Role of 5α-reductase inhibitors in benign prostatic diseases

@article{Azzouni2012RoleO5,
  title={Role of 5$\alpha$-reductase inhibitors in benign prostatic diseases},
  author={Faris Azzouni and James L. Mohler},
  journal={Prostate Cancer and Prostatic Diseases},
  year={2012},
  volume={15},
  pages={222-230}
}
  • F. AzzouniJ. Mohler
  • Published 1 September 2012
  • Biology, Medicine
  • Prostate Cancer and Prostatic Diseases
Testosterone is the most abundant androgen in serum. Intracellularly, testosterone is converted to dihydrotestosterone, the preferred ligand for androgen receptor transactivation, by the enzyme 5α-reductase. Three 5α-reductase isozymes have been discovered and they are expressed ubiquitously in human tissues. Testosterone and dihydrotestosterone have different but complimentary functions. Dihydrotestosterone has 2–5 times higher binding affinity for the androgen receptor than testosterone, and… 

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