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靶向PEG10的siRNA真核表达载体对裸鼠肝癌移植瘤生长的影响 被引量:1

Influence of siRNA eukaryotic expression vectors targeting PEG10 gene on growth of transplanted human hepatocellular carcinoma in nude mice
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摘要 目的探讨靶向PEG10的siRNA真核表达载体(psiRNA-PEG10)对裸鼠人肝癌移植瘤生长的影响。方法建立人肝癌细胞HepG2的荷瘤裸鼠模型,在接种后第14天分别将psiRNA空载体和psiR-NA-PEG10瘤内多点注射进行治疗,观察肿瘤大小变化、组织形态学及超微病理改变。结果psiRNA-PEG10治疗组肿瘤生长受到明显抑制,与生理盐水组和psiRNA组比较差异有显著性(P<0.001),抑瘤率明显高于其他两组,电镜下可见明显的细胞凋亡。结论靶向PEG10的siRNA真核表达载体对裸鼠肝癌移植瘤生长有抑制作用。 [Objective] To investigate the influence of siRNA eukaryotic expression vectors targeting PEG10 gene on growth of human transplanted human hepatocellular carcinoma in nude mice. [Methods] HepG2 cell line was implanted subcutaneously into nude mice. Fourteen days after implantation, psiRNA-PEG10 and psiRNA were injected into nude mice, respectively. The tumor volume was measured. The histopathological changes of the tumors were observed by HE staining and electron microscope. [Results] Growth of hepatoeellular carcinoma was significantly inhibited in the psiRNA-PEG10 therapy group as compared with that in the control group (P 〈0.001). The growth inhibitory rate was remarkably higher than that of the two control groups, electron microscope revealed many apoptotic ceils. [Conduslon] Our finding suggest that psiRNA-PEG10 results in marked inhibition of hepatoeellular carcinoma growth in nude mice.
出处 《中国现代医学杂志》 CAS CSCD 北大核心 2008年第4期402-404,共3页 China Journal of Modern Medicine
基金 国家自然科学基金(30471983)
关键词 PEGl0 SIRNA 裸鼠 肝癌移植瘤 PEG10 siRNA nude mice transplanted hepatocellular carcinoma
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  • 1HubertE.Blum.Molecular therapy and prevention of hepatocellular carcinoma[J].Hepatobiliary & Pancreatic Diseases International,2003,2(1):11-22. 被引量:5
  • 2ELBASHIR S M, HARBORTH J, TUSCHL T, et al. Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells[J]. Nature, 2001, 411: 494-498.
  • 3SCHMECHEL D E, GOLDGABO D, ROSES A D, et al. Cellular localization of messenger RNA encoding amyloid-beta-protein in normai tissue and in Alzheimer disease. Alzheimer Dis. Asso[J]. Disord,1988, 2: 96-111.
  • 4GRAY C W, PATER A J, Regulation of beta-amyloid precursor protein isoform mRNAs by transforming growth factor-beta 1 and interleukin-1beta in astrocytes[J]. Mol. Brain Res, 1993, 19: 251-256.
  • 5ROHAN DE SILVA H A, JEN A, PATEL A J, et al. Cell-specific expression of beta-amyloid precursor protein isoform mRNAs and proteins in neurons and astrocytes. Mol[J]. Brain Res, 1997, 47:147-156.
  • 6TANAKA S, SIOJIRI S, UEDA K, et al. Tissue-specific expression of three types of beta-protein precursor mRNA: enhancement of protease inhibitor-harboring types in Alzheimer' s disease brain.Biochem[J]. Biophys. Res. Commun, 1989, 165: 1406-1414.
  • 7SUI G, SOOHOO C, SHI Y A . DNA vector-based RNAi technology to suppress gene expression in mammalian cells[J]. Proc. Natl. Acad.Sci, 2002, 99: 5515-5520.
  • 8MIYAGISHI M, TAIRA K. U6 promoter-driven siRNAs with four uridine 3'overhangs efficiently suppress targeted gene expression in mammalian cells[J]. Nature Biotechnology, 2002, 20: 497-500.
  • 9PADDISON P J, CANUDY A A, CONKLIN D S, et al. Short hairpin RNAs (shRNAs) induce sequence-sequence specific silencing in mammalian cells[J]. Genes&Development, 2002, 16: 948-958.
  • 10KRETSCHMER -KAZEMI FAR R, SCZAKIEL G. The activity of siRNA in mammalian cells is related to structural target accessibility: a comparison with antisense oligonucleotides [J]. Nucleic Acids Res, 2003, 31: 4417-4424.

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