18β-Glycyrrhetinic Acid Inhibits TGF-β-Induced Epithelial-to-Mesenchymal Transition and Metastasis of Hepatocellular Carcinoma by Targeting STAT3.
| Autor: | Jie, Mo, Zhang, Zhao-Qi, Deng, Ning, Liu, Qiu-Meng, Wang, Chao, Ge, Qian-Yun, Du, Peng-Chen, Song, Sha-Sha, Zhang, Xue-Wu, Long-Xin, Liang, Hui-Fang, Chu, Liang, Zhang, Lei, Chen, Xiao-Ping, Chen, Jin, Dong, Han-Hua, Zhang, Bi-Xiang |
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| Předmět: |
TRANSFORMING growth factors-beta
IN vitro studies HERBAL medicine ANIMAL experimentation WESTERN immunoblotting ONE-way analysis of variance METASTASIS EPITHELIAL-mesenchymal transition HYDROCARBONS FLUORESCENT antibody technique CELL proliferation CELL lines POLYMERASE chain reaction HEPATOCELLULAR carcinoma CARRIER proteins MICE CHINESE medicine |
| Zdroj: | American Journal of Chinese Medicine; 2022, Vol. 50 Issue 1, p313-332, 20p |
| Abstrakt: | 18 β -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- β (TGF- β) -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- β -induced migration, invasion and EMT of HCC cells. However, it had little effect on the inhibition of proliferation by TGF- β. 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- β -induced EMT mainly by reducing the phosphorylation of signal transducer and activator of transcription 3 (STAT3), which played an essential role in TGF- β -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- β -induced EMT and metastasis via the SHP1&SHP2/STAT3/Snail pathway. Our data provide an attractive therapeutic target for future multimodal management of HCC. [ABSTRACT FROM AUTHOR] |
| Databáze: | Complementary Index |
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