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

被引:105
作者
Corn, PG [1 ]
Ricci, MS [1 ]
Scata, KA [1 ]
Arsham, AM [1 ]
Simon, MC [1 ]
Dicker, DT [1 ]
El-Deiry, WS [1 ]
机构
[1] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
关键词
Mxi1; c-Myc; hypoxia; HIF-1; apoptosis;
D O I
10.4161/cbt.4.11.2299
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
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-1 beta), 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.
引用
收藏
页码:1285 / 1294
页数:10
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