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Lack of association between gene polymorphisms of Angiotensin converting enzyme, Nod-like receptor 1, Toll-like receptor 4, FAS/FASL and the presence of Helicobacter pylori-induced premalignant gastric lesions and gastric cancer in Caucasians

BMC Medical Genetics volume 12, Article number: 112 (2011) Cite this article

Abstract

Background

Several polymorphisms of genes involved in the immunological recognition of Helicobacter pylori and regulating apoptosis and proliferation have been linked to gastric carcinogenesis, however reported data are partially conflicting. The aim of our study was to evaluate potential associations between the presence of gastric cancer (GC) and high risk atrophic gastritis (HRAG) and polymorphisms of genes encoding Angiotensin converting enzyme (ACE), Nod-like receptor 1 (NOD1), Toll-like receptor 4 (TLR4) and FAS/FASL.

Methods

Gene polymorphisms were analyzed in 574 subjects (GC: n = 114; HRAG: n = 222, controls: n = 238) of Caucasian origin. ACE I/D (rs4646994), NOD1 796G>A (rs5743336), TLR4 3725G>C (rs11536889), FAS 1377G>A (rs2234767), FAS 670A>G (rs1800682) and FASL 844T>C (rs763110) were genotyped by different PCR approaches and restriction fragment length polymorphism analysis.

Results

Frequencies of genotypes in our study are similar to the data reported on subjects of Caucasian ethnicity. There was a tendency for NOD1 796G/G genotype to be associated with increased risk of HRAG (62.4% vs. 54.5% in controls, p = 0.082). FAS 670G/G genotype was more frequent in HRAG when compared to controls, 23.9% and 17.2% respectively, however it failed to reach significance level (p = 0.077). We did not find any significant associations for all polymorphisms in relation to GC or HRAG. NOD1 796G>A and TLR4 3725G>C gene polymorphisms were also not associated with Helicobacter pylori infection.

Conclusions

ACE, NOD1, TRL4 and FAS/FASL gene polymorphisms are not linked with gastric carcinogenesis in Caucasians, and therefore they should not be considered as potential biomarkers for identifying individuals with higher risk for GC.

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Background

Based on the current paradigm, gastric carcinogenesis is considered as multistep process involving complex interplay between Helicobacter pylori (H. pylori) infection, environmental and host genetic factors [1]. In gastric carcinogenesis two distinct pathways have been suggested for intestinal and diffuse type of gastric cancer (GC) (1). Correa et al. [2] demonstrated that H. pylori infection induces chronic inflammation of the gastric mucosa, leading to atrophic gastritis (AG) and intestinal metaplasia (IM), which are regarded as essential predisposing factors in intestinal-type GC development. Many researchers have shown a close relationship between H. pylori not only for intestinal-type GC, but also for diffuse-type GC [3, 4]. Furthermore, although AG and IM are considered as obligatory predisposing factors in intestinal-type GC, the accumulating evidence suggests that AG and IM are at least partially associated with GC of the diffuse-type as well [3]. Up to date, no molecular screening methods are available for sporadic GC, therefore pathogenetic mechanisms involved in different stages of gastric carcinogenesis need to be further elucidated to allow identification of individuals with increased risk for GC. Recent studies have revealed several genetic polymorphisms related to immune-recognition of H. pylori, cell proliferation, and apoptosis pathways that were linked with premalignant gastric conditions and GC, but further research is needed to establish their role in gastric carcinogenesis [5].

Angiotensin I-converting enzyme (ACE) is expressed by different cell types [6] and generates Angiotensin II, which is a key effector in renin-angiotensin system. Recent reports provided evidence that Angiotensin II is involved in the regulation of cell proliferation, angiogenesis and inflammation through the Angiotensin II type 1 receptors, which are expressed on tumor and endothelial cells [7–9]. Insertion (I) or deletion (D) polymorphism of ACE gene was shown to have functional relevance, since the carriers of D allele have higher ACE activity [10]. ACE I/D polymorphism was linked with early development and spread of GC [11], but the studies report null association with the overall risk for GC [12, 13]. ACE I/D polymorphism was not linked with gastric atrophy in Asian subjects [14]. There are however no reports that evaluate the role ACE I/D polymorphism in premalignant gastric conditions in Caucasians and studies addressing the role of ACE I/D polymorphisms in gastric carcinogenesis are limited.

Nucleotide-binding oligomerisation domain 1 (NOD1) is a member of the Nod-like receptors, which is expressed in the cytoplasm of antigen presenting cells and gastric epithelial cells and is involved in recognition of gram-negative bacteria [15]. It is known that stimulation of gastric epithelial cells with NOD1 ligands leads to production of proinflammatory cytokines [16, 17] and NOD1 participates in host defense against mucosal infection with H. pylori infection [17, 18]. Recently NOD1 was found to respond to peptidoglycan delivered by H. pylori cagPAI [19]. Given the significant role of H. pylori in gastric carcinogenesis, it is hypothesized that genetic variations in gene encoding NOD1 receptor could be related to different outcomes. Gene polymorphism 796G>A of NOD1 has been linked with peptic ulcer disease in H. pylori-positive patients [20] and a significant association with very high odds ratios has been recently reported for the risk of premalignant lesions in the antrum of the stomach [21]. Up to date, the data on NOD1 796G>A gene polymorphism remain very scarce and there are no reports concerning the role of this polymorphism in patients with GC.

