Skip to main content
NCBI home page
Oncotarget logoLink to Oncotarget
. 2017 Mar 11;8(21):34321–34329. doi: 10.18632/oncotarget.16124

Association between hOGG1 polymorphism rs1052133 and gastric cancer

Dingding Zhang 1,#, Xiaoxin Guo 1,#, Jinliang Hu 2,3,#, Guangqun Zeng 4, Maomin Huang 1,5, Dandan Qi 1, Bo Gong 1
PMCID: PMC5470970  PMID: 28415729

Abstract

Purpose

To conduct a comprehensive evaluation of the association of the human8-oxoguanine glycosylase 1 (hOGG1) gene polymorphism rs1052133 with gastric cancer (GC) through a systematic review and meta-analysis of genetic association study.

Results

A total of 15 articles from published papers were included in our analysis. The meta-analyses for hOGG1 rs1052133, composed of 4024GC patients and 6022controls, showed low heterogeneity for the included populations in all the genetic models, except for the Caucasian population under allelic genetic model, the Asian population under addictive model and Caucasian population under dominant model. The analyses of all the genetic models in overall pooled populations did not identify any significant association between GC and hOGG1 rs1052133 (Allelic model: C vs. G, p = 0.746; Addictive model: CC vs. GG, p = 0.888; Recessive model: CC +GC vs. GG, p = 0.628; Dominant model: CC vs. GG+GC, p = 0.147), even though stratified analyses were conducted in different ethnicities under each genetic model.

Materials and Methods

All case-control association studies on hOGG1 and GC reported up to December 15, 2016 in PubMed, Embase, Web of Science, and the Chinese Biomedical Database were retrieved. Odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated for single-nucleotide polymorphism (SNP) using fixed- and random- effects models according to between-study heterogeneity. Publication bias analyses were conducted using Begg test.

Conclusions

This meta-analysis showed there was no association between hOGG1 rs1052133 and GC. Given the limited sample size, further investigations including more ethnic groups are required to validate the association.

Keywords: gastric cancer, meta-analysis, hOGG1 rs1052133, association

INTRODUCTION

Gastric cancer (GC) is one of the most common cancers and the leading causes of cancer death in the world [1], however, there is a gradually decrease in incidence and mortality rates in most developed countries [2]. GC is a multifactorial disease caused by dietary, genetic and environmental factors [3, 4]. Although the pathogenetic mechanism of GC is very complicated and is still not fully understood, more and more evidence has been shown that there is a correlation between genetic polymorphisms and GC risk [5–7].

To date, many genetic polymorphisms in the carcinogen detoxification, antioxidant protection, DNA repair and cell proliferation processes have been reported to play a crucial role in the development of GC [8]. The human 8-oxoguanine glycosylase 1 (hOGG1) gene, specifically involved in the repair of DNA oxidative damage in the base excision response pathway, has been shown to be associated with a variety of cancers [9–13]. As an important component of DNA repair pathway, hOGG1 encodes a DNA glycosylase enzyme that actively removes 8-hydroy-2-deoxyguanine, which is highly mutagenic and a major form of oxidative DNA damage [14, 15]. The dysfunction of hOGG1 might result in the DNA repair deficiency and then induce gene mutation and cell canceration. Functional studies showed that the hOGG1 variant had normal enzymatic activity, but maintained greater sensitivity to oxidation than wildtype hOGG1 protein [16].

The hOGG1 gene has been regarded as a candidate for involvement in the underlying cause of GC and the hOGG1 polymorphism rs1052133 has been widely evaluated in association with GC across different ethnicities [11, 17–31]. hOGG1 polymorphism rs1052133 has been reported to be associated with an altered risk for GC in Chinese, Japanese and Caucasian populations [11, 18, 19, 32]. However, other reported studies on the association between hOGG1 rs1052133 and GC risk are inconclusive and conflicting [20–31]. Such inconsistence and heterogeneity could be caused by different sample sizes and diversities in multiple ethnic cohorts. Meta-analysis, which combined all studies with the same criteria, could be helpful to comprehensively explain the association of hOGG1 rs1052133 with GC and provide some new clues for the research on GC. Therefore, in this study we conduct a systematic review and meta-analysis of all association studies on hOGG1 rs1052133 with GC, to summarize and evaluate the association between hOGG1 rs1052133 and GC.

