Association between polymorphisms of Xeroderma pigmentosum complementation group C gene (XPC) and susceptibility to schizophrenia
Previous studies revealed that polymorphisms in several DNA repair genes are associated with the risk of schizophrenia. The relationship between three polymorphisms (Ala499Val, PAT, and Lys939Gln) of the XPC (MIM: 613208) and the risk of schizophrenia is investigated. A total of 361 schizophrenia ca...
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Published in | Gene Vol. 695; pp. 99 - 100 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
05.05.2019
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ISSN | 0378-1119 1879-0038 1879-0038 |
DOI | 10.1016/j.gene.2019.02.018 |
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Abstract | Previous studies revealed that polymorphisms in several DNA repair genes are associated with the risk of schizophrenia. The relationship between three polymorphisms (Ala499Val, PAT, and Lys939Gln) of the XPC (MIM: 613208) and the risk of schizophrenia is investigated. A total of 361 schizophrenia cases and 360 healthy controls were included in the study. Statistical analysis revealed that the Ala/Val genotype (OR = 0.62, P = 0.004) and the carriers of the Val allele (OR = 0.64, P = 0.006) were negatively associated with the risk of schizophrenia. The other two examined polymorphisms did not reveal significant association. The “Val - Lys” haplotype was associated with decrease risk of schizophrenia (OR = 0.71, P = 0.020). It has been showed that the haplotype “Val - Lys” had the lowest DNA damages, indicating that has higher DNA repair capacity. Here we found that this haplotype is associated with lower risk for schizophrenia.
•Xeroderma pigmentosum complementation group C involved in nucleotide excision repair.•The XPC has several genetic variants including Ala499Val, Lys939Gln, and PAT.•Association between these polymorphisms and risk of schizophrenia was investigated.•The present study was carried out on 361 schizophrenia subjects and 360 healthy controls.•The “Val - Lys” haplotype was associated with decrease risk of schizophrenia. |
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AbstractList | Previous studies revealed that polymorphisms in several DNA repair genes are associated with the risk of schizophrenia. The relationship between three polymorphisms (Ala499Val, PAT, and Lys939Gln) of the XPC (MIM: 613208) and the risk of schizophrenia is investigated. A total of 361 schizophrenia cases and 360 healthy controls were included in the study. Statistical analysis revealed that the Ala/Val genotype (OR = 0.62, P = 0.004) and the carriers of the Val allele (OR = 0.64, P = 0.006) were negatively associated with the risk of schizophrenia. The other two examined polymorphisms did not reveal significant association. The “Val - Lys” haplotype was associated with decrease risk of schizophrenia (OR = 0.71, P = 0.020). It has been showed that the haplotype “Val - Lys” had the lowest DNA damages, indicating that has higher DNA repair capacity. Here we found that this haplotype is associated with lower risk for schizophrenia. Previous studies revealed that polymorphisms in several DNA repair genes are associated with the risk of schizophrenia. The relationship between three polymorphisms (Ala499Val, PAT, and Lys939Gln) of the XPC (MIM: 613208) and the risk of schizophrenia is investigated. A total of 361 schizophrenia cases and 360 healthy controls were included in the study. Statistical analysis revealed that the Ala/Val genotype (OR = 0.62, P = 0.004) and the carriers of the Val allele (OR = 0.64, P = 0.006) were negatively associated with the risk of schizophrenia. The other two examined polymorphisms did not reveal significant association. The "Val - Lys" haplotype was associated with decrease risk of schizophrenia (OR = 0.71, P = 0.020). It has been showed that the haplotype "Val - Lys" had the lowest DNA damages, indicating that has higher DNA repair capacity. Here we found that this haplotype is associated with lower risk for schizophrenia.Previous studies revealed that polymorphisms in several DNA repair genes are associated with the risk of schizophrenia. The relationship between three polymorphisms (Ala499Val, PAT, and Lys939Gln) of the XPC (MIM: 613208) and the risk of schizophrenia is investigated. A total of 361 schizophrenia cases and 360 healthy controls were included in the study. Statistical analysis revealed that the Ala/Val genotype (OR = 0.62, P = 0.004) and the carriers of the Val allele (OR = 0.64, P = 0.006) were negatively associated with the risk of schizophrenia. The other two examined polymorphisms did not reveal significant association. The "Val - Lys" haplotype was associated with decrease risk of schizophrenia (OR = 0.71, P = 0.020). It has been showed that the haplotype "Val - Lys" had the lowest DNA damages, indicating that has higher DNA repair capacity. Here we found that this haplotype is associated with lower risk for schizophrenia. Previous studies revealed that polymorphisms in several DNA repair genes are associated with the risk of schizophrenia. The relationship between three polymorphisms (Ala499Val, PAT, and Lys939Gln) of the XPC (MIM: 613208) and the risk of schizophrenia is investigated. A total of 361 schizophrenia cases and 360 healthy controls were included in the study. Statistical analysis revealed that the Ala/Val genotype (OR = 0.62, P = 0.004) and the carriers of the Val allele (OR = 0.64, P = 0.006) were negatively associated with the risk of schizophrenia. The other two examined polymorphisms did not reveal significant association. The “Val - Lys” haplotype was associated with decrease risk of schizophrenia (OR = 0.71, P = 0.020). It has been showed that the haplotype “Val - Lys” had the lowest DNA damages, indicating that has higher DNA repair capacity. Here we found that this haplotype is associated with lower risk for schizophrenia. •Xeroderma pigmentosum complementation group C involved in nucleotide excision repair.•The XPC has several genetic variants including Ala499Val, Lys939Gln, and PAT.•Association between these polymorphisms and risk of schizophrenia was investigated.•The present study was carried out on 361 schizophrenia subjects and 360 healthy controls.•The “Val - Lys” haplotype was associated with decrease risk of schizophrenia. |
Author | Saadat, Iraj Taghipour, Nahid Saadat, Mostafa |
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Cites_doi | 10.1016/j.psychres.2007.07.014 10.1093/carcin/22.6.917 10.1016/j.schres.2018.06.052 10.1016/j.psychres.2009.03.022 10.1089/gtmb.2015.0168 10.1093/carcin/22.9.1437 10.1002/ijc.20911 10.1016/S1097-2765(00)80132-X 10.1016/j.psychres.2015.05.041 10.1016/j.dnarep.2007.08.006 |
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References | Odemis, Tuzun, Gulec, Semiz, Dasdemir, Kucuk, Yalcınkaya, Bireller, Cakmakoglu, Küçükali (bb0040) 2016; 20 Derakhshandeh, Saadat, Farrashbandi, Saadat (bb0010) 2009; 169 Hu, Smith, Miller, Mohrenweiser, Golden, Case (bb0015) 2001; 22 Saadat, Pakyari, Farrashbandi (bb0045) 2008; 157 Cheng, Guan, Li, Legerski, Einspahr, Bangert, Alberts, Wei (bb0005) 1999; 8 Liu, Wang, Lin, Wei, Zhi, Yuan, Song, Yang, Chen (bb0025) 2012; 28 Sugasawa, Ng, Masutani, Iwai, van der Spek, Eker, Hanaoka, Bootsma, Hoeijmakers (bb0050) 1998; 2 Topak, Ozdel, Dodurga, Secme (bb0055) 2018 Mazaheri, Saadat (bb0035) 2015; 228 Hu, Wang, Wang, Liang, Miao, Xu, Tan, Wei, Lin, Shen (bb0020) 2005; 115 Matullo, Palli, Peluso, Guarrera, Carturan, Celentano, Krogh, Munnia, Tumino, Polidoro, Piazza, Vineis (bb0030) 2001; 22 Zhu, Yang, Chen, Lin, Grossman, Dinney, Wu, Gu (bb0060) 2008; 7 Odemis (10.1016/j.gene.2019.02.018_bb0040) 2016; 20 Matullo (10.1016/j.gene.2019.02.018_bb0030) 2001; 22 Topak (10.1016/j.gene.2019.02.018_bb0055) 2018 Liu (10.1016/j.gene.2019.02.018_bb0025) 2012; 28 Zhu (10.1016/j.gene.2019.02.018_bb0060) 2008; 7 Cheng (10.1016/j.gene.2019.02.018_bb0005) 1999; 8 Saadat (10.1016/j.gene.2019.02.018_bb0045) 2008; 157 Derakhshandeh (10.1016/j.gene.2019.02.018_bb0010) 2009; 169 Sugasawa (10.1016/j.gene.2019.02.018_bb0050) 1998; 2 Hu (10.1016/j.gene.2019.02.018_bb0020) 2005; 115 Mazaheri (10.1016/j.gene.2019.02.018_bb0035) 2015; 228 Hu (10.1016/j.gene.2019.02.018_bb0015) 2001; 22 |
References_xml | – volume: 20 start-page: 11 year: 2016 end-page: 17 ident: bb0040 article-title: Association between polymorphisms of DNA repair genes and risk of schizophrenia publication-title: Genet. Test. Mol. Biomarkers – volume: 7 start-page: 141 year: 2008 end-page: 148 ident: bb0060 article-title: Modulation of DNA damage/DNA repair capacity by publication-title: DNA Repair (Amst) – volume: 8 start-page: 801 year: 1999 end-page: 807 ident: bb0005 article-title: Expression in normal human tissues of five nucleotide excision repair genes measured simultaneously by multiplex reverse transcription-polymerase chain reaction publication-title: Cancer Epidemiol. Biomark. Prev. – volume: 169 start-page: 186 year: 2009 ident: bb0010 article-title: Association between genetic polymorphism of publication-title: Psychiatry Res. – volume: 22 start-page: 1437 year: 2001 end-page: 1445 ident: bb0030 article-title: XRCC1, XRCC3, XPD gene polymorphisms, smoking and (32)P-DNA adducts in a sample of healthy subjects publication-title: Carcinogenesis – volume: 157 start-page: 241 year: 2008 end-page: 245 ident: bb0045 article-title: Genetic polymorphism in the DNA repair gene publication-title: Psychiatry Res. – volume: 22 start-page: 917 year: 2001 