Departments of Biochemistry.
J Virol. 2013 Dec;87(24):13168-78. doi: 10.1128/JVI.01242-13. Epub 2013 Sep 25.
The adenovirus E4orf4 protein selectively kills human cancer cells independently of p53 and thus represents a potentially promising tool for the development of novel antitumor therapies. Previous studies suggested that E4orf4 induces an arrest or a delay in mitosis and that both this effect and subsequent cell death rely largely on an interaction with the B55 regulatory subunit of protein phosphatase 2A. In the present report, we show that the death of human H1299 lung carcinoma cells induced by expression of E4orf4 is typified not by an accumulation of cells arrested in mitosis but rather by the presence of both tetraploid and diploid cells that are arrested in G1 because they are unable to initiate DNA synthesis. We believe that these E4orf4-expressing cells eventually die by various processes, including those resulting from mitotic catastrophe.
腺病毒 E4orf4 蛋白选择性地杀死人类癌细胞,而不依赖于 p53,因此代表了开发新型抗肿瘤疗法的有前途的工具。先前的研究表明,E4orf4 诱导有丝分裂的阻滞或延迟,并且这种效应和随后的细胞死亡在很大程度上依赖于与蛋白磷酸酶 2A 的 B55 调节亚基的相互作用。在本报告中,我们表明,由 E4orf4 表达诱导的人 H1299 肺癌细胞的死亡的特点不是有丝分裂阻滞细胞的积累,而是存在处于 G1 期的四倍体和二倍体细胞,因为它们无法起始 DNA 合成。我们相信,这些表达 E4orf4 的细胞最终通过各种过程死亡,包括那些由于有丝分裂灾难导致的死亡过程。