Počet záznamů: 1  

The cyanobacterial metabolite nocuolin a is a natural oxadiazine that triggers apoptosis in human cancer cells.

  1. 1.
    SYSNO ASEP0474362
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevThe cyanobacterial metabolite nocuolin a is a natural oxadiazine that triggers apoptosis in human cancer cells.
    Tvůrce(i) Voráčová, Kateřina (MBU-M)
    Hájek, Jan (MBU-M) ORCID
    Mareš, Jan (MBU-M) ORCID
    Urajová, Petra (MBU-M)
    Kuzma, Marek (MBU-M) ORCID, RID
    Cheel Horna, José (MBU-M)
    Villunger, A. (AT)
    Kapuscik, Alexandra (MBU-M)
    Bally, M. (CA)
    Novák, Petr (MBU-M) RID, ORCID
    Kabeláč, M. (CZ)
    Krumschnabel, G. (AT)
    Lukeš, Martin (MBU-M) ORCID
    Voloshko, L. (RU)
    Kopecký, Jiří (MBU-M) ORCID
    Hrouzek, Pavel (MBU-M) ORCID
    Číslo článkue0172850
    Zdroj.dok.PLoS ONE. - : Public Library of Science - ISSN 1932-6203
    Roč. 12, č. 3 (2017), s. 1-12
    Poč.str.12 s.
    Jazyk dok.eng - angličtina
    Země vyd.US - Spojené státy americké
    Klíč. slovaENZYMES ; 1,3,4-OXADIAZOLE ; SCAFFOLD
    Vědní obor RIVEE - Mikrobiologie, virologie
    Obor OECDMicrobiology
    CEPGPP503/12/P614 GA ČR - Grantová agentura ČR
    GA14-18067S GA ČR - Grantová agentura ČR
    LO1416 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    EE2.3.30.0059 GA MŠMT - Ministerstvo školství, mládeže a tělovýchovy
    Institucionální podporaMBU-M - RVO:61388971
    UT WOS000396011300042
    EID SCOPUS85014240038
    DOI10.1371/journal.pone.0172850
    AnotaceOxadiazines 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 micro) 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.
    PracovištěMikrobiologický ústav
    KontaktEliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231
    Rok sběru2018
Počet záznamů: 1  

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