Association of NAD(P)H: quinone oxidoreductase 1 (NQO1) C609T polymorphism with esophageal squamous cell carcinoma in a German Caucasian and a northern Chinese population

NAD(P)H: quinone oxidoreductase 1 (NQO1) is an antioxidant enzyme, important in the detoxification of environmental carcinogens. A single base substitution (C → T) polymorphism at nucleotide 609 (null-allele) of NQO1 gene impairs stability and function of the NQO1 protein. To investigate the associa...

Full description

Saved in:
Bibliographic Details
Published inCarcinogenesis (New York) Vol. 24; no. 5; pp. 905 - 909
Main Authors Zhang, Jianhui, Schulz, Wolfgang A., Li, Yan, Wang, Rui, Zotz, Rainer, Wen, Denggui, Siegel, David, Ross, David, Gabbert, Helmut E., Sarbia, Mario
Format Journal Article
LanguageEnglish
Published Oxford Oxford University Press 01.05.2003
Oxford Publishing Limited (England)
Subjects
Online AccessGet full text
ISSN0143-3334
1460-2180
1460-2180
DOI10.1093/carcin/bgg019

Cover

Abstract NAD(P)H: quinone oxidoreductase 1 (NQO1) is an antioxidant enzyme, important in the detoxification of environmental carcinogens. A single base substitution (C → T) polymorphism at nucleotide 609 (null-allele) of NQO1 gene impairs stability and function of the NQO1 protein. To investigate the association of this NQO1 polymorphism with susceptibility to esophageal squamous cell carcinoma (ESCC), the NQO1 C609T genotypes were determined by PCR–RFLP analysis in 450 patients with ESCC (257 German Caucasians and 193 northern Chinese) and 393 unrelated healthy controls (252 German Caucasians and 141 northern Chinese). Additionally, NQO1 protein expression was determined by immunohistochemistry in a subset of 74 ESCC (50 German, 24 Chinese). A significant difference in NQO1 C609T genotype distribution was observed between Caucasian healthy controls (C/C, 73.4%; C/T, 25.0%; T/T, 1.6%) and Chinese healthy controls (C/C, 34.0%; C/T, 49.7%; T/T, 16.3%) (χ2 = 68.40, P < 0.001). The NQO1 T/T genotype significantly increased the risk for developing ESCC in both Caucasian subjects (OR = 4.62, 95% CI = 1.54–13.86) and Chinese subjects (OR = 1.81, 95% CI = 1.04–3.15), compared with the combined C/C and C/T genotypes. In Chinese subjects, this increased susceptibility was pronounced in patients with family history of upper gastrointestinal cancers (OR = 2.18, 95% CI = 1.14–4.17). Immunohistochemical analysis showed NQO1 protein expression in 53 carcinomas, whereas 21 carcinomas were negative. Negativity for NQO1 expression correlated strongly with the NQO1 genotype, being present in 8.6% of cases with C/C, 22.2% of cases with C/T and 100% of cases with T/T genotype (χ2 = 16.60, P < 0.001). In summary, the association of the NQO1 C609T polymorphism with ESCC in genetically distinct populations makes a strong argument for its importance in carcinogenesis of ESCC in the German Caucasian and the northern Chinese population.
AbstractList NAD(P)H: quinone oxidoreductase 1 (NQO1) is an antioxidant enzyme, important in the detoxification of environmental carcinogens. A single base substitution (C --> T) polymorphism at nucleotide 609 (null-allele) of NQO1 gene impairs stability and function of the NQO1 protein. To investigate the association of this NQO1 polymorphism with susceptibility to esophageal squamous cell carcinoma (ESCC), the NQO1 C609T genotypes were determined by PCR-RFLP analysis in 450 patients with ESCC (257 German Caucasians and 193 northern Chinese) and 393 unrelated healthy controls (252 German Caucasians and 141 northern Chinese). Additionally, NQO1 protein expression was determined by immunohistochemistry in a subset of 74 ESCC (50 German, 24 Chinese). A significant difference in NQO1 C609T genotype distribution was observed between Caucasian healthy controls (C/C, 73.4%; C/T, 25.0%; T/T, 1.6%) and Chinese healthy controls (C/C, 34.0%; C/T, 49.7%; T/T, 16.3%) (chi(2) = 68.40, P < 0.001). The NQO1 T/T genotype significantly increased the risk for developing ESCC in both Caucasian subjects (OR = 4.62, 95% CI = 1.54-13.86) and Chinese subjects (OR = 1.81, 95% CI = 1.04-3.15), compared with the combined C/C and C/T genotypes. In Chinese subjects, this increased susceptibility was pronounced in patients with family history of upper gastrointestinal cancers (OR = 2.18, 95% CI = 1.14-4.17). Immunohistochemical analysis showed NQO1 protein expression in 53 carcinomas, whereas 21 carcinomas were negative. Negativity for NQO1 expression correlated strongly with the NQO1 genotype, being present in 8.6% of cases with C/C, 22.2% of cases with C/T and 100% of cases with T/T genotype (chi(2) = 16.60, P < 0.001). In summary, the association of the NQO1 C609T polymorphism with ESCC in genetically distinct populations makes a strong argument for its importance in carcinogenesis of ESCC in the German Caucasian and the northern Chinese population.