RESULTS

Literature search and characteristics

A flow diagram (Figure 1) shows the selection process of studies included in our analysis. The initial search strategy yielded 31 articles. Among them, two review articles were excluded because of the publication type and six articles were excluded because of unrelated topics. The full text of the remaining 23 studies was retrieved and reviewed. Eight articles were excluded after full-text review, five studies were not case-control studies and three articles were experimental studies. Finally, 15 articles were identified that met the inclusion criteria and included for the meta-analysis. The analyzed SNP was successfully genotyped and was within HWE (except the genotype in control subjects from the Takezaki's study) across all the included studies. All of the articles were case-control studies and all the cases were histopathologically confirmed as GC. The characteristics of these included articles are listed in Table 1 and Table 2. The NOS results showed that the score ranged from 7 to 8 with an average of 7.50, which indicated that the methodological quality of these selected articles was generally reliable.

Figure 1. Flow diagram of literature search and study selection for meta-analysis.

Figure 1

Open in a new tab

Table 1. Characteristics of the fifteen studies included in this meta-analysis.

Study Country Study population Ethnicity Study design Genotyping method Mean Age NOS
Case Control Case Control
Lu, et al. 2016 China Chinese Asian CB HB SNaPshot 63.1 ± 10.7 63.3 ± 11.0 8
Hu, et al. 2015 China Chinese Asian HB HB PCR-LDR − − 8
Engin, et al. 2011 Turkey Turkish Others HB HB PCR-RFLP 60.4 ± 1.3 55.5 ±1.3 7
Liu, et al. 2011 China Chinese Asian HB CB PCR-HMR 60.2 ± 10.4 59.3 ± 11.8 8
Canbay, et al. 2010 Turkey Turkish Others CB PB PCR-RFLP 60.1 ± 20.9 52.8 ± 27.2 8
Sun, et al. 2010 China Chinese Asian HB PB PCR-RFLP 59.6 ± 11.2 43.6 ± 10.3 7
Malik, et al. 2010 India Indian Asian CB PB PCR-SSCP 55.9 ± 9.7 58.0 ±12.7 7
Palli, et al. 2010 Italy Italian Caucasian CB PB Taqman 68.8 ± 9.9 55.5 ± 7.0 7
Farinati, et al. 2008 Italy Italian Caucasian CB PB PCR-RFLP 68 46 8
Capella, et al. 2008 Spain Spanish Caucasian CB PB Probe 50.5 ± 20.5 50.5 ± 20.5 8
Poplawskiet al. 2006 Poland Polish Caucasian HB PB PCR-SSCP 62.4 ± 27.4 62.4 ± 27.4 8
Tsukino, et al. 2004 Japan Japanese Asian HB HB PCR-SSCP 57.5 ± 9.5 57.1 ± 9.5 7
Takezaki, et al. 2002 China Chinese Asian CB PB PCR- SSCP 65 ± 15 65 ± 14 7
Hanaoka, et al. 2001 Japan Japanese Brazilian Others HB HB PCR-SSCP 65 ± 13 65 ± 12 7
Hanaoka, et al. 2001 Japan non-Japanese Brazilian Others HB HB PCR-SSCP 59 ± 8 58 ± 8 8
Shinmura, et al. 1998 Japan Japanese Asian HB PB PCR-SSCP − − 7
Open in a new tab

PB, population based; CB, clinic or institute based; HB, hospital based; NOS, Newcastle-Ottawa Scale; -Data unavailable.

Table 2. Genotype frequencies of hOGG1 rs1052133 among gastric cancer cases and controls in the included studies.

Study Sample size Genotypes (Case) Genotypes (Control) Allele Frequency (G) OR, 95%CI
(Allellc Model)		 P
Case Control CC CG GG CC CG GG Case Control
Lu, et al. 2016 1279 1434 477 591 211 525 702 207 0.396 0.389 0.97 (0.87–1.08) 0.604
Hu, et al. 2015 436 372 154 210 72 128 176 68 0.406 0.419 1.06 (0.87–1.29) 0.586
Engin, et al. 2011 106 116 53 42 11 51 47 18 0.302 0.358 1.29 (0.87–1.92) 0.211
Liu, et al. 2011 618 913 114 302 202 144 447 322 0.571 0.594 1.10 (0.95–1.27) 0.199
Canbay, et al. 2010 40 247 24 13 3 171 69 7 0.238 0.168 0.65 (0.37–1.14) 0.131
Sun, et al. 2010 73 255 21 19 33 72 119 64 0.582 0.484 0.67 (0.46–0.98) 0.037
Malik, et al. 2010 108 195 50 51 7 94 89 12 0.301 0.290 0.95 (0.66–1.36) 0.772
Palli, et al. 2010 304 545 192 101 11 325 191 29 0.202 0.228 1.17 (0.92–1.49) 0.212
Farinati, et al. 2008 50 43 33 15 2 36 7 0 0.190 0.081 0.38 (0.15–0.95) 0.033
Capella, et al. 2008 438 1026 279 137 22 621 352 53 0.207 0.223 1.10 (0.91–1.34) 0.320
Poplawski, et al. 2006 28 33 22 6 0 18 15 0 0.107 0.227 2.45 (0.88–6.82) 0.079
Tsukino, 2004 142 271 32 75 35 74 141 56 0.511 0.467 0.84 (0.63–1.12) 0.232
Takezaki, 2002 101 198 20 61 20 30 120 48 0.500 0.545 1.20 (0.85–1.68) 0.292
Hanaoka, 2001 58 127 20 29 9 44 56 27 0.405 0.433 1.12 (0.72–1.75) 0.614
Hanaoka, 2001 208 205 133 67 8 123 74 8 0.200 0.220 1.13 (0.81–1.58) 0.480
Shinmura, 1998 35 42 9 16 10 15 20 7 0.514 0.405 0.64 (0.34–1.22) 0.174
Open in a new tab

