CBME/IBB, DQF/Faculty of Sciences and Technology, University of Algarve, 8005-210, Faro, Portugal.
Curr Drug Metab. 2013 Nov;14(9):969-75. doi: 10.2174/1389200211314090003.
Tumour progression is characterized by a rapid cell growth accompanied by changes in the microenvironment, largely due to hypoxia. The angiogenic switch involves changes in the expression of genes that play key roles in tumour progression, invasion, metastasis and therapeutic response, contributing to tumour aggressiveness. The effect of hypoxia on the cellular concentrations of drug metabolizing enzymes and transporters is much less understood. A brief summary of the signaling mechanisms triggered by hypoxia is presented, followed by a review of the known effects of hypoxia on drug metabolism and transport. Most of the studies available have focused on Cytochromes P450 and ATP-binding cassette transporters, while influx transporters of the SLC family have been less investigated. Given its potential to contribute both to the understanding of the pathogenesis of disease and to the optimization of therapeutics, it is rather surprising that this area of research is still underdeveloped. An increasing number of studies focusing on this subject are bound to provide key information for drug development and optimization of therapeutics.
肿瘤进展的特征是细胞生长迅速,同时微环境发生变化,这主要归因于缺氧。血管生成开关涉及参与肿瘤进展、侵袭、转移和治疗反应的关键基因表达的变化,导致肿瘤侵袭性增强。缺氧对药物代谢酶和转运体细胞浓度的影响知之甚少。本文简要概述了缺氧触发的信号机制,接着综述了已知的缺氧对药物代谢和转运的影响。现有的大多数研究都集中在细胞色素 P450 和三磷酸腺苷结合盒转运体上,而对 SLC 家族的摄取转运体的研究则较少。鉴于缺氧可能有助于理解疾病的发病机制并优化治疗方法,令人惊讶的是,这一研究领域仍未得到充分发展。越来越多的关注这一主题的研究必将为药物开发和治疗优化提供关键信息。