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International Journal of Genomics
Volume 2013 (2013), Article ID 124612, 8 pages
XRCC7 rs#7003908 Polymorphism and Helicobacter pylori Infection-Related Gastric Antrum Adenocarcinoma
1Department of Medicine, The Affiliated Hospital of Youjiang Medical College for Nationalities (AHYMCN), Baise 533000, China
2Department of Pathology, The Affiliated Hospital of Youjiang Medical College for Nationalities (AHYMCN), Baise 533000, China
3Department of Liver Surgery, The Affiliated Ren Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200127, China
Received 26 July 2013; Accepted 29 September 2013
Academic Editor: Elena Pasyukova
Copyright © 2013 Chao Wang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The X-ray repair cross-complementing group 7 (XRCC7) plays a key role in DNA repair that protects against genetic instability and carcinogenesis. To determine whether XRCC7 rs#7003908 polymorphism (XRCC7P) is associated with Helicobacter pylori (H. pylori) infection-related gastric antrum adenocarcinoma (GAA) risk, we conducted a hospital-based case-control study, including 642 patients with pathologically confirmed GAA and 927 individually matched controls without any evidence of tumours or precancerous lesions, among Guangxi population. Increased risks of GAA were observed for individuals with cagA positive (odds ratio (OR) 6.38; 95% confidence interval (CI) 5.03–8.09). We also found that these individuals with the genotypes of XRCC7 rs#7003908 G alleles (XRCC7-TG or -GG) featured increasing risk of GAA (ORs 2.80 and 5.13, resp.), compared with the homozygote of XRCC7 rs#7003908 T alleles (XRCC7-TT). GAA risk, moreover, did appear to differ more significantly among individuals featuring cagA-positive status, whose adjusted ORs (95% CIs) were 15.74 (10.89–22.77) for XRCC7-TG and 38.49 (22.82–64.93) for XRCC7-GG, respectively. Additionally, this polymorphism multiplicatively interacted with XRCC3 codon 241 polymorphism with respect to HCC risk (). These results suggest that XRCC7P may be associated with the risk of Guangxiese GAA related to cagA.
Gastric cancer is the fourth most common cancer worldwide and the second most common cause of death from cancer [1, 2]. The predominant type of this tumor in Guangxi Zhuang Autonomous Region is gastric antrum adenocarcinoma (GAA) . Clinic-epidemiological evidence suggests that Helicobacter pylori (H. pylori) infection is a major risk factor [4, 5]. Increasing evidence has shown that cagA protein, an important H. pylori-produced virulent factor for gastric mucosa injury, could induce many kinds of DNA damage including DNA base damage, DNA double-strand break (DSBs), and oxidative damage [5–10]. Among these DNA damages, DSBs are the most detrimental form [11, 12], because they may lead to both chromosomal breakage and rearrangement and ultimately lead to tumorigenesis of cancers such as GAA.
DNA repair gene “X-ray repair cross-complementing group 7” (XRCC7) is necessary for DNA ligation in the nonhomologous end-joining (NHEJ) pathway, which is responsible for repairing most double-strand breaks [13, 14]. Recently, several studies have shown that XRCC7 rs#7003908 polymorphism (XRCC7P) may be associated with DNA repair capacity and tumor risk [15–17]. However, the association between this polymorphism and GAA has not yet been elucidated. Here, we evaluated whether XRCC7P modifies H. pylori infection-related GAA risk.
