Unknown

Dataset Information

0

Small-molecule inhibitor targeting orphan nuclear receptor COUP-TFII for prostate cancer treatment.


ABSTRACT: The orphan nuclear receptor COUP-TFII is expressed at a low level in adult tissues, but its expression is increased and shown to promote progression of multiple diseases, including prostate cancer, heart failure, and muscular dystrophy. Suppression of COUP-TFII slows disease progression, making it an intriguing therapeutic target. Here, we identified a potent and specific COUP-TFII inhibitor through high-throughput screening. The inhibitor specifically suppressed COUP-TFII activity to regulate its target genes. Mechanistically, the inhibitor directly bound to the COUP-TFII ligand-binding domain and disrupted COUP-TFII interaction with transcription regulators, including FOXA1, thus repressing COUP-TFII activity on target gene regulation. Through blocking COUP-TFII's oncogenic activity in prostate cancer, the inhibitor efficiently exerted a potent antitumor effect in xenograft mouse models and patient-derived xenograft models. Our study identified a potent and specific COUP-TFII inhibitor that may be useful for the treatment of prostate cancer and possibly other diseases.

SUBMITTER: Wang L 

PROVIDER: S-EPMC7190335 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

altmetric image

Publications


The orphan nuclear receptor COUP-TFII is expressed at a low level in adult tissues, but its expression is increased and shown to promote progression of multiple diseases, including prostate cancer, heart failure, and muscular dystrophy. Suppression of COUP-TFII slows disease progression, making it an intriguing therapeutic target. Here, we identified a potent and specific COUP-TFII inhibitor through high-throughput screening. The inhibitor specifically suppressed COUP-TFII activity to regulate i  ...[more]

Similar Datasets

| S-EPMC2535662 | biostudies-literature
| S-EPMC4571324 | biostudies-other
2021-04-27 | PXD024035 | Pride
| S-EPMC5466650 | biostudies-literature
| S-EPMC231058 | biostudies-other
2020-05-12 | GSE142475 | GEO
| S-EPMC4022346 | biostudies-literature