CDC25B is associated with the risk of hepatocellular carcinoma, but not related to persistent infection of hepatitis B virus in a Chinese population

The cell division cycle 25 ( CDC25 ) gene members, including CDC25A , CDC25B and CDC25C , are reported to be associated with several human cancers. Here, we aim to investigate the association of functional polymorphisms of CDC25 gene family with the risk of hepatocellular carcinoma (HCC) and persist...

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Published inMolecular biology reports Vol. 47; no. 5; pp. 3361 - 3368
Main Authors Wang, Peng, Peng, Jing, Gong, Yajie, Shen, Na
Format Journal Article
LanguageEnglish
Published Dordrecht Springer Netherlands 01.05.2020
Springer Nature B.V
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ISSN0301-4851
1573-4978
1573-4978
DOI10.1007/s11033-020-05408-4

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Abstract The cell division cycle 25 ( CDC25 ) gene members, including CDC25A , CDC25B and CDC25C , are reported to be associated with several human cancers. Here, we aim to investigate the association of functional polymorphisms of CDC25 gene family with the risk of hepatocellular carcinoma (HCC) and persistent infection of Hepatitis B virus (HBV) in a Chinese HBV-related population. First, we used bioinformatics tools to systematically screen functional polymorphisms within CDC25 gene family. Second, we evaluated the effects of candidate polymorphisms by recruiting 790 HCC cases, 709 persistent HBV carriers (PHC), and 741 subjects with HBV natural clearance (SHNC). MassARRAY platform was used for genotyping. At last, we conducted functional prediction and assay to further explore the pathogenic mechanism of the identified polymorphism. Our results demonstrated that CDC25B rs2295348 played a protective role in HCC risk in a HBV-related Chinese population (adjusted odds ratio [OR] = 0.77, 95% confidence interval [CI] 0.65–0.93, P  = 0.006). It showed a more significantly reduced HCC risk in the SHNC population (adjusted OR = 0.73, 95% CI 0.59–0.89, P  = 0.002). However, we did not observe the association between CDC25B rs2295348 and the risk of persistent HBV infection. Further functional prediction and assay demonstrated that the mutant A allele of CDC25B rs2295348 might significantly decrease gene expression to modify the HCC risk. Our results suggest that CDC25B rs2295348 may confer a protective effect on HCC risk in a HBV-related Chinese population, but do not influence the susceptibility to persistent HBV infection.
AbstractList The cell division cycle 25 (CDC25) gene members, including CDC25A, CDC25B and CDC25C, are reported to be associated with several human cancers. Here, we aim to investigate the association of functional polymorphisms of CDC25 gene family with the risk of hepatocellular carcinoma (HCC) and persistent infection of Hepatitis B virus (HBV) in a Chinese HBV-related population. First, we used bioinformatics tools to systematically screen functional polymorphisms within CDC25 gene family. Second, we evaluated the effects of candidate polymorphisms by recruiting 790 HCC cases, 709 persistent HBV carriers (PHC), and 741 subjects with HBV natural clearance (SHNC). MassARRAY platform was used for genotyping. At last, we conducted functional prediction and assay to further explore the pathogenic mechanism of the identified polymorphism. Our results demonstrated that CDC25B rs2295348 played a protective role in HCC risk in a HBV-related Chinese population (adjusted odds ratio [OR] = 0.77, 95% confidence interval [CI] 0.65–0.93, P = 0.006). It showed a more significantly reduced HCC risk in the SHNC population (adjusted OR = 0.73, 95% CI 0.59–0.89, P = 0.002). However, we did not observe the association between CDC25B rs2295348 and the risk of persistent HBV infection. Further functional prediction and assay demonstrated that the mutant A allele of CDC25B rs2295348 might significantly decrease gene expression to modify the HCC risk. Our results suggest that CDC25B rs2295348 may confer a protective effect on HCC risk in a HBV-related Chinese population, but do not influence the susceptibility to persistent HBV infection.