2. Materials and Methods
2.1. Study Population
We conducted a hospital-based case-control study that has been previously described [18, 19]. Briefly, all participants, consisting of 642 GAA patients (including 465 previously studied subjects ) and 927 control individuals (including 739 previously studied subjects ), were from Guangxi Zhuang Autonomous Region, and both case and control recruitment is still ongoing. Cases were patients diagnosed with histopathologically confirmed GAA in the Affiliated Hospitals of the three main medical colleges in Guangxi (viz. Guangxi Medical University, Youjiang Medical College for Nationalities, and Guilin Medical College) between September 2008 and December 2010. During the same period, controls without clinical evidence of precancerous lesions or tumors were randomly selected from a pool of volunteers accepting the examination of gastric biopsy because of extended gastric inflammation (superficial chronic gastritis diagnosed by histopathological examination) in the same hospitals. Controls were individually matched to cases by age (±5 years), ethnicity (Han, Minority), sex, smoking habits (never smoking, ever smoking), and alcohol intake (never drinking, ever drinking). In this study, there is one or two controls (who have the aforementioned matching criteria) individually matched to each case. After giving written consent, participants provided demographic information (including age, race, medical history for themselves and their families, and drinking and smoking history) using a standard interviewer-administered questionnaire. A total of 642 cases and 927 controls, representing 99% of eligible cases and 95% of eligible controls, were enrolled and interviewed. The protocol of the study was approved by the Ethics Committees of the hospitals involved in the study.
2.2. DNA Extraction
DNA was extracted from noncancerous gastric biopsy tissues from all cancer patients and control subjects for deparaffinization and proteinase K digestion, described in our previously published study . DNA was stored at −20°C until additional analysis.
2.3. H. pylori Infection-Status Assay
Because our previous report showed that carriers of H. pylori having CagA-present strains would face higher risk of GAA, we evaluated the H. pylori-infection status using cagA-status analysis in this study. CagA status was elucidated through the previously published PCR technique . Briefly, PCR reactions were run in a 25 μL final volume containing 0.625 u of GoTaq DNA polymerase (Promega Corporation, Madison, WI), 0.2 μM of each primer, 200 μM of each dNTPs, and about 100 ng of genomic DNA. Cycling conditions were as follows: PCR program initiated by a 2 min denaturation step at 95°C, followed by 40 cycles of 95°C for 10 s, 54.5°C for 30 s, 72°C for 20 s, and a final elongation step of 72°C for 10 min. The quality control for cagA-status assays was administered by negative and positive controls.
2.4. XRCC7 Genotyping
Laboratory personnel were blinded to case and control status. DNA was extracted from noncancerous gastric biopsy tissues from all cancer patients and control subjects according to the previously described methods . XRCC7 (rs#7003908) genotypes were tested by using the TaqMan-PCR on iCycler iQ real-time PCR detection system (CFX Manager Version 2, Bio-Rad). The primer and probe sequences used for rs#7003908 polymorphism have previously been reported. PCR reactions were run in a 25 μL final volume containing 1 × TaqMan Universal Master Mix II (catalog # 4440041, ABI), 0.2 μM of each probe, 0.2 μM of each primer, and about 100 ng of genomic DNA. Cycling conditions were 95°C for 10 min and 40 cycles of 95°C for 15 s and 60°C for 1 min. To further validate the genotyping results, direct sequencing was randomly tested in about 1% of PCR products, and genotyping was repeated randomly in 10% of the samples.
2.5. Statistical Analysis
All statistical analyses were done using the statistical package for social science (SPSS) version 18 (SPSS Institute, Chicago, IL). The two-sided chi-square test was used to evaluate differences in frequency distributions of demographic characteristics, cagA status, and genotypes of XRCC7 rs#7003908 polymorphism between the cases and controls. Based to individually matched design, conditional logistic regression analyses were carried out to obtain odds ratios (ORs) for risk of GAA and their 95% confidence intervals (CIs). Joint effects between genotypes and H. pylori-infection information were evaluated by using the full regression model that included the main effects of potential risk genotypes, cagA status, and all matching factors with a fully parameterized model (not including interactive variables of both cagA and genotypes). In the present study, the interactive effects between cagA and risk genotypes of XRCC7 rs#7003908 were evaluated according to the following formula [20–22]: where is the odds ratio for the presence of both cagA-positive status and risk genotypes of XRCC7 rs#7003908 (OR > 1), is the odds ratio for cagA-positive status for patients with the low-risk XRCC7 genotype, and is the odds ratio for the high risk XRCC7 genotype in patients with cagA-negative status. A value of <0.05 was considered statistically significant in this study.
