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Hirocidins, Cytotoxic Metabolites from Streptomyces hiroshimensis, Induce Mitochondrion-Mediated Apoptosis.
Han, Esther J; Jeong, Myungeun; Lee, Seoung Rak; Sorensen, Erik J; Seyedsayamdost, Mohammad R.
Afiliação
  • Han EJ; Department of Chemistry, Princeton University, Princeton, NJ 08544, USA.
  • Jeong M; Department of Chemistry, Princeton University, Princeton, NJ 08544, USA.
  • Lee SR; College of Pharmacy, Pusan National University, Busan, 46241, South Korea.
  • Sorensen EJ; Department of Chemistry, Princeton University, Princeton, NJ 08544, USA.
  • Seyedsayamdost MR; Department of Chemistry, Princeton University, Princeton, NJ 08544, USA.
Angew Chem Int Ed Engl ; : e202405367, 2024 Jun 19.
Article em En | MEDLINE | ID: mdl-38898540
ABSTRACT
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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos