Angiogenesis is considered to play an important role in the development of
malignant brain tumors, especially glioblastoma multiforme (GBM). Abnormal
vascular construction with a glomeruloid appearance is characteristic of GE
M, beta -catenin is known as one of the adhesive molecules associated not o
nly with cell adhesion and cell polarity, but also with carcinogenesis. We
postulated the relevance of beta -catenin to vigorous endothelial prolifera
tion in human GEM because the vascular cells (VCs) are apt to lose their ce
ll polarity. The object of this study is to compare the immunohistochemical
localization of beta -catenin in VCs between GBMs and normal brain tissues
. Immunohistochemical analysis of beta -catenin for VCs in 32 GBMs and 10 n
ormal brain tissues was performed. beta -catenin was found concentrated in
the areas of vascular cell-cell junction and internal surface of the vascul
ar lumen in all normal brains. In contrast, beta -catenin, in proliferating
VCs in GBMs, was stained homogeneously and intensely in the cytoplasms of
26 cases (81.3%), in which nuclear staining of beta -catenin was also recog
nized in four cases (12.5%). In conclusion, the intracellular localization
of beta -catenin in VCs of GBMs was found to be different from that of norm
al brain tissues. The changes of expression of beta -catenin may be associa
ted with the angiogenesis or transformation of the VCs in human GEM.