Persistent Intraprostatic Androgen Concentrations after Medical Castration in Healthy Men

Author:

Page Stephanie T.12,Lin Daniel W.32,Mostaghel Elahe A.1,Hess David L.4,True Lawrence D.5,Amory John K.1,Nelson Peter S.16,Matsumoto Alvin M.127,Bremner William J.1

Affiliation:

1. Departments of Medicine (S.T.P., E.A.M., J.K.A., P.S.N., A.M.M., W.J.B.), Seattle, Washington 98195

2. Veterans Affairs Puget Sound Health Care System (S.T.P., D.W.L., A.M.M.), Seattle, Washington 98108

3. Urology (D.W.L.), Seattle, Washington 98195

4. Oregon National Primate Research Center (D.L.H.), Oregon Health & Science University West Campus, Beaverton, Oregon 97006

5. Pathology (L.D.T.), University of Washington School of Medicine, Seattle, Washington 98195

6. Divisions of Human Biology and Clinical Research (P.S.N.), Fred Hutchinson Cancer Research Center, Seattle, Washington 98109-1024

7. Geriatric Research, Education and Clinical Center (A.M.M.), Seattle, Washington 98108

Abstract

Abstract Context: The impact of serum androgen manipulation on prostate tissue hormone levels in normal men is unknown. Studies of men with prostate cancer have suggested that prostatic androgens are preserved in the setting of castration. Tissue androgens might stimulate prostate growth, producing adverse clinical consequences. Objective: The objective of the study was to determine the effect of serum androgen manipulation on intraprostatic androgens in normal men. Design: Thirteen male volunteers ages 35–55 yr (prostate-specific antigen < 2.0 ng/ml; normal transrectal ultrasound) were randomly assigned to: 1) a long-acting GnRH-antagonist, acyline, every 2 wk; 2) acyline plus testosterone (T) gel (10 mg/d); or 3) placebo for 28 d. Serum hormones were assessed weekly. Prostate biopsies were obtained on d 28. Extracted androgens were measured by RIA, and immunohistochemistry for androgen-regulated proteins was performed. Results: The mean decrease in serum T was 94%, whereas prostatic T and dihydrotestosterone levels were 70 and 80% lower, respectively, in subjects receiving acyline alone compared with controls (P < 0.05). Despite this decrease in prostate androgens, there were no detectable differences in prostate epithelial proliferation, apoptosis, prostate-specific antigen, and androgen receptor expression. Conclusion: In this small study of healthy subjects, despite a 94% decrease in serum T with medical castration, intraprostatic T and dihydrotestosterone levels remained 20–30% of control values, and prostate cell proliferation, apoptosis, and androgen-regulated protein expression were unaffected. Our data highlight the importance of assessing tissue hormone levels. The source of persistent prostate androgens associated with medical castration and their potential role in supporting prostate metabolism deserves further study.

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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