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dc.contributor.authorO'Brien, G
dc.contributor.authorCruz-Garcia, L
dc.contributor.authorMajewski, M
dc.contributor.authorGrepl, J
dc.contributor.authorAbend, M
dc.contributor.authorPort, M
dc.contributor.authorTichý, A
dc.contributor.authorSirak, I
dc.contributor.authorMalkova, A
dc.contributor.authorDonovan, E
dc.contributor.authorGothard, L
dc.contributor.authorBoyle, S
dc.contributor.authorSomaiah, N
dc.contributor.authorAinsbury, E
dc.contributor.authorPonge, L
dc.contributor.authorSlosarek, K
dc.contributor.authorMiszczyk, L
dc.contributor.authorWidlak, P
dc.contributor.authorGreen, E
dc.contributor.authorPatel, N
dc.contributor.authorKudari, M
dc.contributor.authorGleeson, F
dc.contributor.authorVinnikov, V
dc.contributor.authorStarenkiy, V
dc.contributor.authorArtiukh, S
dc.contributor.authorVasyliev, L
dc.contributor.authorZaman, A
dc.contributor.authorBadie, C
dc.date.accessioned2018-01-24T15:12:25Z
dc.date.issued2018-01-15
dc.identifier.citationScientific reports, 2018, 8 (1), pp. 684 - ?
dc.identifier.issn2045-2322
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/1023
dc.identifier.eissn2045-2322
dc.identifier.doi10.1038/s41598-017-19043-w
dc.description.abstractPrevious investigations in gene expression changes in blood after radiation exposure have highlighted its potential to provide biomarkers of exposure. Here, FDXR transcriptional changes in blood were investigated in humans undergoing a range of external radiation exposure procedures covering several orders of magnitude (cardiac fluoroscopy, diagnostic computed tomography (CT)) and treatments (total body and local radiotherapy). Moreover, a method was developed to assess the dose to the blood using physical exposure parameters. FDXR expression was significantly up-regulated 24 hr after radiotherapy in most patients and continuously during the fractionated treatment. Significance was reached even after diagnostic CT 2 hours post-exposure. We further showed that no significant differences in expression were found between ex vivo and in vivo samples from the same patients. Moreover, potential confounding factors such as gender, infection status and anti-oxidants only affect moderately FDXR transcription. Finally, we provided a first in vivo dose-response showing dose-dependency even for very low doses or partial body exposure showing good correlation between physically and biologically assessed doses. In conclusion, we report the remarkable responsiveness of FDXR to ionising radiation at the transcriptional level which, when measured in the right time window, provides accurate in vivo dose estimates.
dc.formatElectronic
dc.format.extent684 - ?
dc.languageeng
dc.language.isoeng
dc.publisherNATURE PORTFOLIO
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectHumans
dc.subjectNeoplasms
dc.subjectCurcumin
dc.subjectFerredoxin-NADP Reductase
dc.subjectLipopolysaccharides
dc.subjectRNA
dc.subjectTomography, X-Ray Computed
dc.subjectWhole-Body Irradiation
dc.subjectUp-Regulation
dc.subjectAdult
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectMiddle Aged
dc.subjectFemale
dc.subjectMale
dc.subjectYoung Adult
dc.subjectBiomarkers
dc.titleFDXR is a biomarker of radiation exposure in vivo.
dc.typeJournal Article
dcterms.dateAccepted2017-12-20
rioxxterms.versionofrecord10.1038/s41598-017-19043-w
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2018-01-12
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfScientific reports
pubs.issue1
pubs.notesNo embargo
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Translational Breast Radiobiology
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Translational Breast Radiobiology
pubs.publication-statusPublished
pubs.volume8
pubs.embargo.termsNo embargo
icr.researchteamTranslational Breast Radiobiology
dc.contributor.icrauthorGothard, Lone
dc.contributor.icrauthorSomaiah, Navita


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