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Human papillomavirus oncoproteins and post-translational modifications: generating multifunctional hubs for overriding cellular homeostasis

机译:人乳头瘤病毒癌蛋白和翻译后修饰:为推翻细胞稳态产生多功能集线器

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摘要

Human papillomaviruses (HPVs) are major human carcinogens, causing around 5% of all human cancers, with cervical cancer being the most important. These tumors are all driven by the two HPV oncoproteins E6 and E7. Whilst their mechanisms of action are becoming increasingly clear through their abilities to target essential cellular tumor suppressor and growth control pathways, the roles that post-translational modifications (PTMs) of E6 and E7 play in the regulation of these activities remain unclear. Here, we discuss the direct consequences of some of the most common PTMs of E6 and E7, and how this impacts upon the multi-functionality of these viral proteins, and thereby contribute to the viral life cycle and to the induction of malignancy. Furthermore, it is becoming increasingly clear that these modifications, may, in some cases, offer novel routes for therapeutic intervention in HPV-induced disease.
机译:人乳头瘤病毒(HPV)是主要的人类致癌物质,导致所有人类癌症的5%左右,宫颈癌是最重要的。 这些肿瘤都是由两个HPV癌蛋白E6和E7驱动的。 虽然它们的行动机制越来越清楚,但通过它们对必要的细胞肿瘤抑制和生长控制途径的能力越来越清楚,而E6和E7在这些活动的调节中发挥的翻译改性(PTM)的作用仍不清楚。 在这里,我们讨论了E6和E7中一些最常见的PTM的直接后果,以及这种病毒蛋白的多功能的影响,从而有助于病毒生命周期和诱导恶性肿瘤。 此外,越来越清楚的是,这些修改可能在某些情况下为HPV诱导的疾病提供新的治疗干预途径。

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