Hypoxia-Mediated Biological Control

被引:129
作者
Cassavaugh, Jessica [1 ]
Lounsbury, Karen M. [1 ]
机构
[1] Univ Vermont, Coll Med, Dept Pharmacol, Burlington, VT 05405 USA
关键词
HYPOXIA; HIF; CARDIOVASCULAR PRECONDITIONING; ANGIOGENESIS; ENDOTHELIAL GROWTH-FACTOR; INDUCIBLE FACTOR-I; HUMAN ERYTHROPOIETIN GENE; TUMOR-SUPPRESSOR PROTEIN; HIPPEL-LINDAU PROTEIN; RENAL-CELL-CARCINOMA; TRANSCRIPTIONAL ACTIVITY; UP-REGULATION; UNFAVORABLE PROGNOSIS; NEGATIVE REGULATOR;
D O I
10.1002/jcb.22956
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
When oxygen demand is greater than oxygen supply, cells need to rapidly adjust their metabolism in order for the tissue to survive. Oxygen sensing by an organism influences a host of processes including growth, development, metabolism, pH homeostasis, and angiogenesis. Hypoxia also contributes to a wide number of human diseases including vascular disease, inflammatory conditions and cancer. Recently, major advances have been made in understanding the response of cells and tissues to hypoxia with the goal of providing mechanistic insight and novel therapeutic targets. In this article we review both the normal biological effects of hypoxia as well as the alterations that occur in specific disease conditions with an emphasis on the cell signaling and gene transcription mechanisms that underlie the changes associated with chronic hypoxia. Comparisons of studies in the fields of cardiac ischemia and tumor angiogenesis reveal the complexities within the microenvironment that control responses to hypoxia. It is clear that more interaction between researchers in these fields will improve the development of therapies that either promote or prevent hypoxic responses. J. Cell. Biochem. 112: 735-744, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:735 / 744
页数:10
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