BACKGROUND. Human beta-microseminoprotein (beta-MSP or PSP94) is a small pr
otein secreted by prostatic epithelial cells. We recently reported the pres
ence of low levels of beta-MSP mRNA expression and protein in most prostate
cancer tissues.
METHODS. beta-MSP and mRNA expression was examined by in situ hybridization
in biopsy specimens obtained from 92 patients with prostate cancer. AU tis
sue specimens were obtained by needle biopsies prior to treatment. All pati
ents subsequently received endocrine therapy. To estimate the influence of
beta-MSP mRNA expression and three possible prognostic factors, i.e., patie
nt age, clinical stage, and Gleason score, on time to progression under end
ocrine therapy, univariate and multivariate analyses were performed using C
ox's proportional hazards regression model.
RESULTS. Multivariate survival analysis showed that clinical stage was the
strongest prognostic factor (P =0.006) and that beta-MSP mRNA expression wa
s the second strongest factor (P = 0.038) in 92 patients with stage B-D dis
ease. Analysis of only 51 patients with stage D disease showed that beta-MS
P mRNA expression was the only significant prognosis indicator for progress
ion under endocrine therapy (P = 0.003).
CONCLUSIONS. The presence of cells that express the beta-MSP transcript may
be a novel indicator of potentially aggressive prostate cancer. (C) 1999 W
iley-Liss, Inc.