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Anticancer Effects of Dihydroartemisinin on Human Esophageal Cancer Cells In Vivo

机译:双氢青蒿素对人食管癌细胞的抗癌作用

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摘要

Despite recent advances in chemotherapy and surgical resection, the 5-year survival rate of esophageal cancer still remains at the low level. Therefore, it is very important to discover a new agent to improve the life expectancy of patients with esophageal cancer. Dihydroartemisinin (DHA), a semisynthetic derivative of artemisinin, has recently exhibited promising anticancer activity against various cancer cells. But so far, the specific mechanism remains unclear. We have previously demonstrated that DHA reduced viability of esophageal cancer cells in a dose-dependent manner in vitro and induced cell cycle arrest and apoptosis. Here, we extended our study to further observe the efficacy of DHA on esophageal cancer cells in vivo. In the present study, for the first time, we found that DHA significantly inhibits cell proliferation in xenografted tumor compared with the control. The mechanism was that DHA induced cell apoptosis in both human esophageal cancer cell lines Eca109 and Ec9706 in vivo in a dose-dependent manner. The results suggested that DHA was a promising agent against esophageal cancer in the clinical treatment.
机译:尽管化学疗法和外科切除术最近取得了进展,但食管癌的5年生存率仍然保持在较低水平。因此,寻找一种新的药物来提高食管癌患者的预期寿命非常重要。双氢青蒿素(DHA)是青蒿素的半合成衍生物,最近展现出对各种癌细胞的有希望的抗癌活性。但是到目前为止,具体机制仍不清楚。我们以前已经证明,DHA在体外以剂量依赖性方式降低了食道癌细胞的活力,并诱导了细胞周期停滞和凋亡。在这里,我们扩展了研究范围,以进一步观察DHA在体内对食道癌细胞的疗效。在本研究中,我们首次发现与对照相比,DHA显着抑制异种移植肿瘤中的细胞增殖。其机制是DHA在体内以剂量依赖性方式在人食道癌细胞系Eca109和Ec9706中诱导细胞凋亡。结果表明,DHA是临床治疗食道癌的有前途的药物。

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