期刊文献+

RNAi抑制促血管形成因子治疗结肠癌的研究

Research of inhibiting pro-angiogenic factor in colon cancer by RNA interference
下载PDF
导出
摘要 目的:应用RNA干扰技术抑制促血管形成因子基因的表达,观察结肠癌细胞增殖和凋亡的变化及对结肠癌肿瘤生长的影响,为进一步的临床应用研究提供理论基础。方法:利用60只裸鼠建立肿瘤动物模型,并随机分成5组。通过移植瘤内注射pshRNA-Del1和pshRNA-VEGF载体质粒,观察并比较pshRNA-Del1治疗组、pshRNA-VEGF治疗组和联合治疗组对裸鼠移植瘤生长的影响;通过免疫组化法检测肿瘤组织中Ki-67的表达和微血管密度,进一步探讨基于RNA干扰的治疗对结肠癌疗效的影响。结果:RNAi通过抑制基因VEGF和Del1的表达,能显著抑制结肠肿瘤的生长,减低肿瘤的血管密度,减弱肿瘤细胞增殖。结论:协同阻断基因VEGF和基因Del1的表达能显著抑制结肠肿瘤的生长,并在结肠癌的治疗方面具有明显的作用。 Objective:To observe cell proliferations and apoptosis of colon cancer after inhibiting pro-angiogenic factor gene by the way of RNA interference,and hope that the study would provide a theoretical basis on the further studied in the future.Methods:Animal model was established by using 60 nude mice,which were divided into 5 groups randomly.By injecting pshRNA-Del1 and pshRNA-VEGF plasmid to node mice,the effects of treatments on tumor growth among pshRNA-Del1 treatment group,pshRNA-VEGF treatment group and combined treatment group were observed.Furthermore,in order to explore the efficacy of the treatment of colon cancer,the expression of Ki-67 and the density of micro-vessel by immunohistochemical staining of tumor tissue were detected.Results:On the one hand,RNA interference had the ability to inhibit the expression of VEGF and Del1 to significantly inhibited the growth of colon cancer.On the other hand,the RNAi treatment not only reduced densities of tumor blood vessels but also decreased the proliferations of tumor cells.Conclusion:Blocking the gene expression of VEGF and Del1 together can significantly inhibit the growth of colon cancer.Meanwhile,this kind of RNAi treatment has a significant role in therapeutics of colon cancer.
作者 齐霁 邹小龙
出处 《中国医药导报》 CAS 2011年第36期33-37,共5页 China Medical Herald
基金 黑龙江省教育厅科学技术研究项目(项目编号:11551207)
关键词 RNAI 促血管形成因子 结肠癌 RNAi Pro-angiogenic factor Colon cancer
  • 相关文献

参考文献1

二级参考文献19

  • 1Joyce E. Ohm,Dr. David P. Carbone M.D., Ph.D..VEGF as a mediator of tumor-associated immunodeficiency[J]. Immunologic Research . 2001 (2-3) 被引量:1
  • 2Byzova TV,Goldman CK.Pampori N,et al.A mechanism f-or modulation of cell responses to VEGF: activation of the integrins. Molecular Cell . 2000 被引量:1
  • 3Dias S,Shmelkov SV,Lam G,et al.VEGF(165) promotes survival of leukemic cells by Hsp90-mediated induction of Bcl-2 expression and apoptosis inhibition. Blood . 2002 被引量:1
  • 4Beierle EA,Strande LF,Chen MK.VEGF upregulates Bcl-2 e-xpression and is associated with decreased apoptosis in neuroblastoma cells. Journal of Pediatric Surgery . 2002 被引量:1
  • 5Ferrara N,Gerber H-P,Lecouter J.The biology of VEGF and its receptors. Nature Medicine . 2003 被引量:1
  • 6Lopez-Pedrera C,Barbarroja N,Velasco F.Pathogenic mechanisms of thrombosis in neoplasia: therapeutic implications. Med din (Bare) . 2004 被引量:1
  • 7Ohm,JE,Carbone DP.VEGF as a mediator of tumorasso-ciatedimmunodeficiency. Immunologic Research . 2001 被引量:1
  • 8Dias S,Hattori K,Zhu ZP,et al.Autocrine stimulation of VE-GFR-2 activates human leukemic cell growth and migration. The Journal of Clinical Investigation . 2000 被引量:1
  • 9Kim SJ,Choi IK,Park KH,et al.Serum vascular endothelial growth factor per platelet count in hepatocellular carcinoma: correlations with clinical parameters and survival. Japanese Journal of Clinical Oncology . 2004 被引量:1
  • 10Gerber HP,Dixit V,Ferrara N.VEGF regulates endothelial cell survival by the PI3-kinase/Akt signal transduction pathway.Requirement for flk-1/KDR activation. Journal of Biological Chemistry . 1998 被引量:1

共引文献8

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