Discovery of niclosamide as a p300/transcription factor protein–protein interaction inhibitor
Protein-protein interactions (PPIs) are crucial in various biological processes and are attractive targets for drug discovery. In this study, we identified niclosamide (9) as a novel inhibitor of the hypoxia-inducible factor 1α (HIF-1α)/p300 PPI from the RIKEN NPDepo compound library using a fluorescence anisotropy-based screening method. We synthesized niclosamide azide (10) as a photoaffinity labelling probe to identify the p300 binding site of compound 9 and elucidated the binding mode using photoaffinity labelling experiments and molecular docking simulations. Furthermore, we demonstrated that compound 9 inhibited not only HIF-1α/p300 PPI but also p300-transcription factor PPIs, including interaction with p53 and STAT3, thereby suppressing the expression of BAX and c-MYC, respectively.
Authors
- Kazuki Miura (ORCID: https://orcid.org/0000-0003-4514-6305)
- Satoshi Okada (ORCID: https://orcid.org/0000-0002-6601-5710)
- Hiroyuki Osada
- Hiroyuki Nakamura (ORCID: https://orcid.org/0000-0002-4511-2984)
- Hiroyuki Hirano (ORCID: https://orcid.org/0000-0002-0761-5548)
- Dhina Fitriastuti
Institutions
- Tokyo Institute of Technology (JP)
- RIKEN Center for Sustainable Resource Science (JP)
- Microbial Chemistry Research Foundation (JP)
Publication Details
- Journal
- Bioorganic & Medicinal Chemistry
- Published
- 2025-02-15
- DOI
- https://doi.org/10.1016/j.bmc.2025.118114
- Primary Topic
- Cancer, Hypoxia, and Metabolism
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Nagase Science Technology Foundation