Prediction of DNA damage and G2 chromosomal radio-sensitivity ex vivo in peripheral blood mononuclear cells with label-free Raman micro-spectroscopy

Purpose: Liquid biopsies are a potentially rich store of biochemical information that can be linked to an individual's response to therapeutic treatments, including radiotherapy, and which may ultimately play a role in the individualization of treatment regimens. Peripheral blood mononuclear ce...

Full description

Saved in:
Bibliographic Details
Published inInternational journal of radiation biology Vol. 95; no. 1; pp. 44 - 53
Main Authors Meade, Aidan D., Maguire, Adrian, Bryant, Jane, Cullen, Daniel, Medipally, Dinesh, White, Lisa, McClean, Brendan, Shields, Laura, Armstrong, John, Dunne, Mary, Noone, Emma, Bradshaw, Shirley, Finn, Marie, Shannon, Aoife M., Howe, Orla, Lyng, Fiona M.
Format Journal Article
LanguageEnglish
Published England Taylor & Francis 18.01.2019
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Purpose: Liquid biopsies are a potentially rich store of biochemical information that can be linked to an individual's response to therapeutic treatments, including radiotherapy, and which may ultimately play a role in the individualization of treatment regimens. Peripheral blood mononuclear cells (PBMCs) can be used not only for the biochemical profiling of the individual, but also, being living cells, can provide insights into the individuals response to ionizing radiation exposure. Materials and methods: The present study attempts to link the biochemical profile of lymphocytes within PBMCs obtained through Raman spectroscopy to in vitro measures of low-dose (<0.5Gy) DNA damage response and cytogenetic metrics of radiosensitivity in a cohort of healthy controls and prostate cancer patients (from CTRIAL-IE(ICORG) 08-17, NCT00951535). All parallel metrics to the Raman spectra of the cells were obtained ex vivo in cycling peripheral blood lymphocytes, with radiosensitivity estimated using the G2 chromosomal assay and DNA damage assessed using γH2AX fluorescence. Spectra from a total of 26 healthy volunteers and 22 prostate cancer patients were obtained. Results: The links between both measures of cellular response to ionizing radiation and the Raman spectra were modeled using partial least squares regression (PLSR) and support-vector regression (SVR). It was found that neither regression approach could predict radiation-induced G2 score well, but could predict γH2AX MFI with the SVR outperforming PLSR, implying a non-linear relationship between spectral measurements and measures of DNA damage. Conclusions: Raman spectroscopy of PBMCs represents a label-free approach for prediction of DNA damage levels for either prospective or retrospective analysis.
AbstractList Purpose: Liquid biopsies are a potentially rich store of biochemical information that can be linked to an individual's response to therapeutic treatments, including radiotherapy, and which may ultimately play a role in the individualization of treatment regimens. Peripheral blood mononuclear cells (PBMCs) can be used not only for the biochemical profiling of the individual, but also, being living cells, can provide insights into the individuals response to ionizing radiation exposure. Materials and methods: The present study attempts to link the biochemical profile of lymphocytes within PBMCs obtained through Raman spectroscopy to in vitro measures of low-dose (<0.5Gy) DNA damage response and cytogenetic metrics of radiosensitivity in a cohort of healthy controls and prostate cancer patients (from CTRIAL-IE(ICORG) 08-17, NCT00951535). All parallel metrics to the Raman spectra of the cells were obtained ex vivo in cycling peripheral blood lymphocytes, with radiosensitivity estimated using the G2 chromosomal assay and DNA damage assessed using γH2AX fluorescence. Spectra from a total of 26 healthy volunteers and 22 prostate cancer patients were obtained. Results: The links between both measures of cellular response to ionizing radiation and the Raman spectra were modeled using partial least squares regression (PLSR) and support-vector regression (SVR). It was found that neither regression approach could predict radiation-induced G2 score well, but could predict γH2AX MFI with the SVR outperforming PLSR, implying a non-linear relationship between spectral measurements and measures of DNA damage. Conclusions: Raman spectroscopy of PBMCs represents a label-free approach for prediction of DNA damage levels for either prospective or retrospective analysis.
