The immunophilin ligands cyclosporin A and FK506 suppress prostate cancer cell growth by androgen receptor-dependent and -independent mechanisms

Endocrinology. 2007 Oct;148(10):4716-26. doi: 10.1210/en.2007-0145. Epub 2007 Jul 5.


The androgen receptor (AR) contributes to growth of prostate cancer even under conditions of androgen ablation. Thus, new strategies to target AR activity are needed. The AR interacts with the immunophilin FK506-binding protein 52 (FKBP52), and studies in the FKBP52 knockout mouse have shown that this protein is essential to AR activity in the prostate. Therefore, we tested whether the immunophilin ligand FK506 affected AR activity in prostate cancer cell lines. We also tested the hypothesis that the AR interacts with another immunophilin, cyclophilin 40 (Cyp40), and is regulated by its cognate ligand cyclosporin A (CsA). We show that levels of FKBP52, FKBP51, Cyp40, and a related co-chaperone PP5 were much higher in prostate cancer cells lines [(LNCaP), PC-3, and DU145] compared with primary prostate cells, and that the AR of LNCaP cells can interact with Cyp40. In the absence of androgen, CsA caused inhibition of cell growth in the AR-positive LNCaP and AR-negative PC-3 and DU145 cell lines. Interestingly, FK506 only inhibited LNCaP cells, suggesting a dependence on the AR for this effect. Both CsA and FK506 inhibited growth without inducing apoptosis. In LNCaP cells, CsA completely blocked androgen-stimulated growth, whereas FK506 was partially effective. Further studies in LNCaP cells revealed that CsA and FK506 were able to block or attenuate several stages of AR signaling, including hormone binding, nuclear translocation, and activity at several AR-responsive reporter and endogenous genes. These findings provide the first evidence that CsA and FK506 can negatively modulate proliferation of prostate cells in vitro. Immunophilins may now serve as new targets to disrupt AR-mediated prostate cancer growth.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Androgens / metabolism
  • Androgens / pharmacology
  • Biological Transport / drug effects
  • Cell Division / drug effects
  • Cell Line, Tumor
  • Cell Nucleus / metabolism
  • Cyclophilins / metabolism
  • Cyclosporine / metabolism
  • Cyclosporine / pharmacology*
  • Dihydrotestosterone / pharmacology
  • Humans
  • Immunophilins / metabolism*
  • Ligands
  • Male
  • Nuclear Proteins / metabolism
  • Peptidyl-Prolyl Isomerase F
  • Phosphoprotein Phosphatases / metabolism
  • Prostatic Neoplasms / metabolism*
  • Prostatic Neoplasms / pathology*
  • Receptors, Androgen / genetics
  • Receptors, Androgen / metabolism*
  • Tacrolimus / metabolism
  • Tacrolimus / pharmacology*
  • Tacrolimus Binding Proteins / metabolism
  • Transcription, Genetic / drug effects


  • Androgens
  • Peptidyl-Prolyl Isomerase F
  • Ligands
  • Nuclear Proteins
  • PPIF protein, mouse
  • Receptors, Androgen
  • Dihydrotestosterone
  • Cyclosporine
  • Phosphoprotein Phosphatases
  • protein phosphatase 5
  • Cyclophilins
  • Tacrolimus Binding Proteins
  • tacrolimus binding protein 4
  • Immunophilins
  • tacrolimus binding protein 5
  • Tacrolimus