Nevels Michael, Dobner Thomas
Methods Mol Med. 2007;131:187-95. doi: 10.1007/978-1-59745-277-9_13.
The last 50 yr of molecular biological investigations into human adenoviruses (Ads) have contributed enormously to our understanding of the basic principles of normal and malignant cell growth. Much of this knowledge stems from analyses of the Ad productive infection cycle in permissive host cells. Also, initial observations concerning the transforming potential of human Ads subsequently revealed decisive insights into the molecular mechanisms of the origins of cancer and established Ads as a model system for explaining virus-mediated transformation processes. Today it is well established that cell transformation by human Ads is a multistep process involving several gene products encoded in early transcription units 1A (E1A) and 1B (E1B). Moreover, a large body of evidence now indicates that alternative or additional mechanisms are engaged in Ad-mediated oncogenic transformation involving gene products encoded in early region 4 (E4) as well as epigenetic changes resulting from viral DNA integration. In particular, studies on the transforming potential of several E4 gene products have now revealed new pathways that point to novel general mechanisms of virus-mediated oncogenesis. In this chapter we describe in vitro and in vivo assays to determine the transforming and oncogenic activities of the E1A, E1B, and E4 oncoproteins in primary baby rat kidney cells and athymic nude mice.
过去50年对人类腺病毒(Ads)的分子生物学研究极大地增进了我们对正常和恶性细胞生长基本原理的理解。这些知识大多源于对腺病毒在允许性宿主细胞中产生性感染周期的分析。此外,关于人类腺病毒转化潜能的初步观察随后揭示了对癌症起源分子机制的决定性见解,并将腺病毒确立为解释病毒介导转化过程的模型系统。如今已明确,人类腺病毒介导的细胞转化是一个多步骤过程,涉及早期转录单元1A(E1A)和1B(E1B)中编码的几种基因产物。此外,大量证据表明,腺病毒介导的致癌转化还涉及其他机制,包括早期区域4(E4)中编码的基因产物以及病毒DNA整合导致的表观遗传变化。特别是,对几种E4基因产物转化潜能的研究现已揭示出新的途径,这些途径指向病毒介导肿瘤发生的新的一般机制。在本章中,我们描述了在体外和体内测定E1A、E1B和E4癌蛋白在原代新生大鼠肾细胞和无胸腺裸鼠中的转化和致癌活性的方法。