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Essential role of HCMV deubiquitinase in promoting oncogenesis by targeting anti-viral innate immune signaling pathways

机译:HCMV去泛素酶通过靶向抗病毒先天性免疫信号通路来促进肿瘤发生中的重要作用

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Cancer is a multifactorial disease and virus-mediated carcinogenesis is one of the crucial factors, which is poorly understood. Human cytomegalovirus (HCMV) is a herpesvirus and its components have been evidenced to be associated with cancer of different tissue origin. However, its role in cancer remains unknown. Here, we identified a conserved herpesviral tegument protein known as pUL48 of HCMV, encoding deubiquitinase enzyme, as having a key role in carcinogenesis. We show using deubiquitinase sufficient- and deficient-HCMV that HCMV deubiquitinase is a key in inducing enhanced cellular metabolic activity through upregulation of several anti-apoptotic genes and downregulation of several pro-apoptotic genes expression. Furthermore, HCMV deubiquitinase acquires pro-tumor functions by inhibiting PRR-mediated type I interferon via deubiquitination of TRAF6, TRAF3, IRAK1, IRF7 and STING. Taken together, our results suggest that HCMV infection may promote oncogenesis by inhibiting innate immunity of the host.
机译:癌症是一种多因素疾病,而病毒介导的癌变是关键因素之一,人们对此知之甚少。人类巨细胞病毒(HCMV)是一种疱疹病毒,其成分已被证明与不同组织起源的癌症有关。但是,其在癌症中的作用仍然未知。在这里,我们确定了一种保守的疱疹病毒外皮蛋白,称为HCMV的pUL48,编码去泛素酶,在癌变过程中具有关键作用。我们显示使用去泛素酶足够和不足的HCMV,HCMV去泛素酶是通过上调一些抗凋亡基因和下调一些促凋亡基因表达来诱导增强的细胞代谢活性的关键。此外,HCMV去泛素酶通过TRAF6,TRAF3,IRAK1,IRF7和STING的去泛素化抑制PRR介导的I型干扰素来获得肿瘤前功能。综上所述,我们的结果表明,HCMV感染可通过抑制宿主的先天免疫力来促进肿瘤发生。

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