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Biology subjects

Amundson, S. A.

Publications and source records attributed to Amundson, S. A..

2 recordsLinked to original sources

New Approaches for Quantitative Reconstruction of Radiation Dose in Human Blood Cells

In the event of a nuclear attack or radiation event, there would be an urgent need for assessing and reconstructing the dose to which hundreds or thousands of individuals were exposed. These measurements would need a rapid assay to facilitate triage and medical management for individuals based on dose. Our approaches to development of rapid assays for reconstructing dose, using transcriptomics, have led to identification of gene sets that have potential to be used in the field; but need further testing. This was a proof-of-principle study for new methods using radiation-responsive genes to generate quantitative, rather than categorical, radiation-dose reconstructions based on a blood sample. We used a new normalization method to reduce effects of variability of gene signals in unirradiated samples across studies; developed a quantitative dose-reconstruction method that is generally under-utilized compared to categorical methods; and combined these to determine a gene-set as a reconstructor. Our dose-reconstruction biomarker was trained on two data sets and tested on two independent ones. It was able to predict dose up to 4.5 Gy with root mean squared error (RMSE) of {+/-} 0.35 Gy on test datasets (same platform), and up to 6.0 Gy with RMSE of 1.74 Gy on another (different platform).

genomics

Discordant gene responses to radiation in humans and mice: hematopoietically humanized mice may save the day for radiation biomarker identification.

The mouse (Mus musculus) is an extensively used model of human disease and responses to stresses such as ionizing radiation. As part of our work developing gene expression biomarkers of radiation exposure, dose, and injury, we have found many genes are either up-regulated (e.g. CDKN1A, MDM2, BBC3, and CCNG1) or down-regulated (e.g. TCF4 and MYC) in both species after irradiation. However, we have also found genes that are consistently up-regulated in humans and down-regulated in mice (e.g. DDB2, PCNA, GADD45A, SESN1, RRM2B, KCNN4, IFI30, and PTPRO). Here we test a hematopoietically humanized mouse as a potential in vivo model for biodosimetry studies, measuring the response of these 14 genes one day after radiation exposure, and comparing it with that of human blood irradiated ex vivo, and blood from whole body irradiated mice. We found that human blood cells in the hematopoietically humanized mouse in vivo environment recapitulated the gene expression pattern expected from human cells, not the pattern seen from in vivo irradiated normal mice. The results of this study support the use of hematopoietically humanized mice as an in vivo model for radiation gene expression studies relevant to humans.

genomics