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STI571诱导K562细胞耐药前后基因差异表达的研究

Comparative gene expression profile of K562 cells resistance induced by STI571

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【作者】 樊伟刘晓力张嵩杜庆锋姚锋王瑜周淑芸

【Author】 FAN Wei~1,LIU Xiao-li,ZHANG Song,DU Qing-feng, YAO Feng,WANG Yu,ZHOU Shu-yun(1Qingdao Secondary Sanatorium of Jinan Command,Qingdao 266071,P.R.China)

【机构】 济南军区青岛第二疗养院南方医科大学南方医院南方医科大学南方医院 山东青岛266071

【摘要】 目的研究ST I571诱导K 562细胞耐药前后基因差异表达情况,探讨其耐药机制。方法用药物浓度逐步递增的方法诱导野生型K 562细胞(K 562-W)对ST I571产生耐药,用台盼蓝染色、M TT法对耐药K 562细胞(K 562-R)进行特性鉴定。应用DNA芯片技术对ST I571耐药前后的K 562细胞的基因差异表达进行检测。结果诱导出K 562-R的耐药浓度为0.5μm ol/L,活细胞比例为98.5%。芯片结果发现662个基因出现差异表达,其中335个基因表达上调,327个基因表达下调。结论利用DNA芯片技术挑选与耐药可能相关的基因,可为ST I571耐药机制的研究提供新的切入点。

【Abstract】 [Objective] To study the different gene expression profile of K562 cells resistance to STI571 and to investigate the potential mechanism of acquired resistance.[Methods] The wild-type K562 cells were cultured in gradually increased concentrations of STI571.Trypan blue dye and MTT assay were applied to analyses the characteristics of the resistant K562 cells(K562-R).The gene expression difference between K562-R and K562-W was examined with cDNA array.[Results] The survival percentage of K562-R was 98.5% by Trypan blue dye and MTT assay confirmed K562-R can live steadily at 0.5 μmol/L STI571.We detected different expression of 662 genes in which 335 genes were up-regulated and 327 genes were down-regulated.[Conclusion] To identified genes related to STI571 resistance with cDNA array would provide a way on the potential mechanism of STI571 resistance.

【基金】 国家自然科学基金(30271463);广东省自然科学基金(020086)
  • 【文献出处】 山东医药 ,Shandong Medical Journal , 编辑部邮箱 ,2007年01期
  • 【分类号】R733.7
  • 【被引频次】1
  • 【下载频次】96
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