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Can P glycoprotein mediate resistance to nilotinib in human leukemia cells?

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F13%3A33145121" target="_blank" >RIV/61989592:15110/13:33145121 - isvavai.cz</a>

  • Result on the web

    <a href="http://www.sciencedirect.com/science/article/pii/S1043661812001995" target="_blank" >http://www.sciencedirect.com/science/article/pii/S1043661812001995</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.phrs.2012.10.012" target="_blank" >10.1016/j.phrs.2012.10.012</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Can P glycoprotein mediate resistance to nilotinib in human leukemia cells?

  • Original language description

    The effect of P-glycoprotein (P-gp, ABCB1, MDR1) expression on cell resistance to nilotinib was studied in human leukaemia cells. We used K562/Dox cells overexpressing P-gp and their variants (subclones) with a gradually decreased P-gp expression. Thesesubclones were established by stable transfection of K562/Dox cells with a plasmid vector expressing shRNA targeting the ABCB1 gene. Functional analysis of P-gp using a specific fluorescent probe indicated gradually decreased dye efflux which was proportional to the P-gp expression. We observed that K562/Dox cells overexpressing P gp contained a significantly reduced intracellular level of nilotinib when compared to their counter partner K562 cells, which do not express P-gp. This effect was accompaniedby a decreased sensitivity of the K562/Dox cells to nilotinib. Importantly, cells with downregulated expression of P gp gradually lost their ability to decrease the intracellular level of nilotinib although they still significantly decre

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FR - Pharmacology and apothecary chemistry

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)<br>S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2013

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Pharmacological Research

  • ISSN

    1043-6618

  • e-ISSN

  • Volume of the periodical

    67

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    5

  • Pages from-to

    79-83

  • UT code for WoS article

    000313767400009

  • EID of the result in the Scopus database