18β-Glycyrrhetinic Acid Inhibits TGF-β-Induced Epithelial-to-Mesenchymal Transition and Metastasis of Hepatocellular Carcinoma by Targeting STAT3

被引:10
|
作者
Jie, Mo [1 ,2 ]
Zhang, Zhao-Qi [1 ,2 ,3 ]
Deng, Ning [1 ,2 ]
Liu, Qiu-Meng [1 ,2 ]
Wang, Chao [1 ,2 ]
Ge, Qian-Yun [1 ,2 ]
Du, Peng-Chen [1 ,2 ]
Song, Sha-Sha [1 ,2 ]
Zhang, Xue-Wu [1 ,2 ]
Long-Xin [1 ,2 ]
Liang, Hui-Fang [1 ,2 ]
Chu, Liang [1 ,2 ]
Mang, Lei [1 ,2 ]
Chen, Xiao-Ping [1 ,2 ]
Chen, Jin [1 ,2 ]
Dong, Han-Hua [1 ,2 ]
Zhang, Bi-Xiang [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Hubei Key Lab Hepaio Pancreatobiliaty Dis, Clin Med Res Ctr Hepat Surg Hubei Prov,Minist Edu, Tongji Hosp,Tongji Med Coll,Hepat Surg Ctr,Key La, Wuhan, Hubei, Peoples R China
[2] Minist Publ Hlth, Wuhan, Hubei, Peoples R China
[3] Shanghai Jiao Tong Univ, Dept Gen Surg, Peoples Hosp 1, Shanghai, Peoples R China
来源
AMERICAN JOURNAL OF CHINESE MEDICINE | 2022年 / 50卷 / 01期
基金
中国国家自然科学基金;
关键词
18 beta-Glycyrrhetinic Acid; TGF-beta; Epithelial-to-Mesenchymal Transition; STAT3; Metastasis; HCC; Hepatocellular Carcinoma; GLYCYRRHETINIC ACID; SIGNALING PATHWAY; TUMOR-SUPPRESSOR; CANCER CELLS; MECHANISMS; EXPRESSION; MIGRATION; INVASION; GROWTH;
D O I
10.1142/S0192415X22500124
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
18 beta-glycyrrhetinic acid (GA) is the active ingredient of the traditional Chinese medicinal herb Glycyrrhizae radix et rhizoma. We previously demonstrated that GA inhibited tumor growth in hepatocellular carcinoma (HCC). However, the effect of GA on transforming growth factor-beta (TGF-beta)-induced epithelial-mesenchymal transition (EMT) and metastasis were still unclear. In this study, in vitro transwell assays and immunofluorescence (IF) demonstrated that GA inhibited TGF-beta-induced migration, invasion and EMT of HCC cells. However, it had little effect on the inhibition of proliferation by TGF-beta. Moreover, we confirmed that GA suppressed the metastasis of HCC cells in vivousing an ectopic lung metastasis model. Furthermore, we found that GA inhibited TGF-beta-induced EMT mainly by reducing the phosphorylation of signal transducer and activator of transcription 3 (STAT3), which played an essential role in TGF-beta-induced EMT and cell mobility. Mechanistically, GA inhibited the phosphorylation of STAT3 by increasing the expression of Src homology 2 domain-containing protein tyrosine phosphatases 1 and 2 (SHP1 and SHP2). Therefore, we concluded that GA inhibited TGF-beta-induced EMT and metastasis via the SHP1&SHP2/STAT3/Snail pathway. Our data provide an attractive therapeutic target for future multimodal management of HCC.
引用
收藏
页码:313 / 332
页数:20
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