NAD(P)H: quinone oxidoreductase 1 (NQO1) is an antioxidant enzyme, important in the detoxification of environmental carcinogens. A single base substitution (C [Right arrow] T) polymorphism at nucleotide 609 (null-allele) of NQO1 gene impairs stability and function of the NQO1 protein. To investigate the association of this NQO1 polymorphism with susceptibility to esophageal squamous cell carcinoma (ESCC), the NQO1 C609T genotypes were determined by PCR-RFLP analysis in 450 patients with ESCC (257 German Caucasians and 193 northern Chinese) and 393 unrelated healthy controls (252 German Caucasians and 141 northern Chinese). Additionally, NQO1 protein expression was determined by immunohistochemistry in a subset of 74 ESCC (50 German, 24 Chinese). A significant difference in NQO1 C609T genotype distribution was observed between Caucasian healthy controls (C/C, 73.4%; C/T, 25.0%; T/T, 1.6%) and Chinese healthy controls (C/C, 34.0%; C/T, 49.7%; T/T, 16.3%) ([chi]2 = 68.40, P < 0.001). The NQO1 T/T genotype significantly increased the risk for developing ESCC in both Caucasian subjects (OR = 4.62, 95% CI = 1.54-13.86) and Chinese subjects (OR = 1.81, 95% CI = 1.04-3.15), compared with the combined C/C and C/T genotypes. In Chinese subjects, this increased susceptibility was pronounced in patients with family history of upper gastrointestinal cancers (OR = 2.18, 95% CI = 1.14-4.17). Immunohistochemical analysis showed NQO1 protein expression in 53 carcinomas, whereas 21 carcinomas were negative. Negativity for NQO1 expression correlated strongly with the NQO1 genotype, being present in 8.6% of cases with C/C, 22.2% of cases with C/T and 100% of cases with T/T genotype ([chi]2 = 16.60, P < 0.001). In summary, the association of the NQO1 C609T polymorphism with ESCC in genetically distinct populations makes a strong argument for its importance in carcinogenesis of ESCC in the German Caucasian and the northern Chinese population.
NAD(P)H: quinone oxidoreductase 1 (NQO1) is an antioxidant enzyme, important in the detoxification of environmental carcinogens. A single base substitution (C → T) polymorphism at nucleotide 609 (null-allele) of NQO1 gene impairs stability and function of the NQO1 protein. To investigate the association of this NQO1 polymorphism with susceptibility to esophageal squamous cell carcinoma (ESCC), the NQO1 C609T genotypes were determined by PCR–RFLP analysis in 450 patients with ESCC (257 German Caucasians and 193 northern Chinese) and 393 unrelated healthy controls (252 German Caucasians and 141 northern Chinese). Additionally, NQO1 protein expression was determined by immunohistochemistry in a subset of 74 ESCC (50 German, 24 Chinese). A significant difference in NQO1 C609T genotype distribution was observed between Caucasian healthy controls (C/C, 73.4%; C/T, 25.0%; T/T, 1.6%) and Chinese healthy controls (C/C, 34.0%; C/T, 49.7%; T/T, 16.3%) (χ2 = 68.40, P < 0.001). The NQO1 T/T genotype significantly increased the risk for developing ESCC in both Caucasian subjects (OR = 4.62, 95% CI = 1.54–13.86) and Chinese subjects (OR = 1.81, 95% CI = 1.04–3.15), compared with the combined C/C and C/T genotypes. In Chinese subjects, this increased susceptibility was pronounced in patients with family history of upper gastrointestinal cancers (OR = 2.18, 95% CI = 1.14–4.17). Immunohistochemical analysis showed NQO1 protein expression in 53 carcinomas, whereas 21 carcinomas were negative. Negativity for NQO1 expression correlated strongly with the NQO1 genotype, being present in 8.6% of cases with C/C, 22.2% of cases with C/T and 100% of cases with T/T genotype (χ2 = 16.60, P < 0.001). In summary, the association of the NQO1 C609T polymorphism with ESCC in genetically distinct populations makes a strong argument for its importance in carcinogenesis of ESCC in the German Caucasian and the northern Chinese population.
