A. Vaisanen et al., Matrix metalloproteinase-2 (MMP-2) immunoreactive protein - A new prognostic marker in uveal melanoma?, J PATHOLOGY, 188(1), 1999, pp. 56-62
Citations number
31
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Uveal melanoma is the most common primary intraocular tumour, Once haematog
enous metastasis has occurred, there is no cure for the disease and there i
s an obvious need for new biological prognostic markers to estimate the ris
k of metastasis. In this study, the expression of matrix metalloproteinase-
2 (MMP-2) was characterized immunohistochemically in 29 human uveal melanom
as, Enzyme-linked immunoassays and gelatin zymographies were assessed in or
der to quantify the expression of gelatinases A and B, as well as the tissu
e inhibitor of metalloproteinases (TIMPs), in the vitreous body. A total of
49 per cent of the ureal melanomas displayed a positive immunoreaction for
MMP-2 in melanoma cells, the epithelioid cells showing the most frequent s
taining. There was no correlation between the positivity of MMP-2 staining
and the size of the primary tumour, gender or age. The expression of MMP-2
Has associated sith a dismal prognosis: the 5-year overall survival rate fo
r MMP-2-positive cases was significantly inferior to that of the MMP-2 nega
tive cases, 49 per cent vs. 86 per cent, respectively (p=0.02). A patient g
roup at high risk of metastatic disease was identified; only 38 per cent of
patients with a MMP-2-positive non-spindle cell uveal melanoma survived fo
r 5 years, The analyses of MMPs or TIMPs in the vitreous body had no progno
stic value. Positive immunostaining for MMP-2 was observed in the retinal p
igment epithelium. corneal epithelium, and fibroblasts in the ciliary body
and choroid, It is concluded that immunohistochemical analysis of MMP-2 may
help to predict a risk of metastasis in uveal melanoma, Copyright (C) 1999
John Wiley & Sons, Ltd.