de Oliveira JG, Silva AE. Polymorphisms of the TLR2 and TLR4 genes are associated with risk of gastric cancer in a Brazilian population. World J Gastroenterol 2012; 18(11): 1235-1242
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Ana Elizabete Silva, PhD, Department of Biology, UNESP- São Paulo State University, Rua Cristóvão Colombo, 2265, São José do Rio Preto Campus, 15054-000 SP, Brazil. firstname.lastname@example.org
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Polymorphisms of the TLR2 and TLR4 genes are associated with risk of gastric cancer in a Brazilian population
Juliana Garcia de Oliveira, Ana Elizabete Silva
Juliana Garcia de Oliveira, Ana Elizabete Silva, Department of Biology, UNESP- São Paulo State University, São José do Rio Preto Campus, 15054-000 SP, Brazil
ORCID number: $[AuthorORCIDs]
Author contributions: de Oliveira JG performed the research, analysed the data and drafted the article; Silva AE conceived and designed the research, and critically revised the manuscript.
Supported by The São Paulo State Research Foundation, No. 2010/00507-0; and CNPq, No. 471908/2010-0
Correspondence to: Ana Elizabete Silva, PhD, Department of Biology, UNESP- São Paulo State University, Rua Cristóvão Colombo, 2265, São José do Rio Preto Campus, 15054-000 SP, Brazil. email@example.com
Telephone: +55-17-32212384 Fax: +55-17-32212390
Received: November 29, 2010 Revised: May 7, 2011 Accepted: February 27, 2012 Published online: March 21, 2012
AIM: To investigate toll-like receptor 2 (TLR2) -196 to -174 del, and TLR4 (+896A/G rs4986790 and +1196C/T rs4986791) polymorphisms at risk of chronic gastritis and gastric cancer in a Brazilian population and association of gastric lesions with risk factors such as smoking, alcohol intake and Helicobacter pylori infection.
METHODS: In this case-control study, polymorphism at TLR2 -196 to -174 del was investigated by using the allele-specific polymerase chain reaction (PCR) method, while the PCR-restriction fragment length polymorphism technique was carried out to identify the TLR4 (rs4986790 and rs4986791) genotypes in 607 Brazilian individuals (208 with chronic gastritis-CG, 174 with gastric cancer-GC and 225 controls -C).
RESULTS: The single nucleotide polymorphisms TLR4+1196C/T was not associated with risk of chronic gastritis or gastric cancer and the homozygous genotypes TLR4+896GG and TLR4+1196TT were absent in the studied population. However, the frequency of TLR2 -196 to -174 ins/del + del/del and TLR4+896AG genotypes was significantly higher (P < 0.01 and P = 0.01, respectively) in the cancer group (33.4% and 11.5%, respectively) than in the control group (16.9% and 4.5%, respectively). It was also observed that the G-C haplotype of the TLR4+896A/G+1196C/T (P = 0.02) and the combination of variant alleles of the TLR2/TLR4+896G (P = 0.02) are associated with susceptibility to gastric cancer. In addition, the multiple logistic regression showed that male gender [odds ratio (OR) = 2.70; 95% CI: 1.66-4.41; P < 0.01], alcohol intake (OR = 2.93; 95% CI: 1.76-4.87; P < 0.01), TLR2 -196 to -174 del (OR = 2.64; 95% CI: 1.56-4.44; P < 0.01) and TLR4+896G (OR = 3.19; 95% CI: 1.34- 7.61; P < 0.01) polymorphisms were associated with a higher susceptibility to developing this neoplasm.
CONCLUSION: Our data indicate that TLR2 -196 to -174 del and TLR4+896G may increase the risk of gastric cancer in a Brazilian population.
Citation: de Oliveira JG, Silva AE. Polymorphisms of the TLR2 and TLR4 genes are associated with risk of gastric cancer in a Brazilian population. World J Gastroenterol 2012; 18(11): 1235-1242
Gastric cancer is one of the most serious health problems in many countries, including Brazil, which ranks third in incidence and mortality, and with an estimated incidence in 2010 of about 21 500 new cases, with an incidence of 14.25 per 100 000 males and 7.70 per 100 000 females. The Helicobacter polori (H. pylori) is the major etiological risk factor for this malignancy, which progresses through a multi-step process, developing from gastritis, to gastric atrophy, intestinal metaplasia, dysplasia, and finally to carcinoma. It is widely accepted that chronic H. pylori infection induces a gastric atrophy and hypochlorhydria, which are precursors of all pathophysiological changes of gastric carcinogenesis. However, colonization with H. pylori can lead to various outcomes. Nearly all H. pylori positive subjects have chronic gastritis, and only 1%-2% development of stomach cancer among infected. Hence, other factors are likely to be involved in gastric tumorigenesis such as host genetic factors, as well as the diversity of H. pylori virulence genes.
