New horizons in hypoxia signaling pathways

被引:139
|
作者
Pugh, Christopher W. [1 ]
Ratcliffe, Peter J. [1 ,2 ]
机构
[1] Univ Oxford, Target Discovery Inst, Oxford OX3 7FZ, England
[2] Francis Crick Inst, Midland Rd, London NW1 1AT, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
Hypoxia; Protein hydroxylation; Prolyl hydroxylase; Hypoxia-inducible factor; Transcription; Cancer; INDUCIBLE FACTOR-I; TRANSCRIPTIONAL RESPONSE; HIF; HYDROXYLATION; BINDING; FAMILY; PROKARYOTES; ACTIVATION; ENHANCER; PROTEIN;
D O I
10.1016/j.yexcr.2017.03.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Investigation into the regulation of the erythropoietin gene by oxygen led to the discovery of a process of direct oxygen sensing that transduces many cellular and systemic responses to hypoxia. The oxygen-sensitive signal is generated through the catalytic action of a series of 2-oxoglutarate-dependent oxygenases that regulate the transcription factor hypoxia-inducible factor (HIF) by the post-translational hydroxylation of specific amino acid residues. Here we review the implications of the unforeseen complexity of the HIF transcriptional cascade for the physiology and pathophysiology of hypoxia, and consider the origins of post-translational hydroxylation as a signaling process.
引用
收藏
页码:116 / 121
页数:6
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