NAD(P)H: quinone oxidoreductase 1 (NQO1) is an antioxidant enzyme, important in the detoxification of environmental carcinogens. A single base substitution (C --> T) polymorphism at nucleotide 609 (null-allele) of NQO1 gene impairs stability and function of the NQO1 protein. To investigate the association of this NQO1 polymorphism with susceptibility to esophageal squamous cell carcinoma (ESCC), the NQO1 C609T genotypes were determined by PCR-RFLP analysis in 450 patients with ESCC (257 German Caucasians and 193 northern Chinese) and 393 unrelated healthy controls (252 German Caucasians and 141 northern Chinese). Additionally, NQO1 protein expression was determined by immunohistochemistry in a subset of 74 ESCC (50 German, 24 Chinese). A significant difference in NQO1 C609T genotype distribution was observed between Caucasian healthy controls (C/C, 73.4%; C/T, 25.0%; T/T, 1.6%) and Chinese healthy controls (C/C, 34.0%; C/T, 49.7%; T/T, 16.3%) (chi(2) = 68.40, P < 0.001). The NQO1 T/T genotype significantly increased the risk for developing ESCC in both Caucasian subjects (OR = 4.62, 95% CI = 1.54-13.86) and Chinese subjects (OR = 1.81, 95% CI = 1.04-3.15), compared with the combined C/C and C/T genotypes. In Chinese subjects, this increased susceptibility was pronounced in patients with family history of upper gastrointestinal cancers (OR = 2.18, 95% CI = 1.14-4.17). Immunohistochemical analysis showed NQO1 protein expression in 53 carcinomas, whereas 21 carcinomas were negative. Negativity for NQO1 expression correlated strongly with the NQO1 genotype, being present in 8.6% of cases with C/C, 22.2% of cases with C/T and 100% of cases with T/T genotype (chi(2) = 16.60, P < 0.001). In summary, the association of the NQO1 C609T polymorphism with ESCC in genetically distinct populations makes a strong argument for its importance in carcinogenesis of ESCC in the German Caucasian and the northern Chinese population.NAD(P)H: quinone oxidoreductase 1 (NQO1) is an antioxidant enzyme, important in the detoxification of environmental carcinogens. A single base substitution (C --> T) polymorphism at nucleotide 609 (null-allele) of NQO1 gene impairs stability and function of the NQO1 protein. To investigate the association of this NQO1 polymorphism with susceptibility to esophageal squamous cell carcinoma (ESCC), the NQO1 C609T genotypes were determined by PCR-RFLP analysis in 450 patients with ESCC (257 German Caucasians and 193 northern Chinese) and 393 unrelated healthy controls (252 German Caucasians and 141 northern Chinese). Additionally, NQO1 protein expression was determined by immunohistochemistry in a subset of 74 ESCC (50 German, 24 Chinese). A significant difference in NQO1 C609T genotype distribution was observed between Caucasian healthy controls (C/C, 73.4%; C/T, 25.0%; T/T, 1.6%) and Chinese healthy controls (C/C, 34.0%; C/T, 49.7%; T/T, 16.3%) (chi(2) = 68.40, P < 0.001). The NQO1 T/T genotype significantly increased the risk for developing ESCC in both Caucasian subjects (OR = 4.62, 95% CI = 1.54-13.86) and Chinese subjects (OR = 1.81, 95% CI = 1.04-3.15), compared with the combined C/C and C/T genotypes. In Chinese subjects, this increased susceptibility was pronounced in patients with family history of upper gastrointestinal cancers (OR = 2.18, 95% CI = 1.14-4.17). Immunohistochemical analysis showed NQO1 protein expression in 53 carcinomas, whereas 21 carcinomas were negative. Negativity for NQO1 expression correlated strongly with the NQO1 genotype, being present in 8.6% of cases with C/C, 22.2% of cases with C/T and 100% of cases with T/T genotype (chi(2) = 16.60, P < 0.001). In summary, the association of the NQO1 C609T polymorphism with ESCC in genetically distinct populations makes a strong argument for its importance in carcinogenesis of ESCC in the German Caucasian and the northern Chinese population.
