H. Li et al., HEPATOCYTE GROWTH-FACTOR STIMULATES THE INVASION OF GALLBLADDER CARCINOMA CELL-LINES IN-VITRO, Clinical & experimental metastasis, 16(1), 1998, pp. 74-82
Human gallbladder cancer is highly malignant and its prognosis is usua
lly poor depending on the extent of surrounding tissue invasion. We ex
amined in vitro the invasive activity of four gallbladder cancer cell
lines (GB-d1, GB-h3, GB-d2 and FU-GBC-1) in the absence or presence of
hepatocyte growth factor (HGF). In type 1 collagen gel culture, HGF s
timulated cell proliferation and induced an invasive phenotype of arbo
rizing structures in GB-d1, GB-h3 and GB-d2. In a Matrigel invasion as
say, invasion was also induced in three of these lines by HGF but not
in FU-GBC-1. Cellular motility was, however, stimulated by HGF in all
of the four cell lines to various extents. Zymography for proteolytic
enzymes demonstrated high levels of type IV collagenase and urokinase-
type plasminogen activator (u-PA) activity in GB-d1, GB-h3 and GB-d2 e
ven in the absence of HGF. In the presence of HGF, the 72 kDa type IV
collagenase (MMP-2) activity of GB-h3 and u-PA activities of GB-d1, GB
-h3 and GB-d2 were enhanced. In contrast, the MMPs and PAs activities
of FU-GBC-1 were faint irrespective of the addition of HGF. A Western
blot analysis demonstrated higher levels of 190 kDa c-MET product (HGF
receptor) of GB-d1, GB-h3 and GB-d2 than that of FU-GBC-1. The invasi
on in the Matrigel assay stimulated by HGF was inhibited by protease i
nhibitors, aprotinin and FOY-305, as well as by anti-HGF antibody. The
se results thus suggest that, in addition to the importance of the pro
teolytic activity, the cellular motility induced via the HGF/HGF-recep
tor system is essential for the invasive progression of gallbladder ca
rcinoma cells.