Novel strategies targeting bromodomain-containing protein 4 (BRD4) for cancer drug discovery
As epigenetic readers of the histone code, BRD4 is the most extensively and thoroughly studied member of BET family, which plays a critical role in many human diseases including cancer, inflammation, HIV infections, CNS disorders, and cardiovascular diseases and has been proved to be a promising the...
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Veröffentlicht in: | European journal of medicinal chemistry 2020-08, Vol.200, p.112426, Article 112426 |
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Sprache: | eng |
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Zusammenfassung: | As epigenetic readers of the histone code, BRD4 is the most extensively and thoroughly studied member of BET family, which plays a critical role in many human diseases including cancer, inflammation, HIV infections, CNS disorders, and cardiovascular diseases and has been proved to be a promising therapeutic target for these diseases. To date, many small-molecule BRD4 inhibitors have been discovered, and some of them are in clinical trials for the treatment of different diseases. Due to the lack of selectivity of these small molecules for BRD4 BD1, BRD4 BD2 and/or other BET proteins, they exert some toxic side effects, including dizziness, nausea, and vomit. Now, novel strategies are urgent needed to improve the selectivity and reduce the side effects of current BRD4 inhibitors. Herein, in this article, we made a summary of the recent development of novel strategies targeting BRD4. Opportunities for these strategies to achieve selective and efficacious BRD4 inhibitors for treating human diseases are also highlighted.
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•BRD4 plays an important role in cell cycle control and can affect the processes of cell proliferation, apoptosis and transcription.•Inhibition of BRD4 has been shown to have potential therapeutic applications, making it a promising drug target.•This review introduced three novel strategies targeting BRD4 for cancer drug discovery and summarized the compounds involved in them.. |
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ISSN: | 0223-5234 1768-3254 |
DOI: | 10.1016/j.ejmech.2020.112426 |