周国雄, 丁晓凌, 黄介飞, 张弘, 成建萍, 吴深宝, 魏群. 雷公藤内酯醇对胰腺癌细胞株SW1990基因表达谱的影响[J]. 中国肿瘤临床, 2006, 33(3): 145-147,156.
引用本文: 周国雄, 丁晓凌, 黄介飞, 张弘, 成建萍, 吴深宝, 魏群. 雷公藤内酯醇对胰腺癌细胞株SW1990基因表达谱的影响[J]. 中国肿瘤临床, 2006, 33(3): 145-147,156.
Zhou Guo-xiong, Ding Xiao-ling, Huang Jie-fei, . The Influence of Triptolide on Gene Expression Profile of Pancreatic Cancer Cell Line SW1990[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2006, 33(3): 145-147,156.
Citation: Zhou Guo-xiong, Ding Xiao-ling, Huang Jie-fei, . The Influence of Triptolide on Gene Expression Profile of Pancreatic Cancer Cell Line SW1990[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2006, 33(3): 145-147,156.

雷公藤内酯醇对胰腺癌细胞株SW1990基因表达谱的影响

The Influence of Triptolide on Gene Expression Profile of Pancreatic Cancer Cell Line SW1990

  • 摘要: 目的:应用基因表达谱芯片研究胰腺癌细胞株(SW1990)在雷公藤内酯醇作用后其基因表达的差异性。方法:用Cy5和Cy3两种荧光染料通过逆转录反应将加药组和对照组的SW1990细胞的mRNA分别标记成两种探针,并与载有一组靶基因的表达谱芯片杂交,通过扫描荧光强度,计算机软件分析,寻找经雷公藤内酯醇作用后表达有差异的基因。对芯片结果中两个表达有改变的基因行荧光定量PCR验证。结果:胰腺癌细胞SW1990受雷公藤内酯醇作用4h后,共筛选出11条差异表达基因,且全部下调。结论:雷公藤内酯醇可能部分通过下调C-MYC、ETS2、TGIF、RTP801等基因来发挥其有效的抗肿瘤特性。

     

    Abstract: Objective: To investigate the changes of gene expression profile in pancreatic adenocarcinoma cell line SW1990 after triptolide treatment, in order to find the possible triptolide targets. Methods: Total RNA of triptolide-treated or untreated SW1990 cells was isolated and used as templates for reverse transcriptional labeling of Cy5 and Cy3 fluorescent cDNA probes, respectively. High density DNA microarray chips with a set of 4096 human genes/Ests were used to generate the expression profile by hybridizing with fluorescently labeled probes. Array image was screened and analyzed with array analyzing software GenePixPro3.0. To confirm the expression profiles of these genes, two of the down-regulated genes, C-MYC and ETS2 were selected to undergo analysis by real-time PCR. Results: Incubated with triptolide for 4 h, 11 genes expression in SW1990 cells were significantly suppressed. Conclusion: Potential down-regulated targets from this study include C-MYC, ETS2, TGIF and RTP801, as well as the others. It is suggested that the widely known anti-tumor effects of triptolide are mediated at least in part by suppression of these gene expression.

     

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