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分次放射治疗期间局部和全身照射后基于γ-H2AX定量和细胞遗传学的生物剂量测定

Biodosimetry Based on γ-H2AX Quantification and Cytogenetics after Partial- and Total-Body Irradiation during Fractionated Radiotherapy.

作者信息

Zahnreich Sebastian, Ebersberger Anne, Kaina Bernd, Schmidberger Heinz

机构信息

a  Department of Radiation Oncology and Radiotherapy, University Medical Center Johannes Gutenberg University Mainz, 55131 Mainz, Germany.

出版信息

Radiat Res. 2015 Apr;183(4):432-46. doi: 10.1667/RR13911.1. Epub 2015 Apr 6.

Abstract

The aim of this current study was to quantitatively describe radiation-induced DNA damage and its distribution in leukocytes of cancer patients after fractionated partial- or total-body radiotherapy. Specifically, the impact of exposed anatomic region and administered dose was investigated in breast and prostate cancer patients receiving partial-body radiotherapy. DNA double-strand breaks (DSBs) were quantified by γ-H2AX immunostaining. The frequency of unstable chromosomal aberrations in stimulated lymphocytes was also determined and compared with the frequency of DNA DSBs in the same samples. The frequency of radiation-induced DNA damage was converted into dose, using ex vivo generated calibration curves, and was then compared with the administered physical dose. This study showed that 0.5 h after partial-body radiotherapy the quantity of radiation-induced γ-H2AX foci increased linearly with the administered equivalent whole-body dose for both tumor entities. Foci frequencies dropped 1 day thereafter but proportionality to the equivalent whole-body dose was maintained. Conversely, the frequency of radiation-induced cytogenetic damage increased from 0.5 h to 1 day after the first partial-body exposure with a linear dependence on the administered equivalent whole-body dose, for prostate cancer patients only. Only γ-H2AX foci assessment immediately after partial-body radiotherapy was a reliable measure of the expected equivalent whole-body dose. Local tumor doses could be approximated with both assays after one day. After total-body radiotherapy satisfactory dose estimates were achieved with both assays up to 8 h after exposure. In conclusion, the quantification of radiation-induced γ-H2AX foci, but not cytogenetic damage in peripheral leukocytes was a sensitive and rapid biodosimeter after acute heterogeneous irradiation of partial body volumes that was able to primarily assess the absorbed equivalent whole-body dose.

摘要

本项研究的目的是定量描述分次局部或全身放疗后癌症患者白细胞中辐射诱导的DNA损伤及其分布。具体而言,在接受局部放疗的乳腺癌和前列腺癌患者中,研究了受照射解剖区域和给予剂量的影响。通过γ-H2AX免疫染色对DNA双链断裂(DSB)进行定量。还测定了刺激淋巴细胞中不稳定染色体畸变的频率,并与同一样本中DNA DSB的频率进行比较。利用体外生成的校准曲线将辐射诱导的DNA损伤频率转换为剂量,然后与给予的物理剂量进行比较。本研究表明,局部放疗后0.5小时,两种肿瘤实体的辐射诱导γ-H2AX焦点数量均与给予的等效全身剂量呈线性增加。此后1天焦点频率下降,但与等效全身剂量的比例关系得以维持。相反,仅前列腺癌患者在首次局部照射后0.5小时至1天,辐射诱导的细胞遗传学损伤频率增加,且与给予的等效全身剂量呈线性相关。仅局部放疗后立即进行的γ-H2AX焦点评估是预期等效全身剂量的可靠测量方法。一天后,两种检测方法均可近似估算局部肿瘤剂量。全身放疗后,两种检测方法在照射后8小时内均能获得满意的剂量估计值。总之,在局部身体体积急性异质照射后,辐射诱导的γ-H2AX焦点定量而非外周白细胞中的细胞遗传学损伤是一种敏感且快速的生物剂量计,能够主要评估吸收的等效全身剂量。

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