3.1. Demographic Characteristics of the Subjects
Our final analysis included 642 GAA cases and 927 controls (Table 1). The characteristics of cases and controls showed that there were no significant differences between cases and controls in terms of the distribution of age, sex, race, and smoking and drinking status as a result of individual matching. These results suggest the GAA patient data were comparable to the control data.
3.2. CagA Status and GAA Risk
Table 2 summarizes information on cagA status for the entire study population. The frequency of cagA-positive status among cases (66.5%) was higher than among controls (22.3%), with . Conditional logistic regression analysis exhibited that, compared to individuals with cagA-negative status, these with cagA-positive status would feature higher GAA risk (OR = 6.38).
3.3. XRCC7 rs#7003908 Polymorphism and GAA Risk
The genotypic distribution of XRCC7 rs#7003908 for both cases and controls is shown in Table 3. The genotypic distribution of this gene in controls was in Hardy-Weinberg equilibrium. The frequencies of rs#7003908 G allele were higher in cases (0.53) than controls (0.28).
The adjusted OR for GAA among those heterozygous for XRCC7 rs#7003908 T and G allele (XRCC7-TG) versus those homozygous for XRCC7 rs#7003908 T alleles (XRCC7-TT) was 2.80 (95% CI, 2.15–3.64). The corresponding OR for those homozygous for XRCC7 rs#7003908 G alleles (XRCC7-GG) was 5.13 (95% CI, 3.71–7.11). Thus, GAA risk was associated with the number of XRCC7 rs#7003908 G alleles.
To assess possible interactive effects of matching factors and XRCC7 rs#7003908 polymorphism on GAA risk, we analyzed this polymorphism stratified by matching factors such as age, sex, ethnicity, alcohol stratus, and smoking status. The results demonstrated similar risk estimates of around 3-fold increased GAA risk for the genotypes with XRCC7 rs#7003908 G alleles (data not shown). Likelihood ratio tests for these matching factors did not substantially modulate the effect of this polymorphism on cancer risk.
3.4. Joint Effects of CagA Status and XRCC7 Polymorphism on GAA Risk
The joint effects of cagA status and XRCC7 genotypes on GAA risk are provided in Table 4. In this analysis, we used as a reference the lowest risk group: those who had XRCC7-TT and cagA-negative status. Results showed that cagA-positive status increased GAA risk; moreover, this risk was more pronounced among subjects with XRCC7 risk genotypes. There was evidence of multiplicatively interactive effects of genotypes and cagA status on GAA risk () according to the previously published formula () [20–22].
3.5. Joint Effects of XRCC7 Polymorphism and XRCC3 Polymorphism on GAA Risk
Because our previous study showed that XRCC3 rs#861539 polymorphism , another DNA repair gene involved in DSBR, modifies Guangxiese GAA risk, we explored possible gene-gene interaction between XRCC7 and XRCC3. Because of the small number of subjects with both the homozygotes of the XRCC3 rs#861539 T alleles (XRCC3-TT) and XRCC7-GG, the combination of these two genes was divided into four strata (Table 5). Results exhibited that individuals with both XRCC7-TG/GG and genotypes of the XRCC3 rs#861539 T alleles (XRCC3-CT/TT), in comparison with those with both XRCC7-TT and homozygotes of the XRCC3 rs#861539 T alleles (XRCC3-TT), might face a higher GAA risk (OR, 3.32, 95% CI, 2.54–4.34). A likelihood ratio test showed that there were multiplicatively interactive effects of XRCC7 and XRCC3 on the GAA risk ().
