THE HERBAL MIXTURE XIAO-CHAI-HU TANG (XCHT) INDUCES APOPTOSIS OF HUMAN HEPATOCELLULAR CARCINOMA HUH7 CELLS IN VITRO AND IN VIVO.

Jinyan Zhao, Liya Liu, Yuchen Zhang, Yun Wan, Zhenfeng Hong
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引用次数: 8

Abstract

Background: Xiao-Chai-Hu Tang (XCHT) is an extract of seven herbs with anticancer properties, but its mechanism of action is unknown. In this study, we evaluated XCHT-treated hepatocellular carcinoma (HCC) for anti-proliferative and pro-apoptotic effects.

Materials and methods: Using a hepatic cancer xenograft model, we investigated the in vivo efficacy of XCHT against tumor growth by evaluating tumor volume and weight, as well as measuring apoptosis and cellular proliferation within the tumor. To study the effects of XCHT in vitro, we measured the cell viability of XCHT-treated Huh7 cells, as well as colony formation and apoptosis. To identify a potential mechanism of action, the gene and protein expression levels of Bax, Bcl-2, CDK4 and cyclin-D1 were measured in XCHT-treated Huh7 cells.

Results: We found that XCHT reduced tumor size and weight, as well as significantly decreased cell viability both in vivo and in vitro. XCHT suppressed the expression of the proliferation marker Ki-67 in HCC tissues and inhibited Huh7 colony formation. XCHT induced apoptosis in HCC tumor tissues and in Huh7 cells. Finally, XCHT altered the expression of Bax, Bcl-2, CDK4 and cyclin-D1, which halted cell proliferation and promoted apoptosis.

Conclusion: Our data suggest that XCHT enhances expression of pro-apoptotic pathways, resulting in potent anticancer activity.

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中药复方小柴胡汤对人肝癌huh7细胞的凋亡具有体外和体内诱导作用。
背景:小柴胡汤(XCHT)是7种具有抗癌作用的中药提取物,但其作用机制尚不清楚。在这项研究中,我们评估了xcht治疗的肝细胞癌(HCC)的抗增殖和促凋亡作用。材料与方法:采用肝癌异种移植模型,通过评估肿瘤体积和重量,以及测量肿瘤内细胞凋亡和细胞增殖,研究XCHT在体内对肿瘤生长的抑制作用。为了研究XCHT在体外的作用,我们测量了XCHT处理的Huh7细胞的细胞活力,以及集落形成和凋亡。为了确定其潜在的作用机制,我们检测了xcht处理的Huh7细胞中Bax、Bcl-2、CDK4和cyclin-D1的基因和蛋白表达水平。结果:我们发现XCHT在体内和体外均能减小肿瘤的大小和重量,并显著降低细胞活力。XCHT抑制HCC组织中增殖标志物Ki-67的表达,抑制Huh7集落的形成。XCHT诱导HCC肿瘤组织和Huh7细胞凋亡。最后,XCHT改变Bax、Bcl-2、CDK4和cyclin-D1的表达,抑制细胞增殖,促进细胞凋亡。结论:我们的数据表明XCHT增强了促凋亡通路的表达,从而产生了强大的抗癌活性。
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