Fibroblast growth factor 2 (FGF-2, basic fibroblast growth factor) has been
reported to be elevated in tissues from benign prostatic hyperplasia (BPH)
, the most frequent neoplastic disease in aging men. This suggests that FGF
-2 may play a significant role in the development of BPH. In this study the
cellular distribution pattern of FGF-2 in tissues from BPH has been invest
igated by immunohistochemical and molecular biological methods. Radioimmuno
assay revealed high concentrations of FGF-2, ranging between 450 and 950 ng
per g tissue. Immunoblots confirmed the presence of a 18 kDa FGF-2 in tiss
ue extracts. By immunohistochemistry done with a polyclonal antibody to rec
ombinant FGF-2 on paraffin sections, FGF-2 was localized in fibroblasts, en
dothelial cells and smooth muscle cells of tissue samples of BPH. Nuclei of
these cells were labelled distinctly. Moreover the cytoplasm of smooth mus
cle cells was labelled moderately. No immunostaining was seen in prostatic
epithelium. Nonradioactive in situ hybridization with digoxygenin-labelled
oligonucleotides revealed the presence of mRNA for FGF-2 in smooth muscle c
ells of the prostatic stroma. These results provide evidence that FGF-2 may
be produced locally in the human prostate as a stroma-specific mitogen and
may play a causal role in the development of BPH.