基础医学与临床 ›› 2007, Vol. 27 ›› Issue (9): 975-980.

• 研究论文 • 上一篇    下一篇

外源性三磷酸腺苷对人食管癌Eca-109和肝癌SMMC-7721细胞增殖和周期的影响

秦葵 朱忠宁 任雷鸣 刘江惠   

  1. 河北医科大学药学院药理学研究室 河北医科大学药学院药理学研究室 河北医科大学药学院药理学研究室 河北医科大学第四附属医院 石家庄
  • 收稿日期:2006-06-30 修回日期:2006-09-27 出版日期:2007-09-25 发布日期:2007-09-25
  • 通讯作者: 秦葵

Effects of extracellular adenosine triphosphate on apoptosis of human esophageal carcinoma Eca-109 and hepatoma SMMC-7721 cells

Kui Qin Zhong-ning Zhu Lei-ming Ren Jiang-hui Liu   

  • Received:2006-06-30 Revised:2006-09-27 Online:2007-09-25 Published:2007-09-25
  • Contact: Kui Qin

摘要: 目的 研究三磷酸腺苷(ATP)对于人食管鳞癌Eca-109细胞系和人肝癌细胞SMMC-7721系的抗增殖作用和作用机制。方法 用MTT法测定肿瘤细胞的增殖,AO/EB双荧光染色法观察细胞形态学的改变,流式细胞仪方法定量检测细胞增殖周期、凋亡率及凋亡相关蛋白的改变。结果 ATP在0.01~0.3 mmol/L浓度范围内,可不同程度地抑制Eca-109和SMMC-7721细胞的增殖。分别经0.3 mmol/L的ATP处理72h后,少量SMMC-7721细胞形态出现了凋亡特征,而Eca-109细胞无明显凋亡特征;0.03、0.1和0.3mmol/LATP分别处理细胞72h后,两株细胞的凋亡率及凋亡相关蛋白均无显著变化。0.3 mmol/LATP可使Eca-109细胞的G0/G1细胞数目显著增多,S期细胞显著减少,增殖指数显著降低。结论 ATP通过增加G0/G1期细胞和减少S期细胞,抗食管癌Eca-109细胞增殖,此作用与诱导细胞凋亡无关。而ATP对肝癌SMMC-7721细胞的抗增殖作用与周期无关。

Abstract: Objective To study the effects of adenosine triphosphate (ATP) on the proliferation of human squamous esophageal carcinoma Eca-109 and hepatoma SMMC-7721 cells in vitro and the underlying mechanism. Methods MTT assay was used to determine the proliferation of tumor cells. The AO/EB double stained cells were observed under fluorescence microscope to observe morphological changes. The effects of ATP on the cell cycle, apoptotic rate and apoptosis-related protein were detected by flow cytometry. Results ATP produced inhibitory effects on Eca-109 and SMMC-7721 cells at the concentration between 0.01~0.3 mmol/L. Exposed to 0.3mmol/L ATP for 72h, some of SMMC-7721 cells displayed morphological changes of apoptosis, but Eca-109 cells did not show the characteristics of apoptosis markedly. There was no significant change in the apoptotic rate and apoptosis-related protein of the two tumor cell lines treated with ATP 0.03, 0.1 and 0.3mmol/L for 72h respectively. The proportion of Eca-109 cells in G0/G1-phase of cell cycle was significantly increased, meanwhile the proportion of Eca-109 cells in S-phase and proliferation index value was significantly decreased by treatment with 0.3mmol/L ATP. Conclusion ATP inhibited Eca-109 cell proliferation by changing the distribution of cell cycle phase, and its mechanism might not related to apoptosis, but for SMMC-7721 cell, the inhibition of cell proliferation induced by ATP was not related to the change in cell cycle.