Simone Schüle, Carsten Hackenbroch, Meinrad Beer, Razan Muhtadi, Cornelius Hermann, Samantha Stewart, Daniel Schwanke, Patrick Ostheim, Matthias Port, Harry Scherthan, Michael Abend
{"title":"最近鉴定的EDA2R基因在低水平辐射暴露后的离体剂量反应特征,并与FDXR基因表达和γH2AX焦点分析进行比较。","authors":"Simone Schüle, Carsten Hackenbroch, Meinrad Beer, Razan Muhtadi, Cornelius Hermann, Samantha Stewart, Daniel Schwanke, Patrick Ostheim, Matthias Port, Harry Scherthan, Michael Abend","doi":"10.1080/09553002.2023.2194402","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Recently, promising radiation-induced EDA2R gene expression (GE) changes after low level radiation could be shown. Stimulated by that, in this study, we intended to independently validate these findings and to further characterize dose-response relationships in comparison to FDXR and the γH2AX-DNA double-strand break (DSB) focus assay, since both assays are already widely used for biodosimetry purposes.</p><p><strong>Materials and methods: </strong>Peripheral blood samples from six healthy human donors were irradiated ex vivo (dose: ranging from 2.6 to 49.7 mGy). Subsequently, the fold-differences relative to the sham irradiated reference group were calculated. Radiation-induced changes in GE of <i>FDXR</i> and <i>EDA2R</i> were examined using the quantitative real-time polymerase-chain-reaction (qRT-PCR). DSB foci were quantified in 100 γH2AX + 53BP1 immunostained cells employing fluorescence microscopy. Examinations were performed at single time points enabling sufficient detection of both endpoints.</p><p><strong>Results: </strong>A significant increase in <i>EDA2R</i> GE relative to the unexposed control was observed in the range of 2.6 mGy (1.6-fold, <i>p</i> = .045) to 5.4 mGy (2.2-fold, <i>p</i> = .0002), whereas the copy numbers increased linearly up to 13.1-fold at 49.7 mGy. On the contrary, <i>FDXR</i> upregulation (2.2-fold) became significant after a 22.6 mGy exposure (<i>p</i> ≤ .02) and increased linearly up to 4-fold at 49.7 mGy. A significant increase in radiation-induced foci (relative to unexposed, RIF-fd) was observed after 11.3 mGy (RIF-fd: 1.5 ± 0.5, <i>p</i> ≤ .03), while the foci increased linearly up to 3-fold at 49.7 mGy. From this, the <i>FDXR</i> and RIF-fd slopes have shown comparability, while the <i>EDA2R</i> slope was five times higher. Nevertheless, the coefficient of variation (CV) of <i>EDA2R</i> was about 30% higher than for RIF-fd.</p><p><strong>Conclusion: </strong>Higher radiation-induced EDA2R GE changes and a lower radiation detection level compared to RIF-fd and <i>FDXR</i> GE changes examined under optimal conditions ex vivo on human samples appear promising. Yet, our results represent just the beginning of further studies to be conducted in animal models for further time- and dose-dependent evaluation and additional examinations on radiologically examined patients to evaluate the impact of confounder, such as age, sex, social behavior, or diseases.</p>","PeriodicalId":14261,"journal":{"name":"International Journal of Radiation Biology","volume":null,"pages":null},"PeriodicalIF":2.1000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Ex-vivo dose response characterization of the recently identified <i>EDA2R</i> gene after low level radiation exposures and comparison with <i>FDXR</i> gene expression and the γH2AX focus assay.\",\"authors\":\"Simone Schüle, Carsten Hackenbroch, Meinrad Beer, Razan Muhtadi, Cornelius Hermann, Samantha Stewart, Daniel Schwanke, Patrick Ostheim, Matthias Port, Harry Scherthan, Michael Abend\",\"doi\":\"10.1080/09553002.2023.2194402\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>Recently, promising radiation-induced EDA2R gene expression (GE) changes after low level radiation could be shown. Stimulated by that, in this study, we intended to independently validate these findings and to further characterize dose-response relationships in comparison to FDXR and the γH2AX-DNA double-strand break (DSB) focus assay, since both assays are already widely used for biodosimetry purposes.</p><p><strong>Materials and methods: </strong>Peripheral blood samples from six healthy human donors were irradiated ex vivo (dose: ranging from 2.6 to 49.7 mGy). Subsequently, the fold-differences relative to the sham irradiated reference group were calculated. Radiation-induced changes in GE of <i>FDXR</i> and <i>EDA2R</i> were examined using the quantitative real-time polymerase-chain-reaction (qRT-PCR). DSB foci were quantified in 100 γH2AX + 53BP1 immunostained cells employing fluorescence microscopy. Examinations were performed at single time points enabling sufficient detection of both endpoints.