Lymphangiogenic characteristics of triple negativity in node-negative breast cancer

Int J Surg Pathol. 2009 Dec;17(6):426-31. doi: 10.1177/1066896909337505. Epub 2009 Jun 3.

Abstract

Purpose: Triple-negativity breast cancer (TNBC), being negative for the estrogen receptor, the progesterone receptor, and the human epidermal growth factor receptor 2, represents a subgroup of breast cancer with a poor clinical outcome. The aim of the study was to determine whether TNBC is associated with lymphangiogenesis in node-negative breast carcinomas.

Methods: The authors investigated the clinicopathologic characteristics, lymphatic vessel density (LVD), and expression of 2 lymphangiogenic factors, vascular endothelial growth factor C (VEGF-C) and vascular endothelial growth factor D (VEGF-D), in 21 lymph node-negative TNBCs and 70 lymph node-negative non-TNBCs.

Results: TNBC correlated with younger age (below 35 year) and higher histological grade. It also correlated with a higher intratumoral and peritumoral LVD, positive lymphatic invasion, and positive VEGF-C and VEGF-D expression.

Conclusions: For the first time, this study indicated a link between triple-negativity breast cancer and lymphangiogenesis. Lymphangiogenesis might help explain the special malignant phonotype of breast cancer, and lymphangiogenesis inhibitors might be a novel choice for triple-negativity breast cancer patients.

MeSH terms

  • Adenocarcinoma / metabolism
  • Adenocarcinoma / pathology*
  • Adenocarcinoma / surgery
  • Adult
  • Biomarkers, Tumor / metabolism*
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology*
  • Breast Neoplasms / surgery
  • Estrogen Receptor alpha / metabolism
  • Female
  • Humans
  • Immunoenzyme Techniques
  • Lymph Nodes / metabolism
  • Lymph Nodes / pathology
  • Lymphangiogenesis*
  • Lymphatic Vessels / metabolism
  • Lymphatic Vessels / pathology*
  • Neoplasm Invasiveness
  • Neoplasm Staging
  • Receptor, ErbB-2 / metabolism
  • Receptors, Progesterone / metabolism
  • Vascular Endothelial Growth Factor C / metabolism
  • Vascular Endothelial Growth Factor D / metabolism

Substances

  • Biomarkers, Tumor
  • Estrogen Receptor alpha
  • Receptors, Progesterone
  • Vascular Endothelial Growth Factor C
  • Vascular Endothelial Growth Factor D
  • ERBB2 protein, human
  • Receptor, ErbB-2