NAD(P)H: quinone oxidoreductase 1 (NQO1) is an antioxidant enzyme, important in the detoxification of environmental carcinogens. A single base substitution (C arrow right T) polymorphism at nucleotide 609 (null-allele) of NQO1 gene impairs stability and function of the NQO1 protein. To investigate the association of this NQO1 polymorphism with susceptibility to esophageal squamous cell carcinoma (ESCC), the NQO1 C609T genotypes were determined by PCR-RFLP analysis in 450 patients with ESCC (257 German Caucasians and 193 northern Chinese) and 393 unrelated healthy controls (252 German Caucasians and 141 northern Chinese). Additionally, NQO1 protein expression was determined by immunohistochemistry in a subset of 74 ESCC (50 German, 24 Chinese). A significant difference in NQO1 C609T genotype distribution was observed between Caucasian healthy controls (C/C, 73.4%; C/T, 25.0%; T/T, 1.6%) and Chinese healthy controls (C/C, 34.0%; C/T, 49.7%; T/T, 16.3%) ( chi super(2) = 68.40, P < 0.001). The NQO1 T/T genotype significantly increased the risk for developing ESCC in both Caucasian subjects (OR = 4.62, 95% CI = 1.54-13.86) and Chinese subjects (OR = 1.81, 95% CI = 1.04-3.15), compared with the combined C/C and C/T genotypes. In Chinese subjects, this increased susceptibility was pronounced in patients with family history of upper gastrointestinal cancers (OR = 2.18, 95% CI = 1.14-4.17). Immunohistochemical analysis showed NQO1 protein expression in 53 carcinomas, whereas 21 carcinomas were negative. Negativity for NQO1 expression correlated strongly with the NQO1 genotype, being present in 8.6% of cases with C/C, 22.2% of cases with C/T and 100% of cases with T/T genotype ( chi super(2) = 16.60, P < 0.001). In summary, the association of the NQO1 C609T polymorphism with ESCC in genetically distinct populations makes a strong argument for its importance in carcinogenesis of ESCC in the German Caucasian and the northern Chinese population.
Author Zhang, Jianhui
Gabbert, Helmut E.
Sarbia, Mario
Zotz, Rainer
Ross, David
Siegel, David
Schulz, Wolfgang A.
Li, Yan
Wen, Denggui
Wang, Rui
Author_xml – sequence: 1
  givenname: Jianhui
  surname: Zhang
  fullname: Zhang, Jianhui
  organization: Institute of Pathology, University of Duesseldorf, Moorenstr. 5, D-40225 Duesseldorf, Germany
– sequence: 2
  givenname: Wolfgang A.
  surname: Schulz
  fullname: Schulz, Wolfgang A.
  organization: Department of Urology, University of Duesseldorf, Moorenstr. 5, D-40225 Duesseldorf, Germany
– sequence: 3
  givenname: Yan
  surname: Li
  fullname: Li, Yan
  organization: Laboratory of Molecular Biology, Hebei Cancer Institute, Hebei Medical University, Jiankanglu 12, Shijiazhuang 050011, China
– sequence: 4
  givenname: Rui
  surname: Wang
  fullname: Wang, Rui
  organization: Department of Thoracic Surgery, The Fourth Affiliated Hospital, Hebei Medical University, Jiankanglu 12, Shijiazhuang 050011, China
– sequence: 5
  givenname: Rainer
  surname: Zotz
  fullname: Zotz, Rainer
  organization: Institute of Hemostasis and Transfusion Medicine, University of Duesseldorf, Moorenstr. 5, D-40225 Duesseldorf, Germany
– sequence: 6
  givenname: Denggui
  surname: Wen
  fullname: Wen, Denggui
  organization: Laboratory of Epidemiology, Hebei Cancer Institute, Hebei Medical University, Jiankanglu 12, Shijiazhuang 050011, China
– sequence: 7
  givenname: David
  surname: Siegel
  fullname: Siegel, David
  organization: School of Pharmacy, University of Colorado Health Sciences Center, Denver, CO 80262, USA
– sequence: 8
  givenname: David
  surname: Ross
  fullname: Ross, David
  organization: School of Pharmacy, University of Colorado Health Sciences Center, Denver, CO 80262, USA
– sequence: 9
  givenname: Helmut E.
  surname: Gabbert
  fullname: Gabbert, Helmut E.
