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Relationship between β-catenin expression and epithelial cell proliferation in gastric mucosa with intestinal metaplasia

机译:胃黏膜肠上皮化生过程中β-catenin表达与上皮细胞增殖的关系

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摘要

AIM: To investigate β-catenin expression in patients with intestinal metaplasia, and to look for a possible relationship between β-catenin expression and either epithelial proliferation values or Helicobacter pylori (H pylori) infection.METHODS: Twenty patients with complete type intestinal metaplasia were studied. β-catenin expression and epithelial cell proliferation in antral mucosa were assessed using an immunohistochemical analysis. H pylori infection was detected by histology and a rapid urease test.RESULTS: Reduced β-catenin expression on the surface of metaplastic cells was detected in 13 (65%) out of 20 patients. Moreover, in eight (40%) patients intranuclear expression of β-catenin was found. When patients were analyzed according to H pylori infection, the prevalence of both β-catenin reduction at the cell surface and its intranuclear localization did not significantly differ between infected and uninfected patients. Cell proliferation was higher in patients with intranuclear β-catenin expression as compared to the remaining patients, although the difference failed to reach the statistical significance (36 ± 8.9 vs 27.2 ± 11.4, P = 0.06). On the contrary, a similar cell proliferation value was observed between patients with reduced expression of β-catenin on cell surface and those with a normal expression (28.1 ± 11.8 vs 26.1 ± 8.8, P = 0.7). H pylori infection significantly increased cell proliferation (33.3 ± 10.2% vs 24.6 ± 7.4%, respectively, P = 0.04).CONCLUSION: Both cell surface reduction and intranuclear accumulation of β-catenin were detected in intestinal metaplasia. The intranuclear localization of β-catenin increases cell proliferation. H pylori infection does not seem to play a direct role in β-catenin alterations, whilst it significantly increases cell proliferation.
机译:目的:探讨肠上皮化生患者的β-catenin表达,并探讨β-catenin表达与上皮细胞增殖或幽门螺杆菌感染的关系。方法:20例完全型肠上皮化生患者研究。使用免疫组织化学分析评估了胃黏膜中β-catenin的表达和上皮细胞的增殖。结果:20例患者中有13例(65%)检测到化生细胞表面的β-catenin表达降低。此外,在八名(40%)患者中发现了β-catenin的核内表达。当根据幽门螺杆菌感染对患者进行分析时,感染和未感染患者之间β-catenin在细胞表面的减少及其核内定位的发生率均无显着差异。与其余患者相比,具有核内β-catenin表达的患者的细胞增殖更高,尽管差异未能达到统计学显着性(36±8.9 vs 27.2±11.4,P = 0.06)。相反,在细胞表面表达β-catenin减少的患者与表达正常的患者之间观察到相似的细胞增殖值(28.1±11.8 vs 26.1±8.8,P = 0.7)。幽门螺杆菌感染显着提高了细胞增殖(分别为33.3±10.2%和24.6±7.4%,P = 0.04)。结论:在肠化生过程中检测到了细胞表面减少和β-catenin的细胞核内积聚。 β-catenin的核内定位可增加细胞增殖。幽门螺杆菌感染似乎在β-catenin改变中没有直接作用,但会显着增加细胞增殖。

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