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靶向硒代谢和硒蛋白:药物发现的新途径。

Targeting selenium metabolism and selenoproteins: novel avenues for drug discovery.

机构信息

Burnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL, USA.

出版信息

Metallomics. 2010 Feb;2(2):112-6. doi: 10.1039/b917141j. Epub 2009 Oct 27.

Abstract

Selenoproteins play a wide range of roles in metabolism and oxidative stress defense and are produced by organisms in all three domains of life. Recent evidence has been presented that metal based cancer drugs target the selenol nucleophile of the active site selenocysteine in thioredoxin reductase isoenzymes. Other metals and metalloids, such as tin, arsenic and gold, have also recently been shown to form stable complexes with hydrogen selenide, a required precursor for the synthesis of selenoproteins in all biological organisms. Moreover these metal based compounds have been shown to inhibit growth of pathogens such as Clostridium difficile and Treponema denticola due to their reactivity with this highly reactive metabolic precursor. This review summarizes the recent finding on these two avenues for drug discovery, and puts this work in context with the larger field of selenium biology.

摘要

硒蛋白在代谢和氧化应激防御中发挥着广泛的作用,存在于所有三个生命领域的生物中。最近有证据表明,基于金属的癌症药物靶向硫氧还蛋白还原酶同工酶活性部位硒代半胱氨酸的硒醇亲核试剂。其他金属和类金属,如锡、砷和金,最近也被证明可以与硒化氢形成稳定的配合物,而硒化氢是所有生物合成硒蛋白的必需前体。此外,由于这些金属化合物与这种高反应性代谢前体反应,它们已被证明可以抑制病原体如艰难梭菌和密螺旋体的生长。本综述总结了这两个药物发现途径的最新发现,并将这项工作置于更大的硒生物学领域中。

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