Another important receptor for the recognition of H. pylori is Toll-like receptor 4 (TLR4), a member of Toll-like receptors family. TLR4 recognizes lipopolysaccharide of gram-negative bacteria, and it is thought to interact with macrophage/monocyte in response to H. pylori infection [22]. Expression of TLR4 by gastric epithelium is upregulated in H. pylori-induced gastritis compared to non-inflamed gastric mucosa [23]. Single nucleotide polymorphisms (SNPs) of TLR4 gene are thought to disrupt the normal structure of the extracellular region of the TLR4 and are therefore hypothesized to decrease responsiveness to lipopolysaccharide through alterations in binding. TLR4 896A>G polymorphism was found to be associated with higher risk of H. pylori-induced GC and its precursors [24]. Recently, a novel polymorphism in TLR4 gene 3725G>C (rs11536889) with functional relevance was identified [25] and linked with severe gastric atrophy in Asian population [26]. This is however the only report on TLR4 3725G>C polymorphism and the potential link with premalignant gastric lesions or GC has not been evaluated yet.

The role of apoptosis in tumor genesis has been well established [27]. The FAS and FASL system plays an important role in regulating apoptotic cell death, initiating the extrinsic pathway of apoptosis [28]. Decreased expression levels of FAS and FASL are associated with different malignancies as well as the progression of gastric carcinoma [29]. Several single nucleotide polymorphisms (SNPs) FAS 1377G>A (rs2234767), FAS 670A>G (rs1800682) and FASL 844T>C (rs763110) were shown to affect gene expression [30, 31]. Liu et al. showed an association between these FAS/FASL gene polymorphisms and higher risk of GC [32], while other studies reported null associations [33, 34]. These polymorphisms were also associated with the risk of atrophic gastritis [35], however the data published on the association with risk for GC are still scarce and there are no reports on the role FAS/FASL polymorphisms with respect to GC in Caucasians.

Given the pathophysiological significance of ACE, NOD1, TLR4, FAS and FASL genes in gastric carcinogenesis, it is intriguing to assess the role of these polymorphisms for the development of GC and H. pylori-associated premalignant gastric lesions. Therefore, the aim of our study was to evaluate potential links between the presence of GC or HRAG and ACE I/D, NOD1 796G>A, TLR4 3725G>C, FAS 1377G>A, FAS 670A>G and FASL 844T>C gene polymorphisms in 114 patients with GC, 222 patients with HRAG and 238 controls of Caucasian origin. This study provides further insights in the puzzle of genetic susceptibility for GC and its precursors.

Methods

Study population

Subjects included in the study came from our previous research groups on IL-1B, IL-1RN and NOD2 gene polymorphisms [36–38]. Patients were recruited at three gastroenterological centers in Germany, Lithuania and Latvia. In Germany, patients with GC, HRAG and healthy controls were recruited from the Department of Gastroenterology of the Otto-von-Guericke University Magdeburg between 1998 and 2008. Patients with HRAG were included from the Out-patient Department, and from a clinical study aimed at the long-term follow up of H. pylori infection. Controls were recruited from clinical studies with healthy volunteers and subjects from the Out-patient Department with dyspeptic symptoms.

In Lithuania and Latvia, patients with HRAG and controls were included from the Out-patient Departments of University Hospitals in Kaunas and Riga. All the individuals were referred for upper endoscopy because of dyspeptic symptoms during the period of 2005-2006.

The inclusion criteria of HRAG and controls were no history of malignancy, gastrointestinal disease or surgery. GC was determined by histology. From all participants, DNA for genotyping was available. In total, 346 individuals (114 GC, 140 HRAG, 92 controls) from Germany and 228 individuals from Lithuania and Latvia (82 HRAG, 146 controls) were included. All patients were of Caucasian ethnicity. The study was approved by the Ethics Committees of the OvG University Magdeburg, Lithuanian University of Health Sciences and University of Latvia, and informed consent to participate in the study was obtained from all subjects included.

Histological analysis and H. pyloristatus

Scoring of atrophic gastritis and intestinal metaplasia was done according to the modified Sydney classification [39]. Histological evaluation for GC type was carried out according to the Laurén classification [40]. HRAG was defined as pan-gastritis (similar inflammatory scores in antrum and corpus), corpus-predominant gastritis with or without the presence of gastric atrophy, and intestinal metaplasia either in antrum or corpus as described by Uemura et al. and Meining et al. [41, 42]. H. pylori status was determined by testing for anti-H. pylori IgG antibodies in sera.

Genotyping

Genomic DNA was extracted from peripheral blood mononuclear cells using the QIAamp DNA blood kit (Qiagen, Hilden, Germany) according to the manufacturer's instructions.

ACE I/D

The ACE I/D genotype (rs4646994) was determined by PCR using primers: forward 5'-CTGGAGACCACTCCCATCCTTTCT-3' and reverse, 5'-GATGTGGCCATCACATTCGTCAGAT-3'. An initial 15 minute denaturation at 95° was followed by 40 cycles of 1 min at 64°C, 1 min at 72°C, and 35 s at 95.5°C. Amplified ACE gene polymorphisms were separated on 1.0% agarose gels, and visualized by ethidium bromide staining. D and I alleles were determined by the presence of 190 or 490 bp fragments (Figure 1).

Figure 1
figure 1

Gene polymorphisms were determined by DNA fragment migration profile on agarose gel and visualized by ethidium bromide staining: A . ACE I/D genotypes: D or I alleles were identified by the presence of 190 or 490 bp fragments B . NOD1 796G>A genotypes: wild-type DNA is visible as a double-band 209 bp and 170 bp ( GG ); the mutated DNA is visible as a single 379 bp band ( AA ); heterozygotes give three bands ( GA ); C . TLR4 3725G>C genotypes: wild-type is visible as a double-band 184 and 397 bp ( GG ), mutated DNA is visible as 256 and 397 bp bands ( CC ); heterozygotes give three bands 184, 256, and 397 bp bands ( GC ). Lane L is a 100 bp molecular weight marker (HyperLadder IV, Bioline GmbH, Berlin, Germany).

