Guangdong Key Laboratory of Chiral Molecule and Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou 510006, China.
J Med Chem. 2021 Jun 24;64(12):7900-7925. doi: 10.1021/acs.jmedchem.0c02055. Epub 2021 Feb 18.
Epigenetic regulation of gene expression plays a critical role in various physiological processes, and epigenetic dysregulation is implicated in a number of diseases, prominently including cancer. Epigenetic regulators have been validated as potential therapeutic targets, and significant progress has been made in the discovery and development of epigenetic-based inhibitors. However, successful epigenetic drug discovery is still facing challenges, including moderate selectivity, limited efficacy, and acquired drug resistance. Inspired by the advantages of covalent small-molecule inhibitors, targeted covalent inhibition has attracted increasing interest in epigenetic drug discovery. In this review, we comprehensively summarize the structure-based design and characterization of covalent inhibitors targeting epigenetic writers, readers, and erasers and highlight their potential benefits in enhancing selectivity across the enzyme family and improving in vivo efficacy. We also discuss the challenges and opportunities of covalent small-molecule inhibitors and hope to shed light on future epigenetic drug discovery.
基因表达的表观遗传调控在各种生理过程中起着关键作用,表观遗传失调与许多疾病有关,尤其是癌症。表观遗传调节剂已被验证为潜在的治疗靶点,并且在发现和开发基于表观遗传的抑制剂方面取得了重大进展。然而,成功的表观遗传药物发现仍然面临挑战,包括中等选择性、有限的疗效和获得性药物耐药性。受共价小分子抑制剂优势的启发,靶向共价抑制在表观遗传药物发现中引起了越来越多的关注。在这篇综述中,我们全面总结了针对表观遗传写入器、读取器和擦除器的共价抑制剂的基于结构的设计和表征,并强调了它们在提高酶家族选择性和改善体内疗效方面的潜在益处。我们还讨论了共价小分子抑制剂的挑战和机遇,并希望为未来的表观遗传药物发现提供一些启示。