MAF, minor allele frequency; OR, odds ratio; CI, confidence intervals; P, p value for Z test.

Meta-analysis results

Fifteen studies provided results of the association of hOGG1 rs1052133 with GC and a total of 10046 subjects (4024GC patients and 6022 controls) were tested for hOGG1 rs1052133 in this meta analysis. Stratified analyses were conducted based on three groups, including Asian [11, 18, 24, 26, 27, 29–31], Caucasian [19, 21, 22, 25] and other ethnicities [20, 23, 28], and the heterogeneity of hOGG1 rs1052133 in Asian, Caucasian, other and pooled populations were evaluated firstly. The results showed low heterogeneity for the included populations under all the genetic models by fixed-effect analysis, except for the Caucasian population under allelic genetic model (P = 0.052, I2 = 61.2%), the Asian population under recessive model (P = 0.021, I2 = 57.6%) and Caucasian population under dominant model (P = 0.054, I2 = 60.7%), the random-effect analysis was thus adopted for them under each genetic model (Table 3).

Table 3. Pooled measure for the association of hOGG1 rs1052133 and gastric cancer different allelic models.

Genetic model Ethnicity Pooled OR( 95% CI) Heterogeneity Test for overall effect Begg test
P I2 (%) Z P P▲
Allelic model ( C vs. G) Asian 0.979 (0.879–1.091) 0.121 38.8 0.38 0.705 0.344
CaucasianΔ 1.085 (0.789–1.492) 0.052 61.2 0.50 0.616
others 1.072 (0.841–1.366) 0.265 24.4 0.56 0.574
Overall 1.016 (0.924–1.117) 0.046 40.6 0.32 0.746
Addictive model (CC vs. GG) Asian 0.973 (0.839–1.130) 0.127 38.0 0.35 0.723 0.235
Caucasian 1.171 (0.778–1.764) 0.351 4.5 0.76 0.450
others 1.210 (0.736–1.989) 0.261 25.0 0.75 0.452
Overall 1.010 (0.883–1.155) 0.186 24.2 0.14 0.888
Recessive model (CC + GC vs. GG) AsianΔ 0.939 (0.830–1.064) 0.021 57.6 1.01 0.313 0.322
Caucasian 1.128 (0.752–1.692) 0.405 0.0 0.61 0.543
others 1.223 (0.765–1.956) 0.300 18.1 0.53 0.594
Overall 0.969 (0.864–1.087) 0.052 40.5 0.48 0.628
Dominant model (CC vs. GG +GC) Asian 1.039 (0.930–1.160) 0.692 0.0 0.68 0.498 0.260
CaucasianΔ 1.136 (0.954–1.353) 0.054 60.7 1.43 0.152
others 1.079 (0.828–1.404) 0.470 0.0 0.56 0.575
Overall 1.067 (0.977–1.165) 0.408 4.0 1.45 0.147
Open in a new tab

* OR, odds ratio; CI, confidence intervals; P, p value for Z test; I2 (%), the value to identify heterogeneity.

Δ Pooling model is random effect (Inverse Variance heterogeneity).

▲ Continuity corrected.

