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Cyclovirobuxine D Inhibits Cell Proliferation and Induces Mitochondria-Mediated Apoptosis in Human Gastric Cancer Cells

机译:Cyclovirobuxine D抑制人胃癌细胞增殖并诱导线粒体介导的细胞凋亡。

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摘要

Gastric cancer is one of the most common malignant cancers, with high death rates, poor prognosis and limited treatment methods. Cyclovirobuxine D (CVB-D) is the main active component of the traditional Chinese medicine Buxus microphylla. In the present study, we test the effects of CVB-D on gastric cancer cells and the underlying mechanisms of action. CVB-D reduced cell viability and colony formation ability of MGC-803 and MKN28 cells in a time- and concentration-dependent manner. Flow cytometry showed that cell cycle of CVB-D treated cells was arrested at the S-phase. CVB-D also induced apoptosis in MGC-803 and MKN28 cells, especially early stage apoptosis. Furthermore, mitochondria membrane potential (Δψm) was reduced and apoptosis-related proteins, cleaved Caspase-3 and Bax/Bcl-2, were up-regulated in CVB-D-treated MGC-803 and MKN28 cells. Taken together, our studies found that CVB-D plays important roles in inhibition of gastric tumorigenesis via arresting cell cycle and inducing mitochondria-mediated apoptosis, suggesting the potential application of CVB-D in gastric cancer therapy.
机译:胃癌是最常见的恶性肿瘤之一,死亡率高,预后差且治疗方法有限。 Cyclovirobuxine D(CVB-D)是中药小叶黄杨的主要活性成分。在本研究中,我们测试了CVB-D对胃癌细胞的作用及其潜在的作用机制。 CVB-D以时间和浓度依赖性方式降低了MGC-803和MKN28细胞的细胞活力和集落形成能力。流式细胞仪显示,经CVB-D处理的细胞的细胞周期被阻滞在S期。 CVB-D还诱导了MGC-803和MKN28细胞的凋亡,尤其是早期凋亡。此外,在CVB-D处理的MGC-803和MKN28细胞中,线粒体膜电位(Δψm)降低,裂解Caspase-3和Bax / Bcl-2的凋亡相关蛋白被上调。综上所述,我们的研究发现CVB-D通过阻止细胞周期并诱导线粒体介导的细胞凋亡在抑制胃癌的发生中起着重要作用,提示CVB-D在胃癌治疗中的潜在应用。

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