Host genetic factors, as polymorphisms in inflammatory and immune response genes, are mainly related to the recognition of the bacteria by the immune system and the variation in the level of cytokine response. Among host factors, several inflammatory proteins including cytokines, growth factors, and chemokines have been known to control immune response against H. pylori infection[6,7]. Therefore, many studies have focused on the analyses of polymorphisms in genes associated with the inflammatory response in the gastric mucosa and risk for malignancy[8-11]. Other mediators also have polymorphic variants that modulate the innate immune response pattern, as the toll-like receptors (TLRs), which provide first line of host defense against harmful pathogens.
Among the TLRs, it has been reported that the TLR2, lipoproteins bacterial receptor and the TLR4, the lipopolysaccharide (LPS) receptor, are involved in the response to infection by H. pylori on gastric epithelial cells[3,13-15]. Both the TLR2 and the TLR4 promote transcription of genes involved in immune activation including nuclear factor kappa B (NF-κB) and also mintage-activated protein (MAP) kinase pathways. TLR4 is up regulated in gastric epithelial cell lines infected with H. pylori and in macrophages and expression of TLR4 protein has been demonstrated in chronic active gastritis, in precancerous lesions, and also in gastric tumor cells. TLR2 activates NF-κB in epithelial cells, in response to H. pylori infection, causing the expression of interleukin (IL)-8, macrophage inflammatory protein-3α and growth-regulated oncogene alpha. Thus, it is conceivable that functionally relevant polymorphisms in TLR genes can alter the host immune response to pathogens as infection induced by H. pylori.
Single nucleotide polymorphisms (SNPs) in TLR2 have been associated with susceptibility to various infectious and inflammatory diseases such as leprosy, increased risk of Gram-negative sepsis, asthma, recurrent bacterial infections and sporadic colorectal cancer susceptibility. The specific polymorphism TLR2 -196 to -174 del/del genotype has been reported to show decreased transcriptional activity of the TLR2 gene. Such fact aroused the interest for this polymorphism, and previous studies in the Japanese population demonstrated its association with increased susceptibility to non-cardia gastric cancer and intestinal metaplasia.
Likewise, the TLR4 presents some polymorphisms implicated in increased susceptibility to various diseases such as atherosclerosis, asthma, malaria, and also infection with the H. pylori associated with gastric cancer and its precursors. Two SNPs in TLR4+896A/G (rs4986790) and +1196C/T (rs4986791) have received special attention in some studies, although the results are still controversial[6,28,29].
Therefore, the aim of this study was to evaluate the influence of the 22-bp nucleotide deletion -196 to –174 del, in the promoter region of the gene TLR2 and +896A/G and +1196C/T polymorphisms (Asp299Gly and Thr399Ile) respectively in TLR4 gene on the risk of chronic gastritis and gastric cancer in a Brazilian population and whether there is an association of gastric lesions with risk factors such as smoking, alcohol intake and H. pylori infection.
MATERIALS AND METHODS
This was a case-control study on chronic gastritis and gastric cancer, in which a total of 607 DNA samples from peripheral blood leukocytes were genotyped. The case groups comprised 208 individuals (102 men and 106 women) with a histopathologically confirmed diagnosis of chronic gastritis - CG (Sidney System), with a mean age of 52.8 + 14.5 years (range 19 to 84 years), and 174 individuals (134 men and 40 women) with a histopathologically confirmed diagnosis of gastric cancer - GC (Lauren’s classification), with a mean age of 62.2 ± 12.2 years (range 28 to 93 years). All subjects were recruited from the Hospital de Base in São José do Rio Preto, SP, and from the Pio XII Foundation in Barretos, SP, Brazil. H. pylori infection was histologically established either by the Giemsa staining technique or by the urease test, performed at the Pathology Services of the Hospital de Base and the Pio XII Foundation. Results of H. pylori infection were obtained for the available cases. The cancer-free control group (C) with no previous history of gastric disease was composed of 225 healthy individuals (112 men and 113 women), mainly blood donors, with a mean age of 56.5 + 18.1 years (range 20 to 93 years). Epidemiological data on the study population were collected using a standard interviewer-administered questionnaire, with questions about current and past occupation, smoking habits, alcohol intake and family history of cancer. All the individuals were ethnically classified on their visual appearance as Caucasians in the three groups evaluated. The few cases of African descent were excluded from the study (about 10%).
The National Research Ethics Committee approved this work, and written informed consent was obtained from all individuals.
About 5 mL of whole blood were collected from all study participants in sterile EDTA-coated vacutainers. DNA was extracted according to a previous report, and stored at -20 °C until use for genotyping.