  organization: Institute of Pathology, University of Duesseldorf, Moorenstr. 5, D-40225 Duesseldorf, Germany
– sequence: 10
  givenname: Mario
  surname: Sarbia
  fullname: Sarbia, Mario
  organization: Institute of Pathology, University of Duesseldorf, Moorenstr. 5, D-40225 Duesseldorf, Germany
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14950958$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/12771035$$D View this record in MEDLINE/PubMed
BookMark eNqFklFv0zAQxy00xLrBI6_IQgJtD2F2nMQxb6WDlanqQCoS4sW6Ok7rLbFTOxHbV-JT4q6FSZMQT7bs393__nd3hA6ssxqhl5S8o0SwMwVeGXu2XK0IFU_QiGYFSVJakgM0IjRjCWMsO0RHIVwTQguWi2fokKacU8LyEfo1DsEpA71xFrsaz8fnJ19Op-_xZjBbJexuTeW8rgbVQ9CY4pP51yt6iicFEQvcueaudb5bm9Din6ZfYx1ct4aVhgaHzQCtGwJWumnwrlDXAjYWA77QvgWLJzAoCCbewFbx2Trfr7WPH2tjdRTsXDc09-U9R09raIJ-sT-P0bdPHxeTaTK7uvg8Gc8SleVFnzBdsIpQRmrBCgUl15WuUy50DlldUl7nRc1EplJFNFUcKp0rypVKl2mZkqJix-jtLm_n3WbQoZetCVsLYHV0I3nsaJnl-X9BWpaUUr4FXz8Cr93gbTQhUyoYEyRjEXq1h4ZlqyvZedOCv5N_ZhWBN3sAgoKm9mCVCQ9cJnIi8jJyyY5T3oXgdf2AELndGbkbhdztTOTZI16Z_r7jvQfT_DNqr2JCr2__SoC_kQVnPJfT7z_kfHL5gV7OzuWC_QaMTdcM
CODEN CRNGDP
CitedBy_id crossref_primary_10_1002_ijc_23044
crossref_primary_10_1002_ijc_20375
crossref_primary_10_1515_hsz_2016_0135
crossref_primary_10_3748_wjg_v11_i16_2385
crossref_primary_10_1016_j_gtc_2009_01_009
crossref_primary_10_1111_j_1530_0277_2008_00757_x
crossref_primary_10_1089_dna_2011_1332
crossref_primary_10_1134_S2079059715050020
crossref_primary_10_1002_mgg3_461
crossref_primary_10_2174_0115680096283149240109094710
crossref_primary_10_1089_gtmb_2010_0197
crossref_primary_10_3390_cancers15235604
crossref_primary_10_1080_13547500500382975
crossref_primary_10_1158_1055_9965_1308_13_8
crossref_primary_10_1002_ijc_20576
crossref_primary_10_1002_cbic_201800269
crossref_primary_10_3748_wjg_v11_i23_3623
crossref_primary_10_1080_01635581_2018_1460674
crossref_primary_10_1089_dna_2008_0732
crossref_primary_10_1038_jhg_2014_38
crossref_primary_10_1089_gtmb_2009_0158
crossref_primary_10_1177_1758834016668682
crossref_primary_10_1186_1471_230X_9_76
crossref_primary_10_7314_APJCP_2013_14_4_2349
crossref_primary_10_1038_bjc_2013_357
crossref_primary_10_1016_j_phytochem_2021_112925
crossref_primary_10_1007_s10529_012_1115_0
crossref_primary_10_1016_j_canep_2012_06_004
crossref_primary_10_3748_wjg_v11_i6_858
crossref_primary_10_1111_j_1442_2050_2007_00672_x
crossref_primary_10_1111_j_1442_2050_2009_00947_x
crossref_primary_10_1007_s11033_012_1781_y
crossref_primary_10_1371_journal_pone_0030566
crossref_primary_10_17816_ecogen12247_59
crossref_primary_10_1007_s00280_024_04700_5
crossref_primary_10_1135_cccc2010066
crossref_primary_10_1146_annurev_cancerbio_030518_055905
crossref_primary_10_1186_s12964_020_0518_0
crossref_primary_10_1186_1471_2350_14_31
crossref_primary_10_18093_0869_0189_2008_0_2_68_72
crossref_primary_10_1073_pnas_0307301101
crossref_primary_10_1007_s13277_013_1273_2
crossref_primary_10_1007_s13277_013_1292_z
crossref_primary_10_4238_vol9_1gmr693
crossref_primary_10_1155_2015_892579
crossref_primary_10_1038_bjc_2014_212
crossref_primary_10_1593_neo_11750
crossref_primary_10_1007_s11670_012_0270_0
crossref_primary_10_1134_S1022795409070138
