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Changes in the response of MCF-7 cells to ionizing radiation after the combination of ATM and DNA-PK inhibition

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11150%2F15%3A10293814" target="_blank" >RIV/00216208:11150/15:10293814 - isvavai.cz</a>

  • Alternative codes found

    RIV/60162694:G44__/15:43875359 RIV/00216275:25310/15:39900079

  • Result on the web

    <a href="http://link.springer.com/article/10.1007%2Fs12032-015-0591-1" target="_blank" >http://link.springer.com/article/10.1007%2Fs12032-015-0591-1</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s12032-015-0591-1" target="_blank" >10.1007/s12032-015-0591-1</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Changes in the response of MCF-7 cells to ionizing radiation after the combination of ATM and DNA-PK inhibition

  • Original language description

    The aim of the present study is to evaluate the role of ATM (KU55933) and DNA-PK (NU7441) inhibitors in the repair of double-strand breaks and downstream signaling of DNA damage introduced by ionizing radiation. The irradiation of MCF-7 cells alone increased the proportion of cells in the G1 phase in comparison with mock-treated cells. After ATM inhibitor pretreatment, the cells were more accumulated in the G2 phase, whereas DNA-PK inhibitor application increased the percentage of cells in the G1 phase.ATM and DNA-PK inhibitor application alone increased the sensitivity of MCF-7 cells to ionizing radiation; however, combining both inhibitors together resulted in a further enhancement of cell death. Unexpectedly, combining both inhibitors decreased thepercentage of senescent cells and increased G2 cell cycle arrest 3 days after treatment. After irradiation, the p21 protein was increased and Chk1 and Chk2 were activated. These proteins were not increased in cells pretreated with the AT

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    CE - Biochemistry

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2015

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Medical Oncology

  • ISSN

    1357-0560

  • e-ISSN

  • Volume of the periodical

    32

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    8

  • Pages from-to

  • UT code for WoS article

    000352152000002

  • EID of the result in the Scopus database

    2-s2.0-84925590335