The cell division cycle 25 (CDC25) gene members, including CDC25A, CDC25B and CDC25C, are reported to be associated with several human cancers. Here, we aim to investigate the association of functional polymorphisms of CDC25 gene family with the risk of hepatocellular carcinoma (HCC) and persistent infection of Hepatitis B virus (HBV) in a Chinese HBV-related population. First, we used bioinformatics tools to systematically screen functional polymorphisms within CDC25 gene family. Second, we evaluated the effects of candidate polymorphisms by recruiting 790 HCC cases, 709 persistent HBV carriers (PHC), and 741 subjects with HBV natural clearance (SHNC). MassARRAY platform was used for genotyping. At last, we conducted functional prediction and assay to further explore the pathogenic mechanism of the identified polymorphism. Our results demonstrated that CDC25B rs2295348 played a protective role in HCC risk in a HBV-related Chinese population (adjusted odds ratio [OR] = 0.77, 95% confidence interval [CI] 0.65-0.93, P = 0.006). It showed a more significantly reduced HCC risk in the SHNC population (adjusted OR = 0.73, 95% CI 0.59-0.89, P = 0.002). However, we did not observe the association between CDC25B rs2295348 and the risk of persistent HBV infection. Further functional prediction and assay demonstrated that the mutant A allele of CDC25B rs2295348 might significantly decrease gene expression to modify the HCC risk. Our results suggest that CDC25B rs2295348 may confer a protective effect on HCC risk in a HBV-related Chinese population, but do not influence the susceptibility to persistent HBV infection.The cell division cycle 25 (CDC25) gene members, including CDC25A, CDC25B and CDC25C, are reported to be associated with several human cancers. Here, we aim to investigate the association of functional polymorphisms of CDC25 gene family with the risk of hepatocellular carcinoma (HCC) and persistent infection of Hepatitis B virus (HBV) in a Chinese HBV-related population. First, we used bioinformatics tools to systematically screen functional polymorphisms within CDC25 gene family. Second, we evaluated the effects of candidate polymorphisms by recruiting 790 HCC cases, 709 persistent HBV carriers (PHC), and 741 subjects with HBV natural clearance (SHNC). MassARRAY platform was used for genotyping. At last, we conducted functional prediction and assay to further explore the pathogenic mechanism of the identified polymorphism. Our results demonstrated that CDC25B rs2295348 played a protective role in HCC risk in a HBV-related Chinese population (adjusted odds ratio [OR] = 0.77, 95% confidence interval [CI] 0.65-0.93, P = 0.006). It showed a more significantly reduced HCC risk in the SHNC population (adjusted OR = 0.73, 95% CI 0.59-0.89, P = 0.002). However, we did not observe the association between CDC25B rs2295348 and the risk of persistent HBV infection. Further functional prediction and assay demonstrated that the mutant A allele of CDC25B rs2295348 might significantly decrease gene expression to modify the HCC risk. Our results suggest that CDC25B rs2295348 may confer a protective effect on HCC risk in a HBV-related Chinese population, but do not influence the susceptibility to persistent HBV infection.
The cell division cycle 25 ( CDC25 ) gene members, including CDC25A , CDC25B and CDC25C , are reported to be associated with several human cancers. Here, we aim to investigate the association of functional polymorphisms of CDC25 gene family with the risk of hepatocellular carcinoma (HCC) and persistent infection of Hepatitis B virus (HBV) in a Chinese HBV-related population. First, we used bioinformatics tools to systematically screen functional polymorphisms within CDC25 gene family. Second, we evaluated the effects of candidate polymorphisms by recruiting 790 HCC cases, 709 persistent HBV carriers (PHC), and 741 subjects with HBV natural clearance (SHNC). MassARRAY platform was used for genotyping. At last, we conducted functional prediction and assay to further explore the pathogenic mechanism of the identified polymorphism. Our results demonstrated that CDC25B rs2295348 played a protective role in HCC risk in a HBV-related Chinese population (adjusted odds ratio [OR] = 0.77, 95% confidence interval [CI] 0.65–0.93, P  = 0.006). It showed a more significantly reduced HCC risk in the SHNC population (adjusted OR = 0.73, 95% CI 0.59–0.89, P  = 0.002). However, we did not observe the association between CDC25B rs2295348 and the risk of persistent HBV infection. Further functional prediction and assay demonstrated that the mutant A allele of CDC25B rs2295348 might significantly decrease gene expression to modify the HCC risk. Our results suggest that CDC25B rs2295348 may confer a protective effect on HCC risk in a HBV-related Chinese population, but do not influence the susceptibility to persistent HBV infection.