PURPOSELiquid biopsies are a potentially rich store of biochemical information that can be linked to an individual's response to therapeutic treatments, including radiotherapy, and which may ultimately play a role in the individualization of treatment regimens. Peripheral blood mononuclear cells (PBMCs) can be used not only for the biochemical profiling of the individual, but also, being living cells, can provide insights into the individuals response to ionizing radiation exposure.MATERIALS AND METHODSThe present study attempts to link the biochemical profile of lymphocytes within PBMCs obtained through Raman spectroscopy to in vitro measures of low-dose (<0.5Gy) DNA damage response and cytogenetic metrics of radiosensitivity in a cohort of healthy controls and prostate cancer patients (from CTRIAL-IE(ICORG) 08-17, NCT00951535). All parallel metrics to the Raman spectra of the cells were obtained ex vivo in cycling peripheral blood lymphocytes, with radiosensitivity estimated using the G2 chromosomal assay and DNA damage assessed using γH2AX fluorescence. Spectra from a total of 26 healthy volunteers and 22 prostate cancer patients were obtained.RESULTSThe links between both measures of cellular response to ionizing radiation and the Raman spectra were modeled using partial least squares regression (PLSR) and support-vector regression (SVR). It was found that neither regression approach could predict radiation-induced G2 score well, but could predict γH2AX MFI with the SVR outperforming PLSR, implying a non-linear relationship between spectral measurements and measures of DNA damage.CONCLUSIONSRaman spectroscopy of PBMCs represents a label-free approach for prediction of DNA damage levels for either prospective or retrospective analysis.
Liquid biopsies are a potentially rich store of biochemical information that can be linked to an individual's response to therapeutic treatments, including radiotherapy, and which may ultimately play a role in the individualization of treatment regimens. Peripheral blood mononuclear cells (PBMCs) can be used not only for the biochemical profiling of the individual, but also, being living cells, can provide insights into the individuals response to ionizing radiation exposure. The present study attempts to link the biochemical profile of lymphocytes within PBMCs obtained through Raman spectroscopy to in vitro measures of low-dose (<0.5Gy) DNA damage response and cytogenetic metrics of radiosensitivity in a cohort of healthy controls and prostate cancer patients (from CTRIAL-IE(ICORG) 08-17, NCT00951535). All parallel metrics to the Raman spectra of the cells were obtained ex vivo in cycling peripheral blood lymphocytes, with radiosensitivity estimated using the G2 chromosomal assay and DNA damage assessed using γH2AX fluorescence. Spectra from a total of 26 healthy volunteers and 22 prostate cancer patients were obtained. The links between both measures of cellular response to ionizing radiation and the Raman spectra were modeled using partial least squares regression (PLSR) and support-vector regression (SVR). It was found that neither regression approach could predict radiation-induced G2 score well, but could predict γH2AX MFI with the SVR outperforming PLSR, implying a non-linear relationship between spectral measurements and measures of DNA damage. Raman spectroscopy of PBMCs represents a label-free approach for prediction of DNA damage levels for either prospective or retrospective analysis.
Author Armstrong, John
Meade, Aidan D.
Cullen, Daniel
Shannon, Aoife M.
Dunne, Mary
Finn, Marie
Bradshaw, Shirley
Lyng, Fiona M.
White, Lisa
Medipally, Dinesh
Shields, Laura
Howe, Orla
Noone, Emma
Bryant, Jane
McClean, Brendan
Maguire, Adrian
Author_xml – sequence: 1
  givenname: Aidan D.
  surname: Meade
  fullname: Meade, Aidan D.
