Chromosomal radiosensitivity of human breast carcinoma cells and blood lymphocytes following photon and proton exposures.
Agata KowalskaElena NasonovaPolina KutsaloKonrad CzerskiPublished in: Radiation and environmental biophysics (2023)
Breast carcinomas (BC) are among the most frequent cancers in women. Studies on radiosensitivity and ionizing radiation response of BC cells are scarce and mainly focused on intrinsic molecular mechanisms but do not include clinically relevant features as chromosomal rearrangements important for radiotherapy. The main purpose of this study was to compare the ionizing radiation response and efficiency of repair mechanisms of human breast carcinoma cells (Cal 51) and peripheral blood lymphocytes (PBL) for different doses and radiation qualities ( 60 Co γ-rays, 150 MeV and spread-out Bragg peak (SOBP) proton beams). The radiation response functions obtained using the conventional metaphase assay and premature chromosome condensation (PCC) technique enabled us to determine the number of chromosomal breaks at different time after irradiation. Both cytogenetic assays used confirmed the higher biological radiosensitivity for proton beams in tumor cells compared to PBL, corresponding to higher values of the linear LQ parameter α. additionally, the ratio of the LQ parameters β/α describing efficiency of the repair mechanisms, obtained for chromosome aberrations, showed higher numbers for PBL than for Cal 51 for all exposures. Similar results were observed for the ratio of PCC breaks determined directly after irradiation to that obtained 12 h later. This parameter (t0/t12) showed faster decrease of the repair efficiency with increasing LET value for Cal 51 cells. This finding supports the use of the proton therapy for breast cancer patients.
Keyphrases
- peripheral blood
- copy number
- induced apoptosis
- endothelial cells
- radiation induced
- cell cycle arrest
- air pollution
- high throughput
- early stage
- radiation therapy
- oxidative stress
- squamous cell carcinoma
- adipose tissue
- insulin resistance
- locally advanced
- dna methylation
- signaling pathway
- pregnant women
- pregnancy outcomes
- living cells
- rectal cancer
- single cell
- case control