Liang Huaguo, Chen Zexin, Yang Ruihui, Huang Qingsong, Chen Hongmei, Chen Wanting, Zou Li, Wei Peng, Wei Shijie, Yang Yongxia, Zhang Yongli
School of Life Sciences and Biopharmaceutics, Guangdong Pharmaceutical University, Guangzhou, China.
Guangzhou Key Laboratory of Construction and Application of New Drug Screening Model Systems, Guangdong Pharmaceutical University, Guangzhou, China.
Front Pharmacol. 2022 Jun 13;13:894285. doi: 10.3389/fphar.2022.894285. eCollection 2022.
Methyl gallate (MG), a polyphenolic compound found in plants, is widely used in traditional Chinese medicine. MG is known to alleviate several cancer symptoms. However, most studies that have reported the antitumor effects of MG have done so at the cellular level, and the inhibitory effect and therapeutic mechanism of MG in hepatocellular carcinoma (HCC) have not been extensively explored . We aimed to understand the therapeutic mechanism of MG in HCC and . MTT and colony formation assays were used to determine the impact of MG on the proliferation of a human HCC cell line, BEL-7402; wound healing and transwell assays were used to quantify the migration and invasion of HCC cells. Western blotting was used to quantify the expression of the AMPK/NF-κB signaling pathway proteins. tumor growth was measured in a xenograft tumor nude mouse model treated with MG, and hematoxylin-eosin staining and immunohistochemistry (IHC) were used to visualize the histological changes in the tumor tissue. We found that MG showed anti-proliferative effects both and . MG downregulated the protein expression of AMPK, NF-κB, p-NF-κB, and vimentin and upregulated the expression of E-cadherin in a dose-dependent manner. Additionally, MG inhibited the migration and invasion of HCC cells by decreasing MMP9 and MMP2 expression and increasing TIMP-2 expression. These were consistent with the results of IHC . MG inhibited the proliferation, migration, and invasion of HCC cells. This effect potentially involves the regulation of the AMPK/NF-κB pathway, which in turn impacts epithelial-mesenchymal transition and MMP expression.
没食子酸甲酯(MG)是一种存在于植物中的多酚类化合物,在传统中药中广泛应用。已知MG可缓解多种癌症症状。然而,大多数报道MG抗肿瘤作用的研究都是在细胞水平上进行的,MG在肝细胞癌(HCC)中的抑制作用和治疗机制尚未得到广泛探索。我们旨在了解MG在HCC中的治疗机制。采用MTT和集落形成试验来确定MG对人HCC细胞系BEL-7402增殖的影响;采用伤口愈合试验和Transwell试验来量化HCC细胞的迁移和侵袭。采用蛋白质印迹法来量化AMPK/NF-κB信号通路蛋白的表达。在用MG处理的异种移植瘤裸鼠模型中测量肿瘤生长,并使用苏木精-伊红染色和免疫组织化学(IHC)来观察肿瘤组织的组织学变化。我们发现MG在体内和体外均显示出抗增殖作用。MG以剂量依赖性方式下调AMPK、NF-κB、p-NF-κB和波形蛋白的蛋白表达,并上调E-钙黏蛋白的表达。此外,MG通过降低MMP9和MMP2表达并增加TIMP-2表达来抑制HCC细胞的迁移和侵袭。这些与IHC结果一致。MG抑制HCC细胞的增殖、迁移和侵袭。这种作用可能涉及对AMPK/NF-κB途径的调节,进而影响上皮-间质转化和MMP表达。