Technology ID

Compounds that Interfere with the Androgen Receptor Complex

Lead Inventor
Neckers, Leonard (NCI)
Trepel Neckers, Jane (NCI)
Kim, Yeong (NCI)
Iwai, Aki (NCI)
Ning, Yangmin (FDA)
Cox, Marc (University of Texas, El Paso)
De Leon, Johanny Meneses (University of Texas, El Paso)
Balsiger, Heather (University of Texas, El Paso)
Fletterick, Robert (University of California, San Francisco (UCSF))
Therapeutic Areas
Development Stages
Pre-clinical (in vivo)
Lead IC

Investigators at the National Institutes of Health (NIH) have discovered compounds that have potential as novel anti-androgen therapeutics. The immunophilin protein FKBP52 is part of a protein complex that helps fold the androgen receptor (AR) protein, a target for treating prostate cancer, and enhances its activity. Disruption of the FKPB52-AR interaction greatly reduces the activity of the AR. With the goal of finding potential therapeutic compounds that inhibit the FKBP52-mediated activation of AR, several small molecules were tested and found to be antagonists of FKBP52 and to inhibit AR activity in prostate cells. These compounds can serve as therapeutics for the treatment of prostate cancer and benign prostate enlargement. Moreover, FKBP52 is also implicated in the regulation of other hormone receptors so these compounds could be used to treat other hormone-dependent diseases such as diabetes or even used as contraceptives.

One of the standard treatments for prostate cancer makes use of anti-androgens, like bicalutamide, which compete for binding with the natural male hormones to AR and inhibit their proliferative activity. The problem with available anti-androgen drugs is that prostate tumors eventually become drug resistant resulting in so-called androgen-resistant prostate cancer. One cause of this is an increase in the levels of AR produced by the prostate cancer cells. A solution to this problem may lie in disrupting the protein folding of AR by interfering with its interaction with FKBP52 using these compounds.

The Center for Cancer Research, Urologic Oncology Branch, seeks parties to co-develop, or license antagonists of FKBP52-dependent remodeling of the androgen receptor. 

Competitive Advantages:

  • The compounds do not compete with androgens and specifically inhibit FKBP52-enhanced AR function
  • Potential for synergistic use with conventional anti-androgens for treatment of androgen resistant prostate cancer

Commercial Applications:

  • Use of the compounds for treatment of prostate cancer and benign prostate enlargement
  • Use of the compounds in treating insulin-independent diabetes
  • Use of the compounds as male or female contraceptives
  • Use in screening for compounds that inhibit of FKBP52-enhanced AR activity
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