Our meta-analysis showed that there was no significant association of hOGG1 rs1052133 with GC in the overall pooled populations under all the genetic models (Allelic model: C vs. G, OR = 1.016, 95% CI 0.924 to 1.117, p = 0.746; I2 = 40.6;Addictive model: CC vs. GG, OR = 1.010, 95% CI 0.883 to 1.155, p = 0.888; I2 = 24.2; Recessive model: CC +GC vs. GG, OR = 0.969, 95% CI 0.864 to 1.087, p = 0.628; I2 = 40.5; Dominant model: CC vs. GG+GC, OR = 1.067, 95% CI 0.977 to 1.165, p = 0.147; I2 = 4; Table 3). Figure 2 shows the forest plot of estimates of odds ratios of the association of hOGG1 rs1052133 with GC. When stratified analyses were conducted to explore further association of hOGG1 rs1052133 with GC in different ethnicities under each genetic model, no significant association was detected between hOGG1 rs1052133 and GC, either (Table 3 and Figure 2B–2D).

Figure 2. Forest plots for meta-analysis of hOGG1 rs1052133 and the risk for GC.

Figure 2

Open in a new tab

(A) allelic model (C vs. G); (B) addictive genetic model (CC vs. GG); (C) recessive genetic model (CC + GC vs. GG); (D) dominant genetic model (CC vs. GG+GC).

Publication bias and sensitivity analysis

Publication biases were assessed by the Egger's test quantitatively and the result for hOGG1 rs1052133 based on the 15 included studies did not observe any obvious evidence of publication bias in the overall analyses under all genetic models (Table 3 and Figure 3). The effect of each study on the pooled OR was also assessed by sequential omission of individual studies. We did not find that the exclusion of any single study alter the significance of the final pooled OR.

Figure 3. Funnel plot analysis for publication bias between hOGG1 rs1052133 and GC risk.

Figure 3

Open in a new tab

P for publication bias of this funnel plot for dominant model (CCvs.GG+GC) with all 15 studies is 0.260.

DISCUSSION

As a powerful statistical method, meta-analysis could provide a quantitative approach for pooling the variant results on the same topic to estimate and explain their diversity. This led us to conduct this meta-analysis of 15 published case-control studies, which may help us in distinguishing the truth from the false, and to explore a more robust estimate of the effect of hOGG1 rs1052133 on GC. The hOGG1 rs1052133 has been thought to constitute a candidate genetic risk factor for GC [11, 18, 19, 32]; however, several other studies have investigated the genetic effect of hOGG1 rs1052133 on GC susceptibility with conflicting results [20–31]. In this study, our meta-analysis showed there was no association between hOGG1 rs1052133 and GC in all genetic models, suggesting that hOGG1 rs1052133 may not affect individual susceptibility to GC.

GC is considered to be a common, complex and multifactorial disease, and is estimated to have a significant heritable component. GC ranks as the third leading cause of cancer mortality worldwide and confers a 5-year survival of 20% [33]. Identifying causative genes has helped to understand the disease process and may aid in prevention. About 1%–3% of GC could be attributed to inherited cancer predisposition syndromes. More advances have been made in human GC genetics, but there is still to be known [8]. To date, Germline E-cadherin/CDH1 mutations have been identified in families with an autosomal dominant inherited predisposition to diffuse GC [34]. hOGG1 has been reported to be related to GC risk in several studies [11, 18, 19, 32]. It is an important glycosylase enzyme that plays a critical role in the repair of DNA oxidative damage [14, 15]. The dysfunction of hOGG1 might lead to deficiency of DNA repair and result in cell canceration. hOGG1 variant has been shown to exhibit lower DNA repair activity and greater sensitivity to oxidation than wildtype hOGG1 protein [16].

The association between hOGG1 rs1052133 and GC in previous studies were inconsistent. hOGG1 rs1052133 was reported to be significantly associated with GC in Japanese and Chinese patients with GC [11, 18, 19, 32]. However, no evidence of association between hOGG1 rs1052133 and GC was detected in Turkish, Spanish, Italian, Polish and Indian studies [21–25, 28], meanwhile, the association of hOGG1 rs1052133 with GC was not replicated in other Japanese and Chinese populations [20, 26, 27]. Recently, the association between hOGG1 rs1052133 with GC risks was also accessed in Lu et al’ study with 1,275 GC patients and 1,436 controls [29] and in Hu et al's study with 2745 GC patients and 4588 controls [30], respectively. Both the two studies demonstrated that the significant association was not present between hOGG1 rs1052133 and GC. In order to provide powerful statistical analysis, we conduct this study with more samples (a total of 4024GC patients and 6022 controls) to evaluate the association between hOGG1 rs1052133 and GC. Our results did not show any significant association of hOGG1 rs1052133 with GC, even across different ethnic populations. Therefore, our analyses failed to conclude whether hOGG1 rs1052133 is really a GC-associated SNP and more replication data is needed to validate this association. Of course, other factors, such as environment and different lifestyle, might play roles in these differences as well. Further analysis should be performed in more large-scale cohorts or case-control studies to explore the association of hOGG1 rs1052133 with GC. Future studies on gene-environment interaction should also be considered.