end-page: 922 ident: bb0015 article-title: Amino acid substitution variants of publication-title: Carcinogenesis – volume: 2 start-page: 223 year: 1998 end-page: 232 ident: bb0050 article-title: Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair publication-title: Mol. Cell – volume: 228 start-page: 972 year: 2015 end-page: 973 ident: bb0035 article-title: Susceptibility to schizophrenia and insertion/deletion polymorphism in intron 3 of the publication-title: Psychiatry Res. – volume: 115 start-page: 478 year: 2005 end-page: 483 ident: bb0020 article-title: DNA repair gene publication-title: Int. J. Cancer – volume: 28 start-page: 337 year: 2012 end-page: 345 ident: bb0025 article-title: Interactions between cigarette smoking and XPC-PAT genetic polymorphism enhance bladder cancer risk publication-title: Oncol. Rep. – year: 2018 ident: bb0055 article-title: An evaluation of the differences in DNA damage in lymphocytes and repair efficiencies in patients with schizophrenia and schizoaffective disorder publication-title: Schizophr. Res. – volume: 157 start-page: 241 year: 2008 ident: 10.1016/j.gene.2019.02.018_bb0045 article-title: Genetic polymorphism in the DNA repair gene XRCC1 and susceptibility to schizophrenia publication-title: Psychiatry Res. doi: 10.1016/j.psychres.2007.07.014 – volume: 22 start-page: 917 year: 2001 ident: 10.1016/j.gene.2019.02.018_bb0015 article-title: Amino acid substitution variants of APE1 and XRCC1 genes associated with ionizing radiation sensitivity publication-title: Carcinogenesis doi: 10.1093/carcin/22.6.917 – year: 2018 ident: 10.1016/j.gene.2019.02.018_bb0055 article-title: An evaluation of the differences in DNA damage in lymphocytes and repair efficiencies in patients with schizophrenia and schizoaffective disorder publication-title: Schizophr. Res. doi: 10.1016/j.schres.2018.06.052 – volume: 169 start-page: 186 year: 2009 ident: 10.1016/j.gene.2019.02.018_bb0010 article-title: Association between genetic polymorphism of XRCC1 Arg194Trp and risk of schizophrenia publication-title: Psychiatry Res. doi: 10.1016/j.psychres.2009.03.022 – volume: 20 start-page: 11 year: 2016 ident: 10.1016/j.gene.2019.02.018_bb0040 article-title: Association between polymorphisms of DNA repair genes and risk of schizophrenia publication-title: Genet. Test. Mol. Biomarkers doi: 10.1089/gtmb.2015.0168 – volume: 8 start-page: 801 year: 1999 ident: 10.1016/j.gene.2019.02.018_bb0005 article-title: Expression in normal human tissues of five nucleotide excision repair genes measured simultaneously by multiplex reverse transcription-polymerase chain reaction publication-title: Cancer Epidemiol. Biomark. Prev. – volume: 22 start-page: 1437 year: 2001 ident: 10.1016/j.gene.2019.02.018_bb0030 article-title: XRCC1, XRCC3, XPD gene polymorphisms, smoking and (32)P-DNA adducts in a sample of healthy subjects publication-title: Carcinogenesis doi: 10.1093/carcin/22.9.1437 – volume: 115 start-page: 478 year: 2005 ident: 10.1016/j.gene.2019.02.018_bb0020 article-title: DNA repair gene XPC genotypes/haplotypes and risk of lung cancer in a Chinese population publication-title: Int. J. Cancer doi: 10.1002/ijc.20911 – volume: 2 start-page: 223 year: 1998 ident: 10.1016/j.gene.2019.02.018_bb0050 article-title: Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair publication-title: Mol. Cell doi: 10.1016/S1097-2765(00)80132-X – volume: 28 start-page: 337 year: 2012 ident: 10.1016/j.gene.2019.02.018_bb0025 article-title: Interactions between cigarette smoking and XPC-PAT genetic polymorphism enhance bladder cancer risk publication-title: Oncol. Rep. – volume: 228 start-page: 972 year: 2015 ident: 10.1016/j.gene.2019.02.018_bb0035 article-title: Susceptibility to schizophrenia and insertion/deletion polymorphism in intron 3 of the XRCC4 gene publication-title: Psychiatry Res. doi: 10.1016/j.psychres.2015.05.041 – volume: 7 start-page: 141 year: 2008 ident: 10.1016/j.gene.2019.02.018_bb0060 article-title: Modulation of DNA damage/DNA repair capacity by XPC polymorphisms publication-title: DNA Repair (Amst) doi: 10.1016/j.dnarep.2007.08.006 |
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SubjectTerms | Alleles Case-control DNA damage DNA Damage - genetics DNA repair DNA Repair - genetics DNA-Binding Proteins - genetics Female Genetic Association Studies Genetic Predisposition to Disease Genotype haplotypes Haplotypes - genetics Humans Male photosensitivity disorders Polymorphism, Single Nucleotide - genetics Risk Risk Factors schizophrenia Schizophrenia - genetics Schizophrenia - pathology statistical analysis |
Title | Association between polymorphisms of Xeroderma pigmentosum complementation group C gene (XPC) and susceptibility to schizophrenia |
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