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
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CE - Biochemistry
OECD FORD branch
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Result continuities
Project
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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
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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
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UT code for WoS article
000352152000002
EID of the result in the Scopus database
2-s2.0-84925590335