Intermittent hypoxia is a key regulator of cancer cell and endothelial cell interplay in tumours

被引:172
作者
Toffoli, S. [1 ]
Michiels, C. [1 ]
机构
[1] Fac Univ Notre Dame Paix, Univ Namur, Lab Biochem & Cellular Biol URBC, B-5000 Namur, Belgium
关键词
apoptosis; cancer; chemoresistance; endothelial cell; hypoxia-inducible factor-1; intermittent hypoxia; radioresistance; reactive oxygen species; reoxygenation; tumor cell;
D O I
10.1111/j.1742-4658.2008.06454.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Solid tumours are complex structures in which the interdependent relationship between tumour and endothelial cells modulates tumour development and metastasis dissemination. The tumour microenvironment plays an important role in this cell interplay, and changes in its features have a major impact on tumour growth as well as on anticancer therapy responsiveness. Different studies have shown irregular blood flow in tumours, which is responsible for hypoxia and reoxygenation phases, also called intermittent hypoxia. Intermittent hypoxia induces transient changes, the impact of which has been underestimated for a long time. Recent in vitro and in vivo studies have shown that intermittent hypoxia could positively modulate tumour development, inducing tumour growth, angiogenic processes, chemoresistance, and radioresistance. In this article, we review the effects of intermittent hypoxia on tumour and endothelial cells as well as its impacts on tumour development.
引用
收藏
页码:2991 / 3002
页数:12
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