Cellular androgen content influences enzalutamide agonism of F877L mutant androgen receptor

Daniel J. Coleman, Kathryn Van Hook, Carly J. King, Jacob Schwartzman, Robert Lisac, Joshua Urrutia, Archana Sehrawat, Josha Woodward, Nicholas Wang, Roman Gulati, George V. Thomas, Tomasz M. Beer, Martin Gleave, James E. Korkola, Lina Gao, Laura M. Heiser, Joshi Alumkal

Research output: Contribution to journalArticlepeer-review

11 Scopus citations


Prostate cancer is the most commonly diagnosed and second-most lethal cancer among men in the United States. The vast majority of prostate cancer deaths are due to castration-resistant prostate cancer (CRPC) - the lethal form of the disease that has progressed despite therapies that interfere with activation of androgen receptor (AR) signaling. One emergent resistance mechanism to medical castration is synthesis of intratumoral androgens that activate the AR. This insight led to the development of the AR antagonist enzalutamide. However, resistance to enzalutamide invariably develops, and disease progression is nearly universal. One mechanism of resistance to enzalutamide is an F877L mutation in the AR ligand-binding domain that can convert enzalutamide to an agonist of AR activity. However, mechanisms that contribute to the agonist switch had not been fully clarified, and there were no therapies to block AR F877L. Using cell line models of castration-resistant prostate cancer (CRPC), we determined that cellular androgen content influences enzalutamide agonism of mutant F877L AR. Further, enzalutamide treatment of AR F877L-expressing cell lines recapitulated the effects of androgen activation of F877L AR or wild-type AR. Because the BET bromodomain inhibitor JQ-1 was previously shown to block androgen activation of wild-type AR, we tested JQ-1 in AR F877L-expressing CRPC models. We determined that JQ-1 suppressed androgen or enzalutamide activation of mutant F877L AR and suppressed growth of mutant F877L AR CRPC tumors in vivo, demonstrating a new strategy to treat tumors harboring this mutation.

Original languageEnglish (US)
Pages (from-to)40690
Number of pages1
Issue number26
StatePublished - 2016


  • Androgen receptor mutations
  • BET bromodomain inhibition
  • Genitourinary cancers: Rostate
  • Hormone signaling and inhibitors
  • Regulation of gene expression in drug resistance

ASJC Scopus subject areas

  • Oncology


Dive into the research topics of 'Cellular androgen content influences enzalutamide agonism of F877L mutant androgen receptor'. Together they form a unique fingerprint.

Cite this