Jl. Mohler et al., ANDROGEN AND GLUCOCORTICOID RECEPTORS IN THE STROMA AND EPITHELIUM OFPROSTATIC HYPERPLASIA AND CARCINOMA, Clinical cancer research, 2(5), 1996, pp. 889-895
Differences in stromal and epithelial cell staining for androgen and g
lucocorticoid receptors (ARs and GRs) were investigated in 20 patients
with clinically localized prostatic carcinoma treated by radical pros
tatectomy, Sections of benign prostatic hyperplasia and prostatic carc
inoma from each patient were stained with antibodies to AR and GR usin
g an avidin-biotin peroxidase technique, The specificity of the GR imm
unoreactivity was established in benign prostatic hyperplasia and pros
tatic carcinoma by immunohistochemistry using the GR antibody absorbed
with synthetic peptide and Western blotting, Nuclear staining intensi
ty and percentage of nuclei stained were summed to obtain AR and GR im
munostaining scores, AR staining of prostatic carcinoma epithelial [10
3 +/- 58 (SD)] and stromal (126 +/- 48) nuclei was less than in benign
prostatic hyperplasia (142 +/- 47 and 169 +/- 56; paired Student's t
tests, P = 0.02 and P = 0.01); however, no difference in staining inte
nsity occurred between stroma and epithelium in either tissue type, GR
stained intensely in stromal cells from benign prostatic hyperplasia
(189 +/- 50) and prostatic carcinoma (163 +/- 60), However, prostatic
carcinoma epithelial cells (34 +/- 57) had low levels of glucocorticoi
d receptor staining (P < 10(-7)), and benign prostatic hyperplasia epi
thelium (74 +/- 51) was intermediate, In most patients, GR could not b
e detected in nuclei of prostatic carcinoma epithelial cells but was u
ndiminished in stromal cell nuclei, There was no relationship by multi
variate regression analysis between AR or GR staining and age, serum p
rostate-specific antigen, Gleason grade, or pathological stage. In com
parison with AR, the greater variability of GR staining in epithelium
versus stroma of prostatic carcinoma warrants further study of GR, par
ticularly in the area of stromal-epithelial interaction.