Full size image

NOD1 796G>A

The NOD1 796G>A SNP (rs5743336) was analyzed by PCR restriction fragment length polymorphism analysis (PCR-RFLP) with the following primers: forward 5'-TGA GAC CAT CTT CAT CCT GG-3'; reverse 5'-CTT CCC ACT GAG CAG GTT G-3'. An initial 15 minute denaturation at 95° was followed by 40 cycles of 1 min at 64°C, 1 min at 72°C, and 35 s at 95.5°C. For RFLP analysis, the PCR products were digested with AvaI restriction enzyme (Fermentas, Vilnius, Lithuania) at 37°C overnight, studied by gel electrophoresis on a 2% agarose gel and visualized with ethidium bromide staining. The presence of G allele was indicated by cleavage of the 379 bp amplified PCR product to yield fragments of 209 bp and 170 bp (Figure 1).

TLR4 3725G>C

The TLR4 3725G>C SNP (rs11536889) was genotyped using confronting two-pair primers PCR (PCR-CTPP). The primers were F1: TTT GAT GGA CCT CTG AAT CTC, R1: TTT TCT CAA TGA TAA CAT CCA CTC, F2: CTT GAC CAC ATT TTG GGA AC, and R2: TTC CAA TTT CTC TAT ATC CTT GAT GA. An initial 15 minute denaturation at 95° was followed by 40 cycles of 1 min at 64°C, 1 min at 72°C, and 35 s at 95.5°C. The amplified DNA was visualized on a 2% agarose gel with ethidium bromide staining. The amplified DNA was 184 bp for G allele, 256 bp for C allele, and 397 bp for common band (Figure 1).

FAS 1377G>A, FAS 670A>G, FASL 844T>C

SNPs of FAS 1377G>A (rs2234767), FAS 670A>G (rs1800682) and FASL 844T>C (rs763110) were genotyped by using predesigned TaqMan assays with a BioRad CFX96™ real-time cycler, in accordance with the manufacturer's instructions (Bio-Rad Laboratories Inc, Hercules, USA). Thermal cycling conditions for polymerase chain reaction (PCR) were, first, denaturing at 95°C for 10 min, followed by 40 cycles of 95.5°C for 15 s and 60°C for 1 min (Figure 2).

Figure 2
figure 2

Gene polymorphisms of FAS 1377G>A, FAS 670A>G and FASL 844T>C were determined using Taqman genotyping assays with Biorad CFX96™ real-time cycler (Bio-Rad Laboratories Inc, Hercules, USA).

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Statistical analysis

Concordance of genotype frequencies with the Hardy-Weinberg equilibrium was tested by online software http://ihg.gsf.de/cgi-bin/hw/hwa1.pl. Age is shown as means and standard deviations, and was compared using ANOVA and unpaired Student's t-test. Categorical data (e.g. gender, distribution of genotypes or alleles) are presented as frequencies; comparisons were performed using the Chi-square test. Association between HRAG and GC with gene polymorphisms were calculated using unconditional multiple logistic regression analysis and expressed as odds ratios (OR) with 95% confidence intervals (CI). The ORs presented in the study were not adjusted for confounding factors. The relative risks for mutations were studied using recessive and dominant model that led to a comparison between wildtype+heterozygous vs. homozygous and wildtype vs. heterozygous+homozygous, respectively. Statistical analysis was done using statistical software SPSS Version 16.0 (SPSS Inc., Chicago, Illinois, USA).

Results

The characteristics of the study groups are presented in Table 1. German and Baltic study groups did not differ significantly according to the allele distribution (data not shown), therefore the respective groups with HRAG as well as controls were combined and further analyzed together. Patients differed significantly according to age and gender distribution. Male made up for almost 2/3 of patients with GC, while both other groups demonstrated inverse findings. Furthermore, controls were significantly younger (6 or 9 years) than both other groups (Table 1). Notably, serological H. pylori status were similar among the three groups, the proportion of H. pylori-positive subjects was between 59-62%, and did not differ significantly.

Table 1 Characteristics of groups
Full size table

All individuals were successfully genotyped for ACE I/D, FAS 1377G>A, FAS 670A>G and FASL 844T>C polymorphisms. Four subjects were not genotyped for NOD1 796G>A polymorphism and five subjects for TLR4 3725G>C polymorphism. The genotype distributions for all six polymorphisms in control, HRAG and GC groups were similar to those expected for Hardy-Weinberg equilibrium (data not shown). The genotype frequencies of ACE I/D, NOD1 796G>A, TLR4 3725G>C, FAS 1377G>A, FAS 670A>G and FASL 844T>C among different groups are presented in Table 2. Analysis of genotypes and allele frequencies showed similar distribution between GC, HRAG, and controls. We did not find any significant association between all polymorphisms included in our study with respect to GC and HRAG. We also performed an analysis comparing control group with a risk group (combined GC and HRAG subjects); however it did not reveal significant differences in genotype frequencies (Additional file 1, Table S1).

Table 2 Association of ACE, NOD1, TLR4, FAS and FASL gene polymorphisms with gastric cancer and high risk atrophic gastritis
Full size table

We observed a tendency for NOD1 796G/G genotype for increased risk of atrophic gastritis (62.4% vs. 54.5% in controls, p = 0.082). Similarly, NOD1 allele G was more common in patients with HRAG (77.4%) when compared to controls (72.4%), but without significance (p = 0.081). FAS 670G/G genotype was more frequent in HRAG group when compared to controls, 23.9% and 17.2% respectively, however it failed to reach significance level (p = 0.077). The FAS 670G/A genotype was less frequent in HRAG (45.5%) when compared to controls (53.4%), but the difference was not statistically significant (p = 0.091).

