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.

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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

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article

Discovery of niclosamide as a p300/transcription factor protein–protein interaction inhibitor

Kazuki Miura, Satoshi Okada, Hiroyuki Osada, Hiroyuki Nakamura et al.
Bioorganic & Medicinal Chemistry
Cancer, Hypoxia, and Metabolism
article

Discovery of niclosamide as a p300/transcription factor protein–protein interaction inhibitor

Kazuki Miura, Satoshi Okada, Hiroyuki Osada, Hiroyuki Nakamura, Hiroyuki Hirano, Dhina Fitriastuti
article en

Abstract

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.

Bioorganic & Medicinal ChemistryVol. 121
Tokyo Institute of Technology (JP), RIKEN Center for Sustainable Resource Science (JP), Microbial Chemistry Research Foundation (JP)
Nagase Science Technology Foundation
Openalex Percentile: Top 97%
Cancer, Hypoxia, and Metabolism
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