Department of Anatomical and Cellular Pathology, State Key Laboratory in Oncology in South China and Li Ka Shing Institute of Health Science, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Institutite of Cancer and Genomic Sciences, College of Medical and Dental Sciences, University of Birmingham, Vincent Drive, Edgbaston, Birmingham, United Kingdom.
Int J Cancer. 2017 Oct 15;141(8):1512-1521. doi: 10.1002/ijc.30795. Epub 2017 Jun 7.
The γ-herpesviruses, EBV and KSHV, are closely associated with a number of human cancers. While the signal transduction pathways exploited by γ-herpesviruses to promote cell growth, survival and transformation have been reported, recent studies have uncovered the impact of γ-herpesvirus infection on host cell metabolism. Here, we review the mechanisms used by γ-herpesviruses to induce metabolic reprogramming in host cells, focusing on their ability to modulate the activity of metabolic regulators and manipulate metabolic pathways. While γ-herpesviruses alter metabolic phenotypes as a means to support viral infection and long-term persistence, this modulation can inadvertently contribute to cancer development. Strategies that target deregulated metabolic phenotypes induced by γ-herpesviruses provide new opportunities for therapeutic intervention.
γ 疱疹病毒,如 EBV 和 KSHV,与多种人类癌症密切相关。虽然已经报道了 γ 疱疹病毒利用信号转导通路促进细胞生长、存活和转化,但最近的研究揭示了 γ 疱疹病毒感染对宿主细胞代谢的影响。在这里,我们综述了 γ 疱疹病毒诱导宿主细胞代谢重编程的机制,重点关注它们调节代谢调节剂活性和操纵代谢途径的能力。虽然 γ 疱疹病毒改变代谢表型是支持病毒感染和长期持续存在的一种手段,但这种调节可能会无意中促进癌症的发展。靶向 γ 疱疹病毒诱导的失调代谢表型的策略为治疗干预提供了新的机会。