Swertianin Promotes Anti-Tumor activity by facilitating Macrophage M1 polarization via STING signaling

被引:3
作者
Cao, Chenxi [1 ]
Hu, Biwen [1 ]
Wang, Jin [1 ]
Li, Wenyan [1 ]
Guo, Li [1 ]
Sheng, Jian [1 ]
Zhang, Caiqun [1 ]
机构
[1] Jiaxing Univ, Affiliated Hosp 2, Jiaxing 314001, Peoples R China
关键词
Swertianin; Macrophages; M1; Polarization; Tumor Microenvironment; STING; ACTIVATION;
D O I
10.1016/j.intimp.2024.113182
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To investigate the mechanism by which swertiamarin (swertianin, SWE) regulates the polarization of tumor microenvironment-associated macrophages to M1 phenotype, thereby exerting anti-tumor effects.SWE promoted the formation of M1 cells and increased the proportion of CD86 + cells in both RAW264.7 and primary monocyte-derived macrophages, while activating the STING-NF-kappa B pathway. When STING or P65 was knocked out, the effects of SWE were antagonized, inhibiting the formation of CD86 + M1 cells. At the animal level, SWE inhibited tumor growth, activated STING-NF-kappa B, and promoted the formation of CD86 + cells. STING-KO inhibited the effects of SWE.SWE can activate the STING-NF-kappa B signal to promote macrophage M1 polarization, playing an anti-tumor role.
引用
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页数:9
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