Abstract
BackgroundIn addition to Helicobacter pylori infection, host genetic factors contribute to gastric cancer (GC). Recognition of H. pylori is known to involve Toll-like receptors (TLR), which subsequently leads to activation of NF-κB. Thus, the overall aim of this study was to estimate for the first time the pooled effect size of polymorphisms in TLR2, TLR4 and CD14 on GC development through a meta-analysis.MethodsA case-control study comprising 284 ethnic Chinese individuals (70 non-cardia GC cases and 214 functional dyspepsia controls) was conducted for the genotyping of TLR2 -196 to -174del, CD14 -260 C/T and TLR4 rs11536889 using PCR, RT-PCR and mass spectrometry. Case-control studies of TLR2, TLR4 and CD14 polymorphisms and GC were searched up to June 2012. Pooled odds ratios and 95% confidence intervals were obtained by means of the random effects model.ResultsIn our ethnic Chinese case-control study, the TLR4 rs11536889 C allele increased the risk of GC (OR: 1.89, 95%CI: 1.23–2.92) while the CD14 -260 T allele was protective (OR: 0.62, 95%CI: 0.42–0.91). TLR2 -196 to -174 increased the risk of GC only in H. pylori-infected individuals (OR: 3.10, 95%CI: 1.27–7.60). In the meta-analysis, TLR4 Asp299Gly showed borderline results in the general analysis (pooled OR: 1.58, 95%CI: 0.98–2.60), nevertheless, stratified analysis by ethnicity showed that the mutant allele was a definitive risk factor for GC in Western populations (pooled OR: 1.87, 95%CI: 1.31–2.65). There was a potential association between the TLR2 -196 to -174 deletion allele and GC in Japanese (pooled OR: 1.18, 95%CI: 0.96–1.45). TLR4 Thr399Ile did not provide significant results.Conclusions TLR4 rs11536889 and CD14 -260 C/T are associated with non-cardia GC in Chinese. Based on our meta-analysis, the TLR signalling pathway is involved in gastric carcinogenesis, TLR4 Asp299Gly and TLR2 -196 to -174del showing associations with GC in an ethnic-specific manner.
Highlights
Despite a major decline in incidence and mortality rates over several decades, gastric cancer (GC) still remains a major cause of morbidity and mortality worldwide [1]
Male gender was found to be more predominant in GC patients than in functional dyspepsia (FD) controls, showing a positive association with the development of GC in this ethnic Chinese population (OR: 1.61, 95% confidence intervals (CI): 1.06–2.44)
Comparison of the prevalence of H. pylori infection in GC patients and FD controls showed that H. pylori infection was a risk factor for the development of GC (OR: 2.14, 95% CI: 1.23–3.70)
Summary
Despite a major decline in incidence and mortality rates over several decades, gastric cancer (GC) still remains a major cause of morbidity and mortality worldwide [1]. The incidence of GC in Chinese individuals resident in China represents 42% of the above worldwide estimation, with Chinese ethnicity identified as an independent risk factor for the development of GC in multiracial studies [2,3,4]. Helicobacter pylori has been established as the most important aetiological risk factor for GC, the pathogenesis of GC involves the combined effects of bacterial, host and environmental factors [7,8,9,10,11]. Given that H. pylori is initially targeted by the toll-like receptors (TLR) signalling pathway, it is conceivable that functionally relevant polymorphisms in genes of this arm of the immune system could affect the magnitude and direction of the host response against the infection. In addition to Helicobacter pylori infection, host genetic factors contribute to gastric cancer (GC). The overall aim of this study was to estimate for the first time the pooled effect size of polymorphisms in TLR2, TLR4 and CD14 on GC development through a meta-analysis
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