首页> 美国卫生研究院文献>Frontiers in Oncology >Schistosoma japonicum MiRNA-7-5p Inhibits the Growth and Migration of Hepatoma Cells via Cross-Species Regulation of S-Phase Kinase-Associated Protein 2
【2h】

Schistosoma japonicum MiRNA-7-5p Inhibits the Growth and Migration of Hepatoma Cells via Cross-Species Regulation of S-Phase Kinase-Associated Protein 2

机译:日本血吸虫MiRNA-7-5p通过跨物种调控S相激酶相关蛋白2抑制肝癌细胞的生长和迁移。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

MicroRNAs (miRNAs) play important roles in human diseases, such as cancer. Human miRNA-7-5p is a tumor suppressor miRNA that inhibits tumor growth by regulating multiple oncogenic signal pathways. Recently, studies revealed that plant miRNAs could regulate mammalian gene expression in a cross-kingdom manner. Schistosoma japonicum miRNA-7-5p (designated as sja-miR-7-5p) is conserved between the parasites and mammals. Thus, we investigated whether sja-miR-7-5p has similar antitumor activity to its mammalian counterpart. We first showed that sja-miR-7-5p was detected in host hepatocytes during S. japonicum infection. The sja-miR-7-5p mimics significantly inhibited the growth, migration, and colony formation of mouse and human hepatoma cell lines in vitro, and induced G1/G0 cell cycle arrest. In a xenograft animal model, the tumor volume and weight were significantly reduced in mice inoculated with hepatoma cells transfected with sja-miR-7-5p mimics compared with those transfected with NC miRNAs. Furthermore, the antitumor activity of sja-miR-7-5p was suggested by cross-species downregulation of the S-phase kinase-associated protein 2 gene in the host. Thus, sja-miR-7-5p is translocated into hepatocytes and exerts its anti-cancer activities in mammals, implying that sja-miR-7-5p might strengthen host resistance to hepatocellular carcinoma during schistosome infection.
机译:微小RNA(miRNA)在人类疾病(例如癌症)中起重要作用。人miRNA-7-5p是一种抑制肿瘤的miRNA,可通过调节多种致癌信号途径来抑制肿瘤的生长。最近,研究表明植物miRNA可以以跨王国的方式调节哺乳动物基因的表达。日本血吸虫miRNA-7-5p(命名为sja-miR-7-5p)在寄生虫和哺乳动物之间是保守的。因此,我们调查了sja-miR-7-5p是否具有与其哺乳动物类似物相似的抗肿瘤活性。我们首先显示在日本血吸虫感染期间在宿主肝细胞中检测到sja-miR-7-5p。 sja-miR-7-5p模拟物在体外显着抑制小鼠和人类肝癌细胞系的生长,迁移和集落形成,并诱导G1 / G0细胞周期停滞。在异种移植动物模型中,与用NC miRNA转染的小鼠相比,接种sja-miR-7-5p模拟物转染的肝癌细胞的小鼠的肿瘤体积和重量显着降低。此外,sja-miR-7-5p的抗肿瘤活性是由宿主中S期激酶相关蛋白2基因的跨物种下调暗示的。因此,sja-miR-7-5p在哺乳动物中易位,进入肝细胞并发挥其抗癌活性,这意味着sja-miR-7-5p可能会增强血吸虫感染期间宿主对肝细胞癌的抵抗力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号