Early effects of pharmacological androgen deprivation in human prostate cancer
Article first published online: 6 DEC 2006
Volume 99, Issue 1, pages 60–67, January 2007
How to Cite
Mercader, M., Sengupta, S., Bodner, B. K., Manecke, R. G., Cosar, E. F., Moser, M. T., Ballman, K. V., Wojcik, E. M. and Kwon, E. D. (2007), Early effects of pharmacological androgen deprivation in human prostate cancer. BJU International, 99: 60–67. doi: 10.1111/j.1464-410X.2007.06538.x
- Issue published online: 6 DEC 2006
- Article first published online: 6 DEC 2006
- Accepted for publication 9 August 2006
- prostate cancer;
- radical prostatectomy;
- androgen deprivation;
To assess the early histological effects of pharmacological androgen deprivation (AD), which have been assessed only over longer periods, as surgical castration leads rapidly to diminished cell proliferation and enhanced cell death within the prostate.
PATIENTS AND METHODS
With Institutional Review Board approval, 35 patients were randomly assigned (seven in each group) to receive 0, 7, 14, 21 and 28 days of AD (flutamide, 250 mg orally three times/day, and one injection with leuprolide acetate 7.5 mg) before radical prostatectomy. The surgical specimens were assessed by conventional histology and immunohistochemistry, while macroarray analysis and quantitative real-time polymerase chain reaction (QRT-PCR) were used to examine gene expression.
There were morphological changes within the prostatic tissues as early as 7 days after initiating AD, similar to the response to castration. There was tumour cell vacuolization indicating cellular injury, glandular atrophy and mononuclear cell infiltration as prominent and progressive effects but, by contrast with castration studies, there were no changes in epithelial proliferation or apoptosis. Macroarray analysis, validated by QRT-PCR and immunohistochemistry, showed up-regulation of numerous and potentially counter-effective genes involved in the cell cycle and apoptosis.
Pharmacological AD induces significant involution within prostatic tissues over 7–28 days, but allows the persistence of some viable tumour cells capable of proliferation.