Oliveira Rita I, Guedes Romina A, Salvador Jorge A R
Laboratory of Pharmaceutical Chemistry, Faculty of Pharmacy, University of Coimbra, Coimbra, Portugal.
Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal.
Front Chem. 2022 Sep 15;10:1005727. doi: 10.3389/fchem.2022.1005727. eCollection 2022.
Ubiquitin-specific protease 7 (USP7) is a member of one of the most largely studied families of deubiquitylating enzymes. It plays a key role modulating the levels of multiple proteins, including tumor suppressors, transcription factors, epigenetic modulators, DNA repair proteins, and regulators of the immune response. The abnormal expression of USP7 is found in various malignant tumors and a high expression signature generally indicates poor tumor prognosis. This suggests USP7 as a promising prognostic and druggable target for cancer therapy. Nonetheless, no approved drugs targeting USP7 have already entered clinical trials. Therefore, the development of potent and selective USP7 inhibitors still requires intensive research and development efforts before the pre-clinical benefits translate into the clinic. This mini review systematically summarizes the role of USP7 as a drug target for cancer therapeutics, as well as the scaffolds, activities, and binding modes of some of the most representative small molecule USP7 inhibitors reported in the scientific literature. To wind up, development challenges and potential combination therapies using USP7 inhibitors for less tractable tumors are also disclosed.
泛素特异性蛋白酶7(USP7)是研究最为广泛的去泛素化酶家族之一的成员。它在调节多种蛋白质水平方面发挥关键作用,这些蛋白质包括肿瘤抑制因子、转录因子、表观遗传调节剂、DNA修复蛋白以及免疫反应调节因子。在各种恶性肿瘤中均发现USP7表达异常,高表达特征通常预示着肿瘤预后不良。这表明USP7是一种有前景的癌症治疗预后和可成药靶点。尽管如此,尚无已获批的靶向USP7的药物进入临床试验。因此,在临床前研究成果转化为临床应用之前,开发强效且选择性的USP7抑制剂仍需要大量的研发工作。本综述系统总结了USP7作为癌症治疗药物靶点的作用,以及科学文献中报道的一些最具代表性的小分子USP7抑制剂的骨架、活性和结合模式。最后,还揭示了开发挑战以及使用USP7抑制剂治疗难治性肿瘤的潜在联合疗法。