Polymorphism at TLR2 -196 to -174 del was investigated using the allele-specific polymerase chain reaction (PCR) method, and the PCR-restriction fragment length polymorphism (RFLP) technique was carried out in order to identify the TLR4 (rs4986790 and rs4986791) genotype[33,34] in cases and control groups. In brief, the procedure was carried in a total reaction volume of 25 μL, containing 2.5 μL 10 × PCR buffer, 2 μL deoxyribonucleotide triphosphatess (1.25 μmol/L), 0.5 μL MgCl2 (25 mmol/L), 1.25 μL of each primer (25 mmol/L, Sigma-Aldrich, United States), 15.3 μL dH2O, 2 μL DNA (100 ng/μL), and 0.2 μL Taq DNA polymerase (5 U/μL, Invitrogen, United States). PCR for TLR2 -196 to -174 del was as follows: initial denaturation step at 95 °C for 5 min, amplification was carried out by 35 cycles at 95 °C for 30 s, at 60 °C for 40 s, and at 72 °C for 40 s, followed by a final elongation cycle at 72 °C for 7 min (Table 1). PCR for both TLR4 polymorphisms were as follows: after an initial denaturation step at 94 °C for 3 min, amplification was carried out by 30 cycles at 94 °C for 30 s, at 62 °C for 30 s, and at 72 °C for 30 s, followed by a final elongation cycle at 72 °C for 7 min. Then, 10 μL of TLR4 +896 A/G and TLR4 +1196 C/T polymorphism PCR products were digested with 0.5 μL (5 U/μL) of the BstXI and HinfI specific enzymes, respectively in a 10 μL volume including 2.5 μL 10 × buffer 1 (New England Biolabs, United States) and 7.0 μL dH2O (Table 1). The products were then electrophoresed on a 3% agarose 1000 (Invitrogen, United States) gel, to allow detection by ethidium bromide staining.
Table 1 Primer sequences, restriction enzymes and fragment sizes for toll-like receptor 2 and toll-like receptor 4 gene polymorphisms and interleukin-1β gene.
del -196 to -174
ins/del: 286, 264
F: 5’-AGCATACTTAGACTACCACCTCGATG 3’
R: 5’-GTTGCCATCCGAAATTATAAGAAAAG 3’
37 °C, 1 h
A/G: 131, 108
37 °C, 1 h
C/T: 407, 378
37 °C, 1 h
37 °C, 1 h
TLR: Toll-like receptor; IL: Interleukin; To: Temperature.
In order to confirm the veracity of the results, one confirmed polymorphic case was used as positive control for every RFLP procedure, to attest the good functioning of the restriction enzyme. For the TLR4+896A/G (rs4986790) and +1196C/T (rs4986791) polymorphisms, we also used other fragments of the TLR2 and IL-1β gene that was known to have the enzyme recognition site to verify the correct functioning of the enzymes BstXI and HinfI (Table 1), considering we did not detect any polymorphic homozigous subjects.
Fisher’s exact test was used to compare the groups regarding genotype and allele frequencies, and the chi-square test for determining Hardy-Weinberg equilibrium. Multiple logistic regression models were used to determine the effects of the variables in gastric cancer and chronic gastritis. The models included age (reference: < 61 and 53 years old - median of the groups), gender (reference: female), smoking habits (reference: nonsmokers), drinking habits (reference: nondrinkers), and H. pylori infection (reference: H. pylori-negative). The results are shown as odds ratio (OR), showing 95% CI. ORs were calculated using a dominant model due to low frequency of polymorphic homozygous (i.e., combining heterozygous and homozygous for the minor allele vs homozygous for the major allele) for all SNPs. The haplotype frequencies of TLR4 were inferred by Haploview program (4.0 version). Statistical analyses were performed using the GraphPad Instat, and SPSS (11.5 version) computer software programs. A probability level (P) of less that 0.05 was adopted as a significance criterion.
The samples of the 607 subjects were genotyped for the TLR2 -196 to -174 del and TLR4 (+896A/G rs4986790 and +1196C/T rs4986791). The genotype and allele frequencies for these polymorphisms are presented in Table 2. The genotype and allele frequency distribution of the three polymorphisms complied with Hardy-Weinberg equilibrium in both cases and control groups (data not shown). The banding patterns of these SNPs are represented in Figure 1.
Figure 1 Eletrophoretic pattern of fragments generated by polymerase chain reaction-allele specific and polymerase chain reaction-restriction fragment length polymorphism for the polymorphisms.
A: Toll-like receptor (TLR)2 -196 to -174 del: ins/ins = 286 bp; ins/del = 286 + 264 bp; del/del = 264 bp; B: TLR4 + 896A/G: A/A = 131 bp; A/G = 131 + 108 bp and positive control of enzyme BstXI, TLR2 gene fragment of 286 bp with the enzyme cutting site: 188 + 98 bp (last lane); C: TLR4 + 1196 C/T: C/C = 407 bp; C/T: 407 + 378 bp and positive control of enzyme HinfI, interleukin-1β gene fragment of 370 bp with the enzyme cutting site: 195 + 175 bp (last lane). M: Molecular weight marker of 100 bp.
Table 2 Genotype and allele frequencies of toll-like receptor 2 (-196 to -174 del) and toll-like receptor 4 (rs4986790 and rs4986791) polymorphisms in gastric cancer, chronic gastritis and control groups.
