Youssef Bassem, Feghaly Charbel, Al Choboq Joelle, Bou-Gharios Jolie, Challita Rafka, Azzi Joyce, Bou Hadir Hanine, Abi Antoun Fabienne, Araji Tarek, Taddei Phillip J, Geara Fady, Sfeir Pierre, Jurjus Abdo, Abou-Kheir Wassim, Bodgi Larry
Department of Radiation Oncology, American University of Beirut Medical Center, Beirut 1107 2020, Lebanon.
Department of Anatomy, Cell Biology and Physiological Sciences, Faculty of Medicine, American University of Beirut, Beirut 1107 2020, Lebanon.
Cancers (Basel). 2024 Aug 26;16(17):2968. doi: 10.3390/cancers16172968.
Children with cancer previously treated with radiotherapy face the likelihood of side effects that can be debilitating or fatal. This study aimed to assess the long-term effect of medulloblastoma radiotherapy on the DNA double-strand break (DSB) repair capability of primary fibroblasts derived from lung biopsies of previously irradiated young sheep. This study included biopsies from three control and five irradiated sheep. The treated sheep had previously received spinal radiotherapy at a total dose of 28 Gy, which is equivalent to pediatric medulloblastoma treatment. Lung biopsies were taken 4 years post-irradiation from high-dose (HD, >18 Gy) and low-dose (LD, <2 Gy) regions. Fifteen cell lines were extracted (six control, four LD and five HD). The cells were irradiated, and DNA DSB repair was analyzed by immunofluorescence. Clonogenic, trypan blue and micronuclei assays were performed. Both the HD and LD cell lines had a significantly higher number of residual γH2AX foci 24 h and a significant decrease in pATM activity post-irradiation compared to the control. There was no statistically significant difference in the clonogenic assay, trypan blue and micronuclei results. Our study showed that a previous irradiation can impair the DNA DSB repair mechanism of ovine lung fibroblasts.
先前接受过放射治疗的癌症患儿面临着可能导致虚弱或致命的副作用。本研究旨在评估髓母细胞瘤放疗对先前接受过照射的幼羊肺活检来源的原代成纤维细胞DNA双链断裂(DSB)修复能力的长期影响。本研究包括来自三只对照羊和五只受照射羊的活检样本。受试羊先前接受了总剂量为28 Gy的脊柱放疗,这相当于小儿髓母细胞瘤的治疗剂量。在照射后4年从高剂量(HD,>18 Gy)和低剂量(LD,<2 Gy)区域采集肺活检样本。提取了15个细胞系(6个对照、4个LD和5个HD)。对细胞进行照射,并通过免疫荧光分析DNA DSB修复情况。进行了克隆形成、台盼蓝和微核试验。与对照组相比,HD和LD细胞系在照射后24小时的残留γH2AX病灶数量均显著增加,且pATM活性显著降低。克隆形成试验、台盼蓝和微核结果无统计学显著差异。我们的研究表明,先前的照射会损害绵羊肺成纤维细胞的DNA DSB修复机制。