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淫羊藿素通过调节肝细胞癌中的细胞焦亡和免疫活性发挥抗癌作用。

Icaritin Exerts Anti-Cancer Effects through Modulating Pyroptosis and Immune Activities in Hepatocellular Carcinoma.

作者信息

Jiao Yuanyuan, Li Wenqian, Yang Wen, Wang Mingyu, Xing Yaling, Wang Shengqi

机构信息

College of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Poyanghu Road, Jinghai District, Tianjin 301617, China.

Bioinformatics Center of AMMS, Taiping Road, Haidian District, Beijing 100850, China.

出版信息

Biomedicines. 2024 Aug 21;12(8):1917. doi: 10.3390/biomedicines12081917.

Abstract

Icaritin (ICT), a natural compound extracted from the dried leaves of the genus Epimedium, possesses antitumor and immunomodulatory properties. However, the mechanisms through which ICT modulates pyroptosis and immune response in hepatocellular carcinoma (HCC) remain unclear. This study demonstrated that ICT exhibits pyroptosis-inducing and anti-hepatocarcinoma effects. Specifically, the caspase1-GSDMD and caspase3-GSDME pathways were found to be involved in ICT-triggered pyroptosis. Furthermore, ICT promoted pyroptosis in co-cultivation of HepG2 cells and macrophages, regulating the release of inflammatory cytokines and the transformation of macrophages into a proinflammatory phenotype. In the Hepa1-6+Luc liver cancer model, ICT treatment significantly increased the expression of cleaved-caspase1, cleaved-caspase3, and granzyme B, modulated cytokine secretion, and stimulated CD8 T cell infiltration, resulting in a reduction in tumor growth. In conclusion, the findings in this research suggested that ICT may modulate cell pyroptosis in HCC and subsequently regulate the immune microenvironment of the tumor. These observations may expand the understanding of the pharmacological mechanism of ICT, as well as the therapy of liver cancer.

摘要

淫羊藿素(ICT)是从淫羊藿属植物干燥叶片中提取的一种天然化合物,具有抗肿瘤和免疫调节特性。然而,ICT在肝细胞癌(HCC)中调节细胞焦亡和免疫反应的机制仍不清楚。本研究表明,ICT具有诱导细胞焦亡和抗肝癌作用。具体而言,发现半胱天冬酶1-GSDMD和半胱天冬酶3-GSDME途径参与了ICT触发的细胞焦亡。此外,ICT在HepG2细胞与巨噬细胞共培养中促进细胞焦亡,调节炎性细胞因子的释放以及巨噬细胞向促炎表型的转变。在Hepa1-6+Luc肝癌模型中,ICT治疗显著增加了裂解的半胱天冬酶1、裂解的半胱天冬酶3和颗粒酶B的表达,调节细胞因子分泌,并刺激CD8 T细胞浸润,从而导致肿瘤生长减少。总之,本研究结果表明,ICT可能调节HCC中的细胞焦亡,随后调节肿瘤的免疫微环境。这些观察结果可能会扩展对ICT药理机制以及肝癌治疗的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9873/11351763/01ffbbb1b163/biomedicines-12-01917-g001.jpg

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