For TLR2 -196 to -174 del, the genotype (ins/del and del/del) and allele (del) frequencies were increased statistically (P < 0.01) in gastric cancer group (33.4% and 19% respectively) than in control group (16.0% and 8.5% respectively). In addition, among the groups of chronic gastritis (13.0%) and control (8.5%), the allele frequencies (del) was statistically significant (P = 0.02).
Similarly, for TLR4+896A/G (rs4986790), the genotypes (A/G) and allele (G) frequencies were increased statistically in gastric cancer group (11.5% and 6.0%, respectively; P = 0.01) and chronic gastritis (10.1% and 5.0%, respectively; P = 0.02) than in control group (4.5% and 3%, respectively). This results due to the higher frequency of polymorphic allele (TLR4 +896G) in the gastric cancer and chronic gastritis groups.
In contrast, for TLR4+1196C/T (rs4986791), no significant difference was found between gastric cancer and control group (Table 2). Homozygous genotypes TLR4+896GG and TLR4+1196TT were absent in the studied population. We also compared the genotype and allele frequencies between gastric cancer and gastritis groups and no significant difference was found for the polymorphisms studied (data not shown).
The TLR4 haplotype analysis (Table 3) demonstrated higher frequency of both wild alleles (haplotype A-C) in control subjects compared with gastric cancer (95.7% and 91.4%, respectively; P < 0.01). However, the opposite was observed for frequency of variant haplotype G-C, which was higher in the gastric cancer group compared with control group (63.0% and 31.0%, respectively; P = 0.02).
Table 3 Toll-like receptor 4 haplotype frequency distribution between gastric cancer, chronic gastritis and control groups.
Haplotype G-T not found. NF: Not found; GC: Gastric cancer; CG: Chronic gastritis; C: Control.
In another statistical analysis, which evaluated the combined effect between the three polymorphisms (TLR2 -196 to -174 del, TLR4+896A/G and +1196C/T), the combination of variant alleles of the polymorphisms TLR2 ins/del and del/del with TLR4 +896 AG showed a higher risk of gastric cancer compared to healthy individuals (OR = 4.13; 95% CI: 1.26-13.50; P = 0.02). The other combinations of variant alleles did not show any significant difference (Table 4). The combination of the three variant alleles was found in only one individual of the group of chronic gastritis (data not shown).
Table 4 Combined effect of toll-like receptor 2 (-196 to -174 del) and toll-like receptor 4 (rs4986790 and rs4986791) polymorphisms on risk of gastric cancer and chronic gastritis.
The potential associations between the distributions of TLR2 -196 to -174 del and TLR4 (+896A/G and +1196C/T) genotypes adjusting for risk factors for gastric cancer and chronic gastritis in comparison of control group are presented in Table 5.
Table 5 Distribution of risk factors, genotypes of toll-like receptor 2 (-196 to -174 del) and toll-like receptor 4 (rs4986790 and rs4986791), and odds ratios for gastric cancer, chronic gastritis and control groups.
F (GC/C) %
OR (95% CI)
F (CG/C) %
OR (95% CI)
0.99 (0.66 -1.48)
(< 53 yr) Reference
(≥ 53 yr) 0.64 (0.43-0.95)
1.39 (0.84 -2.28)
TLR4 +896A/G (rs4986790)
TLR4 +1196C/T (rs4986791)
F: Frequency of individual (%); OR: Odds ratio; GC: Gastric cancer; CG: Chronic gastritis; C: Control; TLR: Toll-like receptor.
In the gastric cancer group, the multiple logistic regression shows that male gender (OR = 2.7; 95% CI: 1.66-4.41; P < 0.01), alcohol intake (OR = 2.93; 95% CI: 1.76-4.87; P < 0.01), TLR2 -196 to -174 ins/del+del/del (OR = 2.64; 95% CI: 1.56-4.44; P < 0.01) and TLR4 +896AG (OR = 3.19; 95% CI: 1.34-7.61; P < 0.01) were associated with a higher susceptibility to developing this neoplasm. The comparison between gastritis and control group showed that only TLR4+896AG polymorphism was associated with risk of chronic gastritis (OR = 2.29; 95% CI: 1.02-5.13; P = 0.04), while age above 53 years (OR = 0.64; 95% CI: 0.43-0.95; P = 0.03) and smoking (OR = 0.57; 95% CI: 0.37-0.87; P = 0.01) were negatively associated with the development of gastritis. In another multiple logistic regression analysis considering also the individuals tested for H. pylori infection (95 with gastric cancer and 177 with gastritis), there was no statistically significant association (OR = 0.73, 95% CI: 0.29-1.78; P = 0.49, data not shown in Table 5). There was also no association of three polymorphisms with H. pylori when evaluated negative and positive individuals within a group of gastric cancer and gastritis (data not shown).
