Gruel Gaëtan, Lucchesi Carlo, Pawlik Alexandre, Frouin Vincent, Alibert Olivier, Kortulewski Thierry, Zarour Anissa, Jacquelin Béatrice, Gidrol Xavier, Tronik-Le Roux Diana
Service de Génomique Fonctionnelle, Commissariat a l'Energie Atomique (CEA), 91057 Evry Cedex, France.
Radiat Res. 2006 Nov;166(5):746-56. doi: 10.1667/RR0260.1.
Accurate estimation of the dose of ionizing radiation to which individuals have been exposed is critical for therapeutic treatment. We investigated whether gene expression profiles could be used to evaluate the dose received, thereby serving as a biological dosimeter. We used cDNA microarrays to monitor changes in gene expression profiles induced by ionizing radiation in mouse total blood. The subsets of genes best characterizing each dose were identified by resampling the original data set and calculating the intersection of the dose signatures. This analytical strategy minimizes the impact of potential genetic/epigenetic variation between mice and overcomes the bias in gene selection inherent to microarray technology. The significance of the identified signatures was evaluated by monitoring the type I error rate by in silico negative control simulation. Based on the distribution of the mean ratios of the selected probes, we were able to identify transcription profiles giving 83% to 100% correct estimation of the dose received by test mice, demonstrating that the selected probes could be used to determine the dose of radiation to which the animals had been exposed. This method could potentially be generalized to determine the level of exposure to other toxins and could be used to develop new related clinical applications.
准确估计个体所接受的电离辐射剂量对于治疗至关重要。我们研究了基因表达谱是否可用于评估所接受的剂量,从而作为一种生物剂量计。我们使用cDNA微阵列来监测电离辐射在小鼠全血中诱导的基因表达谱变化。通过对原始数据集进行重采样并计算剂量特征的交集,确定了最能表征每个剂量的基因子集。这种分析策略将小鼠之间潜在的遗传/表观遗传变异的影响降至最低,并克服了微阵列技术固有的基因选择偏差。通过计算机模拟阴性对照来监测I型错误率,评估所识别特征的显著性。基于所选探针平均比值的分布,我们能够识别出转录谱,对测试小鼠所接受的剂量给出83%至100%的正确估计,表明所选探针可用于确定动物所暴露的辐射剂量。这种方法有可能推广到确定对其他毒素的暴露水平,并可用于开发新的相关临床应用。