The cyanobacterial metabolite nocuolin a is a natural oxadiazine that triggers apoptosis in human cancer cells
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
28253280
PubMed Central
PMC5333925
DOI
10.1371/journal.pone.0172850
PII: PONE-D-16-32298
Knihovny.cz E-zdroje
- MeSH
- apoptóza účinky léků MeSH
- chromatografie kapalinová MeSH
- HeLa buňky MeSH
- hmotnostní spektrometrie MeSH
- lidé MeSH
- magnetická rezonanční spektroskopie MeSH
- molekulární struktura MeSH
- multigenová rodina MeSH
- oxaziny chemie farmakologie MeSH
- sekvence aminokyselin MeSH
- sekvenční homologie aminokyselin MeSH
- sinice chemie MeSH
- spektroskopie infračervená s Fourierovou transformací MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- nocuolin A MeSH Prohlížeč
- oxaziny MeSH
Oxadiazines are heterocyclic compounds containing N-N-O or N-N-C-O system within a six membered ring. These structures have been up to now exclusively prepared via organic synthesis. Here, we report the discovery of a natural oxadiazine nocuolin A (NoA) that has a unique structure based on 1,2,3-oxadiazine. We have identified this compound in three independent cyanobacterial strains of genera Nostoc, Nodularia, and Anabaena and recognized the putative gene clusters for NoA biosynthesis in their genomes. Its structure was characterized using a combination of NMR, HRMS and FTIR methods. The compound was first isolated as a positive hit during screening for apoptotic inducers in crude cyanobacterial extracts. We demonstrated that NoA-induced cell death has attributes of caspase-dependent apoptosis. Moreover, NoA exhibits a potent anti-proliferative activity (0.7-4.5 μM) against several human cancer lines, with p53-mutated cell lines being even more sensitive. Since cancers bearing p53 mutations are resistant to several conventional anti-cancer drugs, NoA may offer a new scaffold for the development of drugs that have the potential to target tumor cells independent of their p53 status. As no analogous type of compound was previously described in the nature, NoA establishes a novel class of bioactive secondary metabolites.
Biology Centre v v i Institute of Hydrobiology České Budějovice Czech Republic
British Columbia Cancer Agency Department of Experimental Therapeutics Vancouver BC Canada
Centre Algatech Institute of Microbiology The Czech Academy of Sciences v v i Třeboň Czech Republic
Centre for Phycology Institute of Botany v v i Czech Republic
Laboratory of Molecular Structure Characterization Institute of Microbiology Prague Czech Republic
Saint Petersburg State University St Petersburg Russia
Tyrolean Cancer Research Institute Innsbruck Austria
University of South Bohemia Faculty of Science České Budějovice Czech Republic
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