Wang Luhong, Zhang Yong, Yu Tao, Wu Huijian
Cancer Hospital Affiliated to Dalian University of Technology, Shenyang 110042, China.
Dalian Key Laboratory of Protein Modification and Disease, Faculty of Medicine, School of Biological Engineering, Dalian University of Technology, Dalian 116024, China.
Biomedicines. 2024 Nov 29;12(12):2734. doi: 10.3390/biomedicines12122734.
Deubiquitinating enzymes are a class of proteases that remove ubiquitin tags from proteins, thereby controlling protein stability and function. Tumor inflammation arises from interactions between tumor cells and their microenvironment, which trigger an inflammatory response. The deubiquitinating enzyme USP7 plays a central role in this process. Research suggests that USP7 may modulate various signaling pathways related to inflammatory responses through its deubiquitinating activity, thereby influencing tumor development and progression, including regulating T cell immune activity, improving macrophage anti-tumor activity, and regulating NF-κB signal pathways. Overall, describing the role and mechanism of USP7 in the tumor inflammatory response is of great importance for elucidating the regulatory mechanism of tumor inflammation and developing new therapeutic strategies. This article mainly reviews the structure, function, role, and mechanism of USP7 in the tumor inflammation response.
去泛素化酶是一类蛋白酶,可从蛋白质上去除泛素标签,从而控制蛋白质的稳定性和功能。肿瘤炎症源于肿瘤细胞与其微环境之间的相互作用,这种相互作用会引发炎症反应。去泛素化酶USP7在这一过程中起核心作用。研究表明,USP7可能通过其去泛素化活性调节与炎症反应相关的各种信号通路,从而影响肿瘤的发生发展,包括调节T细胞免疫活性、提高巨噬细胞的抗肿瘤活性以及调节NF-κB信号通路。总体而言,阐述USP7在肿瘤炎症反应中的作用和机制对于阐明肿瘤炎症的调控机制以及开发新的治疗策略具有重要意义。本文主要综述USP7在肿瘤炎症反应中的结构、功能、作用及机制。