  email: aidan.meade@dit.ie
  organization: DIT Centre for Radiation and Environmental Science, Focas Research Institute, Dublin Institute of Technology
– sequence: 2
  givenname: Adrian
  surname: Maguire
  fullname: Maguire, Adrian
  organization: DIT Centre for Radiation and Environmental Science, Focas Research Institute, Dublin Institute of Technology
– sequence: 3
  givenname: Jane
  surname: Bryant
  fullname: Bryant, Jane
  organization: DIT Centre for Radiation and Environmental Science, Focas Research Institute, Dublin Institute of Technology
– sequence: 4
  givenname: Daniel
  surname: Cullen
  fullname: Cullen, Daniel
  organization: School of Biological Sciences, Dublin Institute of Technology
– sequence: 5
  givenname: Dinesh
  surname: Medipally
  fullname: Medipally, Dinesh
  organization: School of Biological Sciences, Dublin Institute of Technology
– sequence: 6
  givenname: Lisa
  surname: White
  fullname: White, Lisa
  organization: School of Biological Sciences, Dublin Institute of Technology
– sequence: 7
  givenname: Brendan
  surname: McClean
  fullname: McClean, Brendan
  organization: Department of Medical Physics, Saint Luke's Radiation Oncology Network, St Luke's Hospital
– sequence: 8
  givenname: Laura
  surname: Shields
  fullname: Shields, Laura
  organization: Department of Medical Physics, Saint Luke's Radiation Oncology Network, St Luke's Hospital
– sequence: 9
  givenname: John
  surname: Armstrong
  fullname: Armstrong, John
  organization: Cancer Trials Ireland
– sequence: 10
  givenname: Mary
  surname: Dunne
  fullname: Dunne, Mary
  organization: Department of Radiation Oncology, Saint Luke's Radiation Oncology Network, St Luke's Hospital
– sequence: 11
  givenname: Emma
  surname: Noone
  fullname: Noone, Emma
  organization: Department of Radiation Oncology, Saint Luke's Radiation Oncology Network, St Luke's Hospital
– sequence: 12
  givenname: Shirley
  surname: Bradshaw
  fullname: Bradshaw, Shirley
  organization: Department of Radiation Oncology, Saint Luke's Radiation Oncology Network, St Luke's Hospital
– sequence: 13
  givenname: Marie
  surname: Finn
  fullname: Finn, Marie
  organization: Department of Radiation Oncology, Saint Luke's Radiation Oncology Network, St Luke's Hospital
– sequence: 14
  givenname: Aoife M.
  surname: Shannon
  fullname: Shannon, Aoife M.
  organization: Cancer Trials Ireland
– sequence: 15
  givenname: Orla
  surname: Howe
  fullname: Howe, Orla
  organization: School of Biological Sciences, Dublin Institute of Technology
– sequence: 16
  givenname: Fiona M.
  surname: Lyng
  fullname: Lyng, Fiona M.
  organization: DIT Centre for Radiation and Environmental Science, Focas Research Institute, Dublin Institute of Technology
BackLink https://www.ncbi.nlm.nih.gov/pubmed/29528761$$D View this record in MEDLINE/PubMed
