The Oncology Department, The Affiliated Hospital of Guilin Medical University, Guilin 541000, China.
Department of Gastrointestinal Oncology, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang Province, China.
Anal Cell Pathol (Amst). 2018 May 17;2018:8759745. doi: 10.1155/2018/8759745. eCollection 2018.
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.
尽管化疗和手术切除有了最近的进展,但食管癌的 5 年生存率仍然很低。因此,发现一种新的药物来提高食管癌患者的预期寿命非常重要。青蒿琥酯(DHA)是青蒿素的半合成衍生物,最近对各种癌细胞表现出有希望的抗癌活性。但到目前为止,具体机制尚不清楚。我们之前的研究表明,DHA 在体外以剂量依赖性方式降低食管癌细胞的活力,并诱导细胞周期停滞和细胞凋亡。在这里,我们将研究扩展到进一步观察 DHA 在体内对食管癌细胞的疗效。在本研究中,我们首次发现 DHA 与对照组相比,显著抑制异种移植瘤中的细胞增殖。其机制是 DHA 以剂量依赖性方式诱导体内人食管癌细胞系 Eca109 和 Ec9706 中的细胞凋亡。结果表明,DHA 是一种有前途的临床治疗食管癌的药物。