TLRs participate in H. pylori bacterium recognition in gastric mucosa, and SNPs in TLRs are associated with impaired immune response, inducing a potent inflammatory response. Therefore, it is relevant to carry out studies on host genetic factors that can be associated with susceptibility of gastric diseases. Hence, we investigated whether TLR2 -196 to –174 del and TLR4 (+896A/G rs4986790 and +1196C/T rs4986791) polymorphisms affect the risk of developing gastric cancer and chronic gastritis in a Brazilian population. Our results have demonstrated for the first time in this population, an association of TLR2 -196 to -174 del and of TLR4+896 G polymorphisms with susceptibility to gastric cancer. The polymorphism TLR4+1196 T was not associated with risk to the gastric lesions evaluated, and the homozygous genotypes TLR4+896GG and TLR4+1196TT were absent in the studied population.
Some studies that investigated the association of TLR2 -196 to -174 del polymorphisms at risk of developing diseases related to an inflammatory process have shown conflicting results. For instance, del allele or del/del genotype of TLR2 -196 to-174 polymorphism was significantly associated with cervical cancer susceptibility and risk of non-cardia gastric cancer in a Japanese population, but not for gastritis, gastric ulcer and duodenal ulcer, while TLR2 -196 to -174 ins allele was associated with more severe intestinal metaplasia in older patients. However, Wang et al failed to show association of TLR2 -196 to -174 del/del and ins/del carriers with ulcerative colitis.
The -196 to -174 del polymorphism in TLR2 gene located on chromosome 4, causes a 22-bp nucleotide deletion that alters the promoter activity of gene. The TLR2 del/del genotype is reported to show decreased transcriptional activity this gene. In our study, we observed significantly higher frequencies of genotypes TLR2 ins/del and del/del in the gastric cancer group compared to the healthy individuals, emphasizing its role in the gastric carcinogenesis.
The TLR4 gene is mapped on chromosome 9 and consists of three exons. In exon 3, two non-synonymous SNPs TLR4+896A/G and +1196C/T allows the substitution of amino acids Asp299Gly and Thr399Ile, respectively. In the analysis by Haploview, the frequencies of TLR4 G-C (299Gly-399Thr) and G allele were higher in patients with gastric cancer indicating an association of this haplotype with increased risk of gastric cancer to its carriers. The substitution of Asp299Gly amino acids disrupt the normal structure of the extracellular region of the TLR4 and may cause decreased ligand recognition or protein interaction, and decreased responsiveness to lipopolysaccharide, disrupting transport of TLR4 to the cell membrane[13,37]. This change leads to an exaggerated inflammatory response with severe tissue destruction, likely due to a failure in stimulating regulatory cells and production of IL-10 cytokine. Arbour et al were the first to report that individuals having either the Asp299Gly and/or Thr399Ile polymorphisms had a blunted response towards inhaled LPS. Thus, during the cascade of progression of gastric carcinogenesis, the subjects with this polymorphism can have an increased risk of severe inflammation followed by development of hypochlorhydria and gastric atrophy, which are regarded as important precursor alterations of gastric cancer.
Both SNPs in TLR4 are presented in about 10% of Caucasian and African populations and are reported to have a positive correlation with susceptibility to infectious diseases, whereas studies in Asian populations have shown the absence of these polymorphisms[26,39]. However, in our study with a Southeastern Brazilian population, we found that both SNPs TLR4 (+896A/G and +1196C/T) were present in heterozygous in about 4.5% to 11.5% and 2.7% to 5.2% respectively in the gastric cancer and control groups. Other studies in the Brazilian population found similar frequencies of heterozygous TLR4+896A/G polymorphism in Chagas disease (5.6%), ulcerative colitis (7.1%) and Crohn’s disease (7%)[40,41]. But, to the best of our knowledge, there are not studies on TLR2 and TLR4 polymorphisms in gastric cancer of Brazilian population.
With regards to TLR4+896A/G and +1196C/T polymorphisms, Garza-Gonzalez et al showed no association with the risk of gastric cancer in the Mexican population, while Trejo de la O et al observed that both SNPs in TLR4 had an association with duodenal ulcer and gastric cancer also in Mexican patients. Yet, other studies have demonstrated association with only one of these polymorphisms and risk of gastric cancer and precancerous lesions, either TLR4+1196C/T (Thr399Ile)[6,42] or TLR4+896A/G (Asp299Gly) polymorphisms are associated with susceptibility to gastric carcinogenesis. In addition, in this study in Caucasian population, homozygous polymorphic TLR4+896 GG was not found, corroborating our results.
Concerning H. pylori infection, we evaluated the association between TLR2 and TLR4 polymorphisms in the case groups with the available information in their medical records (95 with gastric cancer and 177 with gastritis) and no association was found. The reduced number of samples available for statistical analysis may have harmed these results. Rad et al studied the role of various TLRs (2/4/7 and 9) in response to H. pylori using mice mutants lacking these receptors. The results demonstrated the importance of the TLR2 in response to this bacterium, unlike the TLR4. TLR4-receptor lacking mice had little or no change in response to H. pylori compared with controls. Although the role that the effect of polymorphism in TLR2 in the activity of this receptor in gastric cells is not fully understood, this deletion is likely to alter their activity. Since TLR2 has an important role in immune response against the H. pylori bacterium, the change of its function becomes relevant in carcinogenesis of the stomach.