</p><p><strong>Results: </strong>A significant increase in <i>EDA2R</i> GE relative to the unexposed control was observed in the range of 2.6 mGy (1.6-fold, <i>p</i> = .045) to 5.4 mGy (2.2-fold, <i>p</i> = .0002), whereas the copy numbers increased linearly up to 13.1-fold at 49.7 mGy. On the contrary, <i>FDXR</i> upregulation (2.2-fold) became significant after a 22.6 mGy exposure (<i>p</i> ≤ .02) and increased linearly up to 4-fold at 49.7 mGy. A significant increase in radiation-induced foci (relative to unexposed, RIF-fd) was observed after 11.3 mGy (RIF-fd: 1.5 ± 0.5, <i>p</i> ≤ .03), while the foci increased linearly up to 3-fold at 49.7 mGy. From this, the <i>FDXR</i> and RIF-fd slopes have shown comparability, while the <i>EDA2R</i> slope was five times higher. Nevertheless, the coefficient of variation (CV) of <i>EDA2R</i> was about 30% higher than for RIF-fd.</p><p><strong>Conclusion: </strong>Higher radiation-induced EDA2R GE changes and a lower radiation detection level compared to RIF-fd and <i>FDXR</i> GE changes examined under optimal conditions ex vivo on human samples appear promising. Yet, our results represent just the beginning of further studies to be conducted in animal models for further time- and dose-dependent evaluation and additional examinations on radiologically examined patients to evaluate the impact of confounder, such as age, sex, social behavior, or diseases.</p>\",\"PeriodicalId\":14261,\"journal\":{\"name\":\"International Journal of Radiation Biology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Radiation Biology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/09553002.2023.2194402\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/4/17 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Radiation Biology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/09553002.2023.2194402","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/4/17 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOLOGY","Score":null,"Total":0}
Ex-vivo dose response characterization of the recently identified EDA2R gene after low level radiation exposures and comparison with FDXR gene expression and the γH2AX focus assay.
Objective: Recently, promising radiation-induced EDA2R gene expression (GE) changes after low level radiation could be shown. Stimulated by that, in this study, we intended to independently validate these findings and to further characterize dose-response relationships in comparison to FDXR and the γH2AX-DNA double-strand break (DSB) focus assay, since both assays are already widely used for biodosimetry purposes.
Materials and methods: Peripheral blood samples from six healthy human donors were irradiated ex vivo (dose: ranging from 2.6 to 49.7 mGy). Subsequently, the fold-differences relative to the sham irradiated reference group were calculated. Radiation-induced changes in GE of FDXR and EDA2R were examined using the quantitative real-time polymerase-chain-reaction (qRT-PCR). DSB foci were quantified in 100 γH2AX + 53BP1 immunostained cells employing fluorescence microscopy. Examinations were performed at single time points enabling sufficient detection of both endpoints.
Results: A significant increase in EDA2R GE relative to the unexposed control was observed in the range of 2.6 mGy (1.6-fold, p = .045) to 5.4 mGy (2.2-fold, p = .0002), whereas the copy numbers increased linearly up to 13.1-fold at 49.7 mGy. On the contrary, FDXR upregulation (2.2-fold) became significant after a 22.6 mGy exposure (p ≤ .02) and increased linearly up to 4-fold at 49.7 mGy. A significant increase in radiation-induced foci (relative to unexposed, RIF-fd) was observed after 11.3 mGy (RIF-fd: 1.5 ± 0.5, p ≤ .03), while the foci increased linearly up to 3-fold at 49.7 mGy. From this, the FDXR and RIF-fd slopes have shown comparability, while the EDA2R slope was five times higher. Nevertheless, the coefficient of variation (CV) of EDA2R was about 30% higher than for RIF-fd.
Conclusion: Higher radiation-induced EDA2R GE changes and a lower radiation detection level compared to RIF-fd and FDXR GE changes examined under optimal conditions ex vivo on human samples appear promising. Yet, our results represent just the beginning of further studies to be conducted in animal models for further time- and dose-dependent evaluation and additional examinations on radiologically examined patients to evaluate the impact of confounder, such as age, sex, social behavior, or diseases.
期刊介绍:
The International Journal of Radiation Biology publishes original papers, reviews, current topic articles, technical notes/reports, and meeting reports on the effects of ionizing, UV and visible radiation, accelerated particles, electromagnetic fields, ultrasound, heat and related modalities. The focus is on the biological effects of such radiations: from radiation chemistry to the spectrum of responses of living organisms and underlying mechanisms, including genetic abnormalities, repair phenomena, cell death, dose modifying agents and tissue responses. Application of basic studies to medical uses of radiation extends the coverage to practical problems such as physical and chemical adjuvants which improve the effectiveness of radiation in cancer therapy. Assessment of the hazards of low doses of radiation is also considered.