We also analyzed the distribution of genotypes with respect to different histological GC types (Additional file 2, Table S2). Histological type of GC was intestinal, diffuse and mixed type in 47, 47 and 20 patients, respectively. In order to compare intestinal and diffuse type GC, mixed tumor types were excluded from subanalysis. ACE D/D polymorphism was found to be less prevalent in diffuse type GC, when compared to controls (27.7% vs. 12.8%, respectively; OR-0.38, 95% CI 0.15-0.94, p = 0.030). There were no differences between different histological subtypes of GC with respect to the other gene polymorphisms. We also analyzed the seropositivity status of H. pylori with respect to TLR4 3725G>C and NOD1 796G>A polymorphisms, but no significant differences in genotype distribution were observed (Table 3).

Table 3 Distribution of NOD1 and TLR4 gene polymorphisms in Helicobacter pylori positive and negative subjects
Full size table

Discussion

Overall, in our study ACE I/D, NOD1 796G>A, TLR4 3725G>C, FAS 1377G>A, FAS 670A>G and FASL 844T>C gene polymorphisms were not associated with the presence of GC or HRAG. Here, we evaluated six genetic polymorphisms related to the immune-recognition of H. pylori, proliferation and apoptosis that were previously described to be associated with increased risk of GC or premalignant gastric lesions in different case-control studies; however reported data are partially conflicting or just based on one study [11–14, 20, 21, 26, 33–35]. Since ACE, NOD1, TLR4, FAS, and FASL have been shown to be involved in gastric carcinogenesis pathways, we expected that the polymorphisms of genes encoding these proteins could be related to GC.

When analyzing ACE I/D polymorphism we hypothesized that carriers of D allele, which was associated with higher ACE activity [10], could have an increased risk of GC. Ebert et al. [11] identified an association of ACE D/D genotype with the development of early GC, and the same group of researchers showed that this genotype is related to the number of metastatic lymph nodes in GC, but not to the overall risk for GC in German subjects [12]. A Japanese study did not find an association between ACE I/D polymorphism and suseptibility to GC [13]. Another Asian study [14] reported that ACE I/D polymorphism carried a higher risk for GC with odds ratio of 1.59, however the same study did not find significant association of ACE polymorhisms with gastric atrophy. ACE I/D genotype frequencies in our study are in line with previous reports [12]. We did not observe significant link between ACE I/D polymorphisms and the risk for GC or HRAG.

Considering the relationship between H. pylori-induced chronic inflammation and carcinogenesis in the stomach it was tempting to speculate that genetic variation in NOD1 receptor, which is involved in bacterial recognition, could be associated with H. pylori-induced diseases. NOD1 796A/A homozygous mutants were linked with increased risk for peptic ulcer disease in a Hungarian study [20]; however they did not find a significant association with atrophic gastritis. A recent study from Turkey [21] found that subjects with NOD1 796A/A genotype had a significantly increased risk for gastric atrophy and antral intestinal metaplasia with very high odds ratios, 34.2 and 39.7 respectively. Such a strong association reported by Kara et al. [21] urged us to evaluate the possible association of this polymorphism in our subjects with GC and HRAG. The genotype frequencies of NOD1 796G>A in this study correspond to previous reports [20, 21]. In our study we observed a tendency for NOD1 796G/G genotype and allele G for increased risk for atrophic gastritis; however the difference did not reach statistical significance. We did not observe an association between NOD1 796G>A gene polymorphism and HRAG or GC. H. pylori seropositivity status was also not linked with NOD1 796G>A genotypes.

Polymorphisms of TLR4 gene are hypothesized to decrease responsiveness to gram-negative bacteria lipopolysaccharide through alterations in binding. In a recent study TLR4 3725G>C polymorphism was indentified as a risk factor for severe gastric atrophy in H. pylori sero-positive Japanese subjects with OR of 1.43 and 1.47 for G/C and C/C genotypes, respectively [26], however in the same study this polymorphism was not associated with the risk for GC. Another study showed a combined effect of TLR4 3725G>C and miR-146a G>C gene polymorphisms for risk of gastric atrophy, but not for GC [43]. Our data on TLR4 3725G>C genotype frequencies are comparable to the reported frequencies in leukemia study on Caucasian population [44]. We did not find significant association between TLR4 3725G>C genotypes and HRAG or GC. There was also no association between H. pylori seropositivity and TLR4 3725G>C genotypes.

There are only few studies that have evaluated the risk for GC in relation to FAS and FASL gene polymorphisms. Reported results are conflicting and cover Asian subjects only. In two Chinese case-control studies FAS and FASL genotypes had no significant associations with risk of GC [33, 34]. Another study from China suggested that FASL 844T/T or T/C and FAS 1377A/A genotypes could be a risk factor for GC in combination with other gene polymorphisms [32]. Hsu et al. [35] have reported that FAS 1377 allele A was a protective factor for developing intestinal metaplasia in the antrum with odds ratio 0.3, while carrying the FASL 844 allele C was a risk factor for developing gastric atrophy in the corpus with OR of 9.4. The distribution of FAS and FASL genotypes in our cohorts corresponds to the frequencies reported on Caucasian subjects in a lung cancer study [45], but we could not provide any evidence that FAS and FASL gene polymorphism are linked with risk for GC or HRAG in Caucasians.

