Nearly all primary prostatic carcinomas have been found to express the
androgen receptor (AR) protein, which is the intracellular mediator o
f androgen action. To gain a better insight into the mechanisms of and
rogen independence of advanced prostatic carcinoma, it is important to
know whether the AR is also present in metastases of androgen-indepen
dent tumors. We have assessed the status of the AR and the prostate-sp
ecific antigen in 22 metastases of 18 patients with progressive prosta
te cancer. In 18 cases, the metastases were localized in bone, in 3 ca
ses in the epidural space, and in 1 case in the periosteum. All but on
e patient had received some kind of endocrine treatment for prostatic
carcinoma. Paraffin-embedded tissue sections were stained for the AR f
ollowing a streptavidinbiotin-peroxidase protocol with the polyclonal
antibody PG-21, which is directed against amino acids 1 through 21 of
the rat and the human AR. The percentage of AR-positive cells was eval
uated on the basis of an arbitrary 4-point scale. All 22 tumor metasta
ses displayed AR positivity, One AR-positive metastatic lesion did not
stain for prostate-specific antigen, but in all other metastases, thi
s protein was detected by means of immunohistochemistry. The present s
tudy provides evidence that, unlike androgen-independent prostatic car
cinoma cell lines, distant prostatic carcinoma metastases do express t
he AR. These findings indicate that the AR may be involved in the prog
ression of prostate cancer.