18[公式:见文]-甘草次酸抑制TGF-[公式:见文]-靶向STAT3诱导肝癌上皮向间质转化和转移。

IF 5.4 3区 材料科学 Q2 CHEMISTRY, PHYSICAL
ACS Applied Energy Materials Pub Date : 2022-01-01 Epub Date: 2021-12-28 DOI:10.1142/S0192415X22500124
Mo Jie, Zhao-Qi Zhang, Ning Deng, Qiu-Meng Liu, Chao Wang, Qian-Yun Ge, Peng-Chen Du, Sha-Sha Song, Xue-Wu Zhang, Long-Xin, Hui-Fang Liang, Liang Chu, Lei Zhang, Xiao-Ping Chen, Jin Chen, Han-Hua Dong, Bi-Xiang Zhang
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引用次数: 6

摘要

18[分子式:见文]-甘草酸(glycyrrhetinic acid, GA)是中药甘草的有效成分。我们之前证明了GA抑制肝细胞癌(HCC)的肿瘤生长。然而,GA对转化生长因子-[公式:见文](TGF-[公式:见文])诱导的上皮-间质转化(epithelial-mesenchymal transition, EMT)和转移的影响尚不清楚。在本研究中,体外transwell实验和免疫荧光(IF)表明,GA抑制TGF-诱导的HCC细胞迁移、侵袭和EMT。但对TGF-抑制细胞增殖作用不大[公式:见文]。此外,我们在异位肺转移模型中证实了GA抑制HCC细胞的转移。此外,我们发现GA抑制TGF-[公式:见文本]诱导的EMT主要是通过降低信号转导因子和转录激活因子3 (STAT3)的磷酸化,而STAT3在TGF-[公式:见文本]诱导的EMT和细胞迁移中起着至关重要的作用。机制上,GA通过增加Src同源2结构域蛋白酪氨酸磷酸酶1和2 (SHP1和SHP2)的表达来抑制STAT3的磷酸化。因此,我们得出结论,GA通过SHP1&SHP2/STAT3/Snail途径抑制TGF-诱导的EMT和转移。我们的数据为未来HCC的多模式治疗提供了一个有吸引力的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
18[Formula: see text]-Glycyrrhetinic Acid Inhibits TGF-[Formula: see text]-Induced Epithelial-to-Mesenchymal Transition and Metastasis of Hepatocellular Carcinoma by Targeting STAT3.

18[Formula: see text]-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-[Formula: see text] (TGF-[Formula: see text]-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-[Formula: see text]-induced migration, invasion and EMT of HCC cells. However, it had little effect on the inhibition of proliferation by TGF-[Formula: see text]. 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-[Formula: see text]-induced EMT mainly by reducing the phosphorylation of signal transducer and activator of transcription 3 (STAT3), which played an essential role in TGF-[Formula: see text]-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-[Formula: see text]-induced EMT and metastasis via the SHP1&SHP2/STAT3/Snail pathway. Our data provide an attractive therapeutic target for future multimodal management of HCC.

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来源期刊
ACS Applied Energy Materials
ACS Applied Energy Materials Materials Science-Materials Chemistry
CiteScore
10.30
自引率
6.20%
发文量
1368
期刊介绍: ACS Applied Energy Materials is an interdisciplinary journal publishing original research covering all aspects of materials, engineering, chemistry, physics and biology relevant to energy conversion and storage. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrate knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important energy applications.
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