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Combination treatment with artemisinin and oxaliplatin inhibits tumorigenesis in esophageal cancer EC109 cell through Wnt/β‐catenin signaling pathway

机译:通过Wnt /β-catenin信号传导途径抑制食管癌EC109细胞中的肿瘤瘤组合治疗抑制食管癌EC109细胞中的肿瘤

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BACKGROUND:Esophageal cancer (EC) is a prevalent malignant cancer worldwide. Interestingly, the antimalaria compound artemisinin (ART) is also reported to have anticancer potential, although its underlying mechanism in EC is unclear. In this study, we explored the anticancer role of ART in EC109 and further explored the combination of ART and oxaliplatin (OXA) for their synergetic anticancer functions.METHODS:Human EC cell line EC109 was used. After ART or oxaliplatin (OXA) treatment, cell proliferation, migration, and invasion were measured by MTT, transwell, and scratch wound assays, respectively. Flow cytometry was performed to examine the cell cycle and apoptosis. The mRNA and protein levels were determined using qRT-PCR and western blotting.RESULTS:The migration and invasion abilities of EC109 were suppressed by ART. This was due to the inhibitory effect of ART on the Wnt/β-catenin signaling pathway. The levels of β-catenin, c-myc, and survivin were also downregulated by ART. ART inhibits the proliferation of EC109 cells by arresting the cells in the G1-phase of cell cycle. By using LiCl, an activator of the Wnt/β-catenin pathway, we further verified that the inhibition of the Wnt/β-catenin pathway was indeed due to ART. Remarkably, ART enhanced the anticancer effects of OXA in EC109 cells. OXA combined with ART was found to be more efficient in decreasing tumor growth compared to the individual drugs.CONCLUSIONS:ART could suppress tumor progression by inhibiting Wnt/β-catenin signaling pathway, and it may also enhance the antitumor effect of OXA in EC. Thus, ART could be a novel anticancer drug for EC treatment.KEY POINTS:SIGNIFICANT FINDINGS OF THE STUDY: ART could be a novel anticancer drug for esophageal cancer (EC) treatment.WHAT THIS STUDY ADDS:Combination treatment with artemisinin and oxaliplatin inhibits tumorigenesis in esophageal cancer EC109 cells through the Wnt/β-catenin signaling pathway.? 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
机译:背景:食管癌(EC)是全世界普遍存在的恶性癌症。有趣的是,据报道,Antimalaria复合氨化氨基蛋白(ART)还据报道患有抗癌潜力,尽管其在EC中的潜在机制尚不清楚。在这项研究中,我们探讨了EC109中的艺术的抗癌作用,进一步探索了艺术和奥沙利铂(OXA)的组合,以使其协同抗癌功能。方法:使用人类EC细胞系EC109。在艺术或奥沙利铂(OXA)处理后,通过MTT,Transwell和划伤伤口测定来测量细胞增殖,迁移和侵袭。进行流式细胞术以检查细胞周期和细胞凋亡。使用QRT-PCR和Western Blotting测定mRNA和蛋白质水平。结果:EC109的迁移和侵袭能力被艺术抑制。这是由于技术在Wnt /β-连环蛋白信号传导途径上的抑制作用。 β-catenin,c-myc和survivin的水平也通过技术下调。通过在细胞周期的G1相中捕获细胞来抑制EC109细胞的增殖。通过使用LiCl,Wnt /β-catenin途径的活化剂,我们进一步验证了Wnt /β-catenin途径的抑制作为。值得注意的是,艺术增强了EC109细胞中氧气的抗癌效果。与个体药物相比,在减少肿瘤生长中,牛肉与艺术相结合。结论:术语:技术可以通过抑制Wnt /β-连环蛋白信号传导途径来抑制肿瘤进展,并且还可以增强欧氏氧气的抗肿瘤效应。因此,艺术可以是EC治疗的新型抗癌药物。这项研究结果:研究的重要发现:艺术可以是食管癌的新抗癌药物(EC)治疗。本研究补充说:用青蒿素和奥沙利铂治疗抑制肿瘤抑制通过Wnt /β-连环蛋白信号传导途径在食管癌EC109细胞中。 2020作者。中国肺部肿瘤集团和约翰瓦里和儿子澳大利亚发表的胸癌

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