›› 2009, Vol. 40 ›› Issue (3): 423-427.doi: 10.3969/j.issn.0529-1356.2009.03.016

• 论著 • 上一篇    下一篇

三种含硒化合物对K562细胞的抑制作用

杨军英*;徐存拴   

  1. 河南师范大学生命科学学院省部共建细胞分化调控重点实验室,河南 新乡 453007
  • 收稿日期:2008-03-24 修回日期:2008-06-02 出版日期:2009-06-06
  • 通讯作者: 杨军英

Study on the anticancer effect of three new selenium compounds in K562 cells

  1. Key Laboratory for Cell Differentiation Regulation, School of Life Science, BR>He′nan Normal University, He′nan Xinxiang 453007, China
  • Received:2008-03-24 Revised:2008-06-02 Online:2009-06-06
  • Contact: YANG Jun-ying

关键词: 含硒化合物, 四甲基偶氮唑盐, 流式细胞术, K562细胞, 激光扫描共焦显微术, 小鼠

Abstract: Objective To investigate the antitumor activities of three selenium compounds in EM>vitro/EM> as well as EM>in vivo/EM>, and to explore the mechanism. Methods Assay of MTT and growth inhibition of S180 and H22 on tumorbearing mice were used to study the antitumor effect, morphological observation, flow cytometry and confocal laser scanning microscopy assay were used to study the mechanism of three selenium compounds. Results They could significantly inhibit proliferation of K562 cells in vitro(EM>P/EM><0.05), and the growth of S180 and H22 (EM>P/EM><0.01,EM>n/EM>=10). Electron microscopic observation revealed typical apoptotic features, including shrinkage of cellular and nuclear membranes, condensed heterochromatin around the nuclear periphery, and cytoplasmic vacuolation in the K562 cells treated with NaSeVO, SeMoV and SeWV 5 mg/L for 24 hours. The cell cycle was redistributed by selenium compounds and a significantly subG showed at high dosage. The fluorescence intensity of intracellular CaSUP>2+/SUP>,MgEM>SUP>2+/SUP>/EM> and ROS was greatly increased after treatment with selenium compounds as compared with control group(EM>P/EM><0.01). However, the fluorescence intensity of intracellular pH value and MMP decreased(EM>P/EM><0.01). Conclusion Three selenium compounds have antitumor activity EM>in vivo/E

Key words: Selenium compounds, MTT, Flow cytometry, K562 cell, Confocal laser scanning microscopy assay

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