癌变·畸变·突变 ›› 2004, Vol. 16 ›› Issue (1): 39-42.doi: 10.3969/j.issn.1004-616x.2004.01.012

• 研究简报 • 上一篇    下一篇

有机锗多酸衍生物的抗肿瘤作用及其机制

张 煜;王宝贵;张桂英;董晓路   

  1. 吉林大学公共卫生学院, 吉林 长春  130021
  • 收稿日期:2003-09-16 修回日期:2003-10-15 出版日期:2004-01-30 发布日期:2004-01-30
  • 通讯作者: 王宝贵

Study of Anti-tumor and Mechanism of Organogermanium Poly-derivatinmves

ZHANG Yu;WANG Bao-gui;ZHANG Gui-ying;et al   

  1. College of Preventive Medicine, Jilin University, Changchun 130021, China
  • Received:2003-09-16 Revised:2003-10-15 Online:2004-01-30 Published:2004-01-30
  • Contact: WANG Bao-gui

摘要: 背景与目的: 对有机锗多酸衍生物进行体外毒性 、 抑瘤率和对瘤细胞周期影响的研究 , 为临床应用提供科学依据 。 材料与方法:采用MTT法检测有机锗多酸衍生物对FL、L929的体外毒性效应,对SMMC-7721、Hela、K562的体外抑瘤效应,流式细胞仪单荧光染色法检测有机锗多酸衍生物对SMMC-7721的细胞周期影响。结果:①有机锗多酸衍生物在160.00 μg/ml以下时对FL、L929没有任何毒副作用,甚至有促进细胞生长的作用,160.00~1 280.00 μg/ml范围内,随剂量增大毒性也增强。②有机锗多酸衍生物对SMMC-7721、Hela、K562的体外抑瘤效应曲线均为双峰曲线 ,对SMMC-7721 、 K562体外抑瘤率的第一个峰值在2.50 μg/ml时分别是12.6 %、32.8 %,对Hela体外抑瘤率的第一个峰值在5.00 μg/ml时,是10.6 %,之后随剂量增大而减少 , 到80.00~1 280.00 μg/ml范围内, 随剂量增加抑瘤率升高 , 到1 280.00 μg/ml时 , 对上述3种细胞的抑瘤率分别达到66 % 、 59.9 %、65.8 %。③有机锗多酸衍生物对SMMC-7721在5.00 和320.00 μg/ml时作用48 h,均能延长G0/G1期,缩短S、G2期。结论:有机锗多酸衍生物在微量时,对SMMC-7721、Hela、K562的生长有抑制作用,对SMMC-7721细胞周期有影响。

关键词: 有机锗, 多酸衍生物, 体外抑瘤率, 细胞周期

Abstract: BACKGROUND & AIM: To study the cytotoxicity on normal cell , the inhibitive effect of Organogermanium Poly-derivatimves on cancer cell and the effect on cell cycle in vitro, and provide a basis to clinical usage. MATERIAL AND METHODS: The cytotoxicity on FL, L929 and the inhibitive rate of Organogermanium Poly-derivatimves on SMMC-7721, Hela, K562 in vitro were onducted with the method of MTT; The effect of Organogermanium Poly-derivatimves on cell cycle was studied by the way of One-Fluorescence Dying with Flow Cytometer. RESULTS: ①When the dosage reached 160.00 μg/ml, Organogermanium Poly-derivatimves did not show any cytotoxicity on FL and L929, and even stimulated cell growth; When the dosage was 160.00~1280.00 μg/ml, bigger dose showed higher cytotoxicity. ②In vitro, the inhibitive rate curve of Organogermanium Poly-derivatimves on SMMC-7721, Hela, K562 were all two-peak curve. When the dosage reached 2.50 μg/ml, the first peak of the curve, the inhibitive rate of Organogermanium Poly-derivatimves on SMMC-7721, K562 were 12.6 %, 32.8 % respectively, and on Hela, When the dosage reached 5.00 μg/ml, inhibitive rate was 10.6 %, and decreased with higher dose. When the dosage was 80.00~1 280.00 μg/ml, the inhibitive rate rised with higher dose. When the dosage reached 1 280.00 μg/ml, the inhibitive rates were 66.0 %, 59.9 %,65.8 % respectively.③When the dasage reached 5.00 μg/ml, 320.00 μg/ml, after 48 hours, Organogermanium Poly-derivatimves could extend G0/G1 and shorten S,G2 of cell cycle on SMMC-7721. CONCLUSION: At micro-dose, Organogermanium Poly-derivatimves showed obviously inhibiton to SMMC-7721,Hela,K562 and effect to cell cycle on SMMC-7221,have also observed.

Key words: organogermanium, poly-derivatimves, inhibitive rate of tumor in vitro, cell cyc