Tg. Sheidow et al., Expression of vascular endothelial growth factor in uveal melanoma and itscorrelation with metastasis, BR J OPHTH, 84(7), 2000, pp. 750-756
Aims-To evaluate the expression of vascular endothelial growth factor (VEGF
) in uveal melanomas and correlate its presence with tumour characteristics
and systemic metastasis.
Methods-47 cases of ciliochoroidal melanoma enucleated between 1983 and 199
3 were retrieved from the pathology archives at the University of Western O
ntario. Paraffin sections stained with haematoxylin and eosin, periodic aci
d Schiff, and periodic acid Schiff without haematoxylin after bleaching of
melanin were examined. The expression of VEGF protein was examined by an im
munoalkaline phosphatase method following antigen retrieval, using an antib
ody to VEGF and vector red as the chromogen. The intensity of VEGF immunore
activity was graded on a scale of 0-7 and correlated with tumour cell type,
tumour size, presence or absence of necrosis, pigmentation, mitotic activi
ty, microvascular density, and microvascular pattern.
Results-VEGF immunoreactivity was present in 44/47 tumours (94%): the inten
sity was graded as very weak (1-2) in 29/47 (62%) and as weak or greater in
15/47 (32%). VEGF was also found in the ciliary epithelium, smooth muscle
of the ciliary body and iris, retinal ganglion cells, inner photoreceptor s
egments, and the retinal pigment epithelium. Follow up data were available
in 43/47 patients (91.5%), with a median follow up time of 10 years. 16/43
(37%) patients developed metastases. VEGF expression in melanoma was linked
to the presence of tumour necrosis and the degree of pigmentation but no s
tatistically significant relation with microvascular pattern, tumour size,
or microvascular density was found. There was no statistically significant
correlation between VEGF expression and metastasis.
Conclusions-Most ciliochoroidal melanomas express VEGF and expression is co
rrelated with the presence of necrosis but not with the occurrence of syste
mic metastasis or tumour angiogenesis.