This systematic review and meta-analysis has sufficient power to evaluate and review all the published genetics studies in hOGG1 rs1052133, however, some potential limitations of our study on the understanding of hOGG1 in GC genetics should be considered. (1) This meta-analysis was mainly based on the studies with 2950 GC patients and 3817 controls in Japanese and Chinese populations [11, 18, 20, 26, 27, 29–31]. Besides, only 1074 GC patients and 2205 controls in Turkish, Indian, Italian, Spanish and Polish populations were included in the present study. It may restrict our conclusions which indicate the need for larger sample sizes in other ethnic populations. (2) There was a high heterogeneity detected in the Caucasian population under allelic genetic model, in the Asian population under addictive model and in the Caucasian population under dominant model. It is possible that different populations with different clinical patient characteristics were included. (3) GC is a multifactorial disease that results from complex interactions between various genetic factors and other factors. Therefore, our results may be influenced by confronting factors, such as age, gender, environment, and lifestyle. If the investigation of gene-environment interactions in different ethnic subgroups could be carried out, we might get more conclusive claims about the association of hOGG1 rs1052133 with GC.

In conclusion, this meta-analysis showed that hOGG1 rs1052133 is not associated with GC under all the genetic models, suggesting that it may not affect individual susceptibility to GC. Further investigations with larger sample sizes and more ethnic groups are required to validate the association and confirm the roles of hOGG1 in GC.

MATERIALS AND METHODS

Searching strategy

A systematic literature search using the databases PubMed, Embase, Web of Science, and the Chinese Biomedical Database was conducted, to identify all published studies on the association of hOGG1 polymorphisms with GC from their starting date to December 15, 2016. Following keywords were used: ‘‘cancer,’’ ‘‘gastric cancer,’’ ‘‘human 8-oxoguanine glycosylase,’’ ‘‘hOGG1,’’ ‘‘rs1052133,’’ ‘‘polymorphism(s),’’ ‘‘variant(s),’’ and ‘‘mutation(s).’’ The internet was searched using the Google search engine. Reference lists of the retrieved articles and reviews were manually checked for additional articles, to identify studies not yet included in the electronic searches.

Inclusion and exclusion criteria

The eligible articles were considered if they (1) evaluated associations between hOGG1 rs1052133 and GC; (2) used a case–control design to compare GC cases and normal controls in defined populations; (3) gave an OR with 95% CI or other available data from which they could be estimated; and (4) were original research articles, not reviews or comments. Excluded were abstracts from conferences, full texts without raw data available for retrieval, republished data, duplicate studies and reviews.

Data extraction

Two observers (DDZ and XNG) independently abstracted data from all eligible publications onto paper data collection forms. Two reviewers (JLH and GQZ) were blinded to the details (title, author, and academic address) of these studies during assessment. Disagreements were resolved by discussion until a consensus was achieved. Otherwise, a third investigator was consulted to resolve the dispute. The following items were collected from each study: first author's surname, year of publication, statistical data, ethnicity of subjects, whether Hardy-Weinberg equilibrium (HWE) was examined in controls, genotyping method, total numbers of cases and controls, as well as total numbers of cases and controls for each hOGG1genotypes, respectively.

Quality assessment

The Newcastle-Ottawa Scale (NOS) was used to assess the quality of the included studies by two investigators independently. Through the rating system, the NOS was conducted to judge the study quality based on three aspects, which were selection, comparability, and exposure situation in case-control studies. Rating scores range from 0 (worst) to 9 (best). Studies with a score of 7 or greater were thought to have an adequate or good quality.

Statistical analysis

A pooled OR with its corresponding 95% CI was used as a measure of the association of hOGG1 rs1052133 with GC. For genotypic comparison, allelic, addictive, dominant and recessive models were applied in the investigation of the disease association. We conducted stratified analyses by ethnicity, including Asian populations (Japanese, Chinese and Indian), Caucasian populations (Polish, Italian and Spanish), other populations (Turkish, Japanese Brazilian and non-Japanese Brazilian) and pooled populations. Sensitivity analysis was carried out by excluding one study at a time to explore whether the results were influenced by a specific study. Heterogeneity (between-study inconsistency) was investigated and measured using I2 statistic. A p value of I2 < 50% indicated an absence of heterogeneity among studies, the fixed-effect model (Mantel-Haenszel method) was thus used to calculate the pooled ORs. In contrast, if the p value for heterogeneity was I2 ≥ 50%, indicating a high degree of heterogeneity between studies, then the random-effect model (DerSimonian-Laird method) was used to evaluate the summary ORs. Begg liner regression test was used to assess the potential publication bias, where a value of p < 0.05 was considered statistically significant. The Hardy-Weinberg equilibrium (HWE) for each SNP was tested by the χ2 test. All statistical analyses were performed by the Review Manager software (RevMan, version 5.2; The Nordic Cochrane Centre, The Cochrane Collaboration, Copenhagen;2012), and the STATA software (version 12.0, STATA Corp., College Station, TX, USA), as well as the Hardy Weinberg package (version 1.3) in R language (version 2.15.0,http://cran.r-project.org/). Two-sided P values < 0.05 were considered statistically significant.

