4.8 Article

CREB5 Promotes Resistance to Androgen-Receptor Antagonists and Androgen Deprivation in Prostate Cancer

Journal

CELL REPORTS
Volume 29, Issue 8, Pages 2355-+

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2019.10.068

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Funding

  1. PCF/SU2C Prostate Cancer Dream Team
  2. PCF -V Foundation Challenge Award
  3. PCF Young Investigator Award
  4. NIH [K08 CA188615]
  5. American Cancer Society -AstraZeneca postdoctoral fellowship [PF-16-142-01-TBE]
  6. Susan G. Komen postdoctoral fellowship
  7. Terri Brodeur postdoctoral fellowship
  8. DoD Prostate Cancer Research Program postdoctoral training award [W81XWH-15-1-0659]
  9. DoD PCRP Physician Research Training Award [W81XWH-12-1-0062]
  10. NCI [U01 CA176058]
  11. H.L. Snyder Foundation

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Androgen-receptor (AR) inhibitors, including enzalutamide, are used for treatment of all metastatic castration-resistant prostate cancers (mCRPCs). However, some patients develop resistance or never respond. We find that the transcription factor CREB5 confers enzalutamide resistance in an open reading frame (ORF) expression screen and in tumor xenografts. CREB5 overexpression is essential for an enzalutamide-resistant patient-derived organoid. In AR-expressing prostate cancer cells, CREB5 interactions enhance AR activity at a subset of promoters and enhancers upon enzalutamide treatment, including MYC and genes involved in the cell cycle. In mCRPC, we found recurrent amplification and overexpression of CREB5. Our observations identify CREB5 as one mechanism that drives resistance to AR antagonists in prostate cancers.

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