Department of Pediatrics, Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD.
Am J Transplant. 2014 Jun;14(6):1249-58. doi: 10.1111/ajt.12725. Epub 2014 May 19.
Cytomegalovirus (CMV) is increasingly recognized as an accomplished modulator of cell-signaling pathways, both directly via interaction between viral and cellular proteins, and indirectly by activating metabolic/energy states of infected cells. Viral genes, as well as captured cellular genes, enable CMV to modify these pathways upon binding to cellular receptors, up until generation of virus progeny. Deregulation of cell-signaling pathways appears to be a well-developed tightly balanced virus strategy to achieve the desired consequences in each infected cell type. Importantly and perhaps surprisingly, identification of new signaling pathways in cancer cells positioned CMV as a sophisticated user and abuser of many such pathways, creating opportunities to develop novel therapeutic strategies for inhibiting CMV replication (in addition to standard of care CMV DNA polymerase inhibitors). Advances in genomics and proteomics allow the identification of CMV products interacting with the cellular machinery. Ultimately, clinical implementation of candidate drugs capable of disrupting the delicate balance between CMV and cell-signaling will depend on the specificity and selectivity index of newly identified targets.
巨细胞病毒(CMV)越来越被认为是细胞信号通路的出色调节剂,既可通过病毒和细胞蛋白之间的直接相互作用,也可通过激活受感染细胞的代谢/能量状态来间接实现。病毒基因以及捕获的细胞基因使 CMV 能够在与细胞受体结合后对这些途径进行修饰,直到产生病毒后代。细胞信号通路的失调似乎是一种经过精心平衡的病毒策略,旨在在每种受感染的细胞类型中实现预期的结果。重要的是,也许令人惊讶的是,在癌细胞中鉴定出新的信号通路使 CMV 成为许多此类通路的复杂使用者和滥用者,为开发抑制 CMV 复制的新型治疗策略(除了标准的 CMV DNA 聚合酶抑制剂之外)创造了机会。基因组学和蛋白质组学的进步使得能够识别与细胞机制相互作用的 CMV 产物。最终,能够破坏 CMV 与细胞信号之间微妙平衡的候选药物的临床应用将取决于新鉴定的靶标的特异性和选择性指数。