3.6. XRCC7 Polymorphism and Lauren’s Classification
Because Lauren’s classification of gastric cancer is related to the prognosis and the differentiation of this malignant tumor , we analyzed the distribution of XRCC7 rs#7003908 genotypes in the different Lauren’s type: intestinal type and diffuse type (Table 6). We observed a higher frequency of genotypes with mutant alleles (XRCC7-TG/GG) among GAA patients with diffuse type cancer (93.5%) than among those with intestinal type cancer (70.0%). Logistic regression analysis showed that the corresponding risk value was 5.89 (2.89–1.98), with value of .
Additionally, we also investigated the relationship between this polymorphism and primary tumor sites (cardia versus noncardia) among 120 patients with cardia gastric cancer and 642 GAA patients. Among these cases with cardia gastric cancer, the frequency of XRCC7-TT, -TG, and -GG genotype was 52.3% (63/120), 35.8% (43/120), and 11.7% (14/120), respectively. This suggested that GAA patients, compared with those with cardiac gastric cancer, had higher mutant frequency of XRCC7 rs#7003908. Risk analysis next showed the corresponding ORs (95% CIs) were 2.63 (1.70–4.05) for XRCC7-TG and 5.48 (2.96–10.15) for XRCC7-GG, respectively. However, XRCC7 rs#7003908 polymorphism did not modify cardia gastric cancer risk (, data not shown).
To the best of our knowledge, there has been no report on the association between XRCC7P and the risk of GAA, especially from high H. pylori infection areas. In this hospital-based case-control study, we analyzed the association between aforementioned polymorphism and the risk of GAA among Guangxi population from a high H. pylori infection area. Overall, we found that the genotypes with XRCC7 rs#7003908 G alleles had a substantial association with the increasing risk of GAA among Guangxi population (OR = 3.41). We also observed a significant interactive effect between XRCC7P and H. pylori infection status on GAA risk. These results might imply that this polymorphism may have functional significance in the carcinogenesis of H. pylori infection-related GAA.
GAA is one of the major cancer types in the Guangxi Zhuang Autonomous Region; the most environmental cause of which is high H. pylori infection among Guangxi population [3, 5]. Our previous studies [18, 19] and prevent report also show that GAA patients have higher rate of H. pylori infection. However, increasing epidemiological evidence has shown that although many people are infected with H. pylori, only a relatively small proportion of individuals with chronic H. pylori infection develop GAA . This suggests possible individual susceptibility related to genetic factors such as DNA repair capacity [18, 19, 25, 26].
Among these known genetic factors, the NHEJ genes have been reported as a cancer-correlated genetic factor that plays an important role in the repair of DSBs resulting from exogenous attacks such as cagA [10, 27, 28]. XRCC7 (also known as PRKDC/HYRC/HYRC1) is an important DNA repair gene involved in the NHEJ pathway [13, 14, 29]. This gene is located on chromosome 8q11 and consists of 85 exons and 86 introns . The encoded protein of XRCC7 consists of more than 4,000 amino acid residues and constitutes the large catalytic subunit of DNA-PK complex (DNA-PKcs). When DNA-PKcs is recruited to the site of DSBs by the Ku70/Ku80 heterodimer (another subunit of DNA-PK complex), DNA-PK complex then changes into its active form and subsequently initiates NHEJ repair [11, 14]. Murine mutants defective in the XRCC7 have nondetectable DNA-PK activity, suggesting XRCC7 is required for NHEJ pathway .
