Y. Nakayama et al., STROMAL ANGIOGENESIS IN HUMAN GLIOMA - A ROLE OF PLATELET-DERIVED ENDOTHELIAL-CELL GROWTH-FACTOR, Surgical neurology, 49(2), 1998, pp. 181-187
BACKGROUND Although several tumor angiogenic factors have been identif
ied previously and characterized, it is not yet fully clear how tumor
angiogenic factors induce endothelial cell transformation and prolifer
ation. platelet-derived endothelial cell growth factor (PD-ECGF) has b
een recently discovered to be an endothelial cell growth factor initia
lly purified from human platelets. However,there has been no previous
report describing the significance of PD-ECGF in the growth of brain t
umors by angiogenic stimulation. We report the immunohistochemical loc
alization of PD-ECGF in human gliomas and meningiomas, and discuss whe
ther PD-ECGF could play a role in the modulation of stromal angiogenes
is in human glioblastoma multiforme. METHODS Twenty-eight cases of gli
oma (11 glioblastomas and 17 astrocytomas) derived from the neuroectod
erm in embryogenesis and 12 meningiomas from the mesoderm were investi
gated by both immunohistochemical localization of the PD-ECGF and a se
miquantitative assay to determine the degree of stromal angiogenesis.R
ESULTS Numerous PD-ECGF positive cells were observed within and around
the blood vessels of glioblastoma multiforme, especially on the borde
rs of tumor tissue. The PD-ECGF positive cells were negative for anti-
von Willebrand factor (VWF) and antiglial fibrillary acidic protein (G
FAP) antibodies and were positive for antimacrophage (HAM-56). The exp
ression of PD-ECGF by macrophages closely correlated with the degree o
f stromal vascularity in glioblastoma multiforme; no such correlation
was found in either astrocytoma or meningioma. Proliferating cell nucl
ear antigen (PCNA) was found to be positive in some endothelial cells
of stromal vessels in glioblastoma multiforme. These findings suggest
that PD-ECGF expressed by macrophages plays an important role in the g
rowth of glioblastoma multiforme with stromal angiogenesis. (C) 1998 b
y Elsevier Science Inc.