Androgenic modulation of AR-Vs

Endocrine. 2018 Nov;62(2):477-486. doi: 10.1007/s12020-018-1682-5. Epub 2018 Jul 19.

Abstract

Purpose: The importance of androgen receptor variants (AR-Vs) is recognized in prostate cancer. AR-Vs have been the focus of many studies. Expression of AR-Vs has been proposed as a biomarker for resistance to androgen deprivation therapy for metastatic disease. Herein, we show dynamic changes in AR-Vs expression in response to androgen modulation.

Methods: The C4-2B cell line was exposed to low (10-13 M) and high (10-8 M) androgen (dihydrotestosterone, DHT) levels, with or without flutamide. mRNA and protein expression levels were assessed by qPCR and immunohistochemistry, respectively.

Results: We demonstrated that high levels of DHT downregulate AR-FL and AR-Vs. Even though AR-Vs did not present ligand-binding domain, thus were not capable of binding to DHT, they present dynamic changes under androgen treatment. Treatment with flutamide alone or in association with low levels of DHT stimulates growth of prostatic cells.

Conclusions: Importantly, we provide evidence that AR-Vs respond differently to androgenic modulation. These findings have implications for a better understanding of the role of AR-Vs in prostate carcinogenesis.

Keywords: Androgen receptor; Androgen receptor isoforms; Androgen receptor variants; Androgenic modulation; Prostate cancer; Steroids.

MeSH terms

  • Androgens / pharmacology*
  • Cell Line, Tumor
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Ligands
  • Male
  • Mutant Proteins* / agonists
  • Mutant Proteins* / genetics
  • Mutant Proteins* / metabolism
  • Polymorphism, Genetic
  • Prostatic Neoplasms / genetics
  • Prostatic Neoplasms / metabolism
  • Prostatic Neoplasms / pathology
  • Protein Isoforms / agonists
  • Protein Isoforms / metabolism
  • Receptors, Androgen / genetics*
  • Receptors, Androgen / metabolism*

Substances

  • AR protein, human
  • Androgens
  • Ligands
  • Mutant Proteins
  • Protein Isoforms
  • Receptors, Androgen