crossref_primary_10_1371_journal_pone_0123313
crossref_primary_10_1016_j_cbi_2005_03_019
crossref_primary_10_1093_carcin_bgi144
crossref_primary_10_1097_FPC_0b013e32832cf9cf
crossref_primary_10_3109_10408441003742895
crossref_primary_10_3748_wjg_v9_i12_2654
crossref_primary_10_1007_s13577_015_0111_9
crossref_primary_10_1371_journal_pone_0018399
crossref_primary_10_1016_j_fct_2010_07_035
crossref_primary_10_1016_j_mrfmmm_2004_05_023
crossref_primary_10_1038_tpj_2016_32
crossref_primary_10_1097_MBC_0b013e3281eec930
crossref_primary_10_1186_s12906_019_2511_y
ContentType Journal Article
Copyright 2004 INIST-CNRS
Copyright Oxford University Press(England) May 2003
Copyright_xml – notice: 2004 INIST-CNRS
– notice: Copyright Oxford University Press(England) May 2003
DBID BSCLL
AAYXX
CITATION
IQODW
CGR
CUY
CVF
ECM
EIF
NPM
8FD
FR3
P64
RC3
7X8
DOI 10.1093/carcin/bgg019
DatabaseName Istex
CrossRef
Pascal-Francis
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
Technology Research Database
Engineering Research Database
Biotechnology and BioEngineering Abstracts
Genetics Abstracts
MEDLINE - Academic
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Genetics Abstracts
Engineering Research Database
Technology Research Database
Biotechnology and BioEngineering Abstracts
MEDLINE - Academic
DatabaseTitleList MEDLINE


MEDLINE - Academic
Genetics Abstracts
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
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1460-2180
EndPage 909
ExternalDocumentID 345517581
12771035
14950958
10_1093_carcin_bgg019
ark_67375_HXZ_NCJB1JLD_T
Genre Research Support, Non-U.S. Gov't
Journal Article
Comparative Study
GeographicLocations China
Germany
GeographicLocations_xml – name: China
– name: Germany
GroupedDBID ---
-E4
.2P
.55
.GJ
.I3
.ZR
0R~
18M
1TH
29B
2WC
3O-
4.4
482
48X
53G
5GY
5RE
5VS
5WA
5WD
6J9
70D
A8Z
AABZA
AACZT
AAIMJ
AAJKP
AAJQQ
AAMDB
AAMVS
AAOGV
AAPGJ
AAPNW
AAPQZ
AAPXW
AARHZ
AAUAY
AAUQX
AAVAP
AAVLN
AAWDT
ABDFA
ABEFU
ABEJV
ABEUO
ABGNP
ABIME
ABIXL
ABJNI
ABKDP
ABLJU
ABMNT
ABNHQ
ABNKS
ABPIB
ABPQP
ABPTD
ABQLI
ABSMQ
ABVGC
ABWST
ABXVV
ABXZS
ABZBJ
ABZEO
ACFRR
ACGFO
ACGFS
ACNCT
ACPQN
ACPRK
ACUFI
ACUTJ
ACUTO
ACVCV
ACZBC
ADBBV
ADEYI
ADEZT
ADFTL
ADGKP
ADGZP
ADHKW
ADHZD
ADIPN
ADMTO
ADNBA
ADOCK
ADQBN
ADRTK
ADVEK
ADYVW
ADZTZ
ADZXQ
AEGPL
AEGXH
AEHUL
AEJOX
AEKPW
AEKSI
AELWJ
AEMDU
AENEX
AENZO
AEPUE
AETBJ
AEWNT
AFFNX
AFFQV
AFFZL
AFGWE
AFIYH
AFOFC
AFRAH
AFSHK
AFYAG
AGINJ
AGKEF
AGKRT
AGMDO
AGORE
AGQPQ
AGQXC
AGSYK
AHGBF
AHMBA
AHMMS
AHXPO
AIAGR
AIJHB
AJBYB
AJDVS
AJEEA
AJNCP
AKHUL
AKWXX
ALMA_UNASSIGNED_HOLDINGS
ALUQC
ALXQX
ANFBD
APIBT
APJGH
APWMN
AQDSO
AQKUS
ARIXL
ASAOO
ASPBG
ATDFG
ATGXG
ATTQO
AVNTJ
AVWKF
AXUDD
AYOIW
AZFZN
BAWUL
BAYMD
BCRHZ
BEYMZ
BHONS
BQDIO
BSCLL
BSWAC
BTRTY
BVRKM
BZKNY
C1A
C45
CAG
CDBKE
COF
CS3
CXTWN
CZ4
DAKXR
DFGAJ
DIK
DILTD
DU5
D~K
E3Z
EBD
EBS
EE~
EIHJH
EJD
ELUNK
EMOBN
ESTFP
F5P
F9B
FEDTE
FHSFR
FLUFQ
FOEOM
FOTVD
FQBLK
GAUVT
GJXCC
GX1
H13
H5~
HAR
HVGLF
HW0
HZ~
IH2
IOX
J21
JXSIZ
KAQDR
KBUDW
KOP
KQ8
KSI
KSN
M-Z
MBLQV
MBTAY
N9A
NGC
NLBLG
NOMLY
NOYVH
NTWIH
NU-
NVLIB
O0~
O9-
OAWHX
OBFPC
OBOKY
OCZFY
ODMLO
OJQWA
OJZSN
OK1
OPAEJ
OVD
OWPYF
O~Y
P2P
PAFKI
PB-
PEELM
PQQKQ
Q1.