Author Shen, Na
Wang, Peng
Peng, Jing
Gong, Yajie
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CitedBy_id crossref_primary_10_1007_s10565_022_09715_3
crossref_primary_10_1016_j_jmgm_2021_108030
crossref_primary_10_1186_s12876_022_02481_w
Cites_doi 10.1038/nrc2169
10.1038/s41467-018-05694-4
10.1016/j.cell.2004.05.018
10.3322/caac.21551
10.3322/caac.21338
10.1186/1476-4598-7-19
10.1016/j.canep.2019.01.013
10.1016/j.jhep.2018.12.001
10.1093/oxfordjournals.aje.a009876
10.1371/journal.pone.0124266
10.1038/nrg2809
10.1001/jamaoncol.2017.3055
10.1186/s12943-017-0712-x
10.18632/oncotarget.19351
10.1038/s41388-019-1117-7
10.1056/NEJMra1713263
10.1016/j.celrep.2018.03.039
10.1002/mc.23075
10.1038/onc.2017.287
10.1242/jcs.111.16.2445
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References Al-Matouq, Holmes, Hansen (CR11) 2019; 58
Akinyemiju, Abera, Ahmed, Alam, Alemayohu, Allen, Al-Raddadi, Alvis-Guzman, Amoako, Artaman, Ayele, Barac, Bensenor, Berhane, Bhutta, Castillo-Rivas, Chitheer, Choi, Cowie, Dandona, Dandona, Dey, Dicker, Phuc, Ekwueme, Zaki, Fischer, Furst, Hancock, Hay, Hotez, Jee, Kasaeian, Khader, Khang, Kumar, Kutz, Larson, Lopez, Lunevicius, Malekzadeh, McAlinden, Meier, Mendoza, Mokdad, Moradi-Lakeh, Nagel, Nguyen, Nguyen, Ogbo, Patton, Pereira, Pourmalek, Qorbani, Radfar, Roshandel, Salomon, Sanabria, Sartorius, Satpathy, Sawhney, Sepanlou, Shackelford, Shore, Sun, Mengistu, Topor-Madry, Tran, Ukwaja, Vlassov, Vollset, Vos, Wakayo, Weiderpass, Werdecker, Yonemoto, Younis, Yu, Zaidi, Zhu, Murray, Naghavi, Fitzmaurice (CR2) 2017; 3
Zhong, Yang, Xu, Wang, Zheng, Li, He (CR19) 2017; 36
Shen, Li, Xu, Tian, Yang, Zhu, Gong, Ke, Gong, Chang, Zhong, Miao (CR16) 2019; 59
Garcia-Closas, Lubin (CR17) 1999; 149
Alonso, Sasin, Bottini, Friedberg, Friedberg, Osterman, Godzik, Hunter, Dixon, Mustelin (CR7) 2004; 117
Zhu, Wu, Yao, Jiang, Wang, Yang, Wu (CR14) 2015; 10
Boutros, Lobjois, Ducommun (CR8) 2007; 7
Liu, Granieri, Shrestha, Wang, Vorobieva, Rubie, Jones, Ju, Pellecchia, Jiang, Palmerini, Ben-David, Egan, Woodgett, Bader, Datti, Zacksenhaus (CR9) 2018; 23
Siegel, Miller, Jemal (CR1) 2019; 69
Khemlina, Ikeda, Kurzrock (CR5) 2017; 16
Yan, Chua, He, So (CR12) 2008; 7
Zhong, Tian, Fu, Ma, Liu, Li, Shen, Ke, Yang, Gong, Zhu, Wang, Gong, Chang, Lei, Cheng, Huang, Shen, Miao (CR15) 2019
Wu, Lyu, Yang, Liu, Zhang, Shim (CR10) 2018; 9
Liu, Jiang, Yuan, Fang, Cai, Suo, Jin, Zhang, Chen (CR4) 2019; 70
Eichler, Flint, Gibson, Kong, Leal, Moore, Nadeau (CR6) 2010; 11
Chen, Zheng, Baade, Zhang, Zeng, Bray, Jemal, Yu (CR3) 2015; 66
Yin, Chang, Xu (CR13) 2017; 8
Lammer, Wagerer, Saffrich, Mertens, Ansorge, Hoffmann (CR18) 1998; 111
Villanueva (CR20) 2019; 380
X Zhu (5408_CR14) 2015; 10
J Al-Matouq (5408_CR11) 2019; 58
M Garcia-Closas (5408_CR17) 1999; 149
C Wu (5408_CR10) 2018; 9
EE Eichler (5408_CR6) 2010; 11
R Boutros (5408_CR8) 2007; 7
R Zhong (5408_CR15) 2019
W Chen (5408_CR3) 2015; 66
A Alonso (5408_CR7) 2004; 117
L Yin (5408_CR13) 2017; 8
T Akinyemiju (5408_CR2) 2017; 3
Y Zhong (5408_CR19) 2017; 36
Z Liu (5408_CR4) 2019; 70
G Khemlina (5408_CR5) 2017; 16
C Lammer (5408_CR18) 1998; 111
RL Siegel (5408_CR1) 2019; 69
JC Liu (5408_CR9) 2018; 23
