Počet záznamů: 1  

Deazaflavin Inhibitors of TDP2 with Cellular Activity Can Affect Etoposide Influx and/or Efflux

  1. 1.
    0511335 - ÚMG 2020 RIV US eng J - Článek v odborném periodiku
    Komulainen, E. - Pennicott, L. - Le Grand, D. - Caldecott, Keith
    Deazaflavin Inhibitors of TDP2 with Cellular Activity Can Affect Etoposide Influx and/or Efflux.
    ACS Chemical Biology. Roč. 14, č. 6 (2019), s. 1110-1114. ISSN 1554-8929. E-ISSN 1554-8937
    Institucionální podpora: RVO:68378050
    Klíčová slova: 5'-tyrosyl dna phosphodiesterase * small-molecule inhibitors * strand break repair * topoisomerase-ii * enzyme
    Obor OECD: Cell biology
    Impakt faktor: 4.434, rok: 2019
    Způsob publikování: Omezený přístup
    https://pubs.acs.org/doi/10.1021/acschembio.9b00144

    Tyrosyl DNA phosphodiesterase 2 (TDP2) facilitates the repair of topoisomerase II (TOP2)-linked DNA double-strand breaks and, as a consequence, is required for cellular resistance to TOP2 ´poisons´. Recently, a deazaflavin series of compounds were identified as potent inhibitors of TDP2, in vitro. Here, however, we show that while some deazaflavins can induce cellular sensitivity to the TOP2 poison etoposide, they do so independently of TDP2 status. Consistent with this, both the cellular level of etoposide-induced TOP2 cleavage complexes and the intracellular concentration of etoposide was increased by incubation with deazaflavin, suggesting an impact of these compounds on etoposide uptake/efflux. In addition, deazaflavin failed to increase the level of TOP2 cleavage complexes or sensitivity induced by m-AMSA, which is a different class of TOP2 poison to which TDP2-defective cells are also sensitive. In conclusion, while deazaflavins are potent inhibitors of TDP2 in vitro, their limited cell permeability and likely interference with etoposide influx/efflux limits their utility in cells.
    Trvalý link: http://hdl.handle.net/11104/0306729

     
     
Počet záznamů: 1  

  Tyto stránky využívají soubory cookies, které usnadňují jejich prohlížení. Další informace o tom jak používáme cookies.