18β-glycyrrhetinic acid inhibits hepatocellular carcinoma development by reversing hepatic stellate cell-mediated immunosuppression in mice

被引:59
|
作者
Kuang, Penghao [1 ,2 ]
Zhao, Wenxiu [1 ,2 ]
Su, Weixue [1 ,2 ]
Zhang, Zhengqi [1 ,2 ]
Zhang, Lei [1 ,2 ]
Liu, Jianming [1 ,2 ]
Ren, Guangli [1 ,2 ]
Yin, Zhenyu [1 ,2 ]
Wang, Xiaomin [1 ,2 ]
机构
[1] Xiamen Univ, Zhongshan Hosp, Dept Hepatobiliary Surg, Xiamen 361004, Fujian, Peoples R China
[2] Xiamen Univ, Res Inst Digest Dis, Xiamen 361004, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
hepatic stellate cells; 18-glycyrrhetinic acid; immunoregulation; hepatocellular carcinoma; T cells; REGULATORY T-CELLS; GLYCYRRHETINIC ACID; LIVER-CANCER; SORAFENIB; GLYCYRRHIZIN; ANGIOGENESIS; APOPTOSIS; MODEL; POPULATIONS; METASTASIS;
D O I
10.1002/ijc.27852
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 18-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.
引用
收藏
页码:1831 / 1841
页数:11
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