X Yan (5408_CR12) 2008; 7
N Shen (5408_CR16) 2019; 59
A Villanueva (5408_CR20) 2019; 380
References_xml – volume: 7
  start-page: 495
  issue: 7
  year: 2007
  end-page: 507
  ident: CR8
  article-title: CDC25 phosphatases in cancer cells: key players? Good targets?
  publication-title: Nat Rev Cancer
  doi: 10.1038/nrc2169
– volume: 9
  start-page: 3212
  issue: 1
  year: 2018
  ident: CR10
  article-title: Targeting AURKA-CDC25C axis to induce synthetic lethality in ARID1A-deficient colorectal cancer cells
  publication-title: Nat Commun
  doi: 10.1038/s41467-018-05694-4
– volume: 117
  start-page: 699
  issue: 6
  year: 2004
  end-page: 711
  ident: CR7
  article-title: Protein tyrosine phosphatases in the human genome
  publication-title: Cell
  doi: 10.1016/j.cell.2004.05.018
– volume: 69
  start-page: 7
  issue: 1
  year: 2019
  end-page: 34
  ident: CR1
  article-title: Cancer statistics
  publication-title: CA: A Cancer J Clin
  doi: 10.3322/caac.21551
– volume: 66
  start-page: 115
  issue: 2
  year: 2015
  end-page: 132
  ident: CR3
  article-title: He J (2016) Cancer statistics in China
  publication-title: CA: A Cancer J Clin
  doi: 10.3322/caac.21338
– volume: 7
  start-page: 19
  year: 2008
  ident: CR12
  article-title: Small interfering RNA targeting CDC25B inhibits liver tumor growth in vitro and in vivo
  publication-title: Mol Cancer
  doi: 10.1186/1476-4598-7-19
– volume: 59
  start-page: 109
  year: 2019
  end-page: 114
  ident: CR16
  article-title: A missense variant in PTPN12 associated with the risk of colorectal cancer by modifying Ras/MEK/ERK signaling
  publication-title: Cancer Epidemiol
  doi: 10.1016/j.canep.2019.01.013
– volume: 70
  start-page: 674
  issue: 4
  year: 2019
  end-page: 683
  ident: CR4
  article-title: The trends in incidence of primary liver cancer caused by specific etiologies: results from the Global Burden of Disease Study 2016 and implications for liver cancer prevention
  publication-title: J Hepatol
  doi: 10.1016/j.jhep.2018.12.001
– volume: 149
  start-page: 689
  issue: 8
  year: 1999
  end-page: 692
  ident: CR17
  article-title: Power and sample size calculations in case-control studies of gene-environment interactions: comments on different approaches
  publication-title: Am J Epidemiol
  doi: 10.1093/oxfordjournals.aje.a009876
– volume: 10
  start-page: e0124266
  issue: 4
  year: 2015
  ident: CR14
  article-title: MicroRNA let-7c inhibits cell proliferation and induces cell cycle arrest by targeting CDC25A in human hepatocellular carcinoma
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0124266
– volume: 11
  start-page: 446
  issue: 6
  year: 2010
  end-page: 450
  ident: CR6
  article-title: Missing heritability and strategies for finding the underlying causes of complex disease
  publication-title: Nat Rev Genet
  doi: 10.1038/nrg2809
– volume: 3
  start-page: 1683
  issue: 12
  year: 2017
  end-page: 1691
  ident: CR2
  article-title: The burden of primary liver cancer and underlying etiologies from 1990 to 2015 at the global, regional, and national level: results from the Global Burden of Disease Study 2015
  publication-title: JAMA Oncol
