BACKGROUND. Nitric oxide (NO) is synthesized by inducible nitric oxide
synthase (iNOS) and plays an important role in tumor growth and angio
genesis. NO generation by NOS also influences the cytotoxicity of macr
ophages and tumor-induced immunosuppression. Before now, the expressio
n of iNOS in prostate carcinoma tissue had not been determined. METHOD
S. In this study, tissue sections from 16 patients with prostate carci
noma were studied immunohistochemically and compared with tissue speci
mens from 10 patients with benign hyperplasia. RESULTS. Positive iNOS
immunostaining was detected in all sections from patients with prostat
e carcinoma. The malignant epithelial cells were highly positive. The
antibody against iNOS also marked round cells, which had the same cell
shape as that observed for macrophages. These cells were located in s
troma and epithelium adjacent to tumor islets. However, round cells in
benign tissue stained negative for iNOS. None of the benign hyperplas
ia specimens stained positive for iNOS immunohistochemically. CONCLUSI
ONS. Prostate carcinoma tissue had a high iNOS content, whereas benign
tissue did not. The authors suggest that epithelial iNOS expression c
an be used as a specific immunohistochemical marker for prostate carci
noma. NO generation by iNOS may play multiple roles in the development
of this disease. (C) 1998 American Cancer Society.