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Small Molecules as PD-1/PD-L1 Pathway Modulators for Cancer Immunotherapy
被引:28
|作者:
Jiao, Peifu
[1
]
Geng, Qiaohong
[1
]
Jin, Peng
[1
]
Su, Gaoxing
[3
]
Teng, Houyun
[1
]
Dong, Jinlong
[4
]
Yan, Bing
[2
]
机构:
[1] Qilu Normal Univ, Dept Chem, Jinan 250013, Shandong, Peoples R China
[2] Shandong Univ, Sch Environm Sci & Engn, Jinan 250100, Shandong, Peoples R China
[3] Nantong Univ, Sch Pharm, Nantong, Jiangsu 226001, Peoples R China
[4] Jinan Taorui Pharma & Tech Co Ltd, Jinan 250101, Shandong, Peoples R China
关键词:
Immune checkpoint modulators;
sulfonamides;
thiadiazoles;
oxadiazoles;
biphenyl derivatives;
molecular docking;
MONOCLONAL-ANTIBODIES;
PD-1;
EXPRESSION;
B7;
FAMILY;
BLOCKADE;
B7-H1;
INHIBITORS;
MEMBER;
RESISTANCE;
RECEPTOR;
LIGAND;
D O I:
10.2174/1381612824666181112114958
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Blockade of PD-1/PD-L1 interactions using PD-1/PD-L1 pathway modulators has shown unprecedented clinical efficacy in various cancer models. Current PD-1/PD-L1 modulators approved by FDA are exclusively dominated by therapeutic antibodies. Nevertheless, therapeutic antibodies also exhibit several disadvantages such as low tumor penetration, difficulty in crossing physiological barriers, lacking oral bioavailability, high manufacturing costs, inaccessible to intracellular targets, immunogenicity, immune-related adverse events (irAEs). Modulation of PD-1/PD-L1 pathway using small molecules may be an alternative approach to mobilize immune system to fight against cancers. In this review, we focus on summarizing the recently disclosed chemical structures and preliminary structure-activity relationships (SARs) of small molecules as PD-1/PD-L1 modulators for cancer immunotherapy.
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页码:4911 / 4920
页数:10
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