Regulatory mechanisms of hypoxia-inducible factor 1 activity: Two decades of knowledge

被引:182
|
作者
Koyasu, Sho [1 ,2 ]
Kobayashi, Minoru [1 ]
Goto, Yoko [3 ]
Hiraoka, Masahiro [3 ]
Harada, Hiroshi [1 ,4 ]
机构
[1] Kyoto Univ, Lab Canc Cell Biol, Dept Genome Dynam, Ctr Radiat Biol, Kyoto, Japan
[2] Univ Tokyo, Res Ctr Adv Sci & Technol, Tokyo, Japan
[3] Kyoto Univ, Dept Radiat Oncol & Image Appl Therapy, Grad Sch Med, Kyoto, Japan
[4] Japan Sci & Technol Agcy JST, Precursory Res Embryon Sci & Technol, Saitama, Japan
来源
CANCER SCIENCE | 2018年 / 109卷 / 03期
基金
日本科学技术振兴机构;
关键词
gene expression; hypoxia-inducible factor 1 (HIF-1); molecular mechanism; tumor hypoxia; TUMOR-SUPPRESSOR PROTEIN; TRANSCRIPTIONAL ACTIVITY; CANCER-THERAPY; FACTOR; 1-ALPHA; HIF-ALPHA; FACTOR-I; STABILIZES HIF-1-ALPHA; PROLYL; 4-HYDROXYLASES; ERYTHROPOIETIN GENE; BREAST-CANCER;
D O I
10.1111/cas.13483
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hypoxia-inducible factor 1 (HIF-1) is a transcriptional activator of various genes related to cellular adaptive responses to hypoxia. Dysfunctions in the regulatory systems of HIF-1 activity have been implicated in the pathogenesis of various diseases including malignant tumors and, thus, elucidating the molecular mechanisms underlying the activation of HIF-1 is eagerly desired for the development of novel anti-cancer strategies. The importance of oxygen-dependent and ubiquitin-mediated proteolysis of the regulatory subunit of HIF-1 (HIF-1) was first reported in 1997. Since then, accumulating evidence has shown that HIF-1 may become stable and active even under normoxic conditions; for example, when disease-associated genetic and functional alterations in some genes trigger the aberrant activation of HIF-1 regardless of oxygen conditions. We herein review the last two decades of knowledge, since 1997, on the regulatory mechanisms of HIF-1 activity from conventional oxygen- and proteolysis-dependent mechanisms to up-to-the-minute information on cancer-associated genetic and functional alteration-mediated mechanisms.
引用
收藏
页码:560 / 571
页数:12
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