In the present study we evaluated potential links between the risk for GC and several carcinogenesis-related gene polymorphisms that have been rarely or not described, especially in Caucasian population. We did not find significant associations between the presence of GC or HRAG and ACE I/D, NOD1 796G>A, TLR4 3725G>C, FAS 1377G>A, 670A>G and FASL 844T>C gene polymorphisms. We also analyzed the genotype frequencies with respect to different histological GC types. ACE D/D genotype was less prevalent in diffuse-type GC than in controls, however the corresponding subgroups of intestinal and diffuse-type GC are rather small are therefore firm conclusions can not be drawn. Because the studies on ACE I/D, NOD1 796G>A, TLR4 3725G>C, FAS 1377G>A, 670A>G and FASL 844T>C polymorphisms remain limited, evaluation of the association with GC and premalignant gastric lesions requires additional research. Since the strength of the association may depend on the studied population, larger studies of different ethnic groups with different genetic profiles are required. The differences in current data on these polymorphisms may result from study design, H. pylori prevalence, and different histological subtypes of GC. In this study there was no difference in H. pylori positivity among GC, HRAG and control groups. The possible explanation for these findings could be higher prevalence of H. pylori in Baltic countries, when compared to Germany. HRAG and control groups were selected both in Germany and Baltic countries, while GC subjects were recruited only in the German centre, thus possibly affected the H. pylori status within the groups. Alterations in various genes, including oncogenes, tumor-suppressor genes, proinflammatory genes, bacterial recognition and cell-adhesion-related genes have been studied in gastric carcinogenesis [5, 24, 46]. In previous studies we also evaluated the role of IL-1B, IL-1RN and NOD2 gene polymorphisms with respect to risks for GC; however no significant associations were identified [36–38]. Some reports suggested that host genetic factors determine the severity of gastric damage and the eventual clinical outcome of H. pylori infection [47, 48]. These findings however have not been transferred to daily clinical practice, and therefore applicable predisposing genetic factors remain still to be determined.

Conclusions

The study shows that the polymorphisms of ACE, NOD1, TLR4, FAS and FASL genes are not associated with H. pylori-induced premalignant gastric conditions and GC in subjects of Caucasian ethnicity. Based on the data available now, the investigated polymorphisms are not applicable for identifying individuals with higher risk for developing GC.

Abbreviations

GC:

gastric cancer

HRAG:

high risk atrophic gastritis

OR:

odds ratio

CI:

confidence interval

ACE:

Angiotensin converting enzyme

NOD1:

Nod-like receptor 1

TLR4:

Toll-like receptor 4

H. pylori :

Helicobacter pylori

AG:

atrophic gastritis

IM:

intestinal metaplasia

RFLP:

restriction fragment length polymorphism analysis

SNPs:

single nucleotide polymorphisms.

References

  1. Bornschein J, Kandulski A, Selgrad M, Malfertheiner P: From gastric inflammation to gastric cancer. Dig Dis. 2010, 28: 609-614. 10.1159/000320061.

    Article  PubMed  Google Scholar 

  2. Correa P: A human model of gastric carcinogenesis. Cancer Res. 1988, 48: 3554-3560.

    CAS  PubMed  Google Scholar 

  3. Bornschein J, Selgrad M, Warnecke M, Kuester D, Wex T, Malfertheiner P: H. pylori infection is a key risk factor for proximal gastric cancer. Dig Dis Sci. 2010, 55: 3124-3131. 10.1007/s10620-010-1351-x.

    Article  PubMed  Google Scholar 

  4. Komoto K, Haruma K, Kamada T, Tanaka S, Yoshihara M, Sumii K, Kajiyama G, Talley NJ: Helicobacter pylori infection and gastric neoplasia: correlations with histological gastritis and tumor histology. Am J Gastroenterol. 1998, 93: 1271-1276. 10.1111/j.1572-0241.1998.00408.x.

    Article  CAS  PubMed  Google Scholar 

  5. Hishida A, Matsuo K, Goto Y, Hamajima N: Genetic predisposition to Helicobacter pylori-induced gastric precancerous conditions. World J Gastrointest Oncol. 2010, 2: 369-379. 10.4251/wjgo.v2.i10.369.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Bauvois B: Transmembrane proteases in cell growth and invasion: new contributors to angiogenesis?. Oncogene. 2004, 23: 317-329. 10.1038/sj.onc.1207124.

    Article  CAS  PubMed  Google Scholar 

  7. Fujita M, Hayashi I, Yamashina S, Itoman M, Majima M: Blockade of angiotensin AT1a receptor signaling reduces tumor growth, angiogenesis, and metastasis. Biochem Biophys Res Commun. 2002, 294: 441-447. 10.1016/S0006-291X(02)00496-5.

    Article  CAS  PubMed  Google Scholar 

  8. Uemura H, Ishiguro H, Nakaigawa N, Nagashima Y, Miyoshi Y, Fujinami K, Sakaguchi A, Kubota Y: Angiotensin II receptor blocker shows antiproliferative activity in prostate cancer cells: a possibility of tyrosine kinase inhibitor of growth factor. Mol Cancer Ther. 2003, 2: 1139-1147.

    CAS  PubMed  Google Scholar 

  9. Deshayes F, Nahmias C: Angiotensin receptors: a new role in cancer?. Trends Endocrinol Metab. 2005, 16: 293-299. 10.1016/j.tem.2005.07.009.

    Article  CAS  PubMed  Google Scholar 

  10. Rigat B, Hubert C, Alhenc-Gelas F, Cambien F, Corvol P, Soubrier F: An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels. J Clin Invest. 1990, 86: 1343-1346. 10.1172/JCI114844.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Ebert MP, Lendeckel U, Westphal S, Dierkes J, Glas J, Folwaczny C, Roessner A, Stolte M, Malfertheiner P, Rocken C: The angiotensin I-converting enzyme gene insertion/deletion polymorphism is linked to early gastric cancer. Cancer Epidemiol Biomarkers Prev. 2005, 14: 2987-2989. 10.1158/1055-9965.EPI-05-0411.

