首页> 外文期刊>Cancer biology & therapy >Mxi1 is induced by hypoxia in a HIF-1-dependent manner and protects cells from c-Myc-induced apoptosis.
【24h】

Mxi1 is induced by hypoxia in a HIF-1-dependent manner and protects cells from c-Myc-induced apoptosis.

机译:Mxi1由缺氧以HIF-1依赖性方式诱导,并保护细胞免受c-Myc诱导的细胞凋亡。

获取原文
获取原文并翻译 | 示例
           

摘要

HIF-1, a hypoxia inducible transcription factor, plays a pivotal role in the cellular response to hypoxia by activating genes involved in glucose metabolism, vascular remodeling, and erythropoiesis. We identified Mxi1, a c-Myc antagonist, as a novel target gene induced in hypoxia. Mxi1 was not induced in cells deficient in ARNT (HIF-1beta), suggesting that Mxi1 is a transcriptional target of the HIF-1 complex. Notably, c-Myc protein levels decreased during hypoxia but were stabilized by a proteasome inhibitor. Analysis of downstream transcriptional targets of c-Myc during hypoxia revealed that genes regulated by c-Myc, such as ornithine decarboxylase (ODC), were downregulated during hypoxia. In contrast, genes that are regulated by c-Myc and HIF-1, such as LDH-A, were upregulated. Mxi1 protects against c-Myc-dependent sensitization to hypoxia-induced apoptosis. The results suggest a coordinated mechanism for opposing c-Myc signaling during hypoxia that is mediated by a reduction in c-Myc levels, the induction of Mxi1, and a dominant effect of HIF-1 transcriptional activity.
机译:HIF-1是一种低氧诱导型转录因子,它通过激活涉及葡萄糖代谢,血管重塑和促红细胞生成的基因,在细胞对低氧的反应中起关键作用。我们确定Mxi1,c-Myc拮抗剂,作为缺氧诱导的新型靶基因。在缺乏ARNT(HIF-1beta)的细胞中未诱导Mxi1,这表明Mxi1是HIF-1复合体的转录靶标。值得注意的是,缺氧期间c-Myc蛋白水平下降,但被蛋白酶体抑制剂稳定。对缺氧期间c-Myc下游转录靶标的分析显示,缺氧期间c-Myc调控的基因,如鸟氨酸脱羧酶(ODC)被下调。相反,受c-Myc和HIF-1调控的基因(如LDH-A)被上调。 Mxi1可以防止c-Myc依赖性的缺氧诱导的细胞凋亡。结果表明在缺氧过程中,由c-Myc水平降低,Mxi1的诱导和HIF-1转录活性的主导作用介导的对抗c-Myc信号转导的协调机制。

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