3 Biodosimetry

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引用次数: 2

Abstract

The interaction of ionizing radiation with biological systems results in a wide range of responses at the cellular and molecular levels. Using biodosimetry approaches, quantification of these responses can be used to estimate the dose of radiation an individual has received. In the context of radiation triage, a dose estimate serves as a surrogate of potential radiological injury. As biodosimetry techniques incorporate measurements of the actual individual biological response to radiation, biodosimetry may provide more accurate indicators of the potential extent of injury compared with physical dosimetry methods. It is not yet known, however, how closely the various biodosimetry approaches reflect individual injury or predict individual risk, so the current applications of biodosimetry are for the prediction of dose only. Biodosimetry techniques have been previously described in ICRU Report 68. This document aims to provide an up-todate description of biodosimetry methods, introducing newer methods [premature chromosome condensation (PCC), γH2AX, emerging “-omics” technologies] but not including methods no longer used (somatic mutations). The descriptions of some mature methodologies [dicentric chromosome assay (DCA), cytokinesis-block micronucleus (CBMN) assay, translocation analysis by fluorescence in-situ hybridization (FISH)] will overlap with those found in ICRU Report 68 but will also cover updated developments and are included herein to provide a sufficiently comprehensive description of biodosimetry to form a standalone document. A number of characteristics contribute toward the usefulness of biodosimetry and determine the situations in which a particular method will be the most useful. A biodosimeter should be considered regarding the following:
电离辐射与生物系统的相互作用在细胞和分子水平上引起广泛的反应。使用生物剂量学方法,这些反应的量化可用于估计个体所接受的辐射剂量。在辐射分类的背景下,剂量估计可作为潜在辐射损伤的替代。由于生物剂量学技术结合了个体对辐射的实际生物反应的测量,因此与物理剂量学方法相比,生物剂量学可以提供更准确的潜在损伤程度指标。然而,目前尚不清楚各种生物剂量测定方法反映个体损伤或预测个体风险的程度,因此目前生物剂量测定的应用仅用于预测剂量。ICRU报告68先前已对生物剂量测定技术进行了描述。本文档旨在提供生物剂量测定方法的最新描述,介绍较新的方法[过早染色体凝聚(PCC), γ - h2ax,新兴的“组学”技术],但不包括不再使用的方法(体细胞突变)。一些成熟方法的描述[双中心染色体测定法(DCA),细胞分裂-块微核测定法(CBMN),荧光原位杂交易位分析(FISH)]将与ICRU报告68中发现的方法重叠,但也将涵盖最新的发展,并包括在这里,以提供足够全面的生物剂量学描述,形成一个独立的文件。生物剂量测定的一些特点有助于提高其实用性,并决定在何种情况下某一特定方法将是最有用的。在下列情况下应考虑使用生物剂量计:
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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