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乳胞素:首屈一指的蛋白酶体抑制剂,依然卓越非凡,堪称未来抗生素研究的典范。

Lactacystin: first-in-class proteasome inhibitor still excelling and an exemplar for future antibiotic research.

机构信息

Kitasato Institute for Life Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.

出版信息

J Antibiot (Tokyo). 2019 Apr;72(4):189-201. doi: 10.1038/s41429-019-0141-8. Epub 2019 Feb 12.

Abstract

Lactacystin exemplifies the role that serendipity plays in drug discovery and why "finding things without actually looking for them" retains such a pivotal role in the search for the useful properties of chemicals. The first proteasome inhibitor discovered, lactacystin stimulated new possibilities in cancer control. New and innovative uses are regularly being found for lactacystin, including as a model to study dementia, while new formulations and delivery systems may facilitate its use clinically as an anticancer agent. All this provides yet more evidence that we need a comprehensive, collaborative and coordinated programme to fully investigate all new and existing chemical compounds, especially those of microbial origin. We need to do so in order to avoid failing to detect and successfully exploit unsought yet potentially life-saving or extremely advantageous properties of microbial metabolites.

摘要

乳胞菌素就是一个偶然在药物发现中起到作用的例子,也说明了“无心插柳柳成荫”在寻找化学物质有用属性的过程中为何仍起着关键作用。乳胞菌素是第一个被发现的蛋白酶体抑制剂,它为癌症控制带来了新的可能。人们不断发现乳胞菌素的新的、创新的用途,包括将其作为研究痴呆症的模型,而新的配方和输送系统可能会促进其作为抗癌药物在临床上的应用。所有这些都进一步证明,我们需要一个全面、协作和协调的计划来充分研究所有新的和现有的化合物,特别是那些微生物来源的化合物。我们需要这样做,以避免未能发现和成功利用微生物代谢物中那些意外的、但有潜在救生或极其有利的特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c98/6760633/57cca9201fca/41429_2019_141_Fig1_HTML.jpg

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