K. Nabeshima et al., EXPRESSION OF C-MET CORRELATES WITH GRADE OF MALIGNANCY IN HUMAN ASTROCYTIC TUMORS - AN IMMUNOHISTOCHEMICAL STUDY, Histopathology, 31(5), 1997, pp. 436-443
Aims: Recent studies suggest tile involvement of hepatocyte growth fac
tor/scatter factor (HGF/SF) in glioma cell invasion and tumour progres
sion, We investigated the distribution and rate of tumour cells that e
xpress c-Met protein, which is the cell-surface receptor for HGF/SF, i
n astrocytic tumours, The type of cells that express c-Met in tumour t
issues was also identified, Methods and results: c-Met expression was
screened immunohistochemically in a total of 43 astrocytic tumours, in
cluding 14 low-grade astrocytomas (A), 13 anaplastic astrocytomas (AA)
and 16 glioblastoma multiforme (GBM). c-Met reactivity was demonstrat
ed predominantly in the cytoplasm of tumour cells, Bizarre large tumou
r cells tended to stain intensely. Higher c-Met expression levels (gre
ater than or equal to 2+, more than 25 % cells were positive) were not
ed in 21.4%, of (A) vs. 53.8% in (AA) and 87.5% in (GBM) (P < 0.001),
indicating a dear relationship between c-Met protein staining and high
er grade astrocytic tumours, Moreover, c-Met immunoreactivity was also
shown in tumour micro microvasculature. reactive astrocytes, and neur
ones in the cortex infiltrated by glioma cells. In 85.7% of cases cont
aining infiltrated cortex, neurones were positive vs, no neurones in n
on-neoplastic regions (P < 0.002). Conclusions: This evidence suggests
that c-Met expression in the brain could be associated with astrocyto
ma progression and also reactive process. Immunohistochemical determin
ation of c-Met-expressing cell types helps to understand possible role
s of c-Met in tumour tissues.