Acknowledgments

Supported in part by grants from the Natural Science Foundation of China (81670853(B.G.), 81371048 (B.G.), 81470067 (D.Z.) and 81271049 (D.Z.)); grants from Department of Science and Technology of Sichuan Province (2016SZ0022(D.Z.)); grants from health program of Sichuan(2016213(D.Z.)).

Authors’ contributions

Bo Gong conceived and designed the study; Xiaoxin Guo, Guangqun Zeng, Dingding Zhang, Maomin Huang and Dandan Qi collected the data; Jinliang Hu analyzed the data; Bo Gong and Dingding Zhang contributed to the writing of the manuscript.

CONFLICTS OF INTEREST

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

REFERENCES

  • 1.Jemal A, Siegel R, Ward E, Hao Y, Xu J, Thun MJ. Cancer statistics, 2009. CA Cancer J Clin. 2009;59:225–249. doi: 10.3322/caac.20006. [DOI] [PubMed] [Google Scholar]
  • 2.Parkin DM, Bray F, Ferlay J, Pisani P. Global cancer statistics, 2002. CA Cancer J Clin. 2005;55:74–108. doi: 10.3322/canjclin.55.2.74. [DOI] [PubMed] [Google Scholar]
  • 3.Gonzalez CA, Sala N, Capella G. Genetic susceptibility and gastric cancer risk. Int J Cancer. 2002;100:249–260. doi: 10.1002/ijc.10466. [DOI] [PubMed] [Google Scholar]
  • 4.Masuda G, Tokunaga A, Shirakawa T, Togashi A, Kiyama T, Kato S, Matsukura N, Bou H, Watanabe M, Tajiri T. Helicobacter pylori infection, but not genetic polymorphism of CYP2E1, is highly prevalent in gastric cancer patients younger than 40 years. Gastric Cancer. 2007;10:98–103. doi: 10.1007/s10120-007-0414-y. [DOI] [PubMed] [Google Scholar]
  • 5.Gu H, Yang L, Tang N, Zhou B, Zhu H, Sun Q, Cong R, Wang B. Association of endothelin-converting enzyme-1b C-338A polymorphism with gastric cancer risk: a case-control study. Eur J Cancer. 2008;44:1253–1258. doi: 10.1016/j.ejca.2007.09.013. [DOI] [PubMed] [Google Scholar]
  • 6.Qian F, Sun BL, Zhang WY, Ke J, Zhu J. Gly82Ser polymorphism of the receptor for advanced glycation end-product (RAGE) potential high risk in patients with colorectal cancer. Tumour Biol. 2014;35:3171–3175. doi: 10.1007/s13277-013-1414-7. [DOI] [PubMed] [Google Scholar]
  • 7.Yang L, Liu D, Liang S, Guo R, Zhang Z, Xu H, Yang C, Zhu Y. Janus kinase 2 polymorphisms are associated with risk in patients with gastric cancer in a Chinese population. PLoS One. 2013;8:e64628. doi: 10.1371/journal.pone.0064628. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Petrovchich I, Ford JM. Genetic predisposition to gastric cancer. Semin Oncol. 2016;43:554–559. doi: 10.1053/j.seminoncol.2016.08.006. [DOI] [PubMed] [Google Scholar]
  • 9.Zhang J, Dhakal IB, Greene G, Lang NP, Kadlubar FF. Polymorphisms in hOGG1 and XRCC1 and risk of prostate cancer: effects modified by plasma antioxidants. Urology. 2010;75:779–785. doi: 10.1016/j.urology.2009.08.063. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Weiss JM, Goode EL, Ladiges WC, Ulrich CM. Polymorphic variation in hOGG1 and risk of cancer: a review of the functional and epidemiologic literature. Mol Carcinog. 2005;42:127–141. doi: 10.1002/mc.20067. [DOI] [PubMed] [Google Scholar]