    Article  CAS  PubMed  Google Scholar 

  12. Röcken C, Röhl FW, Diebler E, Lendeckel U, Pross M, Carl-McGrath S, Ebert MP: The angiotensin II/angiotensin II receptor system correlates with nodal spread in intestinal type gastric cancer. Cancer Epidemiol Biomarkers Prev. 2007, 16: 1206-1212. 10.1158/1055-9965.EPI-05-0934.

    Article  PubMed  Google Scholar 

  13. Sugimoto M, Furuta T, Shirai N, Ikuma M, Sugimura H, Hishida A: Influences of chymase and angiotensin I-converting enzyme gene polymorphisms on gastric cancer risks in Japan. Cancer Epidemiol Biomarkers Prev. 2006, 15: 1929-1934. 10.1158/1055-9965.EPI-06-0339.

    Article  CAS  PubMed  Google Scholar 

  14. Goto Y, Ando T, Nishio K, Ishida Y, Kawai S, Goto H, Hamajima N: The ACE gene polymorphism is associated with the incidence of gastric cancer among H. pylori seropositive subjects with atrophic gastritis. Asian Pac J Cancer Prev. 2005, 6: 464-467.

    PubMed  Google Scholar 

  15. Strober W, Murray PJ, Kitani A, Watanabe T: Signalling pathways and molecular interactions of NOD1 and NOD2. Nat Rev Immunol. 2006, 6: 9-20. 10.1038/nri1747.

    Article  CAS  PubMed  Google Scholar 

  16. Kim JG, Lee SJ, Kagnoff MF: Nod1 is an essential signal transducer in intestinal epithelial cells infected with bacteria that avoid recognition by toll-like receptors. Infect Immun. 2004, 72: 1487-1495. 10.1128/IAI.72.3.1487-1495.2004.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Masumoto J, Yang K, Varambally S, Hasegawa M, Tomlins SA, Qiu S, Fujimoto Y, Kawasaki A, Foster SJ, Foster SJ, Horie Y, Mak TW, Núñez G, Chinnaiyan AM, Fukase K, Inohara N: Nod1 acts as an intracellular receptor to stimulate chemokine production and neutrophil recruitment in vivo. J Exp Med. 2006, 203: 203-213. 10.1084/jem.20051229.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Fukazawa A, Alonso C, Kurachi K, Gupta S, Lesser CF, McCormick BA, Reinecker HC: GEF-H1 mediated control of NOD1 dependent NF-kappaB activation by Shigella effectors. PLoS Pathog. 2008, 4: e1000228-10.1371/journal.ppat.1000228.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Viala J, Chaput C, Boneca IG, Cardona A, Girardin SE, Moran AP, Athman R, Mémet S, Huerre MR, Coyle AJ, DiStefano PS, Sansonetti PJ, Labigne A, Bertin J, Philpott DJ, Ferrero RL: Nod1 responds to peptidoglycan delivered by the Helicobacter pylori cag pathogenicity island. Nat Immunol. 2004, 5: 1166-1174. 10.1038/ni1131.

    Article  CAS  PubMed  Google Scholar 

  20. Hofner P, Gyulai Z, Kiss ZF, Tiszai A, Tiszlavicz L, Toth G, Szoke D, Molnar B, Lonovics J, Tulassay Z, Mándi Y: Genetic polymorphisms of NOD1 and IL-8, but not polymorphisms of TLR4 genes, are associated with Helicobacter pylori-induced duodenal ulcer and gastritis. Helicobacter. 2007, 12: 124-131. 10.1111/j.1523-5378.2007.00481.x.

    Article  CAS  PubMed  Google Scholar 

  21. Kara B, Akkiz H, Doran F, Bayram S, Erken E, Gumurdullu Y, Sandikci M: The significance of E266K polymorphism in the NOD1 gene on Helicobacter pylori infection: an effective force on pathogenesis?. Clin Exp Med. 2010, 10: 107-112. 10.1007/s10238-009-0077-6.

    Article  CAS  PubMed  Google Scholar 

  22. Maeda S, Akanuma M, Mitsuno Y, Hirata Y, Ogura K, Yoshida H, Shiratori Y, Omata M: Distinct mechanism of Helicobacter pylori-mediated NF-kappa B activation between gastric cancer cells and monocytic cells. J Biol Chem. 2001, 276: 44856-44864. 10.1074/jbc.M105381200.

    Article  CAS  PubMed  Google Scholar 

  23. Schmausser B, Andrulis M, Endrich S, Lee SK, Josenhans C, Müller-Hermelink HK, Eck M: Expression and subcellular distribution of toll-like receptors TLR4, TLR5 and TLR9 on the gastric epithelium in Helicobacter pylori infection. Clin Exp Immunol. 2004, 136: 521-526. 10.1111/j.1365-2249.2004.02464.x.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. El-Omar EM, Ng MT, Hold GL: Polymorphisms in Toll-like receptor genes and risk of cancer. Oncogene. 2008, 27: 244-252. 10.1038/sj.onc.1210912.

    Article  CAS  PubMed  Google Scholar 

  25. Fukusaki T, Ohara N, Hara Y, Yoshimura A, Yoshiura K: Evidence for association between a Toll-like receptor 4 gene polymorphism and moderate/severe periodontitis in the Japanese population. J Periodontal Res. 2007, 42: 541-545. 10.1111/j.1600-0765.2007.00979.x.