More than one hundred polymorphisms have been reported in the XRCC7 gene (dbSNP in NCBI database), some of which are correlated with malignant tumors such as liver cancer [16, 17, 31]. In the present study, we only analyzed XRCC7P, primarily because several studies have shown that this polymorphism may influence the expression of XRCC7 gene and consequently increase the risk of cancers, such as liver, bladder, and prostate cancer [15, 17, 32, 33]. For example, Long et al. investigated the risk effects of XRCC7P on hepatocellular carcinoma (HCC) and found that these individuals carrying XRCC7-GG would face higher cancer risk than those with XRCC7-TT (adjusted OR = 5.04, ) . Similarly, Mandal et al. and Wang et al. also found that this polymorphism might modify the risk of prostate cancer and bladder cancer [32, 33]. Not only did our current data support this hypothesis in view of XRCC7P modifying tumor risk, but we also found that this polymorphism would be able to interact with environmental carcinogens in the process of GAA induced by H. pylori infection. A recent report has shown that XRCC7P increases the levels of DNA adducts and decreases the capacity of NHEJ pathway . Those results suggest that this polymorphism may modulate the normal XRCC7 function, and consequently low NHEJ capacity resulting from XRCC7 function might progress gastric carcinogenesis . Thus, the DNA damage induced by cagA cannot be repaired effectively and duly and, subsequently, may induce genic mutation and gastric mucosal cells canceration. Therefore, XRCC7P may play a role in the carcinogenesis of Guangxiese GAA. In addition, we found some evidence of XRCC7-XRCC3 interactive effects on GAA risk, possibly because this gene-gene interaction results in a more obvious decrease in the NHEJ capacity and consequently correlates with a higher risk for GAA.
In this study, we also investigated the association between XRCC7P and the pathological features of gastric cancer. We observed that these individuals having the mutant genotypes of XRCC7P would feature higher risk of diffuse-type gastric cancer than those with wild genotype of XRCC7P, suggesting that this polymorphism might be correlated with the dedifferentiation of gastric cancer. Furthermore, we also found some evidence of XRCC7P correlating with primary tumor sites of gastric cancer. This is possibly because of the following the reasons: (a) DNA damage induced by H. pylori infection emerging in noncardia gastric mucosa, especially gastric antrum mucosa, because H. pylori mainly infects noncardia gastric mucosa ; (b) high H. pylori infection rate among Guangxi population ; and (c) tissue tumorigenesis and tumor progression easily occurring in these tissues or cells with lots of DNA damage, especially under the condition of low DNA repair capacity [36–38].
When investigating the association between genetic polymorphisms and environmental factors-related cancer risk, it is important to collect sufficiently large samples to test for gene-environment interaction and to avoid the effects of confounders . In this study, the effects of possible confounder, including age, sex, race, and smoking and drinking status, were controlled with an individually matched design. In the stratified analysis, no interactive effects were found, suggesting that these factors do not modify the correlation between XRCC7P and GAA related to H. pylori infection.
In conclusion, this study is, to the best of our knowledge, the first report that describes the polymorphisms in the NHEJ gene XRCC7 and its correlations with H. pylori infection-related GAA risk. We find some evidence to imply that the genotypes of XRCC7 with rs#7003908 G alleles may increase the risk of H. pylori infection-related GAA and the DSBR pathway may play an important role in the mechanism of action of this genotoxin. However, there were several limitations to our study. Although our findings were based on relatively large numbers, potential selection bias might have occurred because the selection of control subjects in our study was hospital-based. Despite XRCC7P being analyzed, we did not investigate the genetic polymorphisms of other DNA repair genes involved in the DSBR such as XRCC5 . Additionally, the relatively small sample size may not have enough power to analyze gene-gene and/or gene-environment interaction. Thus, more genes deserve further elucidation based on a population sample and the combination of genes and H. pylori infection information.
|GAA:||Gastric antrum adenocarcinoma|
|H. pylori:||Helicobacter pylori|
|DSBR:||Double strand break repair|
|PCR:||Polymerase chain reaction|
|XRCC7:||X-ray repair cross-complementing group 7|
|XRCC3-CC:||The homozygotes of XRCC3 rs#861539 C alleles|
|XRCC3-CT:||The heterozygotes of XRCC3 rs#861539 C and T allele|
|XRCC3-CT/TT:||The genotypes with XRCC3 rs#861539 T alleles|
|XRCC3-TT:||The homozygote of XRCC3 rs#861539 T alleles|
|XRCC7-TT:||The homozygotes of XRCC7 rs#7003908 T alleles|
|XRCC7-TG:||The heterozygotes of XRCC7 rs#7003908 T and G allele|
|XRCC7-GG:||The homozygote of XRCC7 rs#7003908 G alleles|
|XRCC7-TG/GG:||The genotypes with XRCC7 rs#7003908 G alleles.|
Conflict of Interests
All authors declare no commercial association, such as consultancies, stock ownership, or other equity interests or patent licensing arrangements.
