Institute of Chinese Medical Sciences, State Key Laboratory of Quality Research in Chinese Medicine, University of Macau, Macao, SAR, China.
Department of Chemistry, Hong Kong Baptist University, Kowloon, 999077, Hong Kong, China.
J Hematol Oncol. 2020 Mar 30;13(1):26. doi: 10.1186/s13045-020-00850-0.
Protein-protein interactions (PPIs) are central to a variety of biological processes, and their dysfunction is implicated in the pathogenesis of a range of human diseases, including cancer. Hence, the inhibition of PPIs has attracted significant attention in drug discovery. Covalent inhibitors have been reported to achieve high efficiency through forming covalent bonds with cysteine or other nucleophilic residues in the target protein. Evidence suggests that there is a reduced risk for the development of drug resistance against covalent drugs, which is a major challenge in areas such as oncology and infectious diseases. Recent improvements in structural biology and chemical reactivity have enabled the design and development of potent and selective covalent PPI inhibitors. In this review, we will highlight the design and development of therapeutic agents targeting PPIs for cancer therapy.
蛋白质-蛋白质相互作用(PPIs)是多种生物过程的核心,其功能障碍与一系列人类疾病的发病机制有关,包括癌症。因此,PPIs 的抑制在药物发现中引起了广泛关注。已报道共价抑制剂通过与靶蛋白中的半胱氨酸或其他亲核残基形成共价键来实现高效性。有证据表明,针对共价药物的耐药性发展风险降低,这是肿瘤学和传染病等领域的主要挑战。结构生物学和化学反应性的最新进展使得设计和开发有效且选择性的共价 PPI 抑制剂成为可能。在这篇综述中,我们将重点介绍针对癌症治疗的靶向 PPI 的治疗剂的设计和开发。