in the cases with low E-cadherin expression (P = 0.000). Tumor recurrence was associated with advanced TNM stage (P = 0.035) and high MVD (P = 0.002). A high MVD was an independent predictor of malignancy recurrence (P = 0.021). The log-rank test showed a significant difference in the disease-free interval in patients stratified according to the MVD value (P = 0.016). Spearman's rank correlation test did not show a significant correlation between E-cadherin and CD105 expression.

Conclusions: CD105-assessed MVD and expression of E-cadherin are promising prognostic factors for the outcome of patients with LSCC. Increased expression of CD105 could help predict patients with an increased risk of developing loco-regional recurrence after surgical treatment. Decreased E-cadherin expression is a potential predictor of lymph node metastases.

Keywords: CD105; E-cadherin; MVD; angiogenesis; immunohistochemistry; laryngeal carcinoma.

MeSH terms

  • Biomarkers, Tumor / metabolism
  • Cadherins
  • Carcinoma, Squamous Cell*
  • Endoglin
  • Humans
  • Laryngeal Neoplasms* / diagnosis
  • Laryngeal Neoplasms* / metabolism
  • Laryngeal Neoplasms* / pathology
  • Male
  • Neovascularization, Pathologic / metabolism
  • Neovascularization, Pathologic / pathology
  • Receptors, Cell Surface / metabolism

Substances

  • Biomarkers, Tumor
  • Cadherins
  • Endoglin
  • Receptors, Cell Surface
  • ENG protein, human
  • CDH1 protein, human