首页> 外文期刊>Asian Pacific Journal of Cancer Prevention >Associations of the -238(G/A) and -308(G/A) TNF-α Promoter Polymorphisms and TNF-α Serum Levels with the Susceptibility to Gastric Precancerous Lesions and Gastric Cancer Related to Helicobacter pylori Infection in a Moroccan Population
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Associations of the -238(G/A) and -308(G/A) TNF-α Promoter Polymorphisms and TNF-α Serum Levels with the Susceptibility to Gastric Precancerous Lesions and Gastric Cancer Related to Helicobacter pylori Infection in a Moroccan Population

机译:-238(g / a)和-308(g / a)TNF-α启动子多态性和TNF-α血清水平的关联与摩洛哥人群中胃癌癌患者有关的胃癌癌症和胃癌的敏感性

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Objective: Helicobacter pylori (H. pylori) induces the production of tumor necrosis factor-alpha (TNF-α), which is closely related to a gastric epithelial injury. TNF-α gene polymorphism and TNF-α serum levels are associated with various malignant conditions. Identification of the ideal marker for gastric cancer (GC) is still the leading aim of several trials. Physio-pathological considerations of GC led us to investigate the association of two TNF-α promoter polymorphisms (-308GA and -238GA), and TNF-α serum levels with the susceptibility to gastric precancerous (PL) and GC. Methods: Patients suffering from gastric lesions (65 chronic gastritis, 50 PL, 40 GC) related to H. pylori ?infection , and 63 healthy controls (HC) were involved in this study. Individuals are genotyped by TNF-α gene promoter sequencing and TNF-α serum levels are measured by ELISA quantitative method. Results: Regarding TNF-α-308 G/A locus, we noticed higher risk for GC (OR=4.3, CI 1.5-11.9, p-value=0.005) and PL (OR=3.4, CI 1.2-9.2, p-value=0.01) for individuals with AA/GA genotypes compared to GG genotype. Concerning TNF-α-238 G/A locus, we noticed higher risk for GC (OR=5.9, CI 1.2-27.5, p-value=0.01) and PL (OR=4.8, CI 1.3-18, p-value=0.01) for individuals with GG genotype compared to AA/GA genotypes. We noticed that TNF-α serum levels have been increased together with gastric lesions severity. Moreover, TNF-α-308 and TNF-α-238 A alleles seemed to, respectively, upregulate and downregulate TNF-α serum levels. Conclusion: The TNF-α -308 A allele has a promotive effect for GC progression, whereas the TNF-α -238 A allele has a protective function against GC progression. High levels of TNF-α seemed to be associated with the aggressiveness of gastric lesions. TNF-α gene polymorphisms and TNF-α serum levels might be helpful to select those patients who are at high risk for GC.
机译:目的:幽门螺杆菌(H. Pylori)诱导肿瘤坏死因子-α(TNF-α)的产生,其与胃上皮损伤密切相关。 TNF-α基因多态性和TNF-α血清水平与各种恶性条件相关。鉴定胃癌(GC)的理想标记仍然是几项试验的主要目的。 GC的物理病理考虑因素导致我们研究了两种TNF-α启动子多态性(-308g> A和-238g> A)和TNF-α血清水平与胃癌癌和GC的敏感性。方法:患有胃病变(65例慢性胃炎,50 pl,40g,40g,40 gc)的患者参与了本研究涉及63例健康对照(HC)。个体是通过TNF-α基因启动子测序的基因分型,通过ELISA定量方法测量TNF-α血清水平。结果:关于TNF-α-308g / A基因座,我们注意到GC的风险较高(或= 4.3,CI 1.5-11.9,P值= 0.005)和PL(或= 3.4,CI 1.2-9.2,P值与GG基因型进行AA / GA基因型的个体,= 0.01)。关于TNF-α-238g / A基因座,我们注意到GC的风险更高(或= 5.9,CI 1.2-27.5,P值= 0.01)和PL(或= 4.8,CI 1.3-18,P值= 0.01 )对于与AA / GA基因型相比具有GG基因型的个体。我们注意到,TNF-α血清水平与胃病变严重程度一起增加。此外,TNF-α-308和TNF-α-238分别似乎分别上调和下调TNF-α血清水平。结论:TNF-α-308 A等位基因对GC进展具有促进效果,而TNF-α-238 A等位基因对GC进展具有保护功能。高水平的TNF-α似乎与胃病变的侵蚀性有关。 TNF-α基因多态性和TNF-α血清水平可能有助于选择高危险性GC的患者。

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