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首页> 外文期刊>Biochemical and Biophysical Research Communications >Enhancement of DEN-induced liver tumorigenesis in heme oxygenase-1 G143H mutant transgenic mice
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Enhancement of DEN-induced liver tumorigenesis in heme oxygenase-1 G143H mutant transgenic mice

机译:DEN引起的血红素加氧酶-1 G143H突变型转基因小鼠肝肿瘤的形成增强

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摘要

Herne oxygenase (HO) is the rate-limiting enzyme in heme metabolism. HO-1 exhibits anti-oxidative and anti-inflammatory function via the actions of its metabolite, respectively. A growing body of evidence demonstrates that HO-1 is implicated in the pathogenesis and progression of several types of cancer. However, whether HO-1 takes part in healthy-premalignant-malignant transformation is still undefined. In this study, we took advantage of transgenic mice which over-expressed HO-1 dominant negative mutant (H0-1 G143H) and observed its susceptibility to DEN-induced hepatocarcinogenesis. Our results indicate that HO-1 G143H mutant accelerates the progression of tumorigenesis and tumor growth. The mechanism is closely related to enhancement of ROS production which induce more hepatocytes death and secretion of inflammatory cytokines, proliferation of surviving hepatocytes. Our result provides the direct evidence that HO-1 plays an important protective role in liver carcinogenesis. Alternatively, we suggest the possible explanation on effect of HO-1 promoter polymorphism which involved in tumorigenesis. (C) 2016 Elsevier Inc. All rights reserved.
机译:赫恩氧化酶(HO)是血红素代谢中的限速酶。 HO-1分别通过其代谢物的作用表现出抗氧化和抗炎功能。越来越多的证据表明,HO-1与几种类型的癌症的发病机理和发展有关。但是,HO-1是否参与健康-恶变前-恶变仍是不确定的。在这项研究中,我们利用了过表达HO-1显性负突变体(H0-1 G143H)的转基因小鼠,并观察了其对DEN诱导的肝癌发生的敏感性。我们的结果表明,HO-1 G143H突变体加速了肿瘤发生和肿瘤生长的进程。该机制与ROS产生的增加密切相关,ROS的产生诱导更多的肝细胞死亡和炎性细胞因子的分泌,存活的肝细胞的增殖。我们的结果提供了直接证据,表明HO-1在肝癌的发生中起着重要的保护作用。或者,我们建议可能参与肿瘤发生的HO-1启动子多态性的解释。 (C)2016 Elsevier Inc.保留所有权利。

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