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Survivin-siRNA在体外诱导Panc-1细胞凋亡的实验研究 被引量:1

The Study of siRNA of Survivin Gene Induced Apoptosis in Panc1 Cell Line in Vitro
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摘要 目的:探讨RNA干扰技术抑制Survivin对人胰癌细胞株Panc-1细胞凋亡的影响。方法:体外设计、合成针对sur-vivin基因的小分子干扰RNA(survivin-siRNA),应用脂质体介导survivin-siRNA转染Panc-1细胞后,MTT试验测定转染细胞的增殖抑制率,RT-PCR检测细胞survivin mRNA表达,琼脂糖凝胶电泳分析其对Panc-1细胞凋亡诱导作用。结果:转染survivin-siR-NA的Panc-1细胞增殖明显受抑制,与对照进行比较,具有显著性差异(P<0.01);经琼脂糖凝胶电泳,转染survivin-siRNA的Panc-1细胞可见到DNA梯形条带,而对照细胞未见到。结论:survivin-siRNA能够显著诱导Panc-1细胞凋亡。 Objective: To explore the effects of surviving-siRNA on induced apoptosis in human pancreatic cancer cell line Panc-1. Methods. The small interference RNA (siRNA) targeting survivin gene was designed and synthesized by transcription in vitro. Survivin siRNA was transferred into Panc-1 cell line by lipofection. The opposite livability on Panc-1 cell line was assayed with MTT test. Expression of survivin was detected by RT-PCR. Apoptosis was detected by DNA gel electrophoresis. Results: Survivin siRNA obviously inhibited the Panc-1 cells growth (P〈0.01). Agarose gel electrophoresis of genomic DNA from Survivin siRNA transferred Pane-1 cells showed typical DNA ladder, but DNA from other cells did not. Conclusion: Survivin siRNA could effectively induce apoptosis in Pane-1 cells.
出处 《数理医药学杂志》 2008年第4期402-404,共3页 Journal of Mathematical Medicine
基金 湖北省自然科学基金(NO.2007ABA186) 湖北省技攻关计划项目(NO.Q200734002) 武汉市高校科研重点项目(NO.02006Z02)资助
关键词 SIRNA SURVIVIN Pane-1 凋亡 siRNA Survivin Panc-1 cell line Apoptosis
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参考文献4

  • 1Chiou SK, Jones MK, Tarnawski AS. Survivin an anti-apoptosis protein: its biological roles and implications for cancer and beyond. Med Sci Monit, 2003, 9 (4):PI25-29.
  • 2Shore S, Raraty MG, Ghaneh P, etal. Review article: chemotherapy for pancreatic cancer. Aliment Pharmacol Ther. 2003 Dec; 18 (11-12) :1049-1069.
  • 3Wrzesien-Kus A, Smolewski P, Sobczak-Pluta A, et al. The inhibitor of apoptosis protein family and its antagonists in acute leukemias. Apoptosis. 2004 Nov. 9 (6) : 705-715.
  • 4Rosel KF, Georg S. The activity of siRNA in mammalian cells is related to structural target accessibility: a comparison with antisense oligonucleotides. Nucleic Acids Res, 2003, 31: 4417-4424.

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