Zheng Xinyu, Rao Xiao-Mei, Gomez-Gutierrez Jorge G, Hao Hongying, McMasters Kelly M, Zhou H Sam
James Graham Brown Cancer Center, University of Louisville School of Medicine, Baxter II, Room 321, 580 S. Preston St., Louisville, KY 40202, USA.
J Virol. 2008 Apr;82(7):3415-27. doi: 10.1128/JVI.01708-07. Epub 2008 Jan 30.
Adenoviruses (Ads) with E1B55K mutations can selectively replicate in and destroy cancer cells. However, the mechanism of Ad-selective replication in tumor cells is not well characterized. We have shown previously that expression of several cell cycle-regulating genes is markedly affected by the Ad E1b gene in WI-38 human lung fibroblast cells (X. Rao, et al., Virology 350:418-428, 2006). In the current study, we show that the Ad E1B55K region is required to enhance cyclin E expression and that the failure to induce cyclin E overexpression due to E1B55K mutations prevents viral DNA from undergoing efficient replication in WI-38 cells, especially when the cells are arrested in the G(0) phase of the cell cycle by serum starvation. In contrast, cyclin E induction is less dependent on the function encoded in the E1B55K region in A549 and other cancer cells that are permissive for replication of E1B55K-mutated viruses, whether the cells are in the S phase or G(0) phase. The small interfering RNA that specifically inhibits cyclin E expression partially decreased viral replication. Our study provides evidence suggesting that E1B55K may be involved in cell cycle regulation that is important for efficient viral DNA replication and that cyclin E overexpression in cancer cells may be associated with the oncolytic replication of E1B55K-mutated viruses.
携带E1B55K突变的腺病毒(Ads)能够在癌细胞中选择性复制并将其破坏。然而,腺病毒在肿瘤细胞中选择性复制的机制尚未完全明确。我们之前已经表明,WI-38人肺成纤维细胞中几个细胞周期调控基因的表达受到腺病毒E1b基因的显著影响(X. Rao等人,《病毒学》350:418 - 428,2006年)。在本研究中,我们发现腺病毒E1B55K区域对于增强细胞周期蛋白E的表达是必需的,并且由于E1B55K突变导致无法诱导细胞周期蛋白E过表达会阻止病毒DNA在WI-38细胞中进行有效复制,尤其是当细胞通过血清饥饿被阻滞在细胞周期的G(0)期时。相比之下,在A549细胞和其他允许E1B55K突变病毒复制的癌细胞中,无论细胞处于S期还是G(0)期,细胞周期蛋白E的诱导对E1B55K区域编码的功能依赖性较小。特异性抑制细胞周期蛋白E表达的小干扰RNA部分降低了病毒复制。我们的研究提供了证据表明,E1B55K可能参与了对有效病毒DNA复制很重要的细胞周期调控,并且癌细胞中细胞周期蛋白E的过表达可能与E1B55K突变病毒的溶瘤复制有关。