  doi: 10.1001/jamaoncol.2017.3055
– volume: 16
  start-page: 149
  issue: 1
  year: 2017
  ident: CR5
  article-title: The biology of Hepatocellular carcinoma: implications for genomic and immune therapies
  publication-title: Mol Cancer
  doi: 10.1186/s12943-017-0712-x
– volume: 8
  start-page: 76305
  issue: 44
  year: 2017
  end-page: 76317
  ident: CR13
  article-title: G2/M checkpoint plays a vital role at the early stage of HCC by analysis of key pathways and genes
  publication-title: Oncotarget
  doi: 10.18632/oncotarget.19351
– year: 2019
  ident: CR15
  article-title: LINC01149 variant modulates MICA expression that facilitates hepatitis B virus spontaneous recovery but increases hepatocellular carcinoma risk
  publication-title: Oncogene
  doi: 10.1038/s41388-019-1117-7
– volume: 380
  start-page: 1450
  issue: 15
  year: 2019
  end-page: 1462
  ident: CR20
  article-title: Hepatocellular carcinoma
  publication-title: N Engl J Med
  doi: 10.1056/NEJMra1713263
– volume: 23
  start-page: 112
  issue: 1
  year: 2018
  end-page: 126
  ident: CR9
  article-title: Identification of CDC25 as a common therapeutic target for triple-negative breast cancer
  publication-title: Cell Rep
  doi: 10.1016/j.celrep.2018.03.039
– volume: 58
  start-page: 1691
  issue: 9
  year: 2019
  end-page: 1700
  ident: CR11
  article-title: CDC25B and CDC25C overexpression in nonmelanoma skin cancer suppresses cell death
  publication-title: Mol Carcinog
  doi: 10.1002/mc.23075
– volume: 36
  start-page: 6177
  issue: 44
  year: 2017
  end-page: 6189
  ident: CR19
  article-title: KCTD12 promotes tumorigenesis by facilitating CDC25B/CDK1/Aurora A-dependent G2/M transition
  publication-title: Oncogene
  doi: 10.1038/onc.2017.287
– volume: 111
  start-page: 2445
  issue: Pt 16
  year: 1998
  end-page: 2453
  ident: CR18
  article-title: The cdc25B phosphatase is essential for the G2/M phase transition in human cells
  publication-title: J Cell Sci
– volume: 59
  start-page: 109
  year: 2019
  ident: 5408_CR16
  publication-title: Cancer Epidemiol
  doi: 10.1016/j.canep.2019.01.013
– volume: 9
  start-page: 3212
  issue: 1
  year: 2018
  ident: 5408_CR10
  publication-title: Nat Commun
  doi: 10.1038/s41467-018-05694-4
– year: 2019
  ident: 5408_CR15
  publication-title: Oncogene
  doi: 10.1038/s41388-019-1117-7
– volume: 111
  start-page: 2445
  issue: Pt 16
  year: 1998
  ident: 5408_CR18
  publication-title: J Cell Sci
  doi: 10.1242/jcs.111.16.2445
– volume: 66
  start-page: 115
  issue: 2
  year: 2015
  ident: 5408_CR3
  publication-title: CA: A Cancer J Clin
  doi: 10.3322/caac.21338
– volume: 16
  start-page: 149
  issue: 1
  year: 2017
  ident: 5408_CR5
  publication-title: Mol Cancer
  doi: 10.1186/s12943-017-0712-x
– volume: 58
  start-page: 1691
  issue: 9
  year: 2019
  ident: 5408_CR11
  publication-title: Mol Carcinog
  doi: 10.1002/mc.23075
– volume: 70
  start-page: 674
  issue: 4
  year: 2019
  ident: 5408_CR4
  publication-title: J Hepatol
  doi: 10.1016/j.jhep.2018.12.001
– volume: 8
  start-page: 76305
  issue: 44
  year: 2017
  ident: 5408_CR13
  publication-title: Oncotarget
  doi: 10.18632/oncotarget.19351
– volume: 380
  start-page: 1450
