The MET oncogene encodes the receptor for Hepatocyte Growth Factor/Sca
tter Factor, a unique growth factor that induces not only proliferatio
n of epithelial cells, but also cell motility and invasiveness. DNA le
vel and expression of the Met/HGF receptor gene were examined with Sou
thern- and Western-blot analyses, respectively, in human ovary, benign
ovarian tumors and epithelial ovarian carcinomas. The Met/ HGF recept
or was detectable in the surface epithelium of normal ovary. The level
of expression was unchanged in benign ovarian tumors of various origi
ns. Fourteen out of 67 malignant carcinomas (20%) showed a 3- to 10-fo
ld increase in expression. in 5 additional cases the Met/HGF protein w
as overexpressed over 50-fold. This represents a total of 28% of cases
. Overexpression was not associated with MET gene amplification. Overe
xpressing tumors belonged to different histotypic variants, but showed
a well-differentiated phenotype. Clinically, overexpression was assoc
iated with disease at any pathologic stage, but was significantly corr
elated with premenopausal status of patients. These data suggest that
expression of the Met/HGF receptor may add a selective growth advantag
e to a narrow subset of differentiated ovarian cancers in premenopausa
l patients. (C) 1994 Wiley-Liss, Inc.