Department of Internal Medicine, District Hospital, Drawsko Pomorskie, Poland.
Exp Mol Pathol. 2010 Jun;88(3):388-93. doi: 10.1016/j.yexmp.2010.03.003. Epub 2010 Mar 15.
This paper shows analysis of the association of the 802C>T polymorphism of the NOD2/CARD15 gene with the occurrence of the chronic inflammation of the gastric mucosa associated with the Helicobacter pylori infections, development of intestinal metaplasia and dysplasia and, in the result of this, gastric cancer. Genomic DNA samples were extracted from paraffin blocks of gastric mucosal biopsies and from peripheral blood. H. pylori infection was confirmed by histological analysis and urease test. Pyrosequencing of 802C>T polymorphism of the NOD2/CARD15 gene was performed for H. pylori infected patients (131) and population group (100). Analysis of the NOD2/CARD15 gene showed that frequency of the T allele was significantly higher (32.8%) in the group of patients in comparison with the population group (18.1%), with the relative risk of 1.8. In the patient group, the frequency of the CC genotype was 51.1%, CT 32.1% and TT 16.8% (relative risk: 0.7, 1.1 and 4.2, respectively), while in the population group it was 69.0%, 25.7% and 5.3% (relative risk: 1.0, 0.9 and 1.3, respectively). The increasing frequency of the T allele and CT and TT genotypes in the patients with increasingly deeper changes in the gastric mucosa becomes apparent. Our findings suggest that polymorphism 802C>T is associated with changes in gastric mucosa and plays a significant role in the initiation and the progression of carcinogenesis. The number of observed mutations in gastric mucosa correlated with severity of disease.
本文分析了 NOD2/CARD15 基因 802C>T 多态性与幽门螺杆菌感染相关的胃黏膜慢性炎症、肠化生和异型增生的发生以及由此导致的胃癌的关系。从胃黏膜活检石蜡块和外周血中提取基因组 DNA 样本。通过组织学分析和尿素酶试验确认幽门螺杆菌感染。对幽门螺杆菌感染患者(131 例)和人群(100 例)进行 NOD2/CARD15 基因 802C>T 多态性的焦磷酸测序。分析 NOD2/CARD15 基因显示,与人群相比,患者组 T 等位基因的频率明显更高(32.8%),相对风险为 1.8。在患者组中,CC 基因型的频率为 51.1%,CT 为 32.1%,TT 为 16.8%(相对风险分别为 0.7、1.1 和 4.2),而在人群中分别为 69.0%、25.7%和 5.3%(相对风险分别为 1.0、0.9 和 1.3)。在胃黏膜病变程度逐渐加深的患者中,T 等位基因和 CT 和 TT 基因型的频率增加更为明显。我们的研究结果表明,802C>T 多态性与胃黏膜变化有关,在胃癌的发生和进展中起重要作用。观察到的胃黏膜突变数量与疾病严重程度相关。