Besides the influence of the H. pylori, other risk factors as gender, age, smoking and alcohol intake were analyzed. There are statistically significant results for male gender and alcohol intake in the gastric cancer group compared with the control group. According to the National Cancer Institute the highest incidence of gastric cancer occurs in men around age 70 years, and about 65% of patients diagnosed with this type of cancer were over 50 years. Another risk factor well established in the literature in relation to gastric carcinogenesis is the excessive consumption of alcohol[43-45]. Really, ethanol oxidation generates acetaldehyde, which presents carcinogenic effects, since it interferes with many DNA synthesis and repair sites, leading to tumor development.
In conclusion, our findings indicate a significant role of both TLR2 -196 to -174 del and TLR4+896G (Asp299Gly) polymorphic variant with susceptibility to gastric cancer in the Southeastern Brazilian population evaluated, whereas no association was observed for TLR4 +1196T polymorphism. Thus, it is feasible to highlight that host genetic factors as the interaction of polymorphisms in genes of toll-like receptors can play an important role in gastric carcinogenesis.
Gastric cancer (GC) has high rate of incidence and mortality in Brazilian population. Thus is important to establish host genetic factors, as polymorphisms in genes related with inflammatory and immune response associated with higher risk of development of this neoplasia. In this study, authors have shown, for the first time association of toll-like receptor (TLR)2 -196 to -174 del and TLR4+896AG (Asp299Gly) polymorphisms with gastric cancer in a sample of Brazilian population.
Epidemiological studies on association of polymorphisms with susceptibility to disease as cancer frequently present conflicting results, possibly due to different factors as ethnicity, sample number, population sub-sampling, which can contribute to this discrepancy. Thus, are relevant studies in different populations that help clarify these aspects.
Innovations and breakthroughs
In this study it was possible to make the combined analysis of three polymorphisms (TLR2 -196 to -174 del, TLR4+896A/G and +1196C/T) and to show that the combination of single nucleotide polymorphisms TLR2 ins/del and del/del with TLR4 +896 AG led to a higher risk of gastric cancer.
Considering the high incidence of gastric cancer in the Brazilian population, the data show that carriers of polymorphisms in genes involved with immune response as TLR2 ins/del and del/del and TLR4 +896 AG, together with other genetic and environmental factors constitute a risk group to gastric carcinogenesis.
This is a cross sectional study on the role of the TLR2 and TLR4 polymorphisms in GC in a Brazilian population. The main point that needs to be further clarified is the ethnic composition of the population. An important observation is that the TLR4 variants are at similar frequencies on the African and Caucasian populations.
Peer reviewers: Sung-Gil Chi, Professor, School of Life Sciences and Biotechnology, Korea University, No. 301, Nok-Ji Building, Seoul 136-701, South Korea; Peter Laszlo Lakatos, MD, PhD, Associate Professor, 1st Department of Medicine, Semmelweis University, Koranyi S 2A, H1083-Budapest, Hungary; Ross McManus, PhD, Senior Lecturer in Molecular Medicine, Institute of Molecular Medicine and Department of Clinical Medicine, Trinity Centre for Health Science, St. James's Hospital, Dublin 8, Ireland
Correa P. A human model of gastric carcinogenesis.Cancer Res. 1988;48:3554-3560.
Hold GL, Rabkin CS, Chow WH, Smith MG, Gammon MD, Risch HA, Vaughan TL, McColl KE, Lissowska J, Zatonski W. A functional polymorphism of toll-like receptor 4 gene increases risk of gastric carcinoma and its precursors.Gastroenterology. 2007;132:905-912.
Scholte GH, van Doorn LJ, Cats A, Bloemena E, Lindeman J, Quint WG, Meuwissen SG, Kuipers EJ. Genotyping of Helicobacter pylori in paraffin-embedded gastric biopsy specimens: relation to histological parameters and effects on therapy.Am J Gastroenterol. 2002;97:1687-1695.
Garza-González E, Bosques-Padilla FJ, El-Omar E, Hold G, Tijerina-Menchaca R, Maldonado-Garza HJ, Pérez-Pérez GI. Role of the polymorphic IL-1B, IL-1RN and TNF-A genes in distal gastric cancer in Mexico.Int J Cancer. 2005;114:237-241.
Achyut BR, Ghoshal UC, Moorchung N, Mittal B. Association of Toll-like receptor-4 (Asp299Gly and Thr399Ileu) gene polymorphisms with gastritis and precancerous lesions.Hum Immunol. 2007;68:901-907.
