Xp. Zhu et Pa. Humphrey, Overexpression and regulation of expression of scatter factor/hepatocyte growth factor in prostatic carcinoma, UROLOGY, 56(6), 2000, pp. 1071-1074
Objectives. Scatter factor (hepatocyte growth factor) (SF/HGF) is a multifu
nctional polypeptide growth factor that has been implicated in tumor prolif
eration, angiogenesis, invasiveness, and metastasis. Little is known of the
expression of SF/HGF in human prostatic carcinoma. The aims of this invest
igation were to quantitate the level of SF/HGF expression in benign versus
malignant human prostatic tissues and to assess regulation of SF/HCF expres
sion by human prostatic stromal myofibroblasts.
Methods. We determined the level of SF/HGF expression in 10 human prostatic
tissue samples (5 benign, 5 carcinoma) by Western blot analysis. Five puri
fied growth factors-basic fibroblast growth factor (bFGF), interleukin-1 be
ta (IL-1 beta), platelet-derived growth factor (PDGF), Vascular endothelial
growth factor (VEGF), and endothelial growth factor (EGF)-were tested for
their capacity to induce SF/HGF expression by a human prostatic stromal myo
fibroblastic cell line, as assessed by enzyme-linked immunosorbent assay. S
upernatant from the normal PrEC prostatic epithelial cell fine and the DU 1
45 carcinoma cell line were assayed for SF/HGF-inducing activity.
Results. SF/HGF exhibited a mean fourfold overexpression in carcinoma tissu
es compared with benign prostatic tissue. Significant stimulation of SF/HGF
expression by prostatic stromal myofibroblasts was detected for IL-1 beta
(8.1-fold), PDGF (6.2-fold), bFGF (4.0-fold), VEGF (3.7-fold), and EGF (2.9
-fold). DU 145-conditioned media, but not the PrEC-conditioned media, conta
ined SF/HGF-inducing activity, which was determined to include IL-1 beta, b
FGF, and PDGF by antibody-blocking experiments.
Conclusions. SF/HGF is overexpressed in human prostatic carcinoma tissues.
Prostatic carcinoma cell stimulation of SF/HCF expression by adjacent benig
n myofibroblastic cells as a type of epithelial-stromal paracrine interacti
on could potentially influence prostatic carcinoma cell behaviors. UROLOGY
56: 1071-1074, 2000. (C) 2000, Elsevier Science Inc.