GSK0660 enhances antitumor immunotherapy by reducing PD-L1 expression

被引:5
作者
Khan, Bibimaryam [1 ,2 ]
Chen, Mingjun [1 ]
Wang, Huijie [1 ]
Khan, Afrasyab [1 ]
Hussain, Shakeel [1 ]
Shi, Juanjuan [1 ]
Yang, Limin [1 ]
Hou, Yongzhong [1 ]
机构
[1] Jiangsu Univ, Sch Life Sci, Zhenjiang 212013, Jiangsu, Peoples R China
[2] Jiangsu Univ, Sch Med, Zhenjiang 212013, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
GSK0660; PD-L1; Transcription; Colon cancer; Immune escape; Immunotherapy; PEROXISOME-PROLIFERATOR; PPAR-GAMMA; BLOCKADE;
D O I
10.1016/j.ejphar.2024.176565
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Blockade of PD-1/PD-L1 immune checkpoint is wildly used for multiple types of cancer treatment, while the low response rate for patients is still completely unknown. As nuclear hormone receptor, PPARS (peroxisome-proliferator-activated receptor) regulates cell proliferation, inflammation, and tumor progression, while the effect of PPARS on tumor immune escape is still unclear. Here we found that PPARS antagonist GSK0660 significantly reduced colon cancer cell PD-L1 protein and gene expression. Luciferase analysis showed that GSK0660 decreased PD-L1 gene transcription activity. Moreover, reduced PD-L1 expression in colon cancer cells led to increased T cell activity. Further analysis showed that GSK0660 decreased PD-L1 expression in a PPARS dependent manner. Implanted tumor model analysis showed that GSK0660 inhibited tumor immune escape and the combined PD-1 antibody with GSK0660 effectively enhanced colorectal cancer immunotherapy. These findings suggest that GSK0660 treatment could be an effective strategy for cancer immunotherapy.
引用
收藏
页数:7
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