Chao Wang, Xiao-Ying Huang, and Jin-Guang Yao contributed equally to this work.
We thank Dr. Qiu-Xiang Liang, Dr. Yun Yi, and Dr. Yuan-Feng Zhou for sample collection and management; Dr. Hua Huang for molecular biochemical technique. We also thank all members of Department of Medical Test and Infective Control, Affiliated Hospital of Youjiang Medical College for Nationalities for their help. This study was supported in part by the National Natural Science Foundation of China (nos. 81160255 and 81372639), the Key Science and Natural Project of Guangxi (GuiKeJiZi no. 2008-98), Innovation Program of Shanghai Municipal Education Commission (no. 13YZ035), the Natural Science Foundation of Guangxi (no. 2013GXNSFAA019251), and the Science Foundation of Youjiang Medical College for Nationalities (nos. 2005 and 2008).
- A. Jemal, R. Siegel, J. Xu, and E. Ward, “Cancer statistics, 2010,” CA-Cancer Journal for Clinicians, vol. 60, no. 5, pp. 277–300, 2010.
- D. M. Parkin, F. Bray, J. Ferlay, and P. Pisani, “Global cancer statistics, 2002,” CA-Cancer Journal for Clinicians, vol. 55, no. 2, pp. 74–108, 2005.
- B. C. Y. Wong, S. K. Lam, C. K. Ching et al., “Differential helicobacter pylori infection rates in two contrasting gastric cancer risk regions of South China,” Journal of Gastroenterology and Hepatology, vol. 14, no. 2, pp. 120–125, 1999.
- A. Cervantes, E. Rodríguez Braun, A. Pérez Fidalgo, and I. Chirivella González, “Molecular biology of gastric cancer,” Clinical & Translational Oncology, vol. 9, no. 4, pp. 208–215, 2007.
- Z. Ali, Y. Deng, and C. Ma, “Progress of research in gastric cancer,” Journal of Nanoscience and Nanotechnology, vol. 12, no. 11, pp. 8241–8248, 2012.
- O. Handa, Y. Naito, and T. Yoshikawa, “CagA protein of Helicobacter pylori: a hijacker of gastric epithelial cell signaling,” Biochemical Pharmacology, vol. 73, no. 11, pp. 1697–1702, 2007.
- N. Murata-Kamiya, “Pathophysiological functions of the CagA oncoprotein during infection by Helicobacter pylori,” Microbes and Infection, vol. 13, no. 10, pp. 799–807, 2011.
- A. Izzotti, S. De Flora, C. Cartiglia et al., “Interplay between Helicobacter pylori and host gene polymorphisms in inducing oxidative DNA damage in the gastric mucosa,” Carcinogenesis, vol. 28, no. 4, pp. 892–898, 2007.
- M. S. P. Ladeira, R. C. A. Bueno, B. F. Dos Santos et al., “Relationship among oxidative DNA damage, gastric mucosal density and the relevance of cagA, vacA and iceA genotypes of Helicobacter pylori,” Digestive Diseases and Sciences, vol. 53, no. 1, pp. 248–255, 2008.
- I. M. Toller, K. J. Neelsen, M. Steger et al., “Carcinogenic bacterial pathogen Helicobacter pylori triggers DNA double-strand breaks and a DNA damage response in its host cells,” Proceedings of the National Academy of Sciences of the United States of America, vol. 108, no. 36, pp. 14944–14949, 2011.
