PD-L1 regulation by SDH5 via β-catenin/ZEB1 signaling

被引:13
作者
Tuo, Zhan [1 ]
Zong, Yan [1 ]
Li, Jie [1 ]
Xiao, Guangqin [1 ]
Zhang, Furong [1 ]
Li, Guiling [1 ]
Wang, Sihua [1 ]
Lv, Yi [1 ]
Xia, Jiahong [1 ]
Liu, Jun [1 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Canc Ctr, Wuhan 430022, Hubei, Peoples R China
来源
ONCOIMMUNOLOGY | 2019年 / 8卷 / 12期
基金
中国国家自然科学基金;
关键词
Lung cancer; PD-L1; SDH5; EMT; immunotherapy; CELL LUNG-CANCER; SUCCINATE-DEHYDROGENASE; 1ST-LINE TREATMENT; COMBINATION; METASTASIS; IPILIMUMAB; EXPRESSION; ANTIBODIES; SYNERGIZES; NIVOLUMAB;
D O I
10.1080/2162402X.2019.1655361
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Programmed death-ligand 1 (PD-L1) is a crucial target for lung cancer immunotherapy. In lung cancer patients with high PD-L1 expression, blocking or reducing its expression can inhibit tumor growth. PD-L1 is regulated by signaling pathways, transcription factors and epigenetic factors, such as the GSK3 beta/beta-catenin pathway, P53 protein and EMT. In our previous study, succinate dehydrogenase 5 (SDH5) was reported to regulate ZEB1 expression, induce EMT and lead to lung cancer metastasis via the GSK3 beta/beta-catenin pathway. It is possible that SDH5 is involved in the mechanisms of PD-L1 regulation.In the present study, we observed a negative correlation between the expression of PD-L1 and SDH5 in vivo and in vitro. The examination of patient tissues also confirmed our results. Furthermore, we also found that SDH5 could reverse PD-L1 expression by the GSK3 beta/beta-catenin/ZEB1 pathways. All these results reveal that SDH5 regulates PD-L1 expression and suggest that SDH5 can be used as a marker to predict tumor immune micro-states and provide guidance for clinical immunotherapy.
引用
收藏
页数:12
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