Disruption of androgen receptor function inhibits proliferation of androgen-refractory prostate cancer cells

Cancer Res. 2002 Feb 15;62(4):1008-13.

Abstract

Prostate cancer cells depend on androgens and the androgen receptor (AR) for survival. However, after androgen ablation therapy, tumors relapse to an androgen-refractory state. To determine whether the androgen receptor is critical for proliferation of androgen-refractory prostate cancer cells, we disrupted the activity of the androgen receptor with an antibody and an AR mRNA hammerhead ribozyme in the following cell lines: LNCaP (androgen-sensitive), LNCaP-Rf and LNCaP-C4 (androgen-refractory), and DU-145 (androgen-insensitive). Microinjection of either antibody or ribozyme inhibited proliferation of androgen-refractory cells. These findings demonstrate that the AR is critical for proliferation of androgen-refractory cells, even in the absence of androgens.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Androgen Antagonists / pharmacology
  • Androgen Receptor Antagonists*
  • Antibodies, Neoplasm / pharmacology
  • Cell Division / physiology
  • Drug Resistance, Neoplasm
  • Humans
  • Male
  • Neoplasms, Hormone-Dependent / pathology
  • Prostatic Neoplasms / pathology*
  • RNA, Catalytic / pharmacology
  • Receptors, Androgen / genetics
  • Receptors, Androgen / immunology
  • Receptors, Androgen / physiology

Substances

  • Androgen Antagonists
  • Androgen Receptor Antagonists
  • Antibodies, Neoplasm
  • RNA, Catalytic
  • Receptors, Androgen
  • hammerhead ribozyme