School of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, United Kingdom ; School of Molecular and Cellular Biology, Garstang Buildling, Faculty of Biological Sciences, University of Leeds, Leeds, LS2 9JT, United Kingdom.
School of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, United Kingdom.
Beilstein J Org Chem. 2013 Nov 19;9:2556-63. doi: 10.3762/bjoc.9.290.
Antimycins (>40 members) were discovered nearly 65 years ago but the discovery of the gene cluster encoding antimycin biosynthesis in 2011 has facilitated rapid progress in understanding the unusual biosynthetic pathway. Antimycin A is widely used as a piscicide in the catfish farming industry and also has potent killing activity against insects, nematodes and fungi. The mode of action of antimycins is to inhibit cytochrome c reductase in the electron transport chain and halt respiration. However, more recently, antimycin A has attracted attention as a potent and selective inhibitor of the mitochondrial anti-apoptotic proteins Bcl-2 and Bcl-xL. Remarkably, this inhibition is independent of the main mode of action of antimycins such that an artificial derivative named 2-methoxyantimycin A inhibits Bcl-xL but does not inhibit respiration. The Bcl-2/Bcl-xL family of proteins are over-produced in cancer cells that are resistant to apoptosis-inducing chemotherapy agents, so antimycins have great potential as anticancer drugs used in combination with existing chemotherapeutics. Here we review what is known about antimycins, the regulation of the ant gene cluster and the unusual biosynthetic pathway.
抗霉素(>40 种成员)早在 65 年前就被发现,但在 2011 年发现编码抗霉素生物合成的基因簇,极大地促进了对抗霉素不寻常生物合成途径的理解。抗霉素 A 广泛用作鲶鱼养殖业中的鱼药,对昆虫、线虫和真菌也具有很强的杀伤活性。抗霉素的作用模式是抑制电子传递链中的细胞色素 c 还原酶,从而阻止呼吸。然而,最近,抗霉素 A 作为线粒体抗凋亡蛋白 Bcl-2 和 Bcl-xL 的有效和选择性抑制剂引起了人们的关注。值得注意的是,这种抑制作用与抗霉素的主要作用模式无关,因此一种名为 2-甲氧基抗霉素 A 的人工衍生物抑制 Bcl-xL 但不抑制呼吸。在对凋亡诱导化疗药物有抗性的癌细胞中,Bcl-2/Bcl-xL 蛋白家族过度表达,因此抗霉素具有与现有化疗药物联合使用的巨大抗癌药物潜力。在这里,我们回顾了对抗霉素的了解,抗基因簇的调控和不寻常的生物合成途径。