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首页> 外文期刊>Proteomics >Proteome analysis of aflatoxin B1-induced hepatocarcinogenesis in tree shrew (Tupaia belangeri chinensis) and functional identification of candidate protein peroxiredoxin II.
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Proteome analysis of aflatoxin B1-induced hepatocarcinogenesis in tree shrew (Tupaia belangeri chinensis) and functional identification of candidate protein peroxiredoxin II.

机译:黄曲霉毒素B1诱导的树sh(Tupaia belangeri chinensis)肝癌发生的蛋白质组分析和候选蛋白质过氧化物酶II的功能鉴定。

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摘要

In order to explore the proteins responsible for hepatocellular carcinoma (HCC), aflatoxin B(1)-induced hepatocarcinogenesis in tree shrew (Tupaia belangeri chinensis) was analyzed with 2-DE and MS. By comparing HCC samples with their own precancerous biopsies and HCC-surrounding tissues, a group of candidate proteins that differentially expressed in HCC were obtained. Peroxiredoxin (Prx) II, one of the candidates with distinct alteration, was further investigated and validated. Western blot and RT-PCR assays confirmed the overexpression of Prx II in both tree shrew and human HCC tissues. RNA interference for silencing Prx II was employed subsequently to explore the function and underlying mechanism of Prx II on liver cancer cell line Hep3B. Results showed the cell proliferation and clone formation decreased obviously when Prx II expression was inhibited, while the flow cytometer analysis showed the percentage of cell apoptosis enhanced. Inhibition of Prx II expression also obviously increased the generation of ROS and malondialdehyde, both are the products from peroxidation. These results imply the important role of Prx II in hepatocarcinogenesis, possibly through its function in regulating peroxidation and hereby to provide a favorable microenvironment for cancer cell surviving and progressing.
机译:为了探索负责肝细胞癌(HCC)的蛋白质,用2-DE和MS分析了树sh(Tupaia belangeri chinensis)中的黄曲霉毒素B(1)诱导的肝癌发生。通过将HCC样品与其自身的癌前活检样品和HCC周围组织进行比较,获得了一组在HCC中差异表达的候选蛋白。 Peroxiredoxin(Prx)II,具有明显改变的候选基因之一,经过进一步研究和验证。 Western印迹和RT-PCR分析证实了树sh和人类HCC组织中Prx II的过度表达。随后采用RNA干扰沉默Prx II,以探索Prx II对肝癌细胞Hep3B的功能和潜在机制。结果显示,抑制Prx II表达后,细胞增殖和克隆形成明显减少,而流式细胞仪分析显示细胞凋亡百分比增加。抑制Prx II表达也明显增加了ROS和丙二醛的生成,两者都是过氧化的产物。这些结果暗示Prx II在肝癌发生中的重要作用,可能是通过其调节过氧化物的功能,从而为癌细胞的生存和发展提供了有利的微环境。

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