4.8 Article

Development of Peptidomimetic Inhibitors of the ERG Gene Fusion Product in Prostate Cancer

Journal

CANCER CELL
Volume 31, Issue 4, Pages 532-+

Publisher

CELL PRESS
DOI: 10.1016/j.ccell.2017.02.017

Keywords

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Funding

  1. Prostate Cancer Foundation Challenge Award
  2. NIH [R01CA132874]
  3. Prostate SPORE [P50CA69568]
  4. Early Detection Research Network [UO1 CA113913]
  5. Department of Defense [PC051081, PC094725]
  6. AACR-Bayer Prostate Cancer Research Fellowship [16-40-44-PITC]
  7. PCF Young Investigator Award
  8. NIH/NCI [R01CA157845, R01CA154980]

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Transcription factors play a key role in the development of diverse cancers, and therapeutically targeting them has remained a challenge. In prostate cancer, the gene encoding the transcription factor ERG is recurrently rearranged and plays a critical role in prostate oncogenesis. Here, we identified a series of peptides that interact specifically with the DNA binding domain of ERG. ERG inhibitory peptides (EIPs) and derived peptidomimetics bound ERG with high affinity and specificity, leading to proteolytic degradation of the ERG protein. The EIPs attenuated ERG-mediated transcription, chromatin recruitment, protein-protein interactions, cell invasion and proliferation, and tumor growth. Thus, peptidomimetic targeting of transcription factor fusion products may provide a promising therapeutic strategy for prostate cancer as well as other malignancies.

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