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首页> 外文期刊>Cancer biology & therapy >Circular RNA ciRS-7 triggers the migration and invasion of esophageal squamous cell carcinoma via miR-7/KLF4 and NF-kappa B signals
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Circular RNA ciRS-7 triggers the migration and invasion of esophageal squamous cell carcinoma via miR-7/KLF4 and NF-kappa B signals

机译:圆形RNA CIRS-7通过MIR-7 / KLF4和NF-Kappa B信号触发食管鳞状细胞癌的迁移和侵袭

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摘要

Esophageal squamous cell carcinoma (ESCC) is one of the most prevalent and deadly cancers worldwide, especially in Eastern Asia. It has been indicated that circular RNAs (circRNA) are the key regulators in the development and progression of human cancers. We therefore evaluated the expression and regulation effects of ciRS-7 on the progression of ESCC, which is a recently identified circRNA and acts as a natural competing endogenous RNA. The expression of ciRS-7 was significantly increased in the ESCC tissues and cells as compared with their corresponding controls. In vitro study showed that ciRS-7 can promote the migration and invasion of ESCC cells. Over expression of miR-7, one of well-known targets of ciRS-7, can attenuate ciRS-7 induced invasion of ESCC cells and over expression of matrix metalloproteinase 2 (MMP2). The expression of stem cell marker Kruppel-like factor-4 (KLF-4), which has been reported as the target of miR7, increased significantly in ciRS-7 transfected ESCC cells. Knockdown of KLF-4 also attenuated over expression of ciRS-7 induced cell invasion. In addition, BAY 11-7082, the inhibitor of NF-kappa B, partially reversed ciRS-7 induced cell invasion. Mechanically studies indicated that ciRS-7 increased the expression of p65 via increasing the phosphorylation of IKK-alpha. Collectively, our present study revealed that ciRS-7 can trigger the migration and invasion of ESCC cells via miR-7/KLF4 and NF-kappa B signals. Targeted inhibition of ciRS-7 might be a potential approach for ESCC treatment.
机译:食管鳞状细胞癌(ESCC)是全球最普遍和最常见的癌症之一,特别是在东亚。已经表明圆形RNA(CircrNA)是人类癌症的开发和进展中的关键调节因素。因此,我们评估了CIRS-7对ESCC进展的表达和调节效应,这是最近鉴定的CircrNA,并作为自然竞争的内源性RNA。与其相应的对照相比,ESCC组织和细胞中CIRS-7的表达显着增加。体外研究表明,CIRS-7可以促进ESCC细胞的迁移和侵袭。在MIR-7的表达式,CIRS-7的众所周知的靶标之一,可以衰减CIRS-7诱导的ESCC细胞侵袭和基质金属蛋白酶2(MMP2)的表达。在CIR-7转染的ESCC细胞中,已经报告为miR7的靶标的干细胞标记物的表达,其作为miR7的靶标显着增加。 KLF-4的敲低也减弱了CIRS-7诱导细胞侵袭的表达。此外,Bay 11-7082,NF-Kappa B的抑制剂,部分反转CIRS-7诱导细胞侵袭。机械研究表明,CIR-7通过增加IKK-α的磷酸化增加P65的表达。统称,我们目前的研究表明,CIRS-7可以通过MiR-7 / KLF4和NF-Kappa B信号触发ESCC细胞的迁移和侵袭。针对ESCC治疗的靶向抑制可能是ESCC治疗的潜在方法。

著录项

  • 来源
    《Cancer biology & therapy》 |2019年第3期|共8页
  • 作者单位

    Second Mil Med Univ Dept Cardiothorac Surg Changhai Hosp 168 Changhai Rd Shanghai 200433;

    Second Mil Med Univ Dept Cardiothorac Surg Changhai Hosp 168 Changhai Rd Shanghai 200433;

    Second Mil Med Univ Dept Cardiothorac Surg Nanjing Clin Med Coll Jinling Hosp Nanjing Jiangsu;

    Second Mil Med Univ Dept Cardiothorac Surg Nanjing Clin Med Coll Jinling Hosp Nanjing Jiangsu;

    Second Mil Med Univ Dept Cardiothorac Surg Nanjing Clin Med Coll Jinling Hosp Nanjing Jiangsu;

    Second Mil Med Univ Dept Cardiothorac Surg Nanjing Clin Med Coll Jinling Hosp Nanjing Jiangsu;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 肿瘤学;
  • 关键词

    ciRS-7; ESCC; miR-7; KLF4; NF-kappa B;

    机译:CRS-7;ESCC;WE-7;KLF4;NF-HEADA B;

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