Insights into non -peptide small-molecule inhibitors of the PD-1/PD-L1 interaction: Development and perspective

被引:13
|
作者
Wu, Xia [1 ]
Meng, Yangyang [1 ]
Liu, Lei [1 ]
Gong, Guowei [3 ]
Zhang, Haotian [2 ]
Hou, Yunlei [1 ]
Liu, Chunyang [1 ]
Wu, Di [1 ]
Qin, Mingze [1 ]
机构
[1] Shenyang Pharmaceut Univ, Key Lab Struct Based Drug Design & Discovery, Minist Educ, Shenyang 110016, Peoples R China
[2] Shenyang Pharmaceut Univ, Dept Pharmacol, Shenyang 110016, Peoples R China
[3] Zunyi Med Univ, Dept Bioengn, Zhuhai Campus, Zhuhai 519041, Peoples R China
关键词
Cancer immunotherapy; The PD-1; PD-L1; blockade; Non-peptide small-molecule inhibitors; Rational drug design; REGULATES PD-L1 EXPRESSION; CANCER-IMMUNOTHERAPY; CHECKPOINT BLOCKADE; IMMUNE CHECKPOINTS; T-CELLS; PROTEIN; LIGANDS; ANTIBODIES; PATHWAY; COMPLEX;
D O I
10.1016/j.bmc.2021.116038
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
The development of immune checkpoint inhibitors has become a research hotspot in cancer immunotherapy in recent years. Anti-PD-1/PD-L1 monoclonal antibodies (mAbs), such as pembrolizumab and nivolumab have been approved for treating different types of cancer. Many peptides, peptidomimetics and non-peptide small-molecule inhibitors targeting the PD-1/PD-L1 axis have been published so far. In comparison with mAbs, small-molecule inhibitors have the potential to overcome inherent shortcomings of mAbs, such as poor oral bioavailability, low tumor penetration, and high manufacturing costs. In this article, we mainly review non-peptide small-molecule inhibitors of the PD-1/PD-L1 interaction, their cocrystal structures, docking studies, and biological activities are also included to guide future study. In addition, we propose several strategies for designing more effective smallmolecule modulators of the PD-1/PD-L1 pathway.
引用
收藏
页数:11
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