低剂量和高剂量辐射和放射性碘对个人电离辐射易感性影响的回顾性生物剂量测定。

Q4 Biochemistry, Genetics and Molecular Biology
Genome Integrity Pub Date : 2017-01-23 eCollection Date: 2017-01-01 DOI:10.4103/2041-9414.198906
Antonina Cebulska-Wasilewska, Mateusz Krzysiek, Grażyna Krajewska, Artur Stępień, Paweł Krajewski
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引用次数: 0

摘要

碘-131(I-131)常用于甲状腺诊断和治疗。体内外暴露于放射性碘会导致外周血淋巴细胞的分子和细胞损伤。本研究旨在探讨低剂量和高剂量 I-131 对电离辐射易感性的影响。研究组包括 30 名无甲状腺疾病者、41 名诊断性暴露于低剂量 I-131 的患者和 37 名治疗性暴露于高剂量 I-131 的甲状腺功能亢进症患者。采用标准化的DNA修复能力测定法来检测G0细胞中DNA快速修复过程的有效性。在体外对细胞进行 X 射线剂量挑战之前和之后,对新鲜血液样本进行了细胞遗传学制备。姐妹染色单体交换(SCE)的频率和SCE数量显著增加的细胞百分比被用作与同源重组相关的细胞遗传学生物标志物,并与早期报道的癌症风险细胞遗传学生物标志物进行比较。在挑战前后,所有调查组的生物标志物都存在很大的个体差异。不过,与未接触 I-131 的对照组相比,接触诊断剂量 I-131 的患者在挑战后的快速修复效率明显较高,这与细胞遗传损伤的减少有关。然而,在使用治疗剂量 5 周后,观察到未修复的挑战后 DNA 和细胞遗传损伤显著增加,这表明存在健康风险。研究结果还表明,直系亲属中出现癌症可能会对暴露于低剂量和高剂量的患者的DNA修复产生不同的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Retrospective Biological Dosimetry at Low and High Doses of Radiation and Radioiodine Impact on Individual Susceptibility to Ionizing Radiation.

Retrospective Biological Dosimetry at Low and High Doses of Radiation and Radioiodine Impact on Individual Susceptibility to Ionizing Radiation.

Retrospective Biological Dosimetry at Low and High Doses of Radiation and Radioiodine Impact on Individual Susceptibility to Ionizing Radiation.

Retrospective Biological Dosimetry at Low and High Doses of Radiation and Radioiodine Impact on Individual Susceptibility to Ionizing Radiation.

Iodine-131 (I-131) is often used in thyroid diagnostics and therapy. External and internal exposure to radioiodine can lead to molecular and cellular damage in peripheral blood lymphocytes. The aim of this study was to explore the influence of low and high doses of I-131 on susceptibility to ionizing radiation. Study groups consisted of 30 individuals free of thyroid diseases, 41 patients exposed diagnostically to low doses of I-131, and 37 hyperthyroidism patients exposed therapeutically to high doses. The standardized DNA repair competence assay was used to test the efficacy of the fast DNA repair process in G0 cells. Cytogenetic preparations were made in fresh blood samples before and after challenging cells in vitro with X-ray dose. The frequency of sister chromatid exchanges (SCE) and percentage of cells with significantly elevated numbers of SCE were used as cytogenetic biomarkers associated to homologous recombination and compared to reported earlier cytogenetic biomarkers of cancer risk. Strong individual variation in the biomarkers is observed in all investigated groups before and after challenging. Nevertheless, the efficiency of post challenging fast repair is significantly high in the patients exposed to diagnostic I-131 doses than in unexposed control group and linked to decreased cytogenetic damage. However, 5 weeks after administration of therapeutic doses, significant increases of unrepaired post challenging DNA and cytogenetic damages were observed indicating a health risk. Results also suggest that the appearance of cancers in immediate families might influence DNA repair differently in patients exposed to low than to high doses.

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Genome Integrity
Genome Integrity Biochemistry, Genetics and Molecular Biology-Genetics
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