基础医学与临床 ›› 2007, Vol. 27 ›› Issue (2): 161-165.

• 研究论文 • 上一篇    下一篇

青蒿琥酯可调控人食管癌CDC25、TGF-beta表达

王静(河北四院) 刘亮 李金梅 刘江惠 郭建文 左连富   

  1. 河北医科大学第四医院河北省肿瘤研究所流式分析室 河北医科大学第四医院河北省肿瘤研究所流式分析室 河北医科大学第四医院河北省肿瘤研究所流式分析室 河北医科大学第四医院河北省肿瘤研究所流式分析室
  • 收稿日期:2006-05-16 修回日期:2006-09-07 出版日期:2007-02-25 发布日期:2007-02-25
  • 通讯作者: 王静(河北四院)

Modulation effect of aresunate on the expression of CDC25A and TGF-beta in human esophageal carcnoma

  

  • Received:2006-05-16 Revised:2006-09-07 Online:2007-02-25 Published:2007-02-25

摘要: 目的 观察青蒿琥酯(artesunate, Art)对人食管癌Eca-109细胞株的抑瘤作用,并进一步探讨Art诱导肿瘤细胞周期阻滞与CDC25A、TGF-β表达的关系。方法 体外培养人食管癌Eca-109细胞株及正常人外周血单个核细胞(hPBMC),利用MTT法测定细胞增殖;采用流式细胞术(FCM)测定细胞周期;应用RT-PCR方法检测CDC25A mRNA表达,应用Western blot方法检测蛋白表达。结果 Art能显著抑制Eca-109细胞的增殖,IC50为(68.80±0.76)μmol/L,而对hPBMC的增殖则没有明显抑制作用。低浓度Art可将细胞阻滞于G0/G1期,S期细胞显著减少,当浓度达到100μmol/L时,细胞阻滞于G2/M期。Art可显著抑制Eca-109细胞CDC25A mRNA及蛋白表达,同时显著上调TGF-β的蛋白表达水平。结论 Art可抑制肿瘤细胞生长,上调TGF-β表达,抑制CDC25A表达。

Abstract: OBJECTIVE To observe the effects of Art on the proliferation of human esophageal carcinoma Eca-109 cell line and explore relationship between cell cycle arrest effect of Art and the expression of CDC25A and TGF-β. METHODS Human esophageal carcinoma Eca-109 cell and healthy human peripheral blood mononuclear cell (hPBMC) were cultured. The inhibitory effects of Art on cell proliferation were determined by MTT method. The changes of cell cycle of tumor cells were assayed by flow cytometry (FCM). The expression of CDC25A mRNA was examined by RT-PCR and the protein expression of CDC25A as well as TGF-β was determined by Western blot. RESULTS Art could significantly inhibit the proliferation of Eca-109. Its IC50 was (68.80±0.76 )μmol/L. It had weaker effect on the proliferation of hPBMC. The cell cycle of Eca-109 was changed greatly after the administration of Art. The number of Eca-109 cells during G0/G1 was increased and that of cells among S phase was reduced under lower doses of Art. However, most of cells were arrested at G2/M phase under the concentration of 100μmol/L. Art could dramatically inhibit the expression of CDC25A in both mRNA and protein levels. The expression of TGF-β was increased at the same concentration of art. CONCLUSION Art inhibited the proliferation of tumor cell, modulated cell cycle by down regulation CDC25A and increased TGF-β.