BookMark eNp9kc1uEzEUhS3UiqaBRwB5yWaCf-LMzI6qhYJUtRWCteWxr4mRfwZ7kpL34IHxKClLVr6Sv3PP0T2X6CymCAi9oWRFSUfek14ITghbMUK7FV0LSsjmBVpQvmENr79naDEzzQxdoMtSfpI6Ed69RBesF6xrN3SB_jxmME5PLkWcLL65v8JGBfUDsIoG3zKstzmFVFJQHmdlXGoKxOImt3fTAcNvvHf7hF3EI2Q3biFXbvApGRxSjbzTHlTGGrwv-MlNW-zVAL6xGQB_rU4RB6dz3TqCnnIqOo2HV-jcKl_g9eldou-fPn67_tzcPdx-ub66a_Sa8qnpjF0zSnvbtobrHsgAre1bYYUaDLVEdJxybVtq2ZoBWGWsaCmnQI0Zes34Er077h1z-rWDMsngyhxVRUi7IutpuaD9fOklEke0Zi0lg5VjdkHlg6REzoXI50JmVSdPhVTd25PFbghg_qmeG6jAhyPgok05qKeUvZGTOviUbVZRuyL5_z3-Asa3nvA
CitedBy_id crossref_primary_10_3390_ijms232112986
crossref_primary_10_3390_ijms221910607
crossref_primary_10_1667_RR15462_1
crossref_primary_10_1002_tbio_202000014
crossref_primary_10_1080_09553002_2021_1931529
crossref_primary_10_1177_1758835920918499
crossref_primary_10_3390_s19183971
crossref_primary_10_3233_BSI_200198
crossref_primary_10_1039_D3AN00686G
crossref_primary_10_3390_cancers15030979
crossref_primary_10_1002_tbio_201900035
crossref_primary_10_1016_j_jpba_2018_11_028
crossref_primary_10_3390_cancers11070925
Cites_doi 10.1016/j.ijrobp.2014.03.009
10.1054/bjoc.2000.1701
10.1016/j.clon.2004.08.008
10.1039/C6AN02100J
10.1007/s10103-016-1959-y
10.1371/journal.pone.0015544
10.1038/nature07762
10.1038/nature08467
10.1080/09553009414551991
10.1371/journal.pone.0047185
10.1162/089976600300015565
10.1088/0031-9155/56/1/002
10.1038/35044005
10.1080/09553000210144484
10.1109/BIBM.2014.6999164
10.1039/C5FD00197H
10.1118/1.3576105
10.1016/0165-4608(95)00279-0
10.1038/bjc.1996.307
10.1080/09553000902781147
10.1039/C5FD00208G
10.1667/RR1775.1
10.1201/9781420059496
10.1088/0031-9155/35/10/301
10.1023/B:STCO.0000035301.49549.88
10.1080/09553000500147642
10.1118/1.4754797
10.1054/bjoc.2001.2086
10.1086/302544
10.1016/j.clon.2004.08.010
10.1080/09553008914551001
10.1667/RR1836.1
10.1016/j.addr.2015.03.009
10.1054/bjoc.2000.1692
10.1016/j.canlet.2016.02.035
10.1017/CBO9780511801389
10.1118/1.2362876
10.1667/RR13342.1
10.1016/j.mrrev.2012.06.002
10.1667/RR13891.1
10.1016/S0002-9440(10)64194-6
10.1093/nar/gkp237
10.1073/pnas.80.18.5612
10.1080/0955300031000150602
10.1016/S0027-5107(98)00245-0
10.1667/RR3454.1
10.1146/annurev.genom.2.1.41
10.1667/RR1851.1
10.1016/j.ijrobp.2009.10.020
10.1038/sj.bjc.6600628
10.1371/journal.pone.0025113
10.1007/s00216-006-0876-5
10.1016/j.toxlet.2003.12.044
10.1016/j.pdpdt.2013.01.008
ContentType Journal Article
Copyright Copyright © 2018 Taylor & Francis Group LLC. 2018
Copyright_xml – notice: Copyright © 2018 Taylor & Francis Group LLC. 2018
DBID NPM
AAYXX
CITATION
7X8
DOI 10.1080/09553002.2018.1451006
DatabaseName PubMed
CrossRef
MEDLINE - Academic
DatabaseTitle PubMed
CrossRef
MEDLINE - Academic
DatabaseTitleList
MEDLINE - Academic
PubMed
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
Sciences (General)
Biology
EISSN 1362-3095
EndPage 53
ExternalDocumentID 10_1080_09553002_2018_1451006
29528761
1451006
Genre Original Articles
Research Support, Non-U.S. Gov't
