dc.contributor.author |
Meadows, Sarah K |
|
dc.contributor.author |
Dressman, Holly K |
|
dc.contributor.author |
Daher, Pamela |
|
dc.contributor.author |
Himburg, Heather |
|
dc.contributor.author |
Russell, J Lauren |
|
dc.contributor.author |
Doan, Phuong |
|
dc.contributor.author |
Chao, Nelson J |
|
dc.contributor.author |
Lucas, Joseph |
|
dc.contributor.author |
Nevins, Joseph R |
|
dc.contributor.author |
Chute, John P |
|
dc.coverage.spatial |
United States |
|
dc.date.accessioned |
2011-06-21T17:31:32Z |
|
dc.date.issued |
2010-07-12 |
|
dc.identifier |
http://www.ncbi.nlm.nih.gov/pubmed/20634956 |
|
dc.identifier.uri |
https://hdl.handle.net/10161/4550 |
|
dc.description.abstract |
In the event of a terrorist-mediated attack in the United States using radiological
or improvised nuclear weapons, it is expected that hundreds of thousands of people
could be exposed to life-threatening levels of ionizing radiation. We have recently
shown that genome-wide expression analysis of the peripheral blood (PB) can generate
gene expression profiles that can predict radiation exposure and distinguish the dose
level of exposure following total body irradiation (TBI). However, in the event a
radiation-mass casualty scenario, many victims will have heterogeneous exposure due
to partial shielding and it is unknown whether PB gene expression profiles would be
useful in predicting the status of partially irradiated individuals. Here, we identified
gene expression profiles in the PB that were characteristic of anterior hemibody-,
posterior hemibody- and single limb-irradiation at 0.5 Gy, 2 Gy and 10 Gy in C57Bl6
mice. These PB signatures predicted the radiation status of partially irradiated mice
with a high level of accuracy (range 79-100%) compared to non-irradiated mice. Interestingly,
PB signatures of partial body irradiation were poorly predictive of radiation status
by site of injury (range 16-43%), suggesting that the PB molecular response to partial
body irradiation was anatomic site specific. Importantly, PB gene signatures generated
from TBI-treated mice failed completely to predict the radiation status of partially
irradiated animals or non-irradiated controls. These data demonstrate that partial
body irradiation, even to a single limb, generates a characteristic PB signature of
radiation injury and thus may necessitate the use of multiple signatures, both partial
body and total body, to accurately assess the status of an individual exposed to radiation.
|
|
dc.language |
eng |
|
dc.language.iso |
en_US |
|
dc.publisher |
Public Library of Science (PLoS) |
|
dc.relation.ispartof |
PLoS One |
|
dc.relation.isversionof |
10.1371/journal.pone.0011535 |
|
dc.subject |
Animals |
|
dc.subject |
Female |
|
dc.subject |
Gene Expression |
|
dc.subject |
Gene Expression Profiling |
|
dc.subject |
Leukocytes, Mononuclear |
|
dc.subject |
Mice |
|
dc.subject |
Mice, Inbred C57BL |
|
dc.subject |
Oligonucleotide Array Sequence Analysis |
|
dc.subject |
Radiation Injuries, Experimental |
|
dc.subject |
Radiation, Ionizing |
|
dc.subject |
Whole-Body Irradiation |
|
dc.title |
Diagnosis of partial body radiation exposure in mice using peripheral blood gene expression
profiles.
|
|
dc.title.alternative |
|
|
dc.type |
Journal article |
|
duke.contributor.id |
Dressman, Holly K|0239213 |
|
duke.contributor.id |
Himburg, Heather|0280633 |
|
duke.contributor.id |
Doan, Phuong|0110004 |
|
duke.contributor.id |
Chao, Nelson J|0137379 |
|
duke.contributor.id |
Lucas, Joseph|0308238 |
|
duke.contributor.id |
Nevins, Joseph R|0084291 |
|
duke.contributor.id |
Chute, John P|0314438 |
|
dc.description.version |
Version of Record |
|
duke.date.pubdate |
2010-7-12 |
|
duke.description.issue |
7 |
|
duke.description.volume |
5 |
|
dc.relation.journal |
Plos One |
|
pubs.author-url |
http://www.ncbi.nlm.nih.gov/pubmed/20634956 |
|
pubs.begin-page |
e11535 |
|
pubs.issue |
7 |
|
pubs.organisational-group |
Basic Science Departments |
|
pubs.organisational-group |
Biostatistics & Bioinformatics |
|
pubs.organisational-group |
Clinical Science Departments |
|
pubs.organisational-group |
Duke |
|
pubs.organisational-group |
Duke Cancer Institute |
|
pubs.organisational-group |
Faculty |
|
pubs.organisational-group |
Global Health Institute |
|
pubs.organisational-group |
Immunology |
|
pubs.organisational-group |
Institutes and Centers |
|
pubs.organisational-group |
Institutes and Provost's Academic Units |
|
pubs.organisational-group |
Medicine |
|
pubs.organisational-group |
Medicine, Cellular Therapy |
|
pubs.organisational-group |
Medicine, Hematological Malignancies |
|
pubs.organisational-group |
Molecular Genetics and Microbiology |
|
pubs.organisational-group |
Pathology |
|
pubs.organisational-group |
School of Medicine |
|
pubs.organisational-group |
Social Science Research Institute |
|
pubs.organisational-group |
University Institutes and Centers |
|
pubs.publication-status |
Published online |
|
pubs.volume |
5 |
|
dc.identifier.eissn |
1932-6203 |
|
duke.contributor.orcid |
Doan, Phuong|0000-0003-1361-2068 |
|