Anti-Tumor Potential of Post-Translational Modifications of PD-1

被引:2
|
作者
Xi, Xiaoming [1 ]
Zhao, Wuli [1 ]
机构
[1] Chinese Acad Med Sci, Inst Med Biotechnol, State Key Lab Resp Hlth & Multimorbid, Sch Basic Med,Peking Union Med Coll, Beijing 100005, Peoples R China
关键词
PD-1; immunotherapy; post-translational modification; ubiquitin-proteasome system; glycosylation; phosphorylation; palmitoylation; T-CELL-ACTIVATION; TUMOR-CELLS; GLYCOSYLATION; EXPRESSION; BINDING; INHIBITOR; PALMITOYLATION; COORDINATION; RECEPTORS; IMMUNITY;
D O I
10.3390/cimb46030136
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Programmed cell death protein-1 (PD-1) is a vital immune checkpoint molecule. The location, stability, and protein-protein interaction of PD-1 are significantly influenced by post-translational modification (PTM) of proteins. The biological information of PD-1, including its gene and protein structures and the PD-1/PD-L1 signaling pathway, was briefly reviewed in this review. Additionally, recent research on PD-1 post-translational modification, including the study of ubiquitination, glycosylation, phosphorylation, and palmitoylation, was summarized, and research strategies for PD-1 PTM drugs were concluded. At present, only a part of PD-1/PD-L1 treated patients (35-45%) are benefited from immunotherapies, and novel strategies targeting PTM of PD-1/PD-L1 may be important for anti-PD-1/PD-L1 non-responders (poor responders).
引用
收藏
页码:2119 / 2132
页数:14
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