Kim Soon-Bin, Hwang Soonjae, Cha Ji-Young, Lee Ho-Jae
Department of Health Sciences and Technology, GAIHST, Gachon University, Incheon 21999, Republic of Korea.
Department of Biochemistry, Lee Gil Ya Cancer and Diabetes Institute, College of Medicine, Gachon University, Incheon 21999, Republic of Korea.
Int J Mol Sci. 2024 Mar 3;25(5):2939. doi: 10.3390/ijms25052939.
Programmed death ligand 1 (PD-L1) plays a pivotal role in cancer immune evasion and is a critical target for cancer immunotherapy. This review focuses on the regulation of PD-L1 through the dynamic processes of ubiquitination and deubiquitination, which are crucial for its stability and function. Here, we explored the intricate mechanisms involving various E3 ubiquitin ligases and deubiquitinating enzymes (DUBs) that modulate PD-L1 expression in cancer cells. Specific ligases are discussed in detail, highlighting their roles in tagging PD-L1 for degradation. Furthermore, we discuss the actions of DUBs that stabilize PD-L1 by removing ubiquitin chains. The interplay of these enzymes not only dictates PD-L1 levels but also influences cancer progression and patient response to immunotherapies. Furthermore, we discuss the therapeutic implications of targeting these regulatory pathways and propose novel strategies to enhance the efficacy of PD-L1/PD-1-based therapies. Our review underscores the complexity of PD-L1 regulation and its significant impact on the tumor microenvironment and immunotherapy outcomes.
程序性死亡配体1(PD-L1)在癌症免疫逃逸中起关键作用,是癌症免疫治疗的关键靶点。本综述聚焦于通过泛素化和去泛素化的动态过程对PD-L1的调控,这对其稳定性和功能至关重要。在此,我们探讨了涉及各种E3泛素连接酶和去泛素化酶(DUBs)的复杂机制,这些机制调节癌细胞中PD-L1的表达。详细讨论了特定的连接酶,强调了它们在标记PD-L1进行降解中的作用。此外,我们讨论了通过去除泛素链来稳定PD-L1的DUBs的作用。这些酶的相互作用不仅决定了PD-L1的水平,还影响癌症进展和患者对免疫治疗的反应。此外,我们讨论了靶向这些调节途径的治疗意义,并提出了增强基于PD-L1/PD-1疗法疗效的新策略。我们的综述强调了PD-L1调控的复杂性及其对肿瘤微环境和免疫治疗结果的重大影响。