Methyl rosmarinate induces cell apoptosis in human hepatocellular carcinoma cells via inhibiting the Akt/mTOR signaling pathways

Yao Xian; Wei Jiang; Runkun Liu; Kangsheng TU; Shijie Gao; Jun Wang; Lei Zhang

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Methyl rosmarinate induces cell apoptosis in human hepatocellular carcinoma cells via inhibiting the Akt/mTOR signaling pathways

VernacularTitle:迷迭香酸甲酯通过抑制Akt/mTOR信号通路诱导人肝癌细胞凋亡
Author: Yao XIAN ¹ ; Wei JIANG ² ; Runkun LIU ³ ; Kangsheng TU ³ ; Shijie GAO ³ ; Jun WANG ⁴ ; Lei ZHANG ⁵
Author Information

1. Department of Nutrition, The First Affliliated Hospital of Xi’an Jiaotong University, Xi’an 710061
2. School of Nursing, Shaoyang University, Shaoyang 422000
3. Department of Hepatobiliary Surgery, The First Affliliated Hospital of Xi’an Jiaotong University, Xi’an 710061
4. Department of Emergency and Intensive Care Unit (East District), The First Affliliated Hospital of Xi’an Jiaotong University, Xi’an 710089
5. Department of Geriatric Surgery, The First Affliliated Hospital of Xi’an Jiaotong University, Xi’an 710061, China
Publication Type:Journal Article
Keywords: methyl rosmarinate; hepatocellular carcinoma (HCC); proliferation; migration; apoptosis; Akt/mTOR pathway
From: Journal of Xi'an Jiaotong University(Medical Sciences) 2023;44(5):802-808
CountryChina
Language:Chinese
Abstract: 【Objective】 To investigate the cell death-inducing effect of methyl rosmarinate (MR) on human hepatoma Hep-3B and SK-Hep1 cells and their potential mechanisms. 【Methods】 The effects of MR on the viability of Hep-3B, SK-Hep1 and MIHA cells were determined by cell counting kit-8 (CCK-8) assay. The morphological changes of three kinds of cells treated with different concentrations of MR were observed by optical microscopy. EdU assay and flow cytometry were used to detect the proliferation and apoptosis of Hep-3B and SK-Hep1 cells. Transwell assay was used to study the effects of MR on the migration and invasion of Hep-3B and SK-Hep1 cells. Western blotting was used to evaluate the protein expression levels of apoptosis, EMT and Akt/mTOR signaling pathways. 【Results】 After treated with different concentrations of MR (0~200 μmol/L) for 48 h, Hep-3B and SK-Hep1 cells activities were significantly decreased in a concentration-dependent manner (P<0.01), while there was no significant effect on MIHA cell activity (P>0.05), and the IC50 of Hep-3B and SK-Hep1 cells were 102.5 and 99.3 μmol/L, respectively. MR treatment (0-150 μmol/L) significantly inhibited the proliferation of Hep-3B and SK-Hep1 cells (P<0.05), while cell detachment and shrinkage were observed by optical microscopy on the Hep-3B and SK-Hep1 cells, while the morphology of MIHA cells was not changed. Compared with the control group, MR (100, 150 μmol/L) induced apoptosis in Hep-3B and SK-Hep1 cells, the expression levels of the pro-apoptotic proteins Bax and cleaved PARP were significantly increased (P<0.05), while the expression level of the anti-apoptotic protein Bcl-2 was significantly decreased (P<0.05). MR (100, 150 μmol/L) also inhibited the migration and invasion of HCC cells, significantly increased the expression of E-cadherin and decreased the expression of N-cadherin and Vimentin compared with the control group (P<0.05). Finally, Western blotting results showed that the expressions of p-Akt and p-mTOR in Hep-3B and SK-Hep1 treated by MR were significantly reduced in a dose-dependent manner, suggesting that MR may play an anti-cancer role by inhibiting Akt/mTOR signaling pathway. 【Conclusion】 MR can promote apoptosis in Hep-3B and SK-Hep1 cells, which may be closely related to the inhibition of Akt/mTOR signaling pathway.