首页> 外文期刊>Cancer Cell >Blockade of miR-150 Maturation by MLL-Fusion/MYC/LIN-28 Is Required for MLL-Associated Leukemia
【24h】

Blockade of miR-150 Maturation by MLL-Fusion/MYC/LIN-28 Is Required for MLL-Associated Leukemia

机译:与MLL相关的白血病需要通过MLL-Fusion / MYC / LIN-28阻断miR-150成熟

获取原文
获取原文并翻译 | 示例
           

摘要

Expression of microRNAs (miRNAs) is under stringent regulation at both transcriptional and posttranscriptional levels. Disturbance at either level could cause dysregulation of miRNAs. Here, we show that MLL fusion proteins negatively regulate production of miR-150, an miRNA widely repressed in acute leukemia, by blocking miR-150 precursors from being processed to mature miRNAs through MYC/LIN28 functional axis. Forced expression of miR-150 dramatically inhibited leukemic cell growth and delayed MLL-fusion-mediated leukemogenesis, likely through targeting FLT3 and MYB and thereby interfering with the HOXA9/MEIS1/FLT3/MYB signaling network, which in turn caused downregulation of MYC/LIN28. Collectively, we revealed a MLL-fusion/MYC/LIN28?miR-150?FLT3/MYB/HOXA9/MEIS1 signaling circuit underlying the pathogenesis of leukemia, where miR-150 functions as a pivotal gatekeeper and its repression is required for leukemogenesis.
机译:microRNA(miRNA)的表达在转录和转录后水平上都受到严格的调控。任何一个水平的干扰都可能导致miRNA失调。在这里,我们显示MLL融合蛋白通过阻止miR-150前体通过MYC / LIN28功能轴加工成成熟的miRNA,从而对miR-150(一种在急性白血病中广泛抑制的miRNA)产生负调控。可能通过靶向FLT3和MYB,miR-150的强制表达可显着抑制白血病细胞生长并延迟MLL融合介导的白血病发生,从而干扰HOXA9 / MEIS1 / FLT3 / MYB信号网络,进而导致MYC / LIN28的下调。 。总的来说,我们揭示了白血病发病机理的MLL-fusion / MYC / LIN28?miR-150?FLT3 / MYB / HOXA9 / MEIS1信号转导通路,其中miR-150起着关键性的守门人的作用,其抑制是白血病发生的必要条件。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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