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Original Studies |
Department of Clinical Physiopathology, Endocrine Unit (A.D.B., C.C., P.G., G.F., M.S.) and Gastroenterology Unit (C.G., S.M.), University of Florence, Florence, Italy
Address all correspondence and requests for reprints to: Dr. Alessandra De Bellis, Department of Clinical Physiopathology, Endocrine Unit, Viale Pieraccini 6, 50139 Florence, Italy.
It is well recognized that the actions of androgens alone do not
explain the hyperplastic development of the gland that occurs in
elderly men. The increasing number of reports confirming the lack of
mitogenic activity of androgens coupled with the powerful mitogenic
activity of growth factors and the discovery of growth factor receptors
led to an increased interest in the putative role of growth factors in
prostate physiopathology. We have previously demonstrated the presence
and the cellular localization of epidermal growth factor and of the
related peptide, transforming growth factor-
, together with their
common receptor in the epithelial compartment of the human hyperplastic
prostate tissue (BPH). In the present study we examined the expression
and cellular localization of messenger ribonucleic acid (RNA) encoding
keratinocyte growth factor (KGF) and its receptor in human hyperplastic
prostate tissue. RT-PCR of total RNA extracted from BPH tissues
documented the presence of transcripts for KGF and its receptor.
In situ hybridization with specific RNA probes
synthesized from the respective complementary DNA demonstrated that KGF
mRNA was mainly localized in the stromal cells, whereas its receptor
was mainly localized in the prostate epithelium. Moreover, the
mitogenic activity of KGF on cultured BPH cells compared to that of
other growth factors has been tested. Our findings clearly indicate
that KGF has the ability to function as a potent mitogen in BPH cells.
Our data support the hypothesis that KGF plays an important role in
prostate growth and that in human prostate it seems to act in a
paracrine fashion.
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