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DNA repair inhibitors sensitize cells differently to high and low LET radiation

The aim of this study was to investigate effects of high LET α-radiation in combination with inhibitors of DDR (DNA-PK and ATM) and to compare the effect with the radiosensitizing effect of low LET X-ray radiation. The various cell lines were irradiated with α-radiation and with X-ray. Clonogenic su...

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Autores principales: Bannik, Kristina, Madas, Balázs, Jarke, Sabrina, Sutter, Andreas, Siemeister, Gerhard, Schatz, Christoph, Mumberg, Dominik, Zitzmann-Kolbe, Sabine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636489/
https://www.ncbi.nlm.nih.gov/pubmed/34853427
http://dx.doi.org/10.1038/s41598-021-02719-9
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author Bannik, Kristina
Madas, Balázs
Jarke, Sabrina
Sutter, Andreas
Siemeister, Gerhard
Schatz, Christoph
Mumberg, Dominik
Zitzmann-Kolbe, Sabine
author_facet Bannik, Kristina
Madas, Balázs
Jarke, Sabrina
Sutter, Andreas
Siemeister, Gerhard
Schatz, Christoph
Mumberg, Dominik
Zitzmann-Kolbe, Sabine
author_sort Bannik, Kristina
collection PubMed
description The aim of this study was to investigate effects of high LET α-radiation in combination with inhibitors of DDR (DNA-PK and ATM) and to compare the effect with the radiosensitizing effect of low LET X-ray radiation. The various cell lines were irradiated with α-radiation and with X-ray. Clonogenic survival, the formation of micronuclei and cell cycle distribution were studied after combining of radiation with DDR inhibitors. The inhibitors sensitized different cancer cell lines to radiation. DNA-PKi affected survival rates in combination with α-radiation in selected cell lines. The sensitization enhancement ratios were in the range of 1.6–1.85 in cancer cells. ATMi sensitized H460 cells and significantly increased the micronucleus frequency for both radiation qualities. ATMi in combination with α-radiation reduced survival of HEK293. A significantly elicited cell cycle arrest in G(2)/M phase after co-treatment of ATMi with α-radiation and X-ray. The most prominent treatment effect was observed in the HEK293 by combining α-radiation and inhibitions. ATMi preferentially sensitized cancer cells and normal HEK293 cells to α-radiation. DNA-PKi and ATMi can sensitize cancer cells to X-ray, but the effectiveness was dependent on cancer cells itself. α-radiation reduced proliferation in primary fibroblast without G(2)/M arrest.
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spelling pubmed-86364892021-12-03 DNA repair inhibitors sensitize cells differently to high and low LET radiation Bannik, Kristina Madas, Balázs Jarke, Sabrina Sutter, Andreas Siemeister, Gerhard Schatz, Christoph Mumberg, Dominik Zitzmann-Kolbe, Sabine Sci Rep Article The aim of this study was to investigate effects of high LET α-radiation in combination with inhibitors of DDR (DNA-PK and ATM) and to compare the effect with the radiosensitizing effect of low LET X-ray radiation. The various cell lines were irradiated with α-radiation and with X-ray. Clonogenic survival, the formation of micronuclei and cell cycle distribution were studied after combining of radiation with DDR inhibitors. The inhibitors sensitized different cancer cell lines to radiation. DNA-PKi affected survival rates in combination with α-radiation in selected cell lines. The sensitization enhancement ratios were in the range of 1.6–1.85 in cancer cells. ATMi sensitized H460 cells and significantly increased the micronucleus frequency for both radiation qualities. ATMi in combination with α-radiation reduced survival of HEK293. A significantly elicited cell cycle arrest in G(2)/M phase after co-treatment of ATMi with α-radiation and X-ray. The most prominent treatment effect was observed in the HEK293 by combining α-radiation and inhibitions. ATMi preferentially sensitized cancer cells and normal HEK293 cells to α-radiation. DNA-PKi and ATMi can sensitize cancer cells to X-ray, but the effectiveness was dependent on cancer cells itself. α-radiation reduced proliferation in primary fibroblast without G(2)/M arrest. Nature Publishing Group UK 2021-12-01 /pmc/articles/PMC8636489/ /pubmed/34853427 http://dx.doi.org/10.1038/s41598-021-02719-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bannik, Kristina
Madas, Balázs
Jarke, Sabrina
Sutter, Andreas
Siemeister, Gerhard
Schatz, Christoph
Mumberg, Dominik
Zitzmann-Kolbe, Sabine
DNA repair inhibitors sensitize cells differently to high and low LET radiation
title DNA repair inhibitors sensitize cells differently to high and low LET radiation
title_full DNA repair inhibitors sensitize cells differently to high and low LET radiation
title_fullStr DNA repair inhibitors sensitize cells differently to high and low LET radiation
title_full_unstemmed DNA repair inhibitors sensitize cells differently to high and low LET radiation
title_short DNA repair inhibitors sensitize cells differently to high and low LET radiation
title_sort dna repair inhibitors sensitize cells differently to high and low let radiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636489/
https://www.ncbi.nlm.nih.gov/pubmed/34853427
http://dx.doi.org/10.1038/s41598-021-02719-9
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