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放疗患者和 C57BL/6 小鼠的基因表达分析,作为衡量电离辐射暴露的指标。

Gene expression analysis in radiotherapy patients and C57BL/6 mice as a measure of exposure to ionizing radiation.

机构信息

Department of Pharmacology and Toxicology, University of Alabama at Birmingham, AL 35294, USA.

出版信息

Radiat Res. 2011 Jul;176(1):49-61. doi: 10.1667/RR2419.1. Epub 2011 Mar 1.

DOI:10.1667/RR2419.1
PMID:21361780
Abstract

Dose assessment after radiological disasters is imperative to decrease mortality through rationally directed medical intervention. Our goal was to identify biomarkers capable of qualitative (nonirradiated/irradiated) and/or quantitative (dose) assessment of radiation exposure. Using real-time quantitative PCR, biodosimetry genes were identified in blood samples from cancer patients undergoing total-body irradiation. Time- (5, 12, 23, 48 h) and dose- (0-8 Gy) dependent changes in gene expression were examined in C57BL/6 mice. A training set was used to derive weighted voting classification algorithms (nonirradiated/irradiated) and continuous regression (dose assessment) models that were tested in a separate validation set of mice. Of eight biodosimetry genes identified in cancer patients ( ACTA2 , BBC3 , CCNG1 , CDKN1A , GADD45A , MDK , SERPINE1 , Tnfrsf10b ), expression of BBC3 , CCNG1 , CDKN1A , SERPINE1 and Tnfrsf10b was significantly (P < 0.05) increased in irradiated mice. CCNG1 and CDKN1A expression segregated irradiated mice from controls with an accuracy, specificity and sensitivity of 96.3, 100.0 and 94.4%, respectively, at 48 h. Multiple linear regression analysis predicted doses for the 0-, 1-, 2-, 4-, 6- and 8-Gy treatment groups as 0.0 ± 0.2, 1.6 ± 1.0, 2.9 ± 1.4, 5.1 ± 2.0, 5.3 ± 0.7 and 10.5 ± 5.6 Gy, respectively. These results suggest that gene expression analysis could be incorporated into biodosimetry protocols for qualitative and quantitative assessment of radiation exposure.

摘要

放射灾难后的剂量评估对于通过合理指导的医疗干预降低死亡率至关重要。我们的目标是确定能够定性(未照射/照射)和/或定量(剂量)评估辐射暴露的生物标志物。使用实时定量 PCR,在接受全身照射的癌症患者的血液样本中鉴定了生物剂量学基因。在 C57BL/6 小鼠中检查了基因表达的时间(5、12、23、48 h)和剂量(0-8 Gy)依赖性变化。使用训练集得出加权投票分类算法(未照射/照射)和连续回归(剂量评估)模型,在单独的小鼠验证集中进行了测试。在癌症患者中鉴定出的 8 个生物剂量学基因(ACTA2、BBC3、CCNG1、CDKN1A、GADD45A、MDK、SERPINE1、Tnfrsf10b)中,BBC3、CCNG1、CDKN1A、SERPINE1 和 Tnfrsf10b 的表达在照射的小鼠中显着增加(P < 0.05)。CCNG1 和 CDKN1A 的表达将照射的小鼠与对照小鼠区分开来,在 48 h 时准确性、特异性和敏感性分别为 96.3%、100.0%和 94.4%。多元线性回归分析预测 0、1、2、4、6 和 8 Gy 处理组的剂量分别为 0.0 ± 0.2、1.6 ± 1.0、2.9 ± 1.4、5.1 ± 2.0、5.3 ± 0.7 和 10.5 ± 5.6 Gy。这些结果表明,基因表达分析可以纳入生物剂量学协议,用于定性和定量评估辐射暴露。

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