Trejo-de la O A, Torres J, Pérez-Rodríguez M, Camorlinga-Ponce M, Luna LF, Abdo-Francis JM, Lazcano E, Maldonado-Bernal C. TLR4 single-nucleotide polymorphisms alter mucosal cytokine and chemokine patterns in Mexican patients with Helicobacter pylori-associated gastroduodenal diseases.Clin Immunol. 2008;129:333-340.
Rad R, Ballhorn W, Voland P, Eisenächer K, Mages J, Rad L, Ferstl R, Lang R, Wagner H, Schmid RM. Extracellular and intracellular pattern recognition receptors cooperate in the recognition of Helicobacter pylori.Gastroenterology. 2009;136:2247-2257.
Kumar S, Kumar A, Dixit VK. Evidences showing association of interleukin-1B polymorphisms with increased risk of gastric cancer in an Indian population.Biochem Biophys Res Commun. 2009;387:456-460.
Melo Barbosa HP, Martins LC, Dos Santos SE, Demachki S, Assumpção MB, Aragão CD, de Oliveira Corvelo TC. Interleukin-1 and TNF-alpha polymorphisms and Helicobacter pylori in a Brazilian Amazon population.World J Gastroenterol. 2009;15:1465-1471.
Partida-Rodríguez O, Torres J, Flores-Luna L, Camorlinga M, Nieves-Ramírez M, Lazcano E, Perez-Rodríguez M. Polymorphisms in TNF and HSP-70 show a significant association with gastric cancer and duodenal ulcer.Int J Cancer. 2010;126:1861-1868.
El-Omar EM, Ng MT, Hold GL. Polymorphisms in Toll-like receptor genes and risk of cancer.Oncogene. 2008;27:244-252.
Arbour NC, Lorenz E, Schutte BC, Zabner J, Kline JN, Jones M, Frees K, Watt JL, Schwartz DA. TLR4 mutations are associated with endotoxin hyporesponsiveness in humans.Nat Genet. 2000;25:187-191.
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.
Ding SZ, Torok AM, Smith MF, Goldberg JB. Toll-like receptor 2-mediated gene expression in epithelial cells during Helicobacter pylori infection.Helicobacter. 2005;10:193-204.
Seya T, Shime H, Ebihara T, Oshiumi H, Matsumoto M. Pattern recognition receptors of innate immunity and their application to tumor immunotherapy.Cancer Sci. 2010;101:313-320.
Kang TJ, Chae GT. Detection of Toll-like receptor 2 (TLR2) mutation in the lepromatous leprosy patients.FEMS Immunol Med Microbiol. 2001;31:53-58.
Schröder NW, Morath S, Alexander C, Hamann L, Hartung T, Zähringer U, Göbel UB, Weber JR, Schumann RR. Lipoteichoic acid (LTA) of Streptococcus pneumoniae and Staphylococcus aureus activates immune cells via Toll-like receptor (TLR)-2, lipopolysaccharide-binding protein (LBP), and CD14, whereas TLR-4 and MD-2 are not involved.J Biol Chem. 2003;278:15587-15594.
Eder W, Klimecki W, Yu L, von Mutius E, Riedler J, Braun-Fahrländer C, Nowak D, Martinez FD. Toll-like receptor 2 as a major gene for asthma in children of European farmers.J Allergy Clin Immunol. 2004;113:482-488.
Kutukculer N, Yeniay BS, Aksu G, Berdeli A. Arg753Gln polymorphism of the human toll-like receptor-2 gene in children with recurrent febrile infections.Biochem Genet. 2007;45:507-514.
Boraska Jelavić T, Barisić M, Drmic Hofman I, Boraska V, Vrdoljak E, Peruzović M, Hozo I, Puljiz Z, Terzić J. Microsatelite GT polymorphism in the toll-like receptor 2 is associated with colorectal cancer.Clin Genet. 2006;70:156-160.
Noguchi E, Nishimura F, Fukai H, Kim J, Ichikawa K, Shibasaki M, Arinami T. An association study of asthma and total serum immunoglobin E levels for Toll-like receptor polymorphisms in a Japanese population.Clin Exp Allergy. 2004;34:177-183.
Tahara T, Arisawa T, Wang F, Shibata T, Nakamura M, Sakata M, Hirata I, Nakano H. Toll-like receptor 2 -196 to 174del polymorphism influences the susceptibility of Japanese people to gastric cancer.Cancer Sci. 2007;98:1790-1794.
Tahara T, Arisawa T, Wang F, Shibata T, Nakamura M, Sakata M, Hirata I, Nakano H. Toll-like receptor 2 (TLR) -196 to 174del polymorphism in gastro-duodenal diseases in Japanese population.Dig Dis Sci. 2008;53:919-924.
Kiechl S, Wiedermann CJ, Willeit J. Toll-like receptor 4 and atherogenesis.Ann Med. 2003;35:164-171.
