Sonveaux Pierre, Jordan Bénédicte F, Gallez Bernard, Feron Olivier
Unit of Pharmacology and Therapeutics, Université catholique de Louvain (UCL), Avenue E. Mounier 52, B-1200 Brussels, Belgium.
Eur J Cancer. 2009 May;45(8):1352-69. doi: 10.1016/j.ejca.2008.12.018. Epub 2009 Jan 17.
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.
缺氧和血流异质性是实体瘤的特征,也是治疗的主要障碍。利用一氧化氮(NO)的生物学特性(一种具有多种功能的小分子自由基)来规避这些耐药源并使肿瘤对放疗和化疗等细胞毒性治疗敏感,尤其具有吸引力。实际上,虽然NO介导血管生成作用,但它也可能促进肿瘤灌注、药物递送和氧合。本文综述了向肿瘤递送NO的不同策略以及与FECS-EJC奖获得者工作相关的内容,重点关注其治疗潜力。还讨论了监测NO递送如何以及在何种程度上影响特定患者体内特定肿瘤表型的技术发展。