Q5Y
QBD
R44
RD5
RNI
ROL
ROX
ROZ
RUSNO
RW1
RXO
RZF
RZO
SV3
TCN
TEORI
TJX
TLC
TMA
TR2
W8F
WOQ
X7H
X7M
XOL
YAYTL
YKOAZ
YXANX
ZGI
ZKB
ZKX
ZXP
~91
AAYXX
CITATION
IQODW
RIG
6.Y
ABNGD
ABQTQ
ABSAR
ADJQC
ADRIX
AFXEN
CGR
CUY
CVF
ECM
EIF
FRP
M49
NPM
RHF
8FD
FR3
P64
RC3
7X8
ID FETCH-LOGICAL-c456t-3e63d0130f936ca87edef279e5a4f817f56f394c2c0e1c7ade5c17cc2b28206d3
ISSN 0143-3334
1460-2180
IngestDate Wed Oct 01 13:55:31 EDT 2025
Sun Sep 28 01:26:27 EDT 2025
Mon Jun 30 12:13:15 EDT 2025
Wed Feb 19 02:35:10 EST 2025
Mon Jul 21 09:12:54 EDT 2025
Thu Apr 24 22:58:25 EDT 2025
Wed Oct 01 01:56:50 EDT 2025
Sat Sep 20 11:01:48 EDT 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 5
Keywords Human
NADPH:quinone reductase
Squamous cell carcinoma
Enzyme
Esophageal disease
Detoxification
Genotype
German
Malignant tumor
Esophagus
Allele
Risk factor
Molecular epidemiology
Digestive diseases
Genetics
Chinese
Drug-metabolizing enzyme
Oxidoreductases
Caucasoid
Polymorphism
Language English
License CC BY 4.0
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c456t-3e63d0130f936ca87edef279e5a4f817f56f394c2c0e1c7ade5c17cc2b28206d3
Notes istex:B20CE784634A8E1F5AA11E9F471CCF1A9F417D50
ark:/67375/HXZ-NCJB1JLD-T
local:bgg019
8To whom correspondence should be addressed Email: sarbia@med.uni-duesseldorf.de
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Article-2
ObjectType-Feature-1
content type line 23
OpenAccessLink https://academic.oup.com/carcin/article-pdf/24/5/905/7086308/bgg019.pdf
PMID 12771035
PQID 219339043
PQPubID 5479
PageCount 5
ParticipantIDs proquest_miscellaneous_73338455
proquest_miscellaneous_18811175
proquest_journals_219339043
pubmed_primary_12771035
pascalfrancis_primary_14950958
crossref_primary_10_1093_carcin_bgg019
crossref_citationtrail_10_1093_carcin_bgg019
istex_primary_ark_67375_HXZ_NCJB1JLD_T
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2003-05-01
PublicationDateYYYYMMDD 2003-05-01
PublicationDate_xml – month: 05
  year: 2003
  text: 2003-05-01
  day: 01
PublicationDecade 2000
PublicationPlace Oxford
PublicationPlace_xml – name: Oxford
– name: England
PublicationTitle Carcinogenesis (New York)
PublicationTitleAlternate Carcinogenesis
PublicationYear 2003
Publisher Oxford University Press
Oxford Publishing Limited (England)
Publisher_xml – name: Oxford University Press
– name: Oxford Publishing Limited (England)
SSID ssj0016359
Score 2.0416403
Snippet NAD(P)H: quinone oxidoreductase 1 (NQO1) is an antioxidant enzyme, important in the detoxification of environmental carcinogens. A single base substitution (C...
SourceID proquest
pubmed
pascalfrancis
crossref
istex
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 905
SubjectTerms Adult
Alleles
Asian Continental Ancestry Group - genetics
Biological and medical sciences
Carcinoma, Squamous Cell - enzymology
Carcinoma, Squamous Cell - ethnology
Carcinoma, Squamous Cell - genetics
Case-Control Studies
China - epidemiology
confidence interval
DNA - genetics
DNA - metabolism
DNA Primers - chemistry
ESCC
Esophageal Neoplasms - enzymology
Esophageal Neoplasms - ethnology
Esophageal Neoplasms - genetics
esophageal squamous cell carcinoma
Esophagus
European Continental Ancestry Group - genetics
Family
Female
Gastroenterology. Liver. Pancreas. Abdomen
Gene Frequency
Genetic Predisposition to Disease
Genotype
Germany - epidemiology
Humans
Immunoenzyme Techniques
Male
Medical sciences
Middle Aged
NAD(P)H Dehydrogenase (Quinone) - genetics
NAD(P)H Dehydrogenase (Quinone) - metabolism
NAD(P)H: quinone oxidoreductase 1
NQO1
odds ratio
PCR
Polymerase Chain Reaction
Polymorphism, Single Nucleotide - genetics
