DNA damage interactions on both nanometer and micrometer scale determine overall cellular damage
Autor: | Thomas Friedrich, Judith Reindl, Stefanie Girst, Christoph Greubel, Christian Siebenwirth, Michael Scholz, K. Ilicic, Matthias Sammer, Thomas E. Schmid, Dietrich W. M. Walsh, Günther Dollinger, Benjamin Schwarz |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
Micrometer scale
DNA damage medicine.medical_treatment Cell Linear energy transfer lcsh:Medicine Article 030218 nuclear medicine & medical imaging Ionizing radiation Lesion 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine medicine lcsh:Science Multidisciplinary Chemistry lcsh:R Radiation therapy medicine.anatomical_structure 030220 oncology & carcinogenesis Biophysics lcsh:Q medicine.symptom ddc:600 DNA |
Zdroj: | Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018) Scientific reports 8(1), 16063 (2018). doi:10.1038/s41598-018-34323-9 Sci. Rep. 8:16063 (2018) Scientific Reports |
ISSN: | 2045-2322 |
Popis: | DNA double strand breaks (DSB) play a pivotal role for cellular damage, which is a hazard encountered in toxicology and radiation protection, but also exploited e.g. in eradicating tumors in radiation therapy. It is still debated whether and in how far clustering of such DNA lesions leads to an enhanced severity of induced damage. Here we investigate - using focused spots of ionizing radiation as damaging agent - the spatial extension of DNA lesion patterns causing cell inactivation. We find that clustering of DNA damage on both the nm and µm scale leads to enhanced inactivation compared to more homogeneous lesion distributions. A biophysical model interprets these observations in terms of enhanced DSB production and DSB interaction, respectively. We decompose the overall effects quantitatively into contributions from these lesion formation processes, concluding that both processes coexist and need to be considered for determining the resulting damage on the cellular level. |
Databáze: | OpenAIRE |
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