Počet záznamů: 1  

Substituted 2-hydroxy-N-(arylalkyl)benzamide sensitizes cancer cells to metabolic stress by disrupting actin cytoskeleton and inhibiting autophagic flux

  1. 1.
    SYSNO ASEP0467237
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevSubstituted 2-hydroxy-N-(arylalkyl)benzamide sensitizes cancer cells to metabolic stress by disrupting actin cytoskeleton and inhibiting autophagic flux
    Tvůrce(i) Pachnikova, G. (CZ)
    Uldrijan, S. (CZ)
    Imramovský, A. (CZ)
    Kryštof, Vladimír (UEB-Q) RID, ORCID
    Slaninová, I. (CZ)
    Celkový počet autorů5
    Zdroj.dok.Toxicology in Vitro. - : Elsevier - ISSN 0887-2333
    Roč. 37, DEC (2016), s. 70-78
    Poč.str.9 s.
    Jazyk dok.eng - angličtina
    Země vyd.GB - Velká Británie
    Klíč. slovahepatocellular-carcinoma cells ; sorafenib ; apoptosis ; death ; maturation ; membrane ; melanoma ; Actin ; Autophagy ; Melanoma ; Metabolic stress ; Sorafenib ; Substituted 2-hydroxy-N-(arylalkyl)benzamide
    Vědní obor RIVCE - Biochemie
    Institucionální podporaUEB-Q - RVO:61389030
    UT WOS000387198300009
    DOI10.1016/j.tiv.2016.09.006
    AnotaceN-((R)-1-(4-chlorophenylcarbamoy1)-2-phenylethyl)-5-chloro-2-hydroxybenzamide (Compound 6k), was recently isolated during the preparation of amino adds esters with salicylanilides. We show here that 6k disrupts the dynamics of actin cytoskeleton in human melanoma cells, affecting processes essential for the maintenance and expansion of tumours such as cell adlision, motility, proliferation, vesicular transport, and autophagic flux. We demonstrated that inhibition of autophagy by 6k increased the sensitivity of melanoma cells to metabolic stress induced by rotenone or nutrient starvation and potentiated the anti-proliferative activity of small molecule multikinase inhibitor sorafenib. Since autophagy plays an important role in survival of cancer cells subjected to chemotherapy, the above mentioned properties are interesting from clinical point of view as 6k could promote metabolic stress within the tumour microenvironment and potentiate the effect of cytostatics in combination therapy.
    PracovištěÚstav experimentální botaniky
    KontaktDavid Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469
    Rok sběru2017
Počet záznamů: 1  

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