Androgen receptor modulation in benign human prostatic tissue and prostatic adenocarcinoma during neoadjuvant endocrine combination therapy

Prostate. 1996 Apr;28(4):227-31. doi: 10.1002/(SICI)1097-0045(199604)28:4<227::AID-PROS3>3.0.CO;2-A.

Abstract

Modulation of androgen receptor (AR) expression during neoadjuvant endocrine therapy in human prostates of patients with localized prostate cancer was investigated by immunohistochemistry. In 8 of 15 untreated prostatectomy specimens, the majority of prostatic glandular cells displayed nuclear immunostaining for AR, whereas only 1 of 26 pretreated cases displayed a similar glandular AR expression. Expression of AR in the prostatic stromal compartment of nontreated cases proved to be quite heterogeneous, since 4 of the 15 (27%) examined specimens did not show stromal AR expression. After preoperative neoadjuvant therapy, this value was 68%, although this difference did not reach statistical significance. Prostatectomy specimens of the treated patients contained carcinomas with a higher Gleason score than those of untreated patients. AR expression in carcinomas of treated patients was diminished (P= 0.05), which may be attributed to their relatively lower differentiation grade. The data strongly suggest that neoadjuvant hormone therapy reduces AR expression by nonneoplastic prostatic glandular cells and carcinoma cells by a selective, but incomplete, elimination of AR-positive cells.

Publication types

  • Comparative Study

MeSH terms

  • Adenocarcinoma / drug therapy
  • Adenocarcinoma / metabolism*
  • Adenocarcinoma / pathology
  • Androgen Antagonists / pharmacology
  • Androgen Antagonists / therapeutic use*
  • Drug Therapy, Combination
  • Epithelial Cells
  • Epithelium / drug effects
  • Epithelium / metabolism
  • Flutamide / pharmacology
  • Flutamide / therapeutic use*
  • Gonadotropin-Releasing Hormone / agonists
  • Humans
  • Immunohistochemistry
  • Male
  • Prostate / cytology
  • Prostate / drug effects
  • Prostate / metabolism*
  • Prostatic Neoplasms / drug therapy
  • Prostatic Neoplasms / metabolism*
  • Prostatic Neoplasms / pathology
  • Receptors, Androgen / drug effects
  • Receptors, Androgen / metabolism*
  • Stromal Cells / cytology
  • Stromal Cells / drug effects
  • Stromal Cells / metabolism

Substances

  • Androgen Antagonists
  • Receptors, Androgen
  • Gonadotropin-Releasing Hormone
  • Flutamide