The role of transforming growth factor-beta (TGF-beta) and nitric oxide (NO
) in ovarian neoplasia is still not clear. We studied the expression of TGF
-beta by enzyme immunoassay, and nitrates las a stable end product of NO) i
n 127 ovarian tissues (36 normal, 37 benign, and 54 malignant). Ploidy stat
us and synthetic phase fraction (SPF) were also assessed by flow cytometry.
Mean ranks of TGF-beta, nitrate, and SPF were significant among different
groups (X-2 = 12.01, P = 0.0025, X-2 = 67.42, P = 0.000, X-2 = 9.06, P = 0.
011 respectively). Nitrate mean ranks were significant among different FIGO
stages of the disease (X-2 = 17.6, P=0.000). A significant correlation was
shown between TGF-beta, and nitrate levels in all tissues (r=0.24, P=0.01)
, as well as in malignant tissues (r = 0.3, P = 0.026). Cutoff values were
determined for both TGF-beta (290 pg/mg protein), and nitrates (310 nmole/m
g non protein nitrogenous substances). At these cut-offs, nitrates showed a
sensitivity of 93% and 84% specificity for malignant versus normal cases,
while TGF-beta had 76% sensitivity, and 82.4% specificity for poor versus g
ood outcome. Patients with epithelial ovarian cancer were followed up for a
total of 40 months. Survival analysis showed that patients with TGF-beta a
bove the cut-off had worse prognosis (X-2 = 12.69, P=0.004). The present re
sults suggest that malignant transformation of ovarian tissues is associate
d with increased TGF-beta and NO production. NO level is related to the dev
elopment and progression of epithelial ovarian cancer, while high levels of
TGF-beta could be of prognostic significance.