首页> 外文期刊>Leukemia and lymphoma >MiR-15a/16-1 enhances retinoic acid-mediated differentiation of leukemic cells and is up-regulated by retinoic acid
【24h】

MiR-15a/16-1 enhances retinoic acid-mediated differentiation of leukemic cells and is up-regulated by retinoic acid

机译:MiR-15a / 16-1增强视黄酸介导的白血病细胞分化,并被视黄酸上调

获取原文
获取原文并翻译 | 示例
           

摘要

miR-15a and miR-16-1 (miR-15a/16-1) have been implicated in apoptosis, cell cycle regulation and chemosensitivity of tumor cells, but little is known about the role of miR-15a/16-1 in the differentiation of leukemic cells. In this study, we found that the expression level of miR-15a/16-1 was up-regulated by all-trans retinoic acid (ATRA) treatment in NB4, HL-60 and U937 cell lines and primary leukemic cells. Overexpression of miR-15a/16-1 could not directly drive cells to undergo differentiation but enhanced ATRA-induced differentiation in NB4 and U937 cells. Up-regulation of miR-15a/16-1 was also observed in 36 patients with acute myeloid leukemia (AML) who achieved a complete remission (CR), and two of them showed sharp down-regulation of miR-15a/16-1 when they had a molecular relapse. These data indicate that miR-15a/16-1 plays an important role in the ATRA-induced differentiation of leukemic and primary AML cells.
机译:miR-15a和miR-16-1(miR-15a / 16-1)与肿瘤细胞的凋亡,细胞周期调控和化学敏感性有关,但对miR-15a / 16-1在肿瘤细胞中的作用了解甚少。白血病细胞的分化。在这项研究中,我们发现在NB4,HL-60和U937细胞系和原代白血病细胞中,全反式维甲酸(ATRA)处理可上调miR-15a / 16-1的表达水平。 miR-15a / 16-1的过表达不能直接驱动细胞分化,但会增强ATRA诱导的NB4和U937细胞分化。在获得完全缓解(CR)的36例急性髓细胞性白血病(AML)患者中,也观察到miR-15a / 16-1的上调,其中两个患者显示miR-15a / 16-1的下调当他们发生分子复发时。这些数据表明,miR-15a / 16-1在ATRA诱导的白血病和原发性AML细胞分化中起重要作用。

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