  issue: 15
  year: 2019
  ident: 5408_CR20
  publication-title: N Engl J Med
  doi: 10.1056/NEJMra1713263
– volume: 23
  start-page: 112
  issue: 1
  year: 2018
  ident: 5408_CR9
  publication-title: Cell Rep
  doi: 10.1016/j.celrep.2018.03.039
– volume: 7
  start-page: 19
  year: 2008
  ident: 5408_CR12
  publication-title: Mol Cancer
  doi: 10.1186/1476-4598-7-19
– volume: 10
  start-page: e0124266
  issue: 4
  year: 2015
  ident: 5408_CR14
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0124266
– volume: 149
  start-page: 689
  issue: 8
  year: 1999
  ident: 5408_CR17
  publication-title: Am J Epidemiol
  doi: 10.1093/oxfordjournals.aje.a009876
– volume: 7
  start-page: 495
  issue: 7
  year: 2007
  ident: 5408_CR8
  publication-title: Nat Rev Cancer
  doi: 10.1038/nrc2169
– volume: 69
  start-page: 7
  issue: 1
  year: 2019
  ident: 5408_CR1
  publication-title: CA: A Cancer J Clin
  doi: 10.3322/caac.21551
– volume: 11
  start-page: 446
  issue: 6
  year: 2010
  ident: 5408_CR6
  publication-title: Nat Rev Genet
  doi: 10.1038/nrg2809
– volume: 36
  start-page: 6177
  issue: 44
  year: 2017
  ident: 5408_CR19
  publication-title: Oncogene
  doi: 10.1038/onc.2017.287
– volume: 3
  start-page: 1683
  issue: 12
  year: 2017
  ident: 5408_CR2
  publication-title: JAMA Oncol
  doi: 10.1001/jamaoncol.2017.3055
– volume: 117
  start-page: 699
  issue: 6
  year: 2004
  ident: 5408_CR7
  publication-title: Cell
  doi: 10.1016/j.cell.2004.05.018
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Snippet The cell division cycle 25 ( CDC25 ) gene members, including CDC25A , CDC25B and CDC25C , are reported to be associated with several human cancers. Here, we...
The cell division cycle 25 (CDC25) gene members, including CDC25A, CDC25B and CDC25C, are reported to be associated with several human cancers. Here, we aim to...
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SubjectTerms Alleles
Animal Anatomy
Animal Biochemistry
Asian Continental Ancestry Group - genetics
Bioinformatics
Biomedical and Life Sciences
Carcinoma, Hepatocellular - genetics
Carcinoma, Hepatocellular - metabolism
Case-Control Studies
cdc25 Phosphatases - genetics
cdc25 Phosphatases - metabolism
Cdc25B phosphatase
Cell division
China - epidemiology
chronic diseases
confidence interval
Gene expression
Gene Frequency - genetics
Genetic Predisposition to Disease - genetics
Genotype
Genotyping
Haplotypes - genetics
Hepatitis B
Hepatitis B - epidemiology
Hepatitis B - genetics
Hepatitis B virus
Hepatitis B virus - genetics
Hepatitis B virus - pathogenicity
Hepatitis B, Chronic - genetics
Hepatocellular carcinoma
hepatoma
Histology
Humans
Infections
Life Sciences
Liver cancer
Liver Neoplasms - genetics
Liver Neoplasms - metabolism
molecular biology
Morphology
mutants
odds ratio
Original Article
Persistent infection
Polymorphism, Single Nucleotide - genetics
Population
prediction
protective effect
risk
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Title CDC25B is associated with the risk of hepatocellular carcinoma, but not related to persistent infection of hepatitis B virus in a Chinese population
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