<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17(10)</volume><submitter>Li MJ</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The aim of this study was to screen molecular biomarkers for biodosimetry from DNA repair-related gene expression profiles.&lt;h4>Material/methods&lt;/h4>Mice were subjected to whole-body exposure with 60Co gamma rays with a dose range of 0-8 Gy at a dose rate of 0.80 Gy/min. RNA was extracted from the peripheral blood of irradiated mice at 4, 8, 12, 24 and 48hrs post-irradiation. The mRNA transcriptional changes of 11 genes related to DNA damage and repair were detected using real-time quantitative polymerase chain reaction (RT-PCR).&lt;h4>Results&lt;/h4>Of the 11 genes examined, CDKN1A (cyclin-dependent kinase inhibitor 1A or p21, Cip1) and ATM (ataxia telangiectasia mutated) expression levels were found to be heavily up- and down-regulated, respectively, with exposure dose increasing at different post-irradiation times. RAD50 (RAD50 homolog), PLK3 (polo-like kinase 3), GADD45A (growth arrest and DNA damage-inducible, alpha), DDB2 (damage-specific DNA-binding protein 2), BBC3 (BCL2-binding component 3) and IER5 (immediate early response 5) gene expression levels were found to undergo significant oscillating changes over a broad dose range of 2-8 Gy at post-exposure time points observed. Three of the genes were found not to change within the observed exposure dose and post-radiation time ranges.&lt;h4>Conclusions&lt;/h4>The results of this study add to the biodosimetry with biomarker data pool and will be helpful for constructing appropriate gene expression biomarker systems to evaluate radiation exposure doses.</pubmed_abstract><journal>Medical science monitor : international medical journal of experimental and clinical research</journal><pagination>BR290-7</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3539470</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Radiation dose effect of DNA repair-related gene expression in mouse white blood cells.</pubmed_title><pmcid>PMC3539470</pmcid><pubmed_authors>Shen Q</pubmed_authors><pubmed_authors>Min R</pubmed_authors><pubmed_authors>Wang WW</pubmed_authors><pubmed_authors>Chen SW</pubmed_authors><pubmed_authors>Li MJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Radiation dose effect of DNA repair-related gene expression in mouse white blood cells.</name><description>&lt;h4>Background&lt;/h4>The aim of this study was to screen molecular biomarkers for biodosimetry from DNA repair-related gene expression profiles.&lt;h4>Material/methods&lt;/h4>Mice were subjected to whole-body exposure with 60Co gamma rays with a dose range of 0-8 Gy at a dose rate of 0.80 Gy/min. RNA was extracted from the peripheral blood of irradiated mice at 4, 8, 12, 24 and 48hrs post-irradiation. The mRNA transcriptional changes of 11 genes related to DNA damage and repair were detected using real-time quantitative polymerase chain reaction (RT-PCR).&lt;h4>Results&lt;/h4>Of the 11 genes examined, CDKN1A (cyclin-dependent kinase inhibitor 1A or p21, Cip1) and ATM (ataxia telangiectasia mutated) expression levels were found to be heavily up- and down-regulated, respectively, with exposure dose increasing at different post-irradiation times. RAD50 (RAD50 homolog), PLK3 (polo-like kinase 3), GADD45A (growth arrest and DNA damage-inducible, alpha), DDB2 (damage-specific DNA-binding protein 2), BBC3 (BCL2-binding component 3) and IER5 (immediate early response 5) gene expression levels were found to undergo significant oscillating changes over a broad dose range of 2-8 Gy at post-exposure time points observed. Three of the genes were found not to change within the observed exposure dose and post-radiation time ranges.&lt;h4>Conclusions&lt;/h4>The results of this study add to the biodosimetry with biomarker data pool and will be helpful for constructing appropriate gene expression biomarker systems to evaluate radiation exposure doses.</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Oct</publication><modification>2024-10-18T01:16:14.573Z</modification><creation>2021-02-20T09:35:42Z</creation></dates><accession>S-EPMC3539470</accession><cross_references><pubmed>21959603</pubmed><doi>10.12659/msm.881976</doi></cross_references></HashMap>