Nuclear damage in peripheral lymphocytes of obese and overweight Italian children as evaluated by the γ-H2AX focus assay and micronucleus test

Childhood obesity, often characterized by a chronic low-grade inflammation, has been associated with an increased risk of developing some types of cancer later in life. Nuclear γ-H2AX foci represent the first detectable response of cells to DNA tumorigenesis lesions, such as the double-strand breaks...

Full description

Saved in:
Bibliographic Details
Published inThe FASEB journal Vol. 25; no. 2; pp. 685 - 693
Main Authors Scarpato, Roberto, Verola, Carmela, Fabiani, Barbara, Bianchi, Vanessa, Saggese, Giuseppe, Federico, Giovanni
Format Journal Article
LanguageEnglish
Published United States The Federation of American Societies for Experimental Biology 01.02.2011
Subjects
Online AccessGet more information

Cover

Loading…
Abstract Childhood obesity, often characterized by a chronic low-grade inflammation, has been associated with an increased risk of developing some types of cancer later in life. Nuclear γ-H2AX foci represent the first detectable response of cells to DNA tumorigenesis lesions, such as the double-strand breaks (DSBs). An excess of micronucleated peripheral lymphocytes was found in subjects with cancer or inflammatation-based diseases. We set out to investigate the expression of genome damage, from DNA lesions to chromosome mutations (micronuclei), in overweight and obese children. Using the γ-H2AX focus assay and micronucleus (MN) test, we analyzed peripheral lymphocytes from 119 Italian children classified as normal weight (n=38), overweight (n=20), or obese (n=61). Cultures treated with bleomycin (BLM) were also set up for each child in both assays to check functioning of the apparatus that ensures DNA integrity. We measured serum TNF-α, IL-6, and C-reactive protein (CRP) as markers of inflammation. Overweight and obese children had significantly higher levels of H2AX phosphorylation (0.0191±0.0039 and 0.0274±0.0029 γ-H2AXF/n) and increased MN frequencies (2.30±0.25 and 2.45±0.22[per thousand]) than normal-weight children (0.0034±0.0006 γ-H2AXF/n, and 0.92±0.12[per thousand] MN), while all subjects responded to BLM induction, irrespective of their weight status. The fold increase of spontaneous MN frequencies in overweight and obese subjects was 2.5 and 2.7, respectively, well below the corresponding increase in the γ-H2AX foci (5.6- and 8.0-fold, respectively). IL-6 and CRP mean values were significantly higher in obese and overweight children than in controls. Here, we demonstrated that peripheral cells of overweight and obese children showed increased levels of DSBs, which were not completely repaired as part of them has been converted into micronuclei. Characterization of childhood obesity inflammation could be implemented using molecular markers of genome damage.--Scarpato, R., Verola, C., Fabiani, B., Bianchi, V., Saggese, G., Federico, G. Nuclear damage in peripheral lymphocytes of obese and overweight Italian children as evaluated by the γ-H2AX focus assay and micronucleus test.
AbstractList Childhood obesity, often characterized by a chronic low-grade inflammation, has been associated with an increased risk of developing some types of cancer later in life. Nuclear γ-H2AX foci represent the first detectable response of cells to DNA tumorigenesis lesions, such as the double-strand breaks (DSBs). An excess of micronucleated peripheral lymphocytes was found in subjects with cancer or inflammation-based diseases. We set out to investigate the expression of genome damage, from DNA lesions to chromosome mutations (micronuclei), in overweight and obese children. Using the γ-H2AX focus assay and micronucleus (MN) test, we analyzed peripheral lymphocytes from 119 Italian children classified as normal weight (n=38), overweight (n=20), or obese (n=61). Cultures treated with bleomycin (BLM) were also set up for each child in both assays to check functioning of the apparatus that ensures DNA integrity. We measured serum TNF-α, IL-6, and C-reactive protein (CRP) as markers of inflammation. Overweight and obese children had significantly higher levels of H2AX phosphorylation (0.0191±0.0039 and 0.0274±0.0029 γ-H2AXF/n) and increased MN frequencies (2.30±0.25 and 2.45±0.22‰) than normal-weight children (0.0034±0.0006 γ-H2AXF/n, and 0.92±0.12‰ MN), while all subjects responded to BLM induction, irrespective of their weight status. The fold increase of spontaneous MN frequencies in overweight and obese subjects was 2.5 and 2.7, respectively, well below the corresponding increase in the γ-H2AX foci (5.6- and 8.0-fold, respectively). IL-6 and CRP mean values were significantly higher in obese and overweight children than in controls. Here, we demonstrated that peripheral cells of overweight and obese children showed increased levels of DSBs, which were not completely repaired as part of them has been converted into micronuclei. Characterization of childhood obesity inflammation could be implemented using molecular markers of genome damage.
