Development of High-Throughput Screening Assays for Inhibitors of ETS Transcription Factors.
Simon L CurrieSteven L WarnerHariprasad VankayalapatiXiaohui LiuSunil SharmaDavid J BearssBarbara J GravesPublished in: SLAS discovery : advancing life sciences R & D (2018)
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.
Keyphrases
- transcription factor
- high throughput
- dna binding
- prostate cancer
- acute lymphoblastic leukemia
- single cell
- radical prostatectomy
- induced apoptosis
- genome wide identification
- benign prostatic hyperplasia
- single molecule
- cell cycle arrest
- randomized controlled trial
- study protocol
- mass spectrometry
- oxidative stress
- capillary electrophoresis