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The effect of chemotherapy on programmed cell death 1/programmed cell death 1 ligand axis: some chemotherapeutical drugs may finally work through immune response
被引:46
|作者:
Luo, Min
[1
]
Fu, Liwu
[1
]
机构:
[1] Sun Yat Sen Univ, Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China, Guangdong Esophageal Canc Inst,Canc Ctr, Guangzhou 510275, Guangdong, Peoples R China
来源:
关键词:
programmed cell death 1;
programmed cell death 1 ligand;
chemotherapy;
immunotherapy;
REGULATORY T-CELLS;
PD-L1 SURFACE EXPRESSION;
BREAST-CANCER CELLS;
B7-H1;
EXPRESSION;
ANTI-PD-L1;
ANTIBODY;
PDL1;
UP-REGULATION;
RESTORES T;
BLOCKADE;
SAFETY;
D O I:
10.18632/oncotarget.7631
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Most tumors are immunogenic which would trigger some immune response. Chemotherapy also has immune potentiating mechanisms of action. But it is unknown whether the immune response is associated with the efficacy of chemotherapy and the development of chemoresistance. Recently, there is a growing interest in immunotherapy, among which the co-inhibitory molecules, programmed cell death 1/programmed cell death 1 ligand (PD-1/PD-L1) leads to immune evasion. Since some reports showed that conventional chemotherapeutics can induce the expression of PD-L1, we try to summarize the effect of chemotherapy on PD-1/PD-L1 axis and some potential molecules relevant to PD-1/PD-L1 in chemoresistance in this review.
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页码:29794 / 29803
页数:10
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