The expression of metalloproteinases was evaluated in a series of 12 mening
iomas of various histological sub-types including 3 meningotheliomatous, 3
fibroblastic, 4 transitional and one psammomatous meningioma (WHO grade I)
as well as one anaplastic meningioma (WHO grade III). No gelatinolytic acti
vity could be detected in all tumor samples pointing towards no or very low
activity of both MMP-2 and MMP-9. At least MMP-2 mRNA could be found in 10
out of 12 tumor samples by the reverse transcription PCR method (RT-PCR) f
ollowed by electrophoresis on silver-stained polyacrylamide gels, which all
ows the detection even of small traces of a specific mRNA. The PCR products
were identified as MMP-2 sequences without introns (mRNA-derived) by direc
t sequencing, thereby demonstrating a low transcriptional activity of the g
ene. The translation of these mRNAs, however, did not result in amounts of
protein detectable by immunohistochemistry or Western blotting. Therefore,
neither MMP-2 nor MMP-9 should play a major role for tumor growth within du
ra mater or bone structures or for brain infiltration in our tumor series.
Therefore, other mechanisms must be responsible for extracellular matrix de
gradation at least in a fraction of meningiomas.