  • 11.Tsukino H, Hanaoka T, Otani T, Iwasaki M, Kobayashi M, Hara M, Natsukawa S, Shaura K, Koizumi Y, Kasuga Y, Tsugane S. hOGG1 Ser326Cys polymorphism, interaction with environmental exposures, and gastric cancer risk in Japanese populations. Cancer Sci. 2004;95:977–983. doi: 10.1111/j.1349-7006.2004.tb03186.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Okasaka T, Matsuo K, Suzuki T, Ito H, Hosono S, Kawase T, Watanabe M, Yatabe Y, Hida T, Mitsudomi T, Tanaka H, Yokoi K, Tajima K. hOGG1 Ser326Cys polymorphism and risk of lung cancer by histological type. J Hum Genet. 2009;54:739–745. doi: 10.1038/jhg.2009.108. [DOI] [PubMed] [Google Scholar]
  • 13.Wang W, Dang S, Li Y, Sun M, Jia X, Wang R, Liu J. hOGG1 Ser326Cys polymorphism and risk of hepatocellular carcinoma among East Asians: a meta-analysis. PLoS One. 2013;8:e60178. doi: 10.1371/journal.pone.0060178. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Collins AR, Gaivao I. DNA base excision repair as a biomarker in molecular epidemiology studies. Mol Aspects Med. 2007;28:307–322. doi: 10.1016/j.mam.2007.05.005. [DOI] [PubMed] [Google Scholar]
  • 15.Boiteux S, Radicella JP. The human OGG1 gene: structure, functions, and its implication in the process of carcinogenesis. Arch Biochem Biophys. 2000;377:1–8. doi: 10.1006/abbi.2000.1773. [DOI] [PubMed] [Google Scholar]
  • 16.Kohno T, Shinmura K, Tosaka M, Tani M, Kim SR, Sugimura H, Nohmi T, Kasai H, Yokota J. Genetic polymorphisms and alternative splicing of the hOGG1 gene, that is involved in the repair of 8-hydroxyguanine in damaged DNA. Oncogene. 1998;16:3219–3225. doi: 10.1038/sj.onc.1201872. [DOI] [PubMed] [Google Scholar]
  • 17.Farinati F, Cardin R, Degan P, Rugge M, Mario FD, Bonvicini P, Naccarato R. Oxidative DNA damage accumulation in gastric carcinogenesis. Gut. 1998;42:351–356. doi: 10.1136/gut.42.3.351. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Takezaki T, Gao CM, Wu JZ, Li ZY, Wang JD, Ding JH, Liu YT, Hu X, Xu TL, Tajima K, Sugimura H. hOGG1 Ser(326)Cys polymorphism and modification by environmental factors of stomach cancer risk in Chinese. Int J Cancer. 2002;99:624–627. doi: 10.1002/ijc.10400. [DOI] [PubMed] [Google Scholar]
  • 19.Farinati F, Cardin R, Bortolami M, Nitti D, Basso D, de Bernard M, Cassaro M, Sergio A, Rugge M. Oxidative DNA damage in gastric cancer: CagA status and OGG1 gene polymorphism. Int J Cancer. 2008;123:51–55. doi: 10.1002/ijc.23473. [DOI] [PubMed] [Google Scholar]
  • 20.Hanaoka T, Sugimura H, Nagura K, Ihara M, Li XJ, Hamada GS, Nishimoto I, Kowalski LP, Yokota J, Tsugane S. hOGG1 exon7 polymorphism and gastric cancer in case-control studies of Japanese Brazilians and non-Japanese Brazilians. Cancer Lett. 2001;170:53–61. doi: 10.1016/s0304-3835(01)00565-1. [DOI] [PubMed] [Google Scholar]
  • 21.Poplawski T, Arabski M, Kozirowska D, Blasinska-Morawiec M, Morawiec Z, Morawiec-Bajda A, Klupinska G, Jeziorski A, Chojnacki J, Blasiak J. DNA damage and repair in gastric cancer--a correlation with the hOGG1 and RAD51 genes polymorphisms. Mutat Res. 2006;601:83–91. doi: 10.1016/j.mrfmmm.2006.06.002. [DOI] [PubMed] [Google Scholar]
  • 22.Capella G, Pera G, Sala N, Agudo A, Rico F, Del Giudicce G, Plebani M, Palli D, Boeing H, Bueno-de-Mesquita HB, Carneiro F, Berrino F, Vineis P, et al. DNA repair polymorphisms and the risk of stomach adenocarcinoma and severe chronic gastritis in the EPIC-EURGAST study. Int J Epidemiol. 2008;37:1316–1325. doi: 10.1093/ije/dyn145. [DOI] [PubMed] [Google Scholar]
  • 23.Canbay E, Agachan B, Gulluoglu M, Isbir T, Balik E, Yamaner S, Bulut T, Cacina C, Eraltan IY, Yilmaz A, Bugra D. Possible associations of APE1 polymorphism with susceptibility and HOGG1 polymorphism with prognosis in gastric cancer. Anticancer Res. 2010;30:1359–1364. [PubMed] [Google Scholar]