Childhood obesity, often characterized by a chronic low-grade inflammation, has been associated with an increased risk of developing some types of cancer later in life. Nuclear γ-H2AX foci represent the first detectable response of cells to DNA tumorigenesis lesions, such as the double-strand breaks (DSBs). An excess of micronucleated peripheral lymphocytes was found in subjects with cancer or inflammatation-based diseases. We set out to investigate the expression of genome damage, from DNA lesions to chromosome mutations (micronuclei), in overweight and obese children. Using the γ-H2AX focus assay and micronucleus (MN) test, we analyzed peripheral lymphocytes from 119 Italian children classified as normal weight (n=38), overweight (n=20), or obese (n=61). Cultures treated with bleomycin (BLM) were also set up for each child in both assays to check functioning of the apparatus that ensures DNA integrity. We measured serum TNF-α, IL-6, and C-reactive protein (CRP) as markers of inflammation. Overweight and obese children had significantly higher levels of H2AX phosphorylation (0.0191±0.0039 and 0.0274±0.0029 γ-H2AXF/n) and increased MN frequencies (2.30±0.25 and 2.45±0.22[per thousand]) than normal-weight children (0.0034±0.0006 γ-H2AXF/n, and 0.92±0.12[per thousand] MN), while all subjects responded to BLM induction, irrespective of their weight status. The fold increase of spontaneous MN frequencies in overweight and obese subjects was 2.5 and 2.7, respectively, well below the corresponding increase in the γ-H2AX foci (5.6- and 8.0-fold, respectively). IL-6 and CRP mean values were significantly higher in obese and overweight children than in controls. Here, we demonstrated that peripheral cells of overweight and obese children showed increased levels of DSBs, which were not completely repaired as part of them has been converted into micronuclei. Characterization of childhood obesity inflammation could be implemented using molecular markers of genome damage.--Scarpato, R., Verola, C., Fabiani, B., Bianchi, V., Saggese, G., Federico, G. Nuclear damage in peripheral lymphocytes of obese and overweight Italian children as evaluated by the γ-H2AX focus assay and micronucleus test.
