G. Anastassiou et al., Expression of the cell adhesion molecules ICAM-1, VCAM-1 and NCAM in uvealmelanoma: A clinicopathological study, ONCOL-BASEL, 58(1), 2000, pp. 83-88
To investigate the relationship between the expression of the cell adhesion
molecules intercellular cell adhesion molecule-1 (ICAM-1), vascular cell a
dhesion molecule-1 (VCAM-1) and neural cell adhesion molecule (NCAM) in uve
al melanoma and the metastatic spread in the first 5 years after diagnosis,
we performed a hospital-based case-control study with human tissue from 90
patients who underwent enucleation for primary uveal melanoma (iris melano
ma excluded). Thirty-five patients developed metastasis within the first 5
years, and 55 patients lived metastasis-free for at least 5 years after enu
cleation. The paraffin-embedded and formalin-fixed globes were studied by i
mmunohistochemistry with monoclonal antibodies for ICAM-1, VCAM-1 and NCAM.
A strong ICAM-1 positivity (more than 75% of the tumor cells stained posit
ive) was detected in 73 tumors (81%). The expression of 75% or less ICAM-1
positive cells in tumors was strongly associated with the development of me
tastases (odds ratio: 7.5, p = 0.001). Multiple logistic regression models
showed that ICAM-1 is an independent risk factor for metastasis even after
control for important prognostic markers like extraocular growth, ciliary b
ody involvement, scleral infiltration and cell type. VCAM-1 was expressed i
n 24 out of 88 tumors (27.3%) and NCAM only in 14 out of 87 tumors (16%). O
nly spindle cells stained positive with anti-NCAM. NCAM and VCAM-1 expressi
on was not related to metastasis. Our results show that the loss of ICAM-1
expression is associated with an increased risk of metastasis within the fi
rst 5 years after diagnosis. Copyright (C) 2000 S. Karger AG. Basel.