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Published on: January 7, 2019
Proto-oncogene expression: a predictive assay for radiation biodosimetry applications
1Applied Cellular Radiobiology Department, Armed Forces Radiobiology Research Institute, 8901 Wisconsin Avenue, Bethesda, MD 20889-5603, USA. millera@mx.afrri.usuhs.mil
Radiation Protection Dosimetry
|August 27, 2002
Summary
Low-dose X-ray radiation increases c-Haras proto-oncogene expression in human lymphocytes. This finding suggests c-Haras mRNA levels could serve as early molecular biomarkers for radiation biodosimetry.
Area of Science:
- Molecular Biology
- Radiation Biology
- Genetics
Background:
- Proto-oncogene expression is critical in cellular regulation.
- Understanding radiation's impact on gene expression is vital for biodosimetry.
- Low-dose radiation effects on specific proto-oncogenes require further investigation.
Purpose of the Study:
- To investigate the effect of low-dose X-ray radiation on proto-oncogene expression in human lymphocytes.
- To identify potential molecular biomarkers for radiation biodosimetry.
Main Methods:
- In vitro human peripheral blood lymphocytes were exposed to low-dose X-ray radiation (0.25-1.50 Gy).
- RNA was extracted at various time points (0.25-17 h) post-irradiation.
- Northern blot hybridization was used to quantify mRNA levels of c-Haras, c-src, c-met, c-jun, c-fos, c-myc, and beta-actin.
Main Results:
- A time- and dose-dependent increase in c-Haras mRNA levels was observed.
- Expression of other proto-oncogenes (c-src, c-met, c-fos, c-jun, c-myc) showed variable responses.
- Beta-actin mRNA levels initially decreased but recovered by 17 hours post-radiation.
- c-Haras transcription rates were higher at 5 h compared to 17 h post-irradiation.
Conclusions:
- Specific proto-oncogene expression, particularly c-Haras, may serve as early diagnostic molecular biomarkers for radiation biodosimetry.
- Real-time PCR technologies can be utilized for quantifying gene expression changes in biodosimetry applications.
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