  • 24.Malik MA, Zargar SA, Mittal B. Lack of influence of DNA repair gene OGG1 codon 326 polymorphisms of gastric cancer risk in the Kashmir valley. Asian Pac J Cancer Prev. 2010;11:165–168. [PubMed] [Google Scholar]
  • 25.Palli D, Polidoro S, D'Errico M, Saieva C, Guarrera S, Calcagnile AS, Sera F, Allione A, Gemma S, Zanna I, Filomena A, Testai E, Caini S, et al. Polymorphic DNA repair and metabolic genes: a multigenic study on gastric cancer. Mutagenesis. 2010;25:569–575. doi: 10.1093/mutage/geq042. [DOI] [PubMed] [Google Scholar]
  • 26.Sun LM, Shang Y, Zeng YM, Deng YY, Cheng JF. HOGG1 polymorphism in atrophic gastritis and gastric cancer after Helicobacter pylori eradication. World J Gastroenterol. 2010;16:4476–4482. doi: 10.3748/wjg.v16.i35.4476. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Liu X, Xiao N, Guo W, Wu Y, Cai Z, He Q, Zhang L, Chen X, Sun C, Wang J, Zhu C, Jin H, Wang Y. The hOGG1 gene 5′-UTR variant c.-53G>C contributes to the risk of gastric cancer but not colorectal cancer in the Chinese population: the functional variation of hOGG1 for gastric cancer risk. J Cancer Res Clin Oncol. 2011;137:1477–1485. doi: 10.1007/s00432-011-1022-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Engin AB, Karahalil B, Engin A, Karakaya AE. DNA repair enzyme polymorphisms and oxidative stress in a Turkish population with gastric carcinoma. Mol Biol Rep. 2011;38:5379–5386. doi: 10.1007/s11033-011-0690-9. [DOI] [PubMed] [Google Scholar]
  • 29.Lu J, Yin Y, Du M, Ma G, Ge Y, Zhang Q, Chu H, Tong N, Wang M, Qiu J, Zhang Z. The association analysis of hOGG1 genetic variants and gastric cancer risk in a Chinese population. Oncotarget. 2016;7:66061–66068. doi: 10.18632/oncotarget.11802. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Hu WG, Pan RJ, Cai W, Wang ZT, Zhu ZG. Lack of association between the hOGG1 gene Ser326Cys polymorphism and gastric cancer risk: evidence from a case-control study and a meta-analysis. Genet Mol Res. 2015;14:14670–14679. doi: 10.4238/2015.November.18.31. [DOI] [PubMed] [Google Scholar]
  • 31.Shinmura K, Kohno T, Kasai H, Koda K, Sugimura H, Yokota J. Infrequent mutations of the hOGG1 gene, that is involved in the excision of 8-hydroxyguanine in damaged DNA, in human gastric cancer. Jpn J Cancer Res. 1998;89:825–828. doi: 10.1111/j.1349-7006.1998.tb00635.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Ni M, Qiu J, He W, Wang X. The functional Ser326Cys polymorphism in hOGG1 is associated with gastric cancer risk: evidence from 1180 cases and 2444 controls. Eur J Gastroenterol Hepatol. 2012;24:683–687. doi: 10.1097/MEG.0b013e328351d1c0. [DOI] [PubMed] [Google Scholar]
  • 33.Torre LA, Bray F, Siegel RL, Ferlay J, Lortet-Tieulent J, Jemal A. Global cancer statistics, 2012. CA Cancer J Clin. 2015;65:87–108. doi: 10.3322/caac.21262. [DOI] [PubMed] [Google Scholar]
  • 34.Oliveira C, Pinheiro H, Figueiredo J, Seruca R, Carneiro F. E-cadherin alterations in hereditary disorders with emphasis on hereditary diffuse gastric cancer. Prog Mol Biol Transl Sci. 2013;116:337–359. doi: 10.1016/B978-0-12-394311-8.00015-7. [DOI] [PubMed] [Google Scholar]

Articles from Oncotarget are provided here courtesy of Impact Journals, LLC

RESOURCES