Nitric oxide delivery to cancer: Why and how?

被引:89
|
作者
Sonveaux, Pierre [1 ]
Jordan, Benedicte F. [2 ]
Gallez, Bernard [2 ]
Feron, Olivier [1 ]
机构
[1] Catholic Univ Louvain, Unit Pharmacol & Therapeut, B-1200 Brussels, Belgium
[2] Catholic Univ Louvain, Unit Biomed Magnet Resonance, B-1200 Brussels, Belgium
关键词
Nitric oxide; Tumour vasculature; Vasodilation; Cell respiration; Blood flow; Tumour oxygenation; Radiotherapy; Chemotherapy; Drug delivery; Imaging; ENDOTHELIAL GROWTH-FACTOR; TUMOR BLOOD-FLOW; ELECTRON-PARAMAGNETIC-RESONANCE; INTERSTITIAL FLUID PRESSURE; HUMAN COLON ADENOCARCINOMA; IN-VIVO; OXYGEN-TENSION; CELL RADIOSENSITIZATION; INDUCED ANGIOGENESIS; VASCULAR REACTIVITY;
D O I
10.1016/j.ejca.2008.12.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hypoxia and blood flow heterogeneities are characteristics of solid tumours and are major obstacles for therapy. Exploiting the biology of nitric oxide (NO), a small radical with multiple functions, is particularly attractive to circumvent these sources of resistance and to sensitise tumour to cytotoxic treatments such as radiotherapy and chemotherapy. Indeed, while NO mediates angiogenic effects, NO may also promote tumour perfusion, drug delivery and oxygenation. Different strategies to deliver NO to tumours and pertaining to the FECS-EJC award laureate's work are reviewed, with a focus on their therapeutic potential. The development of techniques to monitor how and to which extent NO delivery influences the phenotype of a given tumour in a given patient is also discussed. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1352 / 1369
页数:18
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