Journal Article
GrantInformation_xml – fundername: EU FP7 Network of Excellence DoReMi
  grantid: 249689
– fundername: Science Foundation Ireland
  grantid: 11/RFP.1/BMT/3317
GroupedDBID ---
00X
03L
0BK
0R~
29J
36B
4.4
5GY
5RE
A8Z
AAJNR
AALUX
AAMIU
AAPUL
AAPXX
AAQRR
ABBKH
ABDBF
ABEIZ
ABLKL
ABPTK
ABUPF
ACENM
ACFUF
ACGEJ
ACGFS
ACLSK
ADCVX
ADFCX
ADRBQ
ADXPE
AECIN
AENEX
AEOZL
AEXWM
AEYQI
AFKVX
AFWLO
AGDLA
AGFJD
AGRBW
AGYJP
AIJEM
AIRBT
AJWEG
AKBVH
ALIIL
ALMA_UNASSIGNED_HOLDINGS
ALQZU
AMDAE
BABNJ
BLEHA
BOHLJ
CCCUG
CS3
DKSSO
DU5
EAP
EAS
EBB
EBC
EBD
EBO
EBS
EBX
EHN
EJD
EMB
EMK
EMOBN
EPL
EPT
ESX
F5P
H13
HZ~
J.N
KRBQP
KSSTO
KWAYT
KYCEM
LJTGL
M4Z
O9-
P2P
Q~Q
RNANH
RVRKI
SV3
TFDNU
TFL
TFW
TH9
TUS
UEQFS
V1S
~1N
.55
.GJ
53G
5VS
8WZ
A6W
AALIY
AAORF
ABJNI
ABLIJ
ABWCV
ABXYU
ABZEW
ACIEZ
ACKZS
ADFOM
ADFZZ
AEIIZ
AFFNX
AFLEI
AJVHN
ALYBC
AWYRJ
BRMBE
CAG
COF
CYYVM
CZDIS
DRXRE
DWTOO
ESTFP
J5H
JENTW
M44
NPM
NUSFT
QQXMO
TBQAZ
TDBHL
TERGH
TUROJ
UDS
X7M
ZGI
ZXP
AAYXX
CITATION
7X8
ID FETCH-LOGICAL-c413t-8df42119f77d3c9e0be7f975f5abd1f058313cf71f242eefadf57131e1ddb9c23
ISSN 0955-3002
IngestDate Fri Oct 25 04:18:17 EDT 2024
Fri Aug 23 01:22:03 EDT 2024
Wed Oct 16 00:51:57 EDT 2024
Tue Jun 13 19:28:21 EDT 2023
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords support vector regression
γH2AX fluorescence
individual radiation sensitivity
partial least squares regression
DNA damage
G2 radiosensitivity
Raman spectroscopy
Language English
License free
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c413t-8df42119f77d3c9e0be7f975f5abd1f058313cf71f242eefadf57131e1ddb9c23
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://www.tandfonline.com/doi/pdf/10.1080/09553002.2018.1451006?needAccess=true
PMID 29528761
PQID 2013519955
PQPubID 23479
PageCount 10
ParticipantIDs pubmed_primary_29528761
informaworld_taylorfrancis_310_1080_09553002_2018_1451006
crossref_primary_10_1080_09553002_2018_1451006
proquest_miscellaneous_2013519955
PublicationCentury 2000
PublicationDate 1/18/2019
PublicationDateYYYYMMDD 2019-01-18
PublicationDate_xml – month: 01
  year: 2019
  text: 1/18/2019
  day: 18
PublicationDecade 2010
PublicationPlace England
PublicationPlace_xml – name: England
PublicationTitle International journal of radiation biology
PublicationTitleAlternate Int J Radiat Biol
PublicationYear 2019
Publisher Taylor & Francis
Publisher_xml – name: Taylor & Francis
References CIT0030
CIT0032
CIT0031
CIT0034
CIT0033
CIT0036
CIT0035
CIT0038
CIT0037
CIT0041
CIT0040
CIT0043
CIT0042
CIT0001
CIT0045
CIT0044
CIT0003
CIT0047
CIT0002
CIT0046
CIT0005
CIT0049
CIT0004
CIT0048
CIT0007
CIT0006
CIT0009
CIT0008
CIT0050
CIT0052
CIT0051
CIT0010
CIT0054
CIT0053
CIT0012
CIT0011
CIT0055
Redon CE (CIT0039) 2012; 1819
CIT0014
CIT0013
CIT0016
CIT0015
CIT0018
CIT0017
CIT0019
CIT0021
CIT0020
CIT0023
CIT0022
CIT0025
CIT0024
CIT0027
CIT0026
CIT0029
CIT0028
References_xml – volume: 1819
  start-page: 743
