Immunohistochemical analysis of L1 cell adhesion molecule and high endothelial venules in breast cancer brain metastasis

Pathol Res Pract. 2021 Jul:223:153484. doi: 10.1016/j.prp.2021.153484. Epub 2021 May 13.

Abstract

Background: The vasculature is a crucial factor in tumor development. Vascular co-option achieved by the L1 cell adhesion molecule (L1CAM) and lymphocyte recruitment inside tumors by high endothelial venules (HEVs) are important prognostic factors in primary breast cancer. Their status in breast cancer brain metastasis is unknown.

Aim of the study: To explore the status of L1CAMs and HEVs in this tumor compartment.

Material and methods: Thirty resected breast cancer brain metastases were immunohistochemically studied for L1CAM and MECA-79, an HEV marker. Clinicopathological factors were recorded.

Results: Age at brain metastasis diagnosis ranged from 37 to 80 years (median 55). The time to brain metastasis development after primary tumor diagnosis ranged from 12 to 187 months (median 57). Median overall survival after brain metastasis diagnosis was 29 months. None of the tumors expressed the factors studied.

Conclusion: L1CAM and high endothelial venules are not found in breast cancer brain metastasis.

Keywords: Brain metastasis; Breast cancer; L1CAM; MECA-79; Microenvironment; Vascular co-option.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers, Tumor / analysis*
  • Brain Neoplasms / chemistry*
  • Brain Neoplasms / secondary
  • Breast Neoplasms / pathology*
  • Endothelial Cells / chemistry*
  • Endothelial Cells / pathology
  • Female
  • Humans
  • Immunohistochemistry*
  • Middle Aged
  • Neural Cell Adhesion Molecule L1 / analysis*
  • Predictive Value of Tests
  • Retrospective Studies
  • Tumor Microenvironment
  • Venules / chemistry*
  • Venules / pathology

Substances

  • Biomarkers, Tumor
  • L1CAM protein, human
  • Neural Cell Adhesion Molecule L1