- B. Pardo, B. Gómez-González, and A. Aguilera, “DNA double-strand break repair: How to fix a broken relationship,” Cellular and Molecular Life Sciences, vol. 66, no. 6, pp. 1039–1056, 2009.
- A. T. Natarajan and F. Palitti, “DNA repair and chromosomal alterations,” Mutation Research, vol. 657, no. 1, pp. 3–7, 2008.
- B. P. C. Chen, M. Li, and A. Asaithamby, “New insights into the roles of ATM and DNA-PKcs in the cellular response to oxidative stress,” Cancer Letters, vol. 327, no. 1-2, pp. 103–110, 2012.
- E. J. Gapud and B. P. Sleckman, “Unique and redundant functions of ATM and DNA-PKcs during V(D)J recombination,” Cell Cycle, vol. 10, no. 12, pp. 1928–1935, 2011.
- I. Saadat, R. Vakili-Ghartavol, M. Farvardin-Jahromi, and M. Saadat, “Association between exudative age-related macular degeneration and the G6721T polymorphism of XRCC7 in outdoor subjects,” Korean Journal of Ophthalmology, vol. 26, no. 6, pp. 423–427, 2012.
- M. Rahimi, S. Fayaz, A. Fard-Esfahani, M. H. Modarressi, S. M. Akrami, and P. Fard-Esfahani, “The role of Ile3434Thr XRCC7 gene polymorphism in differentiated thyroid cancer risk in an Iranian population,” Iranian Biomedical Journal, vol. 16, no. 4, pp. 218–222, 2012.
- X. D. Long, J. G. Yao, Y. Z. Huang, et al., “DNA repair gene XRCC7 polymorphisms (rs#7003908 and rs#10109984) and hepatocellular carcinoma related to AFB1 exposure among Guangxi population, China,” Hepatology Research, vol. 41, no. 11, pp. 1085–1093, 2011.
- L. Zhao, X.-D. Long, J.-G. Yao et al., “Genetic polymorphism of XRCC3 codon 241 and Helicobacter pylori infection-related gastric antrum adenocarcinoma in Guangxi Population, China: a hospital-based case-control study,” Cancer Epidemiology, vol. 35, no. 6, pp. 564–568, 2011.
- X.-D. Long, Y. Ma, Y.-Z. Huang et al., “Genetic polymorphisms in DNA repair genes XPC, XPD, and XRCC4, and susceptibility to helicobacter pylori infection-related gastric antrum adenocarcinoma in Guangxi population, China,” Molecular Carcinogenesis, vol. 49, no. 6, pp. 611–618, 2010.
- X. D. Long, D. Zhao, C. Wang, et al., “Genetic polymorphisms in DNA repair genes XRCC4 and XRCC5 and aflatoxin B1-related hepatocellular carcinoma,” Epidemiology, vol. 24, no. 5, pp. 671–681, 2013.
- X. D. Long, J. G. Yao, Z. Zeng, et al., “Polymorphisms in the coding region of X-ray repair complementing group 4 and aflatoxin B1-related hepatocellular carcinoma,” Hepatology, vol. 58, no. 1, pp. 171–181, 2013.
- X.-D. Long, Y. Ma, Y.-F. Zhou, A.-M. Ma, and G.-H. Fu, “Polymorphism in xeroderma pigmentosum complementation group C codon 939 and aflatoxin B1-related hepatocellular carcinoma in the Guangxi population,” Hepatology, vol. 52, no. 4, pp. 1301–1309, 2010.
- M. Vauhkonen, H. Vauhkonen, and P. Sipponen, “Pathology and molecular biology of gastric cancer,” Best Practice & Research Clinical Gastroenterology, vol. 20, no. 4, pp. 651–674, 2006.
