Gene expression signatures that predict radiation exposure in mice and humans

被引:162
作者
Dressman, Holly K.
Muramoto, Garrett G.
Chao, Nelson J.
Meadows, Sarah
Marshall, Dawn
Ginsburg, Geoffrey S.
Nevins, Joseph R.
Chute, John P.
机构
[1] Institute for Genome Sciences and Policy, Duke University Medical Center, Durham, NC
[2] Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC
[3] Division of Cellular Therapy, Department of Medicine, Duke University Medical Center, Durham, NC
关键词
D O I
10.1371/journal.pmed.0040106
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background: The capacity to assess environmental inputs to biological phenotypes is limited by methods that can accurately and quantitatively measure these contributions. One such example can be seen in the context of exposure to ionizing radiation. Methods and Findings: We have made use of gene expression analysis of peripheral blood (PB) mononuclear cells to develop expression profiles that accurately reflect prior radiation exposure. We demonstrate that expression profiles can be developed that not only predict radiation exposure in mice but also distinguish the level of radiation exposure, ranging from 50 cGy to 1,000 cGy. Likewise, a molecular signature of radiation response developed solely from irradiated human patient samples can predict and distinguish irradiated human PB samples from nonirradiated samples with an accuracy of 90%, sensitivity of 85%, and specificity of 94%. We further demonstrate that a radiation profile developed in the mouse can correctly distinguish PB samples from irradiated and nonirradiated human patients with an accuracy of 77%, sensitivity of 82%, and specificity of 75%. Taken together, these data demonstrate that molecular profiles can be generated that are highly predictive of different levels of radiation exposure in mice and humans. Conclusions: We suggest that this approach, with additional refinement, could provide a method to assess the effects of various environmental inputs into biological phenotypes as well as providing a more practical application of a rapid molecular screening test for the diagnosis of radiation exposure. © 2007 Dressman et al.
引用
收藏
页码:690 / 701
页数:12
相关论文
共 41 条
[1]
Cardis E., Kesmeniene A., Ivanov V., Malakhova I., Shibata Y., Et al., Risk of thyroid cancer after exposure to 131I in childhood, J Natl Cancer Inst, 97, pp. 724-732, (2005)
[2]
Pobel D., Viel J., Case control study of leukemia among young people near La Hague nuclear reprocessing plant: The environmental hypothesis revisited, BMJ, 314, pp. 101-106, (1997)
[3]
Wing S., Richardson D., Wolf S., Mihlan G., Crawford-Brown D., Et al., A case control study of multiple myeloma at four nuclear facilities, Ann Epidemiol, 10, pp. 144-153, (2000)
[4]
Iwamoto K., Mizuno T., Tokuoka S., Mabuchi K., Seyama T., Frequency of p53 mutations in hepatocellular carcinomas from atomic bomb survivors, J Natl Cancer Inst, 90, pp. 1167-1168, (1998)
[5]
Hirai Y., Kusonoki Y., Kyoizumi S., Awa A., Pawel D., Et al., Mutant frequency at the HPRT locus in peripheral blood T lymphocytes of atomic bomb survivors, Mutat Res, 329, pp. 183-196, (1995)
[6]
Takeshima Y., Seyama T., Bennet W., Akiyama M., Tokuoka S., Et al., p53 mutations in lung cancers from from non-smoking atomic bomb survivors, Lancet, 342, pp. 1520-1521, (1993)
[7]
Neel J., Lewis S., The comparison radiation genetics of humans and mice, Annu Rev Genet, 24, pp. 327-362, (1990)
[8]
Yoshimoto Y., Schull W., Kato H., Neel J., Mortality among the offspring (F1) of atomic bomb survivors, 1946-1985, J Radiat Res (Tokyo), 32, pp. 327-351, (1991)
[9]
Satoh C., Takahashi N., Asakawa J., Kodaira M., Kuick R., Et al., Genetic analysis of children of atomic bomb survivors, Environ Health Perspect, 104, pp. 511-519, (1996)
[10]
Wasalenko J., MacVittie T., Blakely W., Pesik N., Wiley A., Et al., Medical management of the acute radiation syndrome: Recommendations of the Strategic National Stockpile Radiation Working Group, Ann Intern Med, 140, pp. 1037-1051, (2004)