    Article  CAS  PubMed  Google Scholar 

  26. Hishida A, Matsuo K, Goto Y, Mitsuda Y, Hiraki A, Naito M, Wakai K, Tajima K, Hamajima N: Toll-like receptor 4 +3725 G/C polymorphism, Helicobacter pylori seropositivity, and the risk of gastric atrophy and gastric cancer in Japanese. Helicobacter. 2009, 14: 47-53. 10.1111/j.1523-5378.2009.00659.x.

    Article  CAS  PubMed  Google Scholar 

  27. Zörnig M, Hueber A, Baum W, Evan G: Apoptosis regulators and their role in tumorigenesis. Biochim Biophys Acta. 2001, 1551: F1-37.

    PubMed  Google Scholar 

  28. Suda T, Takahashi T, Golstein P, Nagata S: Molecular cloning and expression of the Fas ligand, a novel member of the tumor necrosis factor family. Cell. 1993, 75: 1169-1178. 10.1016/0092-8674(93)90326-L.

    Article  CAS  PubMed  Google Scholar 

  29. Takahama Y, Yamada Y, Emoto K, Fujimoto H, Takayama T, Ueno M, Uchida H, Hirao S, Mizuno T, Nakajima Y: The prognostic significance of overexpression of the decoy receptor for Fas ligand (DcR3) in patients with gastric carcinomas. Gastric Cancer. 2002, 5: 61-68. 10.1007/s101200200011.

    Article  CAS  PubMed  Google Scholar 

  30. Kanemitsu S, Ihara K, Saifddin A, Otsuka T, Takeuchi T, Nagayama J, Kuwano M, Hara T: A functional polymorphism in fas (CD95/APO-1) gene promoter associated with systemic lupus erythematosus. J Rheumatol. 2002, 29: 1183-1188.

    CAS  PubMed  Google Scholar 

  31. Sibley K, Rollinson S, Allan JM, Smith AG, Law GR, Roddam PL, Skibola CF, Smith MT, Morgan GJ: Functional FAS promoter polymorphisms are associated with increased risk of acute myeloid leukemia. Cancer Res. 2003, 63: 4327-4330.

    CAS  PubMed  Google Scholar 

  32. Liu L, Wu C, Wang Y, Zhong R, Wang F, Zhang X, Duan S, Lou J, Yu D, Tan W, Yuan J, Wu T, Nie S, Miao X, Lin D: Association of candidate genetic variations with gastric cardia adenocarcinoma in Chinese population: a multiple interaction analysis. Carcinogenesis. 2011, 32: 336-342. 10.1093/carcin/bgq264.

    Article  CAS  PubMed  Google Scholar 

  33. Wang M, Wu D, Tan M, Gong W, Xue H, Shen H, Zhang Z: FAS and FAS ligand polymorphisms in the promoter regions and risk of gastric cancer in Southern China. Biochem Genet. 2009, 47: 559-568. 10.1007/s10528-009-9264-0.

    Article  CAS  PubMed  Google Scholar 

  34. Zhou RM, Wang N, Chen ZF, Duan YN, Sun DL, Li Y: Polymorphisms in promoter region of FAS and FASL gene and risk of cardia gastric adenocarcinoma. J Gastroenterol Hepatol. 2010, 25: 555-561. 10.1111/j.1440-1746.2009.06116.x.

    Article  CAS  PubMed  Google Scholar 

  35. Hsu PI, Lu PJ, Wang EM, Ger LP, Lo GH, Tsay FW, Chen TA, Yang HB, Chen HC, Lin WS, Lai KH: Polymorphisms of death pathway genes FAS and FASL and risk of premalignant gastric lesions. Anticancer Res. 2008, 28: 97-103.

    CAS  PubMed  Google Scholar 

  36. Wex T, Ebert MP, Kropf S, Dierkes J, Schüttler K, Röcken C, Höcker M, Malfertheiner P: Gene polymorphisms of the NOD-2/CARD-15 gene and the risk of gastric cancer in Germany. Anticancer Res. 2008, 28: 757-762.

    CAS  PubMed  Google Scholar 

  37. Wex T, Leodolter A, Bornschein J, Kuester D, Kähne T, Kropf S, Albrecht C, Naumann M, Roessner A, Malfertheiner P: Interleukin 1 beta (IL1B) gene polymorphisms are not associated with gastric carcinogenesis in Germany. Anticancer Res. 2010, 30: 505-511.

    CAS  PubMed  Google Scholar 

  38. Kupcinskas L, Wex T, Kupcinskas J, Leja M, Ivanauskas A, Jonaitis LV, Janciauskas D, Kiudelis G, Funka K, Sudraba A, Chiu HM, Lin JT, Malfertheiner P: Interleukin-1B and interleukin-1 receptor antagonist gene polymorphisms are not associated with premalignant gastric conditions: a combined haplotype analysis. Eur J Gastroenterol Hepatol. 2010, 22: 1189-1195. 10.1097/MEG.0b013e32833cf3d5.

    Article  CAS  PubMed  Google Scholar 

  39. Dixon MF, Genta RM, Yardley JH, Correa P: Classification and grading of gastritis. The updated Sydney System. International Workshop on the Histopathology of Gastritis, Houston 1994. Am J Surg Pathol. 1996, 20: 1161-1181.

    Article  CAS  PubMed  Google Scholar 

  40. Lauren P: The two histological main types of gastric carcinoma: diffuse and so called intestinal-type carcinoma. An attempt at a histo-clinical classification. Acta Pathol Microbiol Scand. 1965, 64: 31-49.

    CAS  PubMed  Google Scholar 

  41. Uemura N, Okamoto S, Yamamoto S, Matsumura N, Yamaguchi S, Yamakido M, Taniyama K, Sasaki N, Schlemper RJ: Helicobacter pylori infection and the development of gastric cancer. N Engl J Med. 2001, 345: 784-789. 10.1056/NEJMoa001999.

