期刊文献+

小干扰RNA抑制胃癌细胞肝素酶表达及侵袭的实验研究 被引量:8

Inhibitory effect of siRNA on heparanase expression and invasion ability of gastric cancer cells:an in vitro experiment
原文传递
导出
摘要 目的利用 RNA 干扰(RNAi)技术封闭胃癌细胞系 SGC7901肝素酶表达,观察其对肿瘤细胞侵袭能力的影响。方法体外转录合成小于扰 RNA(siRNA),经脂质体转染胃癌细胞系;结合逆转录(RT)-PCR,Western 印迹检测类肝素酶 mRNA 及蛋白质表达;通过体外侵袭实验评价肝素酶RNAi 后胃癌细胞系的侵袭能力变化。结果肝素酶 siRNA 分子可以特异性地抑制 SGC7901细胞肝素酶 mRNA,抑制率达(70±6)%;肝素酶 RNAi 后 SGC7901细胞的侵袭抑制率达(61±36)%。结论靶向肝素酶基因的 siRNA 分子能特异性抑制其蛋白表达水平,降低肿瘤细胞的侵袭能力。肝素酶是促进胃癌细胞侵袭转移的关键分子,并可为抑制胃癌侵袭转移提供新策略。 Objective To investigate the inhibitory effect of siRNA on heparanase expression and invasion ability gastric cancer cells. Methods A heparanase mRNA-targeting double-stranded siRNA was designed with the bioinformatics technology. Human gastric cancer cells of the line SGC7901 were cultured and transfected with the siRNA of the concentrations of 5,10,20, and 40 nmol/L respectively. Forty-eight hours later RT-PCR and Western blotting were applied to detect the mRNA and protein expression of heparanase. Millicell chamber assay was performed to detect the invasion ability of the SGC7901 cells. Blank control group and negative control group were set. Results The mRNA expression level of the cells transfected with the siRNA of the concentrations 20 nmol/L and 40 nmol/L were 0. 207 ± 0. 095 and 0.200 ± 0.085 respectively, both significantly lower than that of the control group (0.60 ± 0.09, both P 〈 0. 05). Western blotting showed that the protein expression of heparanase of the different siRN.A subgroups were all decreased dose-dependently; and no heparanase band was seen in the 40 nmol/L subgroup. The invasion rate of the siRNA group was significantly lower than that of the control group with a mean inhibition rate of (61 ±36)%. Conclusion RNAi inhibits the expression of heparanase and the invasion ability of human gastric cancer cells. Heparanase may be a new target in treatment of gastric cancer's metastasis.
出处 《中华医学杂志》 CAS CSCD 北大核心 2007年第24期1717-1720,共4页 National Medical Journal of China
基金 国家自然科学基金(30300342) 辽宁省高 校优秀人才支持计划基金(RC-05-02)
关键词 肝素裂合酶 肿瘤侵润 RNA干扰 Heparin lyase Neoplasm invasiveness RNA interfering
  • 相关文献

参考文献3

二级参考文献32

  • 1Zhen-NingWang,Hui-MianXu,LiJiang,XinZhou,ChongLu,XueZhang.Expression of survivin in primary and metastatic gastric cancer cells obtained by laser capture microdissection[J].World Journal of Gastroenterology,2004,10(21):3094-3098. 被引量:23
  • 2Gazzaniga P, Gradilone A, Giuliani L, et al. Expression and prognostic significance of LININ, survivin and other apoptosisrelated genes in the progression of superficial bladder cancer[J]. Ann Oncol, 2003,14( 1 ): 85-90. 被引量:1
  • 3Ikeguchi M, Kaibara N. survivin messenger RNA expression is a good prognostic biomarker for oesophageal carcinoma [J].Br J Cancer, 2002,87(8) :883-887. 被引量:1
  • 4Wall NR, O'Connor SD, Plescia J, et al. Suppression of survivin phosphorylation on Thr34 by Flavopiridol enhances tumor cell apoptosis [ J ]. Cancer Res, 2003,63 ( 1 ): 230-235. 被引量:1
  • 5Willians NS, Gaynor RB, Scoggin S, et al. Identification and validation of genes involved in the pathogenesis of colorectal cancer using cDNA microarrays and RNA interference [J].Clinical Cancer Res, 2003,9 (3): 931-946. 被引量:1
  • 6Ikeguchl M, Hirooka Y, Kalbara N. Quantitative analysis of apoptosis-related gene expression in hepatocellular carcinoma[J]. Cancer, 2003,95(9):1938-1945. 被引量:1
  • 7Mahotka C, Krieg T, Krieg A, et al. Distinct in vivo expression patterns of surviving splice variants in renal cell carcinomas [J]. Int J Cancer, 2002, 100( 1 ) :30-36. 被引量:1
  • 8Xing N, Qian J, Bostwick D, et al. Neuroendocrine cells in human prostate over-express the anti-apoptosis protein survivin[J]. Prostate, 2001,48( 1 ): 7-15. 被引量:1
  • 9Elbashir SM, Harborth J, Weber K, et al. Analysis of gene function in somatic mammalian cells using interfering RNAs[J]. Methods, 2002,26(2): 199-213. 被引量:1
  • 10Crnkovic-Mertens I, Hoppe-Seyler F, Butz K. Induction of apoptosis in tumor cells by siRNA-mediated silencing of the livin/ML-IAP/KIAP gene [J]. Oncogene, 2003,22(51 ):8330-8336. 被引量:1

共引文献73

同被引文献105

引证文献8

二级引证文献22

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