Increasing evidence suggests that endothelial cells are involved in tumor g
rowth and metastasis. E-selectin, an adhesion molecule specifically express
ed or secreted by activated endothelial cells, may enhance tumor angiogenes
is and the adhesion of tumor cells to endothelial cells at distant sites. T
he aim of this study was to assess the relationship between concentrations
of circulating soluble E-selectin and clinical, pathological and biological
features in patients with breast cancer (BC). sE-selectin concentrations w
ere analyzed by an ELISA method in sera from 113 patients with metastatic B
C, 30 patients with primary inflammatory, BC, 105 patients with primary non
-inflammatory BC, 456 patients with node-negative BC, and 42 healthy contro
ls, sE-selectin in the metastatic BC group was significantly higher than in
the healthy control group. In metastatic BC, sE-selectin was significantly
higher in patients with liver metastases than in patients without Ih,er me
tastases. In patients with primary non-inflammatory BC, a negative correlat
ion was found between sE-selectin concentrations and tumoral microvessel co
unt. In over-all and disease-free survival studies performed in the node-ne
gative population (median follow-up duration 7.5 years), multivariate analy
ses demonstrated a prognostic value of sE-selectin and tumor size. This stu
dy suggests that endothelial activation might play a role in the developmen
t of BC. This role seems not to be related to angiogenesis.