4.7 Review

Androgen receptor: structure, role in prostate cancer and drug discovery

Journal

ACTA PHARMACOLOGICA SINICA
Volume 36, Issue 1, Pages 3-23

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/aps.2014.18

Keywords

androgen; androgen receptor; prostate cancer; nuclear receptor; drug discovery; rational drug design; structural biology; castration resistance; antiandrogen

Funding

  1. Singapore National Medical Research Council [R-174-000-137-275]
  2. Jay and Betty Van Andel Foundation
  3. Amway (China) Limited
  4. National Institutes of Health [5R01DK071662-08, GM102545, GM104212]
  5. NUS Graduate School for Integrative Sciences Engineering
  6. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK071662] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM104212, R01GM102545] Funding Source: NIH RePORTER

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Androgens and androgen receptors (AR) play a pivotal role in expression of the male phenotype. Several diseases, such as androgen insensitivity syndrome (AIS) and prostate cancer, are associated with alterations in AR functions. Indeed, androgen blockade by drugs that prevent the production of androgens and/or block the action of the AR inhibits prostate cancer growth. However, resistance to these drugs often occurs after 2-3 years as the patients develop castration-resistant prostate cancer (CRPC). In CRPC, a functional AR remains a key regulator. Early studies focused on the functional domains of the AR and its crucial role in the pathology. The elucidation of the structures of the AR DNA binding domain (DBD) and ligand binding domain (LBD) provides a new framework for understanding the functions of this receptor and leads to the development of rational drug design for the treatment of prostate cancer. An overview of androgen receptor structure and activity, its actions in prostate cancer, and how structural information and high-throughput screening have been or can be used for drug discovery are provided herein.

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