  year: 2012
  ident: CIT0039
  publication-title: BBA Gene Regul Mech
  contributor:
    fullname: Redon CE
– ident: CIT0043
  doi: 10.1016/j.ijrobp.2014.03.009
– ident: CIT0005
  doi: 10.1054/bjoc.2000.1701
– ident: CIT0008
  doi: 10.1016/j.clon.2004.08.008
– ident: CIT0031
  doi: 10.1039/C6AN02100J
– ident: CIT0017
  doi: 10.1007/s10103-016-1959-y
– ident: CIT0038
  doi: 10.1371/journal.pone.0015544
– ident: CIT0050
  doi: 10.1038/nature07762
– ident: CIT0020
  doi: 10.1038/nature08467
– ident: CIT0047
  doi: 10.1080/09553009414551991
– ident: CIT0013
  doi: 10.1371/journal.pone.0047185
– ident: CIT0046
  doi: 10.1162/089976600300015565
– ident: CIT0026
  doi: 10.1088/0031-9155/56/1/002
– ident: CIT0055
  doi: 10.1038/35044005
– ident: CIT0007
  doi: 10.1080/09553000210144484
– ident: CIT0028
  doi: 10.1109/BIBM.2014.6999164
– ident: CIT0037
  doi: 10.1039/C5FD00197H
– ident: CIT0032
  doi: 10.1118/1.3576105
– ident: CIT0045
  doi: 10.1016/0165-4608(95)00279-0
– ident: CIT0035
  doi: 10.1038/bjc.1996.307
– ident: CIT0002
  doi: 10.1080/09553000902781147
– ident: CIT0029
  doi: 10.1039/C5FD00208G
– ident: CIT0042
  doi: 10.1667/RR1775.1
– ident: CIT0052
  doi: 10.1201/9781420059496
– ident: CIT0024
  doi: 10.1088/0031-9155/35/10/301
– ident: CIT0049
  doi: 10.1023/B:STCO.0000035301.49549.88
– ident: CIT0019
  doi: 10.1080/09553000500147642
– ident: CIT0023
  doi: 10.1118/1.4754797
– ident: CIT0040
  doi: 10.1054/bjoc.2001.2086
– ident: CIT0041
  doi: 10.1086/302544
– ident: CIT0009
  doi: 10.1016/j.clon.2004.08.010
– ident: CIT0044
  doi: 10.1080/09553008914551001
– ident: CIT0027
  doi: 10.1667/RR1836.1
– ident: CIT0022
  doi: 10.1016/j.addr.2015.03.009
– ident: CIT0034
  doi: 10.1054/bjoc.2000.1692
– ident: CIT0014
  doi: 10.1016/j.canlet.2016.02.035
– ident: CIT0010
  doi: 10.1017/CBO9780511801389
– ident: CIT0012
  doi: 10.1118/1.2362876
– ident: CIT0015
  doi: 10.1667/RR13342.1
– ident: CIT0051
  doi: 10.1016/j.mrrev.2012.06.002
– ident: CIT0025
  doi: 10.1667/RR13891.1
– ident: CIT0054
  doi: 10.1016/S0002-9440(10)64194-6
– ident: CIT0003
  doi: 10.1093/nar/gkp237
– ident: CIT0036
  doi: 10.1073/pnas.80.18.5612
– ident: CIT0048
  doi: 10.1080/0955300031000150602
– ident: CIT0001
  doi: 10.1016/S0027-5107(98)00245-0
– ident: CIT0018
  doi: 10.1667/RR3454.1
– ident: CIT0033
  doi: 10.1146/annurev.genom.2.1.41
– ident: CIT0006
  doi: 10.1667/RR1851.1
– ident: CIT0011
  doi: 10.1016/j.ijrobp.2009.10.020
– ident: CIT0004
  doi: 10.1038/sj.bjc.6600628
– ident: CIT0016
  doi: 10.1371/journal.pone.0025113
– ident: CIT0030
  doi: 10.1007/s00216-006-0876-5
– ident: CIT0053
  doi: 10.1016/j.toxlet.2003.12.044
– ident: CIT0021
  doi: 10.1016/j.pdpdt.2013.01.008
SSID ssj0002038
Score 2.3567538
Snippet Purpose: Liquid biopsies are a potentially rich store of biochemical information that can be linked to an individual's response to therapeutic treatments,...