Author Scarpato, Roberto
Verola, Carmela
Saggese, Giuseppe
Bianchi, Vanessa
Fabiani, Barbara
Federico, Giovanni
Author_xml – sequence: 1
  fullname: Scarpato, Roberto
– sequence: 2
  fullname: Verola, Carmela
– sequence: 3
  fullname: Fabiani, Barbara
– sequence: 4
  fullname: Bianchi, Vanessa
– sequence: 5
  fullname: Saggese, Giuseppe
– sequence: 6
  fullname: Federico, Giovanni
BackLink https://www.ncbi.nlm.nih.gov/pubmed/21068397$$D View this record in MEDLINE/PubMed
BookMark eNo1kEtOwzAYhC1URB-wYw2-QMB2EsdeVhXQShUsoBK76I_zp0mVl-ykKKfgMNyDMxFeq5FGn2ZGMyeTuqmRkEvObjjT8jY7jOpxqQIRnZAZD33mSSXZhMyY0sKT0ldTMnfuwBjjjMszMhWcSeXraEbeH3tTIliaQgV7pEVNW7RFm6OFkpZD1eaNGTp0tMlok6BDCnVKmyPaNyz2eUc3HZQF1NTkRZlarCk4ikcoe-gwpclAuxzp54e3FstXmjWmdyPhYPjJqQpjm_p7wmiPLd05Oc2gdHjxpwuyu797Wa297dPDZrXcesbXYeShz3mUgEHIlEGlDOjUz7j2udIhYhTJdHTCMGFBKoNMBchEAAnjymgtwIgFufrNbfukwjRubVGBHeL_Z0bg-hfIoIlhbwsX754F4z4bWxRnSnwBFlZzZQ
CitedBy_id crossref_primary_10_1080_10807039_2020_1736985
crossref_primary_10_1002_em_22115
crossref_primary_10_1016_j_cell_2016_07_031
crossref_primary_10_1093_mutage_geu042
crossref_primary_10_1016_j_dnarep_2021_103049
crossref_primary_10_1016_j_dnarep_2022_103323
crossref_primary_10_1016_j_mrrev_2013_02_001
crossref_primary_10_18632_aging_103008
crossref_primary_10_1016_j_mrgentox_2020_503194
crossref_primary_10_1080_15548627_2021_1899440
crossref_primary_10_18632_oncotarget_4032
crossref_primary_10_1146_annurev_nutr_062322_022751
crossref_primary_10_1111_obr_13389
crossref_primary_10_1016_j_genrep_2017_10_012
crossref_primary_10_1080_10520295_2023_2210848
crossref_primary_10_1007_s00204_021_03009_z
crossref_primary_10_3390_medicina61010021
crossref_primary_10_1016_j_mad_2023_111775
crossref_primary_10_1016_j_fct_2019_03_025
crossref_primary_10_1038_s41598_023_35533_6
crossref_primary_10_3390_ijms20051146
crossref_primary_10_1002_oby_21888
crossref_primary_10_1053_j_gastro_2014_07_056
crossref_primary_10_17517_ksutfd_942657
crossref_primary_10_1016_j_molmet_2024_102065
crossref_primary_10_1016_j_bbagrm_2012_02_021
crossref_primary_10_1017_erm_2022_22
crossref_primary_10_1080_03014460_2020_1714728
crossref_primary_10_1007_s00394_018_1782_2
crossref_primary_10_1016_j_mrfmmm_2023_111827
crossref_primary_10_1093_mutage_get024
crossref_primary_10_1016_j_mrfmmm_2014_08_005
crossref_primary_10_3390_biology14040324
crossref_primary_10_2217_nnm_2018_0316
crossref_primary_10_1016_j_mrrev_2019_108295
crossref_primary_10_1016_j_mrrev_2021_108395
crossref_primary_10_1016_j_mrrev_2015_07_001
crossref_primary_10_1515_bjmg_2017_0024
crossref_primary_10_1016_j_gendis_2018_03_001
crossref_primary_10_3390_biomedicines10030529
crossref_primary_10_1007_s00411_016_0654_5
crossref_primary_10_1038_s41419_024_06922_0
crossref_primary_10_1089_dna_2014_2705
crossref_primary_10_1371_journal_pone_0147968
crossref_primary_10_1016_j_mrgentox_2014_06_006
crossref_primary_10_1093_mutage_geab036
crossref_primary_10_1002_mnfr_201500110
crossref_primary_10_1002_cam4_5274
crossref_primary_10_1016_j_mrgentox_2018_03_001
crossref_primary_10_3390_ijerph17041208
crossref_primary_10_1016_j_jhep_2011_09_020
crossref_primary_10_1016_j_envpol_2021_117346
crossref_primary_10_1016_j_trecan_2018_03_004
crossref_primary_10_1007_s00580_012_1671_7
crossref_primary_10_1007_s11033_019_04764_0
