Literature DB >> 15700316

DNA repair gene XPC genotypes/haplotypes and risk of lung cancer in a Chinese population.

Zhibin Hu1, Yonggang Wang, Xinru Wang, Gang Liang, Xiaoping Miao, Yaochu Xu, Wen Tan, Qingyi Wei, Dongxin Lin, Hongbing Shen.   

Abstract

DNA repair is central to normal cellular functions, and polymorphisms of DNA repair genes may cause variation in DNA repair capacity in the general population. Newly identified polymorphisms of xeroderma pigmentosum group C (XPC), one of the nucleotide excision repair genes, were shown to contribute to genetic susceptibility to cancer. In this study, we hypothesized that 2 exonic variants C499T and A939C and their haplotypes in XPC are associated with lung cancer risk. To test this hypothesis, we performed a case-control study of 320 histologically confirmed lung cancer patients and 322 age and sex frequency-matched cancer-free controls in a Chinese population. Multivariate logistic regression analyses revealed that the risks [adjusted odds ratios (ORs) and 95% confidence intervals (CIs)] associated with the XPC variant genotypes were 1.57 (95% CI = 1.13-2.19) for 499CT/TT and 1.21 (95% CI = 0.87-1.69) for 939AC/CC compared with the 499CC and 939AA wild-type homozygotes, respectively. Individuals with both putative risk genotypes (499CT/TT and 939AC/CC) had a greater risk of lung cancer (adjusted OR = 2.37; 95% CI = 1.33-4.21) compared with individuals with both wild-type genotypes (499CC and 939AA). When we performed the haplotype analysis and assumed the XPC 499T and 939C as risk alleles, the adjusted ORs increased as the number of variants in the haplotype genotypes increased (p(trend) < 0.001). In the stratified analysis, the greatest risk was found in smokers having the combined variant genotypes (adjusted OR = 7.36; 95% CI = 3.19-17.00) compared with nonsmokers having both wild-type genotypes and in smokers with 2 or 3 haplotype variants (adjusted OR = 7.27; 95% CI = 3.37-15.68) compared with nonsmokers having 0 haplotype variant. These findings indicate that XPC exonic variants may contribute to the risk of lung cancer in the Chinese population, and these variant genotypes may modulate the risk of lung cancer associated with smoking. (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15700316     DOI: 10.1002/ijc.20911

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  32 in total

1.  Correlating observed odds ratios from lung cancer case-control studies to SNP functional scores predicted by bioinformatic tools.

Authors:  Yong Zhu; Aaron Hoffman; Xifeng Wu; Heping Zhang; Yawei Zhang; Derek Leaderer; Tongzhang Zheng
Journal:  Mutat Res       Date:  2007-11-26       Impact factor: 2.433

2.  XPC Lys939Gln and Ala499Val polymorphisms in colorectal cancer susceptibility: a meta-analysis of case-control studies.

Authors:  Chuan Liu; Qinghua Yin; Mingzhen Ying; Junhui Lin; Lian Li; Guangjun Jiao; Mei Wang; Yajie Wang
Journal:  Mol Biol Rep       Date:  2014-01-03       Impact factor: 2.316

3.  Modulation of DNA damage/DNA repair capacity by XPC polymorphisms.

Authors:  Yimin Zhu; Hushan Yang; Qin Chen; Jie Lin; H Barton Grossman; Colin P Dinney; Xifeng Wu; Jian Gu
Journal:  DNA Repair (Amst)       Date:  2007-10-17

Review 4.  Host nucleotide polymorphism in hepatitis B virus-associated hepatocellular carcinoma.

Authors:  Shilu Mathew; Hany Abdel-Hafiz; Abbas Raza; Kaneez Fatima; Ishtiaq Qadri
Journal:  World J Hepatol       Date:  2016-04-08

5.  Predictive impact of genetic polymorphisms in DNA repair genes on susceptibility and therapeutic outcomes to colorectal cancer patients.

Authors:  Kang Sun; Aixia Gong; Pin Liang
Journal:  Tumour Biol       Date:  2014-10-30

6.  A meta-analysis of evidences on XPC polymorphisms and lung cancer susceptibility.

Authors:  Chuan Liu; Qinghua Yin; Jianbing Hu; Lian Li; Yingyi Zhang; Yajie Wang
Journal:  Tumour Biol       Date:  2013-02-06

7.  DNA Repair Gene Polymorphisms in the Nucleotide Excision Repair Pathway and Lung Cancer Risk: A Meta-analysis.

Authors:  Chao-Rong Mei; Meng Luo; Hong-Mei Li; Wen-Jun Deng; Qing-Hua Zhou
Journal:  Chin J Cancer Res       Date:  2011-06       Impact factor: 5.087

8.  Assessment of the XPC (A2920C), XPF (T30028C), TP53 (Arg72Pro) and GSTP1 (Ile105Val) polymorphisms in the risk of cutaneous melanoma.

Authors:  Cristiane Oliveira; José Augusto Rinck-Junior; Gustavo Jacob Lourenço; Aparecida Machado Moraes; Carmen Silvia Passos Lima
Journal:  J Cancer Res Clin Oncol       Date:  2013-04-09       Impact factor: 4.553

9.  Using haplotype analysis to elucidate significant associations between genes and Hodgkin lymphoma.

Authors:  Anthony M D'Amelio; Claudia Monroy; Randa El-Zein; Carol J Etzel
Journal:  Leuk Res       Date:  2012-08-14       Impact factor: 3.156

10.  Body mass index and smoking-related lung cancer risk in the Singapore Chinese Health Study.

Authors:  W-P Koh; J-M Yuan; R Wang; H-P Lee; M C Yu
Journal:  Br J Cancer       Date:  2009-12-15       Impact factor: 7.640

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