Silverman Robert H
Department of Cancer Biology, NB40 Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
Cytokine Growth Factor Rev. 2007 Oct-Dec;18(5-6):381-8. doi: 10.1016/j.cytogfr.2007.06.012. Epub 2007 Jul 27.
The antiviral and antitumor actions of interferons are caused, in part, by a remarkable regulated RNA cleavage pathway known as the 2-5A/RNase L system. 2'-5' linked oligoadenylates (2-5A) are produced from ATP by interferon-inducible synthetases. 2-5A activates pre-existing RNase L, resulting in the cleavage of RNAs within single-stranded regions. Activation of RNase L by 2-5A leads to an antiviral response, although precisely how this happens is a subject of ongoing investigations. Recently, RNase L was identified as the hereditary prostate cancer 1 gene. That finding has led to the discovery of a novel human retrovirus, XMRV. My scientific journey through the 2-5A system recounts some of the highlights of these efforts. Knowledge gained from studies on the 2-5A system could have an impact on development of therapies for important viral pathogens and cancer.
干扰素的抗病毒和抗肿瘤作用部分是由一种显著的受调控的RNA切割途径引起的,该途径被称为2-5A/RNase L系统。2'-5'连接的寡腺苷酸(2-5A)由ATP通过干扰素诱导合成酶产生。2-5A激活预先存在的RNase L,导致单链区域内的RNA切割。2-5A对RNase L的激活引发抗病毒反应,尽管具体机制仍在研究中。最近,RNase L被鉴定为遗传性前列腺癌1基因。这一发现导致了一种新型人类逆转录病毒XMRV的发现。我在2-5A系统方面的科学历程讲述了这些研究工作的一些亮点。从2-5A系统研究中获得的知识可能会对重要病毒病原体和癌症的治疗方法开发产生影响。