crossref_primary_10_1016_j_mrfmmm_2013_11_005
crossref_primary_10_1038_s41366_021_00879_2
crossref_primary_10_1155_2017_2050194
crossref_primary_10_1016_j_mrrev_2020_108345
crossref_primary_10_1016_j_mrrev_2018_08_002
crossref_primary_10_1016_j_mrrev_2020_108343
crossref_primary_10_35407_bag_2024_35_01_02
crossref_primary_10_1002_ajh_23463
crossref_primary_10_1093_mutage_geab041
crossref_primary_10_1021_acs_est_4c06411
crossref_primary_10_1155_2017_3574840
crossref_primary_10_1038_s41598_018_29581_6
crossref_primary_10_1016_j_mrfmmm_2016_05_001
crossref_primary_10_3390_ijms22042163
crossref_primary_10_1016_j_mrrev_2018_07_001
crossref_primary_10_1016_j_mrrev_2018_11_001
crossref_primary_10_1051_bioconf_20249101013
crossref_primary_10_1016_j_mrgentox_2022_503526
crossref_primary_10_1080_01635581_2021_1952627
ContentType Journal Article
DBID FBQ
CGR
CUY
CVF
ECM
EIF
NPM
DOI 10.1096/fj.10-168427
DatabaseName AGRIS
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
DatabaseTitleList MEDLINE

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
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 3
  dbid: FBQ
  name: AGRIS
  url: http://www.fao.org/agris/Centre.asp?Menu_1ID=DB&Menu_2ID=DB1&Language=EN&Content=http://www.fao.org/agris/search?Language=EN
  sourceTypes: Publisher
DeliveryMethod no_fulltext_linktorsrc
Discipline Biology
EISSN 1530-6860
EndPage 693
ExternalDocumentID 21068397
US201301938108
Genre Research Support, Non-U.S. Gov't
Journal Article
GeographicLocations Italy
GeographicLocations_xml – name: Italy
GroupedDBID ---
-DZ
-~X
.55
0R~
0VX
123
18M
1OB
1OC
29H
2WC
33P
34G
39C
3O-
4.4
53G
5GY
5RE
85S
AAHHS
AANLZ
ABCUV
ABDNZ
ABEFU
ABJNI
ABOCM
ABPTK
ACCFJ
ACCZN
ACGFS
ACIWK
ACNCT
ACPOU
ACPRK
ACXQS
ACYGS
ADKYN
ADZMN
AEEZP
AEIGN
AENEX
AEQDE
AEQTP
AEUYR
AFDAS
AFFNX
AFFPM
AFMIJ
AFRAH
AGCDD
AI.
AIURR
AIWBW
AJBDE
ALMA_UNASSIGNED_HOLDINGS
ALUQN
AMYDB
BFHJK
C1A
CS3
DCZOG
DU5
D~5
E3Z
EBS
EJD
F20
F5P
F9R
FBQ
FRP
HZ~
H~9
J5H
L7B
LATKE
LEEKS
MEWTI
MVM
NEJ
O9-
OHT
OVD
Q-A
RHF
RHI
RJQFR
ROL
SAMSI
SJN
SUPJJ
TEORI
TFA
TR2
TWZ
VH1
W8F
WH7
WHG
WOQ
WXSBR
X7M
XJT
XOL
XSW
Y6R
YBU
YCJ
YHG
YKV
YNH
YSK
Z0Y
ZA5
ZCA
ZE2
ZGI
ZXP
~KM
AAHQN
AAMNL
AAYCA
AFWVQ
AGHNM
AHBTC
AITYG
AIZAD
ALVPJ
BIYOS
CGR
CUY
CVF
ECM
EIF
H13
HGLYW
NPM
U18
ID FETCH-LOGICAL-c3957-e3117baceaf8ce88ca9d3f1931895ee776da9d55b04d64f84e024ab018c992ac2
ISSN 0892-6638
IngestDate Thu Apr 03 06:59:52 EDT 2025
Wed Dec 27 19:18:05 EST 2023
IsPeerReviewed true
IsScholarly true
Issue 2
Language English
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c3957-e3117baceaf8ce88ca9d3f1931895ee776da9d55b04d64f84e024ab018c992ac2
PMID 21068397
PageCount 9
ParticipantIDs pubmed_primary_21068397
fao_agris_US201301938108
PublicationCentury 2000
PublicationDate February 2011
PublicationDateYYYYMMDD 2011-02-01
PublicationDate_xml – month: 02
  year: 2011
  text: February 2011
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle The FASEB journal
PublicationTitleAlternate FASEB J
PublicationYear 2011
Publisher The Federation of American Societies for Experimental Biology
Publisher_xml – name: The Federation of American Societies for Experimental Biology
SSID ssj0001016
Score 2.311432
Snippet Childhood obesity, often characterized by a chronic low-grade inflammation, has been associated with an increased risk of developing some types of cancer later...
