Astragaloside III inhibits MAPK-mediated M2 tumor-associated macrophages to suppress the progression of lung Cancer cells via Akt/ mTOR signaling pathway

被引:0
作者
Sun, Yan [1 ,2 ]
Liu, Jia-Qi [1 ,2 ]
Chen, Wen-Jing [1 ,2 ]
Tang, Wei-Feng [1 ,2 ]
Zhou, Yao-Long [1 ,2 ]
Liu, Bao-Jun [1 ,2 ]
Wei, Ying [1 ,2 ]
Dong, Jing-Cheng [1 ,2 ]
机构
[1] Fudan Univ, Huashan Hosp, Dept Integrat Med, Shanghai, Peoples R China
[2] Fudan Univ, Inst Integrat Med, Shanghai, Peoples R China
关键词
Astragaloside III; Lung cancer; Tumor microenvironment; Tumor-associated macrophages; Macrophage polarization; IMMUNOTHERAPY; MICROENVIRONMENT; CHEMOTHERAPY; INFLAMMATION; METASTASIS; CARCINOMA; VEGF;
D O I
10.1016/j.intimp.2025.114546
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tumor-associated macrophages (TAMs) play a key role in facilitating a range of cancerous processes by modulating the tumor microenvironment thus being a target for cancer treatment. Astragaloside III (AS-III), a compound derived from Astragalus triterpenoid saponins, has demonstrated immunomodulatory and anticancer properties, but the underlying mechanism remains unclear. Here, we demonstrated that AS-III suppressed metastasis, angiogenesis and induced apoptosis of lung cancer in vitro and in vivo by inhibiting macrophage M2 polarization and inducing M1 phenotype transformation. This was achieved through the inhibition of the MAPK signaling pathway. Furthermore, the tumor inhibitory effects of AS-III were found to be mediated by the Akt/ mTOR pathway. Overall, these results highlight the role of AS-III in modifying the TAMs in TME, offering fresh perspectives on tumor immunotherapy by means of targeting macrophage.
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页数:16
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