Aromatization of androstenedione to estrogen by benign prostatic hyperplasia, prostate cancer and expressed prostatic secretions Journal Article


Authors: Stone, N. N.; Laudone, V. P.; Fair, W. R.; Fishman, J.
Article Title: Aromatization of androstenedione to estrogen by benign prostatic hyperplasia, prostate cancer and expressed prostatic secretions
Abstract: Human prostatic tissue and expressed prostatic secretions (EPS) efrom patients with benign prostatic hyperplasia (BPH) and prostate cancer were incubated with (1 β 3H) androstenedione. The extent of aromatization was determined by measuring the transfer of 3H from the 1 β position into water. The amount of 3H2O recovered corresponds to the estrogens formed. Tissue from 5 patients with BPH yielded 2.13 (±1.05) pmol/mg protein/h while the EPS from the same patients yielded 727 fmol/mg protein/h. In patients with prostate cancer the mean formation of estrogens was 388 fmol/mg protein/h (±75). 4-hydroxyandrostenedione, an aromatase inhibitor, successfully inhibited aromatization in BPH and prostate cancer 53-98%. © 1987 Springer-Verlag.
Keywords: estrogens; dose-response relationship, drug; prostate cancer; prostatic neoplasms; prostate; hyperplasia; carrier proteins; androstenedione; aromatization; bph; human; male; priority journal; prostatic secretions
Journal Title: Urological Research
Volume: 15
Issue: 3
ISSN: 0300-5623
Publisher: Springer  
Date Published: 1987-06-01
Start Page: 165
End Page: 167
Language: English
DOI: 10.1007/bf00254430
PUBMED: 3629751
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 5 February 2021 -- Source: Scopus
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  1. William R Fair
    342 Fair