Development of High-Throughput Screening Assays for Inhibitors of ETS Transcription Factors

SLAS Discov. 2019 Jan;24(1):77-85. doi: 10.1177/2472555218798571. Epub 2018 Sep 11.

Abstract

ETS transcription factors from the ERG and ETV1/4/5 subfamilies are overexpressed in the majority of prostate cancer patients and contribute to disease progression. Here, we have developed two in vitro assays for the interaction of ETS transcription factors with DNA that are amenable to high-throughput screening. Using ETS1 as a model, we applied these assays to screen 110 compounds derived from a high-throughput virtual screen. We found that the use of lower-affinity DNA binding sequences, similar to those that ERG and ETV1 bind to in prostate cells, allowed for higher inhibition from many of these test compounds. Further pilot experiments demonstrated that the in vitro assays are robust for ERG, ETV1, and ETV5, three of the ETS transcription factors that are overexpressed in prostate cancer.

Keywords: Alphascreen; ETS transcription factors; fluorescence polarization (FP); prostate cancer.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • DNA-Binding Proteins / genetics
  • High-Throughput Screening Assays / methods*
  • Humans
  • Male
  • Prostate / metabolism
  • Prostatic Neoplasms / genetics
  • Proto-Oncogene Proteins c-ets / genetics*
  • Transcriptional Regulator ERG / genetics

Substances

  • DNA-Binding Proteins
  • Proto-Oncogene Proteins c-ets
  • Transcriptional Regulator ERG