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Mitoxantrone in Combination with a DNA-PK Inhibitor: Possible Therapy of Promyelocytic Leukaemia Resistant Forms

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11150%2F11%3A10106825" target="_blank" >RIV/00216208:11150/11:10106825 - isvavai.cz</a>

  • Alternative codes found

    RIV/60162694:G44__/11:00002579

  • Result on the web

    <a href="http://fb.cuni.cz/file/5600/FB2011A0029.pdf" target="_blank" >http://fb.cuni.cz/file/5600/FB2011A0029.pdf</a>

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Mitoxantrone in Combination with a DNA-PK Inhibitor: Possible Therapy of Promyelocytic Leukaemia Resistant Forms

  • Original language description

    The aim of the study was to sensitize cells of human promyelocytic leukaemia HL-60/MX2 (resistant to mitoxantrone and further substances interacting with topoisomerase II - TI II) to the effect of mitoxantrone (MTX). We demonstrated that the main mechanism of the HL-60/MX2 cell atypical multiple drug resistance is not only their altered activity of TI II and reduced levels of TI II ? and ?. The resistance of the HL-60/MX2 cells to MTX is associated with their increased ability to repair DSB. The HL-60/MX2 cells, compared to HL-60 cells (which are MTX-sensitive), contain large amounts of DNA-PK, which is responsible for the main pathway of the DSB repair, non-homogenous end joining (NHEJ), and they also contain large amounts of further repair proteins Rad50 and Nbs1, which are important in both NHEJ and homologous re-combination. We demonstrated that specific DNA-PK inhibitor NU7026 in HL60/MX2 prevented DSB repair through the NHEJ pathway and essentially abolished the resistance to MTX

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    BO - Biophysics

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2011

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Folia Biologica

  • ISSN

    0015-5500

  • e-ISSN

  • Volume of the periodical

    57

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    CZ - CZECH REPUBLIC

  • Number of pages

    6

  • Pages from-to

    200-205

  • UT code for WoS article

    000297182800004

  • EID of the result in the Scopus database