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Spermine oxidase a polyamine catabolic enzyme that links Helicobacter pylori CagA and gastric cancer risk

机译:精胺氧化酶一种多胺分解代谢酶将幽门螺杆菌CagA与胃癌风险联系起来

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摘要

We have recently reported that Helicobacter pylori strains expressing the virulence factor cytotoxin-associated gene A (CagA) stimulate increased levels of spermine oxidase (SMO) in gastric epithelial cells, while cagA strains did not. SMO catabolizes the polyamine spermine and produces H2O2 that results in both apoptosis and DNA damage. Exogenous overexpression of CagA confirmed these findings, and knockdown or inhibition of SMO blocked CagA-mediated apoptosis and DNA damage. The strong association of SMO, apoptosis, and DNA damage was also demonstrated in humans infected with cagA+, but not cagA strains. In infected gerbils and mice, DNA damage was CagA-dependent and only present in epithelial cells that expressed SMO. We also discovered SMOhigh gastric epithelial cells from infected animals with dysplasia that are resistant to apoptosis despite high levels of DNA damage. Inhibition of polyamine synthesis or SMO could abrogate the development of this cell population that may represent precursors for neoplastic transformation.
机译:最近,我们报道了表达毒力因子细胞毒素相关基因A(CagA)的幽门螺杆菌菌株刺激胃上皮细胞中精胺氧化酶(SMO)水平升高,而cagA 菌株却没有。 SMO分解多胺精胺并产生H2O2,导致凋亡和DNA损伤。 CagA的外源性过表达证实了这些发现,而敲除或抑制SMO可以阻断CagA介导的细胞凋亡和DNA损伤。在感染了cagA + 的人中也证实了SMO,细胞凋亡和DNA损伤的强相关性,但没有感染cagA 株。在感染的沙鼠和小鼠中,DNA损伤是CagA依赖性的,仅存在于表达SMO的上皮细胞中。我们还从发育异常的受感染动物中发现了SMO 胃上皮细胞,尽管其DNA损伤程度很高,但它对细胞凋亡具有抗性。多胺合成或SMO的抑制作用可以消除这种细胞群的发展,这种细胞群可以代表肿瘤转化的前体。

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