Centre de Recherche en Cancérologie de Lyon, INSERM 1052, CNRS 5286, Univ Lyon, Université Claude Bernard, Lyon 1, Lyon, F-69424, France.
Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, Falmer, Brighton, BN1 9RQ, United Kingdom.
Mutat Res Rev Mutat Res. 2017 Jan-Mar;771:59-84. doi: 10.1016/j.mrrev.2017.01.001. Epub 2017 Jan 16.
Recent epidemiology studies highlighted the detrimental health effects of exposure to low dose and low dose rate ionizing radiation (IR): nuclear industry workers studies have shown increased leukaemia and solid tumour risks following cumulative doses of <100mSv and dose rates of <10mGy per year; paediatric patients studies have reported increased leukaemia and brain tumours risks after doses of 30-60mGy from computed tomography scans. Questions arise, however, about the impact of even lower doses and dose rates where classical epidemiological studies have limited power but where subsets within the large cohorts are expected to have an increased risk. Further progress requires integration of biomarkers or bioassays of individual exposure, effects and susceptibility to IR. The European DoReMi (Low Dose Research towards Multidisciplinary Integration) consortium previously reviewed biomarkers for potential use in IR epidemiological studies. Given the increased mechanistic understanding of responses to low dose radiation the current review provides an update covering technical advances and recent studies. A key issue identified is deciding which biomarkers to progress. A roadmap is provided for biomarker development from discovery to implementation and used to summarise the current status of proposed biomarkers for epidemiological studies. Most potential biomarkers remain at the discovery stage and for some there is sufficient evidence that further development is not warranted. One biomarker identified in the final stages of development and as a priority for further research is radiation specific mRNA transcript profiles.
最近的流行病学研究强调了暴露于低剂量和低剂量率电离辐射(IR)对健康的有害影响:核工业工人的研究表明,累积剂量<100mSv 和剂量率<10mGy/年时,白血病和实体瘤的风险增加;儿科患者的研究报告称,在接受 30-60mGy 的计算机断层扫描(CT)扫描后,白血病和脑瘤的风险增加。然而,对于更低剂量和剂量率的影响,出现了一些问题,因为经典的流行病学研究的影响力有限,但预计在大型队列的子集中风险会增加。进一步的进展需要整合个体暴露、效应和对 IR 易感性的生物标志物或生物测定。以前,欧洲多利米(低剂量研究走向多学科整合)联盟审查了潜在用于 IR 流行病学研究的生物标志物。鉴于对低剂量辐射反应的机制理解的提高,目前的综述提供了涵盖技术进展和最近研究的更新。确定的一个关键问题是决定要推进哪些生物标志物。提供了从发现到实施的生物标志物开发路线图,并用于总结拟议用于流行病学研究的生物标志物的当前状态。大多数潜在的生物标志物仍处于发现阶段,对于某些生物标志物,有足够的证据表明进一步开发是不必要的。一个在最后开发阶段确定的、作为进一步研究的优先事项的生物标志物是辐射特异性 mRNA 转录谱。