Objectives. To determine the cell-specific expression of the two major isof
orms of cyclooxygenase (COX-1 and COX-2) in human noncancerous and cancerou
s prostatic tissues.
Methods. Thirty-one specimens of prostate carcinoma (CaP) and 10 specimens
of benign prostatic hyperplasia (BPH) were stained with mouse antihuman COX
-1 and COX-2 monoclonal antibodies. The stained specimens were analyzed bot
h descriptively and in a semiquantitative manner by assigning an immunoreac
tive intensity score (0 to 4). The averaged results were compared for diffe
rent histologic tissue types, including luminal and basal epithelium of BPH
, the peripheral zone, high-grade prostatic intraepithelial neoplasia (PIN)
, and CaP of varying Gleason grades.
Results. COX-1 expression in noncancerous prostatic tissue was seen predomi
nantly in the basal epithelial cells of BPH (90% positive staining). COX-1
expression was minimal in noncancerous luminal epithelial cells (0% to 10%)
but was upregulated in CaP (63% of CaP specimens). Strong COX-2 expression
was demonstrated in the smooth muscle cells of the prostate. COX-2 was als
o expressed in the basal epithelial cells (60% BPH, 94% peripheral zone, 75
% PIN]. Luminal epithelial cells derived from BPH, the peripheral zone, and
PIN expressed COX-2 in 0%, 26%, and 86% of samples, respectively. COX-2 ex
pression in CaP was intense and uniform, with 87% of samples demonstrating
immunoreactivity.
Conclusions. The results of the present study indicate that expression of b
oth COX-1 and COX-2 in human CaP is increased. COX-2 expression is also inc
reased in the basal and luminal epithelial cells of PIN. These data indicat
e that COX-1 and COX-2 (and/or their prostaglandin products) may play a rol
e in the malignant transformation of the prostate. UROLOGY 56: 671-676, 200
0. (C) 2000, Elsevier Science Inc.