Development of the Inhibitors That Target the PD-1/PD-L1 InteractionA Brief Look at Progress on Small Molecules, Peptides and Macrocycles

被引:131
作者
Guzik, Katarzyna [1 ]
Tomala, Marcin [1 ]
Muszak, Damian [1 ]
Konieczny, Magdalena [1 ]
Hec, Aleksandra [2 ]
Blaszkiewicz, Urszula [2 ]
Pustula, Marcin [1 ]
Butera, Roberto [3 ]
Doemling, Alexander [3 ]
Holak, Tad A. [1 ]
机构
[1] Jagiellonian Univ, Fac Chem, Gronostajowa 2, PL-30387 Krakow, Poland
[2] Recepton Sp Zoo, Michala Bobrzynskiego 14, PL-30348 Krakow, Poland
[3] Univ Groningen, Dept Drug Design, A Deusinglaan 9, NL-9713 AV Groningen, Netherlands
基金
欧盟地平线“2020”;
关键词
peptide-based and small synthetic molecule inhibitors; lead optimization; scaffold hopping; PD-1; PD-L1; pathway; rational drug design; cancer immunotherapy; cocrystal structures; structure-activity relationship; MONOCLONAL-ANTIBODIES; CHECKPOINT BLOCKADE; PROTEIN; PD-1; EXPRESSION; PATHWAY; SURFACE; B7-H1;
D O I
10.3390/molecules24112071
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
Cancer immunotherapy based on antibodies targeting the immune checkpoint PD-1/PD-L1 pathway has seen unprecedented clinical responses and constitutes the new paradigm in cancer therapy. The antibody-based immunotherapies have several limitations such as high production cost of the antibodies or their long half-life. Small-molecule inhibitors of the PD-1/PD-L1 interaction have been highly anticipated as a promising alternative or complementary therapeutic to the monoclonal antibodies (mAbs). Currently, the field of developing anti-PD-1/PD-L1 small-molecule inhibitors is intensively explored. In this paper, we review anti-PD-1/PD-L1 small-molecule and peptide-based inhibitors and discuss recent structural and preclinical/clinical aspects of their development. Discovery of the therapeutics based on small-molecule inhibitors of the PD-1/PD-L1 interaction represents a promising but challenging perspective in cancer treatment.
引用
收藏
页数:30
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