Hirocidins, Cytotoxic Metabolites from Streptomyces hiroshimensis, Induce Mitochondrion-Mediated Apoptosis

被引:3
作者
Han, Esther J. [1 ]
Jeong, Myungeun [1 ]
Lee, Seoung Rak [2 ]
Sorensen, Erik J. [1 ]
Seyedsayamdost, Mohammad R. [1 ,3 ]
机构
[1] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
[2] Pusan Natl Univ, Coll Pharm, Busan 46241, South Korea
[3] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Natural Products; Antiproliferative Metabolites; Streptomyces hiroshimensis; Caspase-9; Mitochondrion-dependent Apoptosis; MICROBIAL NATURAL-PRODUCTS; UNDECYLPRODIGIOSIN; METABOLOMICS; RIBOFLAVIN; ACTIVATION; LUMICHROME; INHIBITOR; CASPASE-9; DISCOVERY; MBT76;
D O I
10.1002/anie.202405367
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recent advances in whole genome sequencing have revealed an immense microbial potential for the production of therapeutic small molecules, even from well-known producers. To access this potential, we subjected prominent antimicrobial producers to alternative antiproliferative assays using persistent cancer cell lines. Described herein is our discovery of hirocidins, novel secondary metabolites from Streptomyces hiroshimensis with antiproliferative activities against colon and persistent breast cancer cells. Hirocidin A is an unusual nine-membered carbocyclic maleimide and hirocidins B and C are relatives with an unprecedented, bridged azamacrocyclic backbone. Mode of action studies show that hirocidins trigger mitochondrion-dependent apoptosis by inducing expression of the key apoptotic effector caspase-9. The discovery of new cytotoxins contributes to scaffold diversification in anticancer drug discovery and the reported modes of action and concise total synthetic route for variant A set the stage for unraveling specific targets and biochemical interactions of the hirocidins.
引用
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页数:7
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