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MiR-378 inhibits progression of human gastric cancer MGC-803 cells by targeting MAPK1 in vitro

机译:MiR-378通过靶向MAPK1体外抑制人胃癌MGC-803细胞的进展

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摘要

Gastric cancer (GC) is one of the most common cancers and the leading cause of cancer-related deaths globally. The discovery of microRNAs (miRNAs) provides a new avenue for GC diagnostic and treatment regiments. Currently, a large number of miRNAs have been reported to be associated with the progression of GC, among which miR-378 has been examined to be downregulated in GC tissues and several cell lines. However, the function of miR-378 on GC cells and the mechanisms were less known. Here we found that ectopic expression of miR-378 could inhibit cell proliferation, cell cycle progression, cell migration as well as invasion, and induced cell apoptosis in GC cell line MGC-803. Moreover, we found that oncogene mitogen-activated protein kinase 1 (MAPK1) was a target gene of miR-378 in GC cells, and the tumor-suppressive role of miR-378 might be achieved by the direct interaction with MAPK1. Taken together, our results showed that miR-378 might act as tumor suppressors in GC, and it may provide novel diagnostic and therapeutic options for human GC clinical operation in the future.
机译:胃癌(GC)是全球癌症相关死亡最常见的癌症之一。 MicroRNAS(MIRNA)的发现为GC诊断和治疗法律提供了新的大道。目前,据报道,据报道大量miRNA与GC的进展相关,其中已经检查miR-378在GC组织和几种细胞系中下调。然而,MIR-378对GC细胞和机制的功能较少。在这里,我们发现miR-378的异位表达可以抑制细胞增殖,细胞周期进展,细胞迁移以及侵袭和诱导GC细胞系MGC-803中的细胞凋亡。此外,我们发现癌基因丝裂解剂蛋白激酶1(MAPK1)是GC细胞中miR-378的靶基因,MiR-378的肿瘤抑制作用可能通过与MAPK1的直接相互作用来实现。我们的结果表明,MIR-378可能担任GC中的肿瘤抑制剂,它可能在未来为人类GC临床操作提供新的诊断和治疗选择。

著录项

  • 来源
    《Oncology Research》 |2013年第12期|共8页
  • 作者

    FeiB.; WuH.;

  • 作者单位

    Department of General Surgery Second Affiliated Hospital of Soochow University SooChow Jiangsu;

    Department of General Surgery Second Affiliated Hospital of Soochow University SooChow 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

    Cell progression; Gastric cancer (GC); MAPK; MiR-378;

    机译:细胞进展;胃癌(GC);MAPK;MIR-378;

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