Bromodomain and extraterminal (BET) proteins: biological functions, diseases and targeted therapy

BET proteins, which influence gene expression and contribute to the development of cancer, are epigenetic interpreters. Thus, BET inhibitors represent a novel form of epigenetic anticancer treatment. Although preliminary clinical trials have shown the anticancer potential of BET inhibitors, it appea...

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Veröffentlicht in:Signal transduction and targeted therapy 2023-11, Vol.8 (1), p.420-26, Article 420
Hauptverfasser: Wang, Zhi-Qiang, Zhang, Zhao-Cong, Wu, Yu-Yang, Pi, Ya-Nan, Lou, Sheng-Han, Liu, Tian-Bo, Lou, Ge, Yang, Chang
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Sprache:eng
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Zusammenfassung:BET proteins, which influence gene expression and contribute to the development of cancer, are epigenetic interpreters. Thus, BET inhibitors represent a novel form of epigenetic anticancer treatment. Although preliminary clinical trials have shown the anticancer potential of BET inhibitors, it appears that these drugs have limited effectiveness when used alone. Therefore, given the limited monotherapeutic activity of BET inhibitors, their use in combination with other drugs warrants attention, including the meaningful variations in pharmacodynamic activity among chosen drug combinations. In this paper, we review the function of BET proteins, the preclinical justification for BET protein targeting in cancer, recent advances in small-molecule BET inhibitors, and preliminary clinical trial findings. We elucidate BET inhibitor resistance mechanisms, shed light on the associated adverse events, investigate the potential of combining these inhibitors with diverse therapeutic agents, present a comprehensive compilation of synergistic treatments involving BET inhibitors, and provide an outlook on their future prospects as potent antitumor agents. We conclude by suggesting that combining BET inhibitors with other anticancer drugs and innovative next-generation agents holds great potential for advancing the effective targeting of BET proteins as a promising anticancer strategy.
ISSN:2059-3635
2095-9907
2059-3635
DOI:10.1038/s41392-023-01647-6