SourceID pubmed
fao
SourceType Index Database
Publisher
StartPage 685
SubjectTerms Adolescent
Cell Nucleus - pathology
Child
DNA Damage
DNA Repair
Female
Gene Expression Regulation - physiology
Histones - genetics
Histones - metabolism
Humans
Italy
Lymphocytes - cytology
Male
Micronucleus Tests
Overweight - genetics
Overweight - metabolism
Title Nuclear damage in peripheral lymphocytes of obese and overweight Italian children as evaluated by the γ-H2AX focus assay and micronucleus test
URI https://www.ncbi.nlm.nih.gov/pubmed/21068397
Volume 25
hasFullText
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Jb9NAFB4lICQuFXtboJoDN8tgO2N7fExRo8ChEmpT5Ra9GY-rotiuavcQfga_pT-QN4sXFZAKFyuacZyJ36e3L4R8CASTWSzBZ4XIfSZY7gNI7oNSUYbyQjJlEmRPk-WKfV3H68nkbpS1dNuKj_LHH-tK_oequIZ01VWy_0DZ_qG4gJ-RvnhFCuP1QTQ-1c2I4cbLodSpNyYhHJmALqnaetsdEqqWu9a2la2FamyooDa50Noo97601s3Rl3RD0_X_dpopougSyhL8ZTRfe0Utbxu8qQHbtqnU6XyVPgUut12k6vuAwMX87OTYG_-ZLugDZn6Ty-yuu60LdYO2tstEKdW2FxoL0M3Rr0YhksG9j8A1o4m9C9CMG8aeDO2a7bNCVMd90ZbldsBAx55tXbSDYTTitYmd9fObDECjTBMOhUDghzrMmI5vQwpelwYPaOwmqB4-YPdeR-5ua0qmaJvoYavaQ-Skv_aGuAILPMin8TFM42n7VdRkCqjvmTJGpTl_RvacLULnFljPyURVL8gTO51095L8dPCiFl70qqIDvOgIXrQuqIEXRUzQAV7UwYt28KLQ0B5eVOwowosO8KIGXtTAyzxqDC-q4fWKrBYn55-Xvhvh4UsdAPbVLAxTAVJBwaXiXEKWzwo0GkKexUqlaZLjShyLgOUJKzhTqDOCCEIusywCGb0mj6q6UvuERjJkRYqymRU5E5JDjk9RM2A5xFym6oDs4yvdwCUKx83qLNIhefwhHgb8gLyx73lzbVu4bDo6HP515y15OmD0HXlcIM9Q71EBbcURmS6Ovx0Zuv8ChzKLuA
linkProvider National Library of Medicine
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=Nuclear+damage+in+peripheral+lymphocytes+of+obese+and+overweight+Italian+children+as+evaluated+by+the+gamma-H2AX+focus+assay+and+micronucleus+test&rft.jtitle=The+FASEB+journal&rft.au=Scarpato%2C+Roberto&rft.au=Verola%2C+Carmela&rft.au=Fabiani%2C+Barbara&rft.au=Bianchi%2C+Vanessa&rft.date=2011-02-01&rft.eissn=1530-6860&rft.volume=25&rft.issue=2&rft.spage=685&rft_id=info:doi/10.1096%2Ffj.10-168427&rft_id=info%3Apmid%2F21068397&rft_id=info%3Apmid%2F21068397&rft.externalDocID=21068397
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0892-6638&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0892-6638&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0892-6638&client=summon