Liquid biopsies are a potentially rich store of biochemical information that can be linked to an individual's response to therapeutic treatments, including...
PURPOSELiquid biopsies are a potentially rich store of biochemical information that can be linked to an individual's response to therapeutic treatments,...
SourceID proquest
crossref
pubmed
informaworld
SourceType Aggregation Database
Index Database
Publisher
StartPage 44
SubjectTerms DNA damage
G2 radiosensitivity
individual radiation sensitivity
partial least squares regression
Raman spectroscopy
Space life sciences
support vector regression
γH2AX fluorescence
Title Prediction of DNA damage and G2 chromosomal radio-sensitivity ex vivo in peripheral blood mononuclear cells with label-free Raman micro-spectroscopy
URI https://www.tandfonline.com/doi/abs/10.1080/09553002.2018.1451006
https://www.ncbi.nlm.nih.gov/pubmed/29528761
https://search.proquest.com/docview/2013519955
Volume 95
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3JbtswECXcBC16KRp3czewQA8tDBqiKEXS0Y6bBAES9JAAuQkSRaYGYiuQ7SDpd_S3-k-dISlLrlN0uwi2bEm039NwOJp5Q8h7L8hFrIVkEeeKBbsyZIn2JAtk6CmcEWJTC3N8snt4Fhydh-edzvdW1tJykQ_k1zvrSv4FVdgHuGKV7F8guzop7IDXgC9sAWHY_hHGnyt8zFL7fOOTYb_IppiEg9HwA78vv2Cy3byconp_VkxKNsd8ddcwQt30ryfXpc0jB9uBlViXNpO9Dz-hnKHUcVb1MbbviuCAMuqS6Qq7PWQY_Z9iPh8z5Zooi1lerT0lXg83tkQqcDCWeU4EaoV7rQM8nBRw-vGgiZhf1BVpw6JqcXpU3WZWO-Eoa1IE9lBVfNbU0LeDG1hPxZmzx6Y8bqPPyFoAM2TC86wtV9Z8Yw2Y8Gzbztq-u3dtHltjbYUn3bRvJYs3JhSXgZlgdyVTuMfjATY39ryfBLztisp-co9s-2D3wOBuD0fj0f7KNfA901p9NfS6pAzF3u-6xJqztCal--sFkXGMTh-TR25FQ4eWnjuko2Zdct_2OL3tkgfHLnujS3bcRDKnH5za-ccn5FtDYlpqCiSmlsQUSEwPfNoiMd0gMVU3FElMJzPakJgaEtMWiakhMUUS04bE1JCYbpL4KTnb_3S6d8hcqxAmwQtbsLjQAWoV6igqhEyUl6tIJ1GowywvuPbCWHAhdcQ1uKRK6azQYcQFV7wo8kT64hnZgiGpF4TKIkx0FgsZ-yIQWZxwZcrDQ3T24ijpkUGNSXplFWFSXgvtOhBTBDF1IPZI0kYuXRhSa8vnVPzm2Hc1zCnYffyv4F4ql3P8FvbWhIN65LnFfzUcPwl98HL4y_-48ivysLkhX5OtRbVUb8D_XuRvHat_APZa2QI
link.rule.ids 315,783,787,27936,27937
linkProvider EBSCOhost
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Prediction+of+DNA+damage+and+G2+chromosomal+radio-sensitivity+ex+vivo+in+peripheral+blood+mononuclear+cells+with+label-free+Raman+micro-spectroscopy&rft.jtitle=International+journal+of+radiation+biology&rft.au=Meade%2C+Aidan+D.&rft.au=Maguire%2C+Adrian&rft.au=Bryant%2C+Jane&rft.au=Cullen%2C+Daniel&rft.date=2019-01-18&rft.pub=Taylor+%26+Francis&rft.issn=0955-3002&rft.eissn=1362-3095&rft.volume=95&rft.issue=1&rft.spage=44&rft.epage=53&rft_id=info:doi/10.1080%2F09553002.2018.1451006&rft.externalDocID=1451006
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0955-3002&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0955-3002&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0955-3002&client=summon