Cellular atypia is negatively correlated with immunohistochemical reactivity of CD31 and vWF expression levels in canine hemangiosarcoma

J Vet Med Sci. 2018 Feb 9;80(2):213-218. doi: 10.1292/jvms.17-0561. Epub 2018 Jan 1.

Abstract

Canine hemangiosarcoma (HSA) is one of the most common mesenchymal tumors in dogs. Its high metastatic and growth rates are usually associated with poor prognosis. Neoplastic cells of HSA can show various levels of cellular atypia in the same mass and may consist of various populations at different differentiated stages. Up to present, however, there is no report analyzing their differentiation states by comparing cellular atypia with differentiation-related protein expressions. To evaluate whether cellular atypia can be used as a differentiation marker in HSA, we analyzed correlation between cellular atypia and intensities of CD31 and von Willebrand Factor (vWF) staining in HSA cases. We also compared cellular atypia and expression levels of CD31 and vWF in each growth patterns. Our results show that cellular atypia was negatively correlated to CD31 and vWF expression levels but no significant correlation was found between growth patterns and cellular atypia or CD31 and vWF expression levels. Our study suggests that cellular atypia is useful for identifying differentiation levels in HSA cases. This study also provides useful information to determine differentiation levels of cell populations within HSA based only on morphological analysis, which will aid further HSA research such as identifying undifferentiation markers of endothelial cells or finding undifferentiated cell population in tissue sections.

Keywords: CD31; canine hemangiosarcoma; cellular atypia; growth pattern; vWF.

MeSH terms

  • Animals
  • Dog Diseases / metabolism*
  • Dog Diseases / pathology
  • Dogs
  • Female
  • Gene Expression Regulation, Neoplastic
  • Hemangiosarcoma / metabolism
  • Hemangiosarcoma / pathology
  • Hemangiosarcoma / veterinary*
  • Male
  • Platelet Endothelial Cell Adhesion Molecule-1 / immunology*
  • von Willebrand Factor / metabolism*

Substances

  • Platelet Endothelial Cell Adhesion Molecule-1
  • von Willebrand Factor