Angiogenesis is an important part of normal and pathological processes, inc
luding tumour growth, metastasis, inflammation and wound healing. VEGF is t
he best known angiogenic factor, implicated in tumour-associated microvascu
lar hyperpermeability and carcinogenesis. We investigated 103 malignant ple
ural mesotheliomas, analysing the expression of vascular endothelial growth
factor using immunohistochemistry and insitu hybridization. The grade of m
icrovessel density was assessed with the aid of anti-factor-VIII antibodies
. An increased expression of VEGF was found in biphasic and epithelioid mes
otheliomas, correlating in a statistically significant manner (P<0.042). In
situ hybridization confirmed the specificity of VEGF mRNA expression. There
was a robust correlation between VEGF expression and increased microvessel
density (P<0.001), and positive mesotheliomas had significantly higher mic
rovessel densities than negative specimens. There was also a significant co
rrelation between microvessel density and histological pattern. As growth p
attern tended towards biphasic and sarcomatoid mesotheliomas the density of
micovessels decreased (P<0.05).