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药物代谢中的偶氮还原酶。

Azoreductases in drug metabolism.

作者信息

Ryan Ali

机构信息

Faculty of Science, Engineering and Computing, Kingston University, Kingston upon Thames, UK.

出版信息

Br J Pharmacol. 2017 Jul;174(14):2161-2173. doi: 10.1111/bph.13571. Epub 2016 Sep 2.

Abstract

UNLABELLED

Azoreductases are flavoenzymes that have been characterized in a range of prokaryotes and eukaryotes. Bacterial azoreductases are associated with the activation of two classes of drug, azo drugs for the treatment of inflammatory bowel disease and nitrofuran antibiotics. The mechanism of reduction of azo compounds is presented; it requires tautomerisation of the azo compound to a quinoneimine and provides a unifying mechanism for the reduction of azo and quinone substrates by azoreductases. The importance of further work in the characterization of azoreductases from enteric bacteria is highlighted to aid in the development of novel drugs for the treatment of colon related disorders. Human azoreductases are known to play a crucial role in the metabolism of a number of quinone-containing cancer chemotherapeutic drugs. The mechanism of hydride transfer to quinones, which is shared not only between eukaryotic and prokaryotic azoreductases but also the wider family of NAD(P)H quinone oxidoreductases, is outlined. The importance of common single nucleotide polymorphisms (SNPs) in human azoreductases is described not only in cancer prognosis but also with regard to their effects on the efficacy of quinone drug-based cancer chemotherapeutic regimens. This highlights the need to screen patients for azoreductase SNPs ahead of treatment with these regimens.

LINKED ARTICLES

This article is part of a themed section on Drug Metabolism and Antibiotic Resistance in Micro-organisms. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v174.14/issuetoc.

摘要

未标注

偶氮还原酶是一类黄素酶,已在多种原核生物和真核生物中得到表征。细菌偶氮还原酶与两类药物的激活有关,即用于治疗炎症性肠病的偶氮药物和硝基呋喃抗生素。文中介绍了偶氮化合物的还原机制;它需要偶氮化合物互变异构为醌亚胺,并为偶氮还原酶还原偶氮和醌底物提供了统一机制。强调了进一步研究肠道细菌偶氮还原酶特性的重要性,以助力开发治疗结肠相关疾病的新型药物。已知人类偶氮还原酶在多种含醌类癌症化疗药物的代谢中起关键作用。概述了氢化物向醌转移的机制,这不仅在真核和原核偶氮还原酶之间存在共性,而且在更广泛的NAD(P)H醌氧化还原酶家族中也存在。描述了人类偶氮还原酶中常见单核苷酸多态性(SNP)的重要性,这不仅涉及癌症预后,还涉及其对基于醌类药物的癌症化疗方案疗效的影响。这突出了在用这些方案治疗前对患者进行偶氮还原酶SNP筛查的必要性。

相关文章

本文是关于微生物中药物代谢与抗生素耐药性主题部分的一部分。若要查看本部分的其他文章,请访问http://onlinelibrary.wiley.com/doi/10.1111/bph.v174.14/issuetoc。

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