Mockenhaupt FP, Cramer JP, Hamann L, Stegemann MS, Eckert J, Oh NR, Otchwemah RN, Dietz E, Ehrhardt S, Schröder NW. Toll-like receptor (TLR) polymorphisms in African children: common TLR-4 variants predispose to severe malaria.J Commun Dis. 2006;38:230-245.
Lorenz E, Frees KL, Schwartz DA. Determination of the TLR4 genotype using allele-specific PCR.Biotechniques. 2001;31:22-24.
Wu MS, Cheng TY, Shun CT, Lin MT, Chen LC, Lin JT. Functional polymorphisms of CD14 and toll-like receptor 4 in Taiwanese Chinese with Helicobacter pylori-related gastric malignancies.Hepatogastroenterology. 2006;53:807-810.
Garza-Gonzalez E, Bosques-Padilla FJ, Mendoza-Ibarra SI, Flores-Gutierrez JP, Maldonado-Garza HJ, Perez-Perez GI. Assessment of the toll-like receptor 4 Asp299Gly, Thr399Ile and interleukin-8 -251 polymorphisms in the risk for the development of distal gastric cancer.BMC Cancer. 2007;7:70.
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.
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.
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells.Nucleic Acids Res. 1988;16:1215.
Lachheb J, Dhifallah IB, Chelbi H, Hamzaoui K, Hamzaoui A. Toll-like receptors and CD14 genes polymorphisms and susceptibility to asthma in Tunisian children.Tissue Antigens. 2008;71:417-425.
Soares SC, Abé-Sandes K, Nascimento Filho VB, Nunes FM, Silva WA. Genetic polymorphisms in TLR4, CR1 and Duffy genes are not associated with malaria resistance in patients from Baixo Amazonas region, Brazil.Genet Mol Res. 2008;7:1011-1019.
Pandey S, Mittal RD, Srivastava M, Srivastava K, Singh S, Srivastava S, Mittal B. Impact of Toll-like receptors [TLR] 2 (-196 to -174 del) and TLR 4 (Asp299Gly, Thr399Ile) in cervical cancer susceptibility in North Indian women.Gynecol Oncol. 2009;114:501-505.
Wang F, Tahara T, Arisawa T, Shibata T, Nakamura M, Fujita H, Iwata M, Kamiya Y, Nagasaka M, Takahama K. Genetic polymorphisms of CD14 and Toll-like receptor-2 (TLR2) in patients with ulcerative colitis.J Gastroenterol Hepatol. 2007;22:925-929.
Schröder NW, Schumann RR. Non-LPS targets and actions of LPS binding protein (LBP).J Endotoxin Res. 2005;11:237-242.
Higgins SC, Lavelle EC, McCann C, Keogh B, McNeela E, Byrne P, O'Gorman B, Jarnicki A, McGuirk P, Mills KH. Toll-like receptor 4-mediated innate IL-10 activates antigen-specific regulatory T cells and confers resistance to Bordetella pertussis by inhibiting inflammatory pathology.J Immunol. 2003;171:3119-3127.
Cheng PL, Eng HL, Chou MH, You HL, Lin TM. Genetic polymorphisms of viral infection-associated Toll-like receptors in Chinese population.Transl Res. 2007;150:311-318.
Queiroz DM, Oliveira AG, Saraiva IE, Rocha GA, Rocha AM, das Graças Pimenta Sanna M, Guerra JB, Dani R, Ferrari Mde L, Castro LP. Immune response and gene polymorphism profiles in Crohn's disease and ulcerative colitis.Inflamm Bowel Dis. 2009;15:353-358.
Ramasawmy R, Cunha-Neto E, Fae KC, Borba SC, Teixeira PC, Ferreira SC, Goldberg AC, Ianni B, Mady C, Kalil J. Heterozygosity for the S180L variant of MAL/TIRAP, a gene expressing an adaptor protein in the Toll-like receptor pathway, is associated with lower risk of developing chronic Chagas cardiomyopathy.J Infect Dis. 2009;199:1838-1845.
Santini D, Angeletti S, Ruzzo A, Dicuonzo G, Galluzzo S, Vincenzi B, Calvieri A, Pizzagalli F, Graziano N, Ferraro E. Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms in gastric cancer of intestinal and diffuse histotypes.Clin Exp Immunol. 2008;154:360-364.
Doll R, Forman D, La Vecchia C. Alcoholic beverages and cancers of the digestive tract and larynx.Health Issues Related to Alcohol Consumption. 2nd ed. Bodmin Cornwall: MPG Books; 1999;351-393.
Seitz HK, Matsuzaki S, Yokoyama A, Homann N, Väkeväinen S, Wang XD. Alcohol and cancer.Alcohol Clin Exp Res. 2001;25:137S-143S.
Pöschl G, Seitz HK. Alcohol and cancer.Alcohol Alcohol. 2004;39:155-165.
Jelski W, Szmitkowski M. Alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH) in the cancer diseases.Clin Chim Acta. 2008;395:1-5.