- J. Parsonnet, G. D. Friedman, N. Orentreich, and H. Vogelman, “Risk for gastric cancer in people with CagA positive or CagA negative Helicobacter pylori infection,” Gut, vol. 40, no. 3, pp. 297–301, 1997.
- C. de Martel, D. Forman, and M. Plummer, “Gastric cancer: epidemiology and risk factors,” Gastroenterology Clinics of North America, vol. 42, no. 2, pp. 219–240, 2013.
- Y. Hong, G. Wang, and R. J. Maier, “A Helicobacter hepaticus catalase mutant is hypersensitive to oxidative stress and suffers increased DNA damage,” Journal of Medical Microbiology, vol. 56, no. 4, pp. 557–562, 2007.
- F. Farinati, R. Cardin, M. Bortolami et al., “Oxidative DNA damage in gastric cancer: CagA status and OGG1 gene polymorphism,” International Journal of Cancer, vol. 123, no. 1, pp. 51–55, 2008.
- O. H. Ambur, T. Davidsen, S. A. Frye et al., “Genome dynamics in major bacterial pathogens,” FEMS Microbiology Reviews, vol. 33, no. 3, pp. 453–470, 2009.
- J. D. Sipley, J. C. Menninger, K. O. Hartley, D. C. Ward, S. P. Jackson, and C. W. Anderson, “Gene for the catalytic subunit of the human DNA-activated protein kinase maps to the site of the XRCC7 gene on chromosome 8,” Proceedings of the National Academy of Sciences of the United States of America, vol. 92, no. 16, pp. 7515–7519, 1995.
- A. Errami, W. J. I. Overkamp, D. M. He et al., “A new X-ray sensitive CHO cell mutant of ionizing radiation group 7, XR- C2, that is defective in DSB repair but has only a mild defect in V(D)J recombination,” Mutation Research, vol. 461, no. 1, pp. 59–69, 2000.
- J. Zhang, X. H. Wu, and Y. Gan, “Current evidence on the relationship between three polymorphisms in the XRCC7 gene and cancer risk,” Molecular Biology Reports, vol. 40, no. 1, pp. 81–86, 2013.
- R. K. Mandal, R. Kapoor, and R. D. Mittal, “Polymorphic variants of DNA repair gene XRCC3 and XRCC7 and risk of prostate cancer: a study from North Indian population,” DNA and Cell Biology, vol. 29, no. 11, pp. 669–674, 2010.
- S.-Y. Wang, L. Peng, C.-P. Li et al., “Genetic variants of the XRCC7 gene involved in DNA repair and risk of human bladder cancer,” International Journal of Urology, vol. 15, no. 6, pp. 534–539, 2008.
- H. S. Lee, G. Choe, K. U. Park et al., “Altered expression of DNA-dependent protein kinase catalytic subunit (DNA-PKcs) during gastric carcinogenesis and its clinical implications on gastric cancer,” International Journal of Oncology, vol. 31, no. 4, pp. 859–866, 2007.
- C. Montecucco and R. Rappuoli, “Living dangerously: how helicobacter pylori survives in the human stomach,” Nature Reviews Molecular Cell Biology, vol. 2, no. 6, pp. 457–466, 2001.
- Q. Xia, X. Y. Huang, F. Xue, et al., “Genetic polymorphisms of DNA repair genes and DNA repair capacity related to aflatoxin b1 (AFB1)-induced DNA damages,” in New Research Directions in DNA Repair, C. Chen, Ed., pp. 377–412, InTech, Rijeka, Croatia, 1st edition, 2013.
- D. M. Wilson III and L. H. Thompson, “Life without DNA repair,” Proceedings of the National Academy of Sciences of the United States of America, vol. 94, no. 24, pp. 12754–12757, 1997.
- W. Yasui, K. Sentani, J. Motoshita, and H. Nakayama, “Molecular pathobiology of gastric cancer,” Scandinavian Journal of Surgery, vol. 95, no. 4, pp. 225–231, 2006.