    Article  CAS  PubMed  Google Scholar 

  42. Meining A, Bayerdörffer E, Müller P, Miehlke S, Lehn N, Hölzel D, Hatz R, Stolte M: Gastric carcinoma risk index in patients infected with Helicobacter pylori. Virchows Arch. 1998, 432: 311-314. 10.1007/s004280050171.

    Article  CAS  PubMed  Google Scholar 

  43. Hishida A, Matsuo K, Goto Y, Naito M, Wakai K, Tajima K, Hamajima N: Combined effect of miR-146a rs2910164 G/C polymorphism and Toll-like receptor 4 +3725 G/C polymorphism on the risk of severe gastric atrophy in Japanese. Dig Dis Sci. 2011, 56: 1131-1137. 10.1007/s10620-010-1376-1.

    Article  CAS  PubMed  Google Scholar 

  44. Miedema KG, Te Poele EM, Tissing WJ, Postma DS, Koppelman GH, de Pagter AP, Kamps WA, Alizadeh BZ, Boezen HM, de Bont ES: Association of polymorphisms in the TLR4 gene with the risk of developing neutropenia in children with leukemia. Leukemia. 2011, 25: 995-1000. 10.1038/leu.2011.27.

    Article  CAS  PubMed  Google Scholar 

  45. Ter-Minassian M, Zhai R, Asomaning K, Su L, Zhou W, Liu G, Heist RS, Lynch TJ, Wain JC, Lin X, De Vivo I, Christiani DC: Apoptosis gene polymorphisms, age, smoking and the risk of non-small cell lung cancer. Carcinogenesis. 2008, 29: 2147-2152. 10.1093/carcin/bgn205.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Perri F, Piepoli A, Bonvicini C, Gentile A, Quitadamo M, Di Candia M, Cotugno R, Cattaneo F, Zagari MR, Ricciardiello L, et al: Cytokine gene polymorphisms in gastric cancer patients from two Italian areas at high and low cancer prevalence. Cytokine. 2005, 30: 293-302. 10.1016/j.cyto.2005.01.011.

    Article  CAS  PubMed  Google Scholar 

  47. El-Omar EM, Carrington M, Chow WH, McColl KE, Bream JH, Young HA, Herrera J, Lissowska J, Yuan CC, Rothman N, Lanyon G, Martin M, Fraumeni JF, Rabkin CS: Interleukin-1 polymorphisms associated with increased risk of gastric cancer. Nature. 2000, 404: 398-402. 10.1038/35006081.

    Article  CAS  PubMed  Google Scholar 

  48. Machado JC, Figueiredo C, Canedo P, Pharoah P, Carvalho R, Nabais S, Castro Alves C, Campos ML, Van Doorn LJ, Caldas C, Seruca R, Carneiro F, Sobrinho-Simões M: A proinflammatory genetic profile increases the risk for chronic atrophic gastritis and gastric carcinoma. Gastroenterology. 2003, 125: 364-371. 10.1016/S0016-5085(03)00899-0.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

We thank Ursula Stolz and Marion Holley for their support in this study. The study was partially co-funded by Ministries of Education and Research in Latvia and Lithuania, by Science Foundation of Lithuanian University of Health Sciences and State Research Program in Health in Latvia. The study was funded by the "LOM-Program" of the Medical Faculty of the Otto-von-Guericke University Magdeburg.

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    Authors and Affiliations

    1. Department of Gastroenterology, Lithuanian University of Health Sciences, Eiveniu 2, 50009, Kaunas, Lithuania

      Juozas Kupcinskas, Gediminas Kiudelis & Laimas Jonaitis

    2. Clinic of Gastroenterology, Hepatology and Infectious Diseases, Otto von Guericke University, Leipziger Str. 44, 39120, Magdeburg, Germany

      Thomas Wex, Jan Bornschein, Michael Selgrad & Peter Malfertheiner

    3. Faculty of Medicine, University of Latvia, Digestive Diseases Center, Hospital Lizeners, 6 Linezera iela, LV1006, Riga, Latvia

      Marcis Leja

    4. Department of Oncology, Lithuanian University of Health Sciences, Eiveniu 2, 50009, Kaunas, Lithuania

      Elona Juozaityte

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    The authors declare that they have no competing interests.

    Authors' contributions

    JK performed acquisition of data, SNP genotyping, statistical analysis, drafted the manuscript; TW was involved in study design, coordination, drafting and final revision of the manuscript; JB, MS, EJ, GK, LJ performed acquisition of data; ML was involved in study design and data collection; PM was involved in study design, and final revision of the manuscript. All authors read and approved the final manuscript.

    Juozas Kupcinskas, Thomas Wex contributed equally to this work.

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    12881_2011_843_MOESM1_ESM.DOC

    Additional file 1: Table S1. Distribution of ACE, NOD1, TLR4, FAS and FASL gene polymorphisms in control and risk group (gastric cancer and high risk atrophic gastritis patients). (DOC 58 KB)

    12881_2011_843_MOESM2_ESM.DOC

    Additional file 2: Table S2. Distribution of ACE, NOD1, TLR4, FAS and FASL gene polymorphisms in controls, intestinal and diffuse type gastric cancer groups. (DOC 106 KB)

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    Kupcinskas, J., Wex, T., Bornschein, J. et al. Lack of association between gene polymorphisms of Angiotensin converting enzyme, Nod-like receptor 1, Toll-like receptor 4, FAS/FASL and the presence of Helicobacter pylori-induced premalignant gastric lesions and gastric cancer in Caucasians. BMC Med Genet 12, 112 (2011). https://0-doi-org.brum.beds.ac.uk/10.1186/1471-2350-12-112

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