Regulation of cancer cell metabolism by hypoxia-inducible factor 1

被引:369
作者
Semenza, Gregg L. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Sch Med, Vasc Program, Inst Cell Engn,Dept Pediat, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Sch Med, Vasc Program, Inst Cell Engn,Dept Med, Baltimore, MD 21218 USA
[4] Johns Hopkins Univ, Sch Med, Vasc Program, Inst Cell Engn,Dept Oncol, Baltimore, MD 21218 USA
[5] Johns Hopkins Univ, Sch Med, Vasc Program, Inst Cell Engn,Dept Radiat Oncol, Baltimore, MD 21218 USA
关键词
BNIP3; Glucose transporter; Glycolysis; HIF-1; Lactate dehydrogenase; MCT4; Mitochondrial autophagy; NHE1; Oxygen; PDK1; Warburg effect; UBIQUITIN-PROTEASOME PATHWAY; FACTOR; 1-ALPHA; UNFAVORABLE PROGNOSIS; BREAST-CANCER; GROWTH-FACTOR; CERVICAL-CANCER; HIF-ALPHA; PROLINE HYDROXYLATION; RADICAL RADIOTHERAPY; LUNG-CANCER;
D O I
10.1016/j.semcancer.2008.11.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The induction of hypoxia-inducible factor 1 (HIF-1) activity, either as a result of intratumoral hypoxia or loss-of-function mutations in the VHL gene, leads to a dramatic reprogramming of cancer cell metabolism involving increased glucose transport into the cell, increased conversion of glucose to pyruvate, and a concomitant decrease in mitochondrial metabolism and mitochondrial mass. Blocking these adaptive metabolic responses to hypoxia leads to cell death due to toxic levels of reactive oxygen species. Targeting HIF-1 or metabolic enzymes encoded by HIF-1 target genes may represent a novel therapeutic approach to cancer. (c) 2008 Published by Elsevier Ltd.
引用
收藏
页码:12 / 16
页数:5
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