Polymorphism, Single-Stranded Conformational
restriction fragment length polymorphism analysis
RFLP
Risk Factors
Tumors
UGIC
upper gastrointestinal cancer
Title Association of NAD(P)H: quinone oxidoreductase 1 (NQO1) C609T polymorphism with esophageal squamous cell carcinoma in a German Caucasian and a northern Chinese population
URI https://api.istex.fr/ark:/67375/HXZ-NCJB1JLD-T/fulltext.pdf
https://www.ncbi.nlm.nih.gov/pubmed/12771035
https://www.proquest.com/docview/219339043
https://www.proquest.com/docview/18811175
https://www.proquest.com/docview/73338455
Volume 24
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVAFT
  databaseName: Open Access Digital Library
  customDbUrl:
  eissn: 1460-2180
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0016359
  issn: 0143-3334
  databaseCode: KQ8
  dateStart: 19960101
  isFulltext: true
  titleUrlDefault: http://grweb.coalliance.org/oadl/oadl.html
  providerName: Colorado Alliance of Research Libraries
– providerCode: PRVBFR
  databaseName: Free Medical Journals - Free Access to All
  customDbUrl:
  eissn: 1460-2180
  dateEnd: 20241001
  omitProxy: true
  ssIdentifier: ssj0016359
  issn: 0143-3334
  databaseCode: DIK
  dateStart: 19960101
  isFulltext: true
  titleUrlDefault: http://www.freemedicaljournals.com
  providerName: Flying Publisher
– providerCode: PRVFQY
  databaseName: GFMER Free Medical Journals
  customDbUrl:
  eissn: 1460-2180
  dateEnd: 20241001
  omitProxy: true
  ssIdentifier: ssj0016359
  issn: 0143-3334
  databaseCode: GX1
  dateStart: 19960101
  isFulltext: true
  titleUrlDefault: http://www.gfmer.ch/Medical_journals/Free_medical.php
  providerName: Geneva Foundation for Medical Education and Research
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1tb9MwELbKJiG-IN4pg-EPCG0qYXWcN_NtdLCqYmOgTit8iZzE7iq2di-tNPhJ_AB-H3e2m6RAJeBLFDnuuck9vpwv53sIeSaCto65iDymQ-0FReZ7GZPC42Gu2irRUma4d3hvP-oeBr1BOGg0ftSylmbT7GX-7Y_7Sv5Hq9AGesVdsv-g2VIoNMA56BeOoGE4_pWOa8_WrPy3d8BfPIDFfRcX-uezEaztVWtyNUI6ESzsCq-sFjMEPB_eMwwIdKK26CNTw9fTCTxxZMwwkVmF7AZganA3yflMYnyghTF-rGSdg9hTiYES2dpFwz5udSRyp6GtMLVfW2P8GoQca0jPrWDQs5InrO4Nd6ywIdrb0eUiMVAZoChD2j2QfzwbVZ-OjmcnJvx9NDnRQ4nhnTK9yOQofKqQf-RkfHS_n8c5almFZeiTe5y70Kez3Xb_tcNoWDPEwmzm_v0FYYtn2WcFJ9lw2LYmuwaXs1ODF-bH4H7ZYiq_1OSeX7pGVv04ipA5Y3dQphaBi2tI-sp_7Gq7wthbduQtOy5WrHWSFtyiVZzhV5imKy9hpmpLsbJ8DWR8of4tctMtYui2ReRt0lDjO-T6nkvTuEu-14BJJ5oCMDcONruvqIMkXYQkZXQDAblJDRxpHY4U4UgrONI5HCnCkZZwpKMxldTCkZZwpABHaJ7DkTo40gqO98jh2zf9TtdzpCBeDr7-1OMq4gV-bteCR7lMYlUo7cdChTLQCYt1GGkugtzP24rlsSxUmLM4z_3MR6qCgt8nK3inDwlNAhZoaI8jFQaiKGSSMS20AhctE1wXTfJirpM0dxXzkbjlJLWZGzy1N5labTbJ87L7mS0Vs7SjUXDZS158wfzKOEy7g8_pfqf3mvXe7aT9JllfQEAlNhDg6IdJk6zNIZE6u3SZgg_CuWgHvEmellfhpYFqkWMFGkpZkjCs0bu8Rwy4TYIQejywSKvGdoh9tPTKGrlRTeDHZGV6MVNPwHWfZutmnvwEmo3xMw
linkProvider Geneva Foundation for Medical Education and Research
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=Association+of+NAD%28P%29H%3A+quinone+oxidoreductase+1+%28NQO1%29+C609T+polymorphism+with+esophageal+squamous+cell+carcinoma+in+a+German+Caucasian+and+a+northern+Chinese+population&rft.jtitle=Carcinogenesis+%28New+York%29&rft.au=Zhang%2C+Jianhui&rft.au=Schulz%2C+Wolfgang+A&rft.au=Li%2C+Yan&rft.au=Wang%2C+Rui&rft.date=2003-05-01&rft.issn=0143-3334&rft.volume=24&rft.issue=5&rft.spage=905&rft_id=info:doi/10.1093%2Fcarcin%2Fbgg019&rft_id=info%3Apmid%2F12771035&rft.externalDocID=12771035
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0143-3334&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0143-3334&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0143-3334&client=summon