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首页> 外文期刊>Gut: Journal of the British Society of Gastroenterology >Vitamin D upregulated protein 1 deficiency promotes N-methyl-N-nitrosourea and Helicobacter pylori-induced gastric carcinogenesis in mice.
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Vitamin D upregulated protein 1 deficiency promotes N-methyl-N-nitrosourea and Helicobacter pylori-induced gastric carcinogenesis in mice.

机译:维生素D上调的蛋白1缺乏症会促进N-甲基-N-亚硝基脲和幽门螺杆菌诱导的小鼠胃癌发生。

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摘要

OBJECTIVE: Vitamin D(3) upregulated protein 1 (VDUP1) is a potent tumour suppressor whose expression is dramatically reduced in various types of human cancers, including gastric cancer. However, the precise mechanisms underlying tumour development remain unclear. In the present study, the authors examined the effect of VDUP1 on Helicobacter pylori-induced gastric carcinogenesis in mice. DESIGN: Gastric cancer was generated in VDUP1 knockout (KO) and wild-type mice using a combination of N-methyl-N-nitrosourea treatment and H pylori infection. Fifty weeks after treatment, gastric tissues from both types of mice were examined by histopathology, immunohistochemistry and immunoblotting. In vitro tests on the human gastric cancer cell line, AGS, were also performed to identify the underlying mechanisms of cancer development. RESULTS: The overall incidence of gastric cancer was significantly higher in VDUP1 KO mice than in wild-type mice. Similarly, VDUP1 KO mice showed more severe chronic gastritis, glandular atrophy, foveolar hyperplasia, metaplasia and dysplasia. Although no differences in the apoptotic index were apparent, lack of VDUP1 increased the rate of gastric epithelial cell proliferation in non-cancerous stomachs, with corresponding increases in tumour necrosis factor alpha (TNFalpha) level, nuclear transcription factor kappa B (NF-kappaB) activation and cyclooxygenase-2 (COX-2) expression. An in vitro study showed that H pylori-associated cell proliferation and induction of TNFalpha, NF-kappaB and COX-2 were inhibited in cells transfected with VDUP1. In addition, overexpression of VDUP1 in AGS cells suppressed TNFalpha-induced NF-kappaB activation and COX-2 expression. CONCLUSION: Our data show that VDUP1 negatively regulates H pylori-associated gastric carcinogenesis, in part by disrupting cell growth and inhibiting the induction of TNFalpha, NF-kappaB and COX-2. These findings provide important insights into the role of VDUP1 in H pylori-associated tumourigenesis.
机译:目的:维生素D(3)上调蛋白1(VDUP1)是一种有效的肿瘤抑制因子,其表达在包括胃癌在内的各种人类癌症中均显着降低。但是,尚不清楚肿瘤发生的确切机制。在本研究中,作者检查了VDUP1对幽门螺杆菌诱导的小鼠胃癌发生的作用。设计:结合使用N-甲基-N-亚硝基脲治疗和幽门螺杆菌感染,在VDUP1基因敲除(KO)和野生型小鼠中产生了胃癌。治疗后五十周,通过组织病理学,免疫组织化学和免疫印迹检查了两种小鼠的胃组织。还对人胃癌细胞系AGS进行了体外测试,以确定癌症发展的潜在机制。结果:VDUP1 KO小鼠的胃癌总发病率明显高于野生型小鼠。同样,VDUP1 KO小鼠表现出更严重的慢性胃炎,腺体萎缩,小叶增生,化生和发育异常。尽管凋亡指数没有明显差异,但缺乏VDUP1可以增加非癌性胃中胃上皮细胞增殖的速率,并相应增加肿瘤坏死因子α(TNFalpha),核转录因子kappa B(NF-kappaB)激活和环氧合酶2(COX-2)表达。一项体外研究表明,在用VDUP1转染的细胞中,幽门螺杆菌相关的细胞增殖以及TNFα,NF-κB和COX-2的诱导受到抑制。此外,AGS细胞中VDUP1的过表达抑制了TNFalpha诱导的NF-κB活化和COX-2表达。结论:我们的数据显示VDUP1负调控幽门螺杆菌相关的胃癌发生,部分是通过破坏细胞生长并抑制TNFα,NF-κB和COX-2的诱导。这些发现为VDUP1在幽门螺杆菌相关的肿瘤发生中的作用提供了重要的见识。

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