Membrane testosterone binding sites in prostate carcinoma as a potential new marker and therapeutic target: study in paraffin tissue sections

BMC Cancer. 2005 Nov 17:5:148. doi: 10.1186/1471-2407-5-148.

Abstract

Background: Steroid action is mediated, in addition to classical intracellular receptors, by recently identified membrane sites, that generate rapid non-genomic effects. We have recently identified a membrane androgen receptor site on prostate carcinoma cells, mediating testosterone rapid effects on the cytoskeleton and secretion within minutes.

Methods: The aim of this study was to investigate whether membrane androgen receptors are differentially expressed in prostate carcinomas, and their relationship to the tumor grade. We examined the expression of membrane androgen receptors in archival material of 109 prostate carcinomas and 103 benign prostate hyperplasias, using fluorescein-labeled BSA-coupled testosterone.

Results: We report that membrane androgen receptors are preferentially expressed in prostate carcinomas, and they correlate to their grade using the Gleason's microscopic grading score system.

Conclusion: We conclude that membrane androgen receptors may represent an index of tumor aggressiveness and possibly specific targets for new therapeutic regimens.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Binding Sites
  • Biomarkers, Tumor*
  • Cell Differentiation
  • Cell Membrane / metabolism*
  • Fluorescein / pharmacology
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Male
  • Middle Aged
  • Paraffin
  • Prostatic Neoplasms / metabolism*
  • Receptors, Androgen / metabolism
  • Reproducibility of Results
  • Steroids / metabolism

Substances

  • Biomarkers, Tumor
  • Receptors, Androgen
  • Steroids
  • Paraffin
  • Fluorescein