Post-translational regulations of PD-L1 and PD-1: Mechanisms and opportunities for combined immunotherapy

被引:48
|
作者
Dai, Xiaoming [1 ]
Gao, Yang [1 ,2 ]
Wei, Wenyi [1 ,3 ]
机构
[1] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02115 USA
[2] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Urol, Xian 710061, Peoples R China
[3] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Dept Pathol, 330 Brookline Ave, Boston, MA 02215 USA
关键词
PD-L1; Immunotherapy; Post -translational modification; Ubiquitination; PROTAC; Glycosylation; Phosphorylation; Acetylation; Palmitoylation; IMMUNE-CHECKPOINT BLOCKADE; ANTITUMOR IMMUNITY; CANCER; EXPRESSION; PROTEINS; SURFACE; PALMITOYLATION; UBIQUITINATION; DEGRADATION; RESISTANCE;
D O I
10.1016/j.semcancer.2021.04.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Antibodies targeting programmed cell death protein 1 (PD-1) or its ligand programmed death-ligand 1 (PD-L1) are profoundly changing the methods to treat cancers with long-term clinical benefits. Unlike conventional methods that directly target tumor cells, PD-1/PD-L1 blockade exerts anti-tumor effects largely through reactivating or normalizing cytotoxic T lymphocyte in the tumor microenvironment to combat cancer cells. However, only a small fraction of cancer patients responds well to PD-1/PD-L1 blockade and clinical outcomes have reached a bottleneck without substantial advances. Therefore, better understanding the molecular mechanisms underlying how PD-1/PD-L1 expression is regulated will provide new insights to improve the efficacy of current anti-PD-1/PD-L1 therapy. Here, we provide an update of current progress of PD-L1 and PD-1 post-translational regulations and highlight the mechanism-based combination therapy strategies for a better treatment of human cancer.
引用
收藏
页码:246 / 252
页数:7
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