Dose and Dose-Rate Effects of Low-Dose Ionizing Radiation on Activation of Trp53 in Immortalized Murine Cells

2004 ◽  
Vol 162 (3) ◽  
pp. 296-307 ◽  
Author(s):  
Takashi Sugihara ◽  
Junji Magae ◽  
Renu Wadhwa ◽  
Sunil C. Kaul ◽  
Yasushi Kawakami ◽  
...  
2005 ◽  
Vol 1276 ◽  
pp. 179-180
Author(s):  
Takashi Sugihara ◽  
Junji Magae ◽  
Renu Wadhwa ◽  
Sunil C. Kaul ◽  
Yasushi Kawakami ◽  
...  

2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Yusuke Matsuya ◽  
Stephen J. McMahon ◽  
Kaori Tsutsumi ◽  
Kohei Sasaki ◽  
Go Okuyama ◽  
...  

2017 ◽  
Vol 56 (4) ◽  
pp. 433-441 ◽  
Author(s):  
Nguyen T. K. Vo ◽  
Colin B. Seymour ◽  
Carmel E. Mothersill

Author(s):  
Linda Walsh ◽  
Roy Shore ◽  
Tamara V. Azizova ◽  
Werner Rühm

AbstractRecently, several compilations of individual radiation epidemiology study results have aimed to obtain direct evidence on the magnitudes of dose-rate effects on radiation-related cancer risks. These compilations have relied on meta-analyses of ratios of risks from low dose-rate studies and matched risks from the solid cancer Excess Relative Risk models fitted to the acutely exposed Japanese A-bomb cohort. The purpose here is to demonstrate how choices of methodology for evaluating dose-rate effects on radiation-related cancer risks may influence the results reported for dose-rate effects. The current analysis is intended to address methodological issues and does not imply that the authors recommend a particular value for the dose and dose-rate effectiveness factor. A set of 22 results from one recent published study has been adopted here as a test set of data for applying the many different methods described here, that nearly all produced highly consistent results. Some recently voiced concerns, involving the recalling of the well-known theoretical point—the ratio of two normal random variables has a theoretically unbounded variance—that could potentially cause issues, are shown to be unfounded when aimed at the published work cited and examined in detail here. In the calculation of dose-rate effects for radiation protection purposes, it is recommended that meta-estimators should retain the full epidemiological and dosimetric matching information between the risks from the individual low dose-rate studies and the acutely exposed A-bomb cohort and that a regression approach can be considered as a useful alternative to current approaches.


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