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A frequency-based gene selection method to identify robust biomarkers for radiation dose prediction

机译:一种基于频率的基因选择方法,可识别用于辐射剂量预测的可靠生物标记

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Purpose: A fast, radiation-specific and highly accurate prediction of the radiation dose of accidentally exposed individuals is essential for medical decision-making. The aim of the present study is to identify small gene signatures allowing the discrimination between low and medium dose exposure of low linear energy transfer (LET)-radiation. Material and methods: We developed a framework for dose prediction using a frequency-based gene selection approach, based on a p-value and fold-change criterion applied to microarray expression data. A repeated cross-validated classification guarantees unbiased performance results. Human blood from six healthy donors was irradiated ex vivo with 0.5, 1, 2 and 4 Gy (Cs-137 γ-rays). Expression levels of isolated blood lymphocytes were measured at 6, 24 and 48 h after irradiation. Results: We identified radiation-responsive genes, most of them functionally linked to apoptosis, DNA-damage or cell-cycle regulation. We extracted small subsets of genes, with which 95.7% of all samples can be correctly predicted, regardless of the time post irradiation. Seven of these genes were used for validation by Quantitative Real-Time Polymerase Chain Reaction (qRT-PCR). Conclusion: The genes identified are potential robust biomarkers, which are particularly suitable for dose level discrimination at a window of time that would be appropriate for life-saving medical triage.
机译:目的:对意外暴露的个体的辐射剂量进行快速,针对辐射的准确预测,对于医疗决策至关重要。本研究的目的是鉴定小的基因特征,从而区分低线性能量转移(LET)辐射的中低剂量暴露。材料和方法:我们基于应用于微阵列表达数据的p值和倍数变化标准,使用基于频率的基因选择方法开发了剂量预测框架。重复的交叉验证分类可确保实现公正的性能结果。用0.5、1、2和4 Gy(Cs-137γ射线)离体辐照来自六个健康供体的人血。在照射后6、24和48小时测量分离的血液淋巴细胞的表达水平。结果:我们确定了辐射响应基因,其中大多数与凋亡,DNA损伤或细胞周期调控功能相关。我们提取了小的基因子集,无论辐照后的时间如何,都可以正确预测所有样品的95.7%。这些基因中的七个用于实时定量聚合酶链反应(qRT-PCR)的验证。结论:鉴定出的基因是潜在的强健生物标志物,特别适用于在一定时间范围内进行剂量水平的鉴别,这对于挽救生命的医疗分类很合适。

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