期刊文献+

新型多酸化合物对人乳腺癌细胞增殖的抑制作用

The growth inhibition of human breast cancer cells induced with new polyoxometalates
下载PDF
导出
摘要 采用MTT法、形态学方法和Western blot方法,检测了3种新型多酸化合物[SbW9、(SbW9)2-(SnR)4、(SbW9)2-(SnR-CH3)4]对人乳腺癌MCF7和MDA-MB-231细胞生长抑制作用,细胞形态学变化及细胞PCNA蛋白表达变化,并探讨该3种化合物抑癌的机制.实验结果表明:3种化合物对人乳腺癌细胞MCF7和MDA-MB-231的生长均具有明显的抑制作用(P<0.01),细胞形态发生明显变化,细胞皱缩并且增殖速度明显减慢;其中,(SbW9)2-(SnR)4可使MCF7细胞PCNA蛋白表达下降(P<0.05),且呈浓度剂量依赖性.说明该3种新型多酸化合物均具有抗肿瘤活性,其活性部位可能是以{SbW9}为基本建筑单元的聚阴离子,作用机制可能与其抑制细胞DNA的合成有关. The purpose of the current study is to investigate the growth inhibition and the mechanism of MCF7 and MDA-MB-231 cells induced with new trivacant Keggin-type polyoxometalates [SbW9、(SbW9)2-(SnR)4、(SbW9)2-(SnR-CH3)4],and explore the underlying molecular mechanism.The antiproliferative effective of compounds on MCF7 and MDA-MB-231 cells was measured with MTT.Morphological changes were observed by microscopic.The protein expression of PCNA was determined by Western blotting.MTT assay shows that proliferation of MCF7 and MDA-MB-231 cells were significantly inhibited,the compounds(P〈0.01).Microscopic observation of cell morphology changed significantly,and the cells were shrinked and the proliferation were reduced significantly.In particular,the expression of PCNA protein was decreased significantly(P〈0.05) in a dose-dependent manner by(SbW9)2-(SnR)4.The results of the study indicated that the decisive site of anti-tumor activity which has SbW9 as its basic building unit maybe relate to inhibition of cell complexes on DNA synthesis.
出处 《辽宁师范大学学报(自然科学版)》 CAS 2012年第1期98-102,共5页 Journal of Liaoning Normal University:Natural Science Edition
基金 国家自然科学基金项目(30570225)
关键词 多酸化合物 乳腺癌 增殖 polyoxometalate breast cancer proliferation
  • 相关文献

参考文献3

二级参考文献59

  • 1王朕华,丰有吉,王以政.钾离子通道与肿瘤细胞的关系[J].国外医学(肿瘤学分册),2005,32(10):733-736. 被引量:4
  • 2Norman S D,Ladd M M,Marcus R B,et al.Inorg Chem[J],1997,36:1 424.
  • 3Carl J Carrano,Ruben Verastgue,Marcus R.Bond Inorg Chem[J],1993,32:3 589.
  • 4Manzer L E.Organomet Chem[J],1975,102:167.
  • 5Ellen Kime-Hunt,Spartalian K,DeRusha M,et al.Inorg Chem[J],1989,28:4 392.
  • 6Holmes S M,Carrano C J,et al.Inorg Chem[J],1991,30:1 231.
  • 7Carrano C J,Mohan M,Holmes S M,et al. Inorg Chem[J],1994,33:646.
  • 8Reglinski J,Garner M,Cassidy I D,et al.Chem Soc Dalton Trans[J],1999:2 119.
  • 9Trofimenko S.Am Chem Soc[J],1967:6 288.
  • 10OUADID-AHIDOUCH H, CHAUSSADE F, ROUDBARAKi M,et al. Kvl. 1 K^+ channels identification in human breast carcinoma cellst involvement in cell prollferation[J]. Biochem Biophys Res Commun, 2000, 278:272-277.

共引文献18

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部