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Prevention of tumor growth by needle-free jet injection of anti-C7orf24 siRNA

机译:通过无针喷射抗C7orf24 siRNA预防肿瘤生长

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摘要

Chromosome 7 open reading frame 24 (C7orf24), which was identified by proteome analysis, is upregulated in various types of cancer and is associated with cellular proliferation. However, in vivo antitumor effect by knockdown of C7orf24 has not been clarified. In this study, we investigated that the antitumor effect of anti-C7orf24 small interfering RNA (siRNA) administered by needle-free jet injection (JI) on lung cancer-bearing mice. Transfection of anti-C7orf24 siRNA induced cytotoxicity in cultured human lung cancer cells through specific knockdown of C7orf24. Furthermore, JI could effectively deliver anti-C7orf24 siRNA to tumor tissues, and as a result tumor growth was significantly inhibited. Immunohistochemical analysis revealed that C7orf24 levels were significantly reduced within tumor tissues collected from anti-C7orf24 siRNA-administered mice, indicating that the knockdown of C7orf24 induced cytotoxicity in tumor tissue. In conclusion, these data show for the first time that knockdown of C7orf24 prevents tumor growth in vivo following JI-mediated the siRNA delivery.
机译:通过蛋白质组分析鉴定的7号染色体开放阅读框24(C7orf24)在各种类型的癌症中上调,并与细胞增殖有关。但是,尚不清楚通过敲低C7orf24的体内抗肿瘤作用。在这项研究中,我们调查了通过无针喷射注射(JI)施用的抗C7orf24小干扰RNA(siRNA)对荷瘤小鼠的抗肿瘤作用。抗C7orf24 siRNA的转染通过C7orf24的特异性敲除在培养的人肺癌细胞中诱导了细胞毒性。此外,JI可以有效地将抗C7orf24 siRNA递送至肿瘤组织,因此,肿瘤的生长受到了显着抑制。免疫组织化学分析显示,从抗C7orf24 siRNA给予的小鼠收集的肿瘤组织中,C7orf24水平显着降低,表明C7orf24的敲低诱导了肿瘤组织中的细胞毒性。总之,这些数据首次表明,在JI介导的siRNA递送后,C7orf24的敲低阻止了体内肿瘤的生长。

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