PD-L1 表达和 PD-1 检查点通路在癌症中
中文名称
通路描述
程序性细胞死亡 1(PD1)及其配体(PDL1)是关键的生理免疫检查点,通过调节 T 和 B 细胞等其他免疫细胞类型的激活程度来维持机体自我耐受。在实体肿瘤中,PD-1/PD-L1 抑制通路可以通过增加肿瘤细胞表面的 PD-L1 表达而(错误)被用来沉默免疫系统。PD-L1 的上调是由 MAPK 和 PI3K/Akt 促生存通路的激活以及转录因子 HIF-1、STAT3 和 NF-kappa B 引起的。MAPK 和 PI3K 信号通路由基因突变和生长因子激活。肿瘤细胞上的 PD-L1 可能随后与 PD-1 受体结合,导致 T 细胞介导的免疫反应受到抑制。靶向 PD-L1 或 PD-1 的阻断 PD-1/PD-L1 通路的治疗性抗体在挽救 T 细胞抗肿瘤效应方面非常有效。
英文描述
Programmed cell death 1 (PD1) and its ligand (PDL1) are key regulatory physiological immune checkpoints that maintain self-tolerance in the organism by regulating the degree of activation of T and B cells amongst other immune cell types. In solid tumors, the PD-1/PD-L1 inhibitory pathway can be (mis-)used to silence the immune system by increasing the expression of PD-L1 on the tumor cell surface. Up-regulation of PD-L1 is caused by activation of pro-survival pathways MAPK and PI3K/Akt as well as transcriptional factors HIF-1, STAT3 and NF-kappa B. The MAPK and PI3K signalling pathways are activated by gene mutations and growth factors. PD-L1 on tumor cells may then engage the PD-1 receptors resulting in suppression of T-cell mediated immune response. Therapeutic antibodies blocking the PD-1/PD-L1 pathway by targeting PD-L1 or PD-1 are highly effective in rescuing T cell anti-tumor effector functions.
所含基因
90 个基因
AKT1
AKT2
AKT3
ALK
BATF
BATF2
BATF3
CD247
CD274
CD28
CD3D
CD3E
CD3G
CD4
CHUK
CSNK2A1
CSNK2A2
CSNK2A3
CSNK2B
EGF
EGFR
EML4
FOS
HIF1A
HRAS
IFNG
IFNGR1
IFNGR2
IKBKB
IKBKG
JAK1
JAK2
JUN
KRAS
LAT
LCK
MAP2K1
MAP2K2
MAP2K3
MAP2K6
MAP3K3
MAPK1
MAPK11
MAPK12
MAPK13
MAPK14
MAPK3
MTOR
MYD88
NFATC1
NFATC2
NFATC3
NFKB1
NFKBIA
NFKBIB
NFKBIE
NRAS
P3R3URF-PIK3R3
PDCD1
PIK3CA
PIK3CB
PIK3CD
PIK3R1
PIK3R2
PIK3R3
PLCG1
PPP3CA
PPP3CB
PPP3CC
PPP3R1
PPP3R2
PRKCQ
PTEN
PTPN11
PTPN6
RAF1
RASGRP1
RELA
RPS6KB1
RPS6KB2
STAT1
STAT3
TICAM1
TICAM2
TIRAP
TLR2
TLR4
TLR9
TRAF6
ZAP70