Department of Hepatobiliary Surgery, Zhongshan Hospital, Xiamen University, Xiamen, Fujian, China.
Int J Cancer. 2013 Apr 15;132(8):1831-41. doi: 10.1002/ijc.27852. Epub 2012 Oct 20.
Hepatic stellate cells (HSCs) have immunosuppressive capabilities and contribute to the occurrence and development of hepatocellular carcinoma (HCC). Thus, activated HSCs may be a suitable target for HCC therapy. Our study used mixed leukocyte reactions (MLR) in vitro to demonstrate that 18β-glycyrrhetinic acid (GA) could reverse HSC-mediated immunosuppression by reducing T-cell apoptosis and regulatory T (Treg) cells expression, thereby enhancing the ability of T cells to attack tumor cells and attenuating HCC cell invasiveness. Moreover, we established a HCC orthotopic implantation model in immunocompetent C57BL/6 mice, which suggested that GA played a protective role in HCC development by reducing immunosuppression mediated by HSCs in the tumor microenvironment.
肝星状细胞(HSCs)具有免疫抑制能力,并有助于肝细胞癌(HCC)的发生和发展。因此,激活的 HSCs 可能是 HCC 治疗的合适靶点。我们的研究使用混合淋巴细胞反应(MLR)体外实验表明,18β-甘草酸(GA)可通过减少 T 细胞凋亡和调节性 T(Treg)细胞表达来逆转 HSC 介导的免疫抑制,从而增强 T 细胞攻击肿瘤细胞的能力,并减弱 HCC 细胞的侵袭性。此外,我们在免疫活性 C57BL/6 小鼠中建立了 HCC 原位移植模型,该模型表明 GA 通过减少肿瘤微环境中 HSCs 介导的免疫抑制来发挥对 HCC 发展的保护作用。