The animal study, led by researchers at The Ohio State Comprehensive Cancer Center - Arthur G. James Cancer Hospital and Richard J. Solove Research Institute (OSUCCC - James), shows that X-rays or gamma rays alter the levels of certain molecules called microRNA in the blood in a predictable way.
If verified in human subjects, the findings could lead to new methods for rapidly identifying people at risk for acute radiation syndrome after occupational exposures or accidents such as the recent Fukushima Daiichi nuclear reactor incident. The microRNA markers might also help doctors plan radiation therapy for individual patients by taking into account how different people respond to radiation treatment, the researchers say.
The findings are reported in the journal PLOS ONE.
"Our paper reports the identification of a panel of microRNA markers in mice whose serum levels provide an estimate of radiation response and of the dose received after an exposure has occurred," says senior author Dr. Arab Chakravarti, chair and professor of Radiation Oncology, the Max Morehouse Chair in Cancer Research and co-director of the Brain Tumor Program.
"Accurate dose evaluation is critical for making medical decisions and for the timely administration of therapy to prevent or reduce acute and late effects."
The findings might also one day allow doctors to evaluate radiation toxicity during the course of therapy based on an individual's biology. "This would particularly benefit leukemia and lymphoma patients who receive total body irradiation in preparation for stem-cell transplantation," Chakravarti says.
First author Dr. Naduparambil Jacob, a research assistant professor in radiation oncology, noted that the study could be an important step in the development of biological dosimetry, or biodosimetry, a technology for identifying people at risk for acute radiation illnesses that develop within weeks of radiation exposure, and cancers and degenerative diseases that can occur months or years later.
"Biodosimetry is an emerging concept that could enable us to identify individuals who need immediate treatment after a radiation exposure and to better develop personalized radiation treatment plans for patients," Jacob says.
For this study, Chakravarti, Jacob and their colleagues evaluated dose-dependent changes in levels of 88 individual microRNAs in serum from mice after a single acute radiation exposure, and after fractionated doses of radiation that are typical of radiation treatment prior to stem-cell transplantation. Samples were collected from exposed and control animals 24 or 48 hours after exposure.
Key technical findings include:
Funding from the NIH/National Cancer Institute (grant CA148190, CA108633) and a Brain Tumor Funders Collaborative grant supported this research.
Other researchers involved in this study were James V. Cooley, Tamara N. Yee, Jidhin Jacob and Hansjuerg Alder, The Ohio State University; Priyankara Wickramasinghe, The Wistar Institute; and Kirsteen H. Maclean, NanoString Technologies.
The Ohio State University Comprehensive Cancer Center - Arthur G. James Cancer Hospital and Richard J. Solove Research Institutestrives to create a cancer-free world by integrating scientific research with excellence in education and patient-centered care, a strategy that leads to better methods of prevention, detection and treatment. Ohio State is one of only 41 National Cancer Institute (NCI)-designated Comprehensive Cancer Centers and one of only seven centers funded by the NCI to conduct both phase I and phase II clinical trials. The NCI recently rated Ohio State's cancer program as "exceptional," the highest rating given by NCI survey teams. As the cancer program's 210-bed adult patient-care component, The James is a "Top Hospital" as named by the Leapfrog Group and one of the top cancer hospitals in the nation as ranked by U.S.News & World Report.
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