Modelling the In Vivo and Ex Vivo DNA Damage Response after Internal Irradiation of Blood from Patients with Thyroid Cancer.
Sarah SchumannHarry ScherthanPhilipp E HartrampfLukas GöringAndreas K BuckMatthias PortMichael LassmannUta EberleinPublished in: International journal of molecular sciences (2024)
This work reports on a model that describes patient-specific absorbed dose-dependent DNA damage response in peripheral blood mononuclear cells of thyroid cancer patients during radioiodine therapy and compares the results with the ex vivo DNA damage response in these patients. Blood samples of 18 patients (nine time points up to 168 h post-administration) were analyzed for radiation-induced γ-H2AX + 53BP1 DNA double-strand break foci (RIF). A linear one-compartment model described the absorbed dose-dependent time course of RIF (Parameters: c characterizes DSB damage induction; k 1 and k 2 are rate constants describing fast and slow repair). The rate constants were compared to ex vivo repair rates. A total of 14 patient datasets could be analyzed; c ranged from 0.012 to 0.109 mGy -1 , k 2 from 0 to 0.04 h -1 . On average, 96% of the damage is repaired quickly with k 1 (range: 0.19-3.03 h -1 ). Two patient subgroups were distinguished by k 1 -values ( n = 6, k 1 > 1.1 h -1 ; n = 8, k 1 < 0.6 h -1 ). A weak correlation with patient age was observed. While induction of RIF was similar among ex vivo and in vivo, the respective repair rates failed to correlate. The lack of correlation between in vivo and ex vivo repair rates and the applicability of the model to other therapies will be addressed in further studies.
Keyphrases
- dna damage response
- radiation induced
- end stage renal disease
- dna repair
- ejection fraction
- newly diagnosed
- chronic kidney disease
- case report
- pulmonary tuberculosis
- radiation therapy
- oxidative stress
- prognostic factors
- stem cells
- mycobacterium tuberculosis
- patient reported outcomes
- bone marrow
- mesenchymal stem cells
- circulating tumor
- rna seq
- single cell
- nucleic acid