Andersen J B, Hassel B A
University of Maryland, Marlene and Stewart Greenebaum Cancer Center, Baltimore, MD 21201, USA.
Cytokine Growth Factor Rev. 2006 Dec;17(6):411-21. doi: 10.1016/j.cytogfr.2006.10.001. Epub 2006 Nov 13.
The interferon-stimulated gene, 15 kDa (ISG15) is an interferon regulated gene that is induced as a primary response to diverse microbial and cell stress stimuli, and encodes the founding member of the ubiquitin-like protein family. ISG15 post-translationally modifies proteins via a pathway parallel to, and partially overlapping with, that of ubiquitin. In addition, ISG15 is released from cells to mediate extracellular cytokine-like activities. Although the biological activities of ISG15 have yet to be fully elucidated, it is clear that ISG15 has the capacity to modulate diverse cellular and physiologic functions. Consistent with this view, alterations in the ISG15 pathway have been identified in human tumors and in tumor cell lines. Here we review evidence of a role for ISG15 as an endogenous tumor suppressor that, when dysregulated in malignant cells, can be subverted to promote oncogenesis.
干扰素刺激基因15千道尔顿蛋白(ISG15)是一种受干扰素调节的基因,作为对多种微生物和细胞应激刺激的主要反应而被诱导表达,它编码泛素样蛋白家族的创始成员。ISG15通过一条与泛素途径平行且部分重叠的途径对蛋白质进行翻译后修饰。此外,ISG15从细胞中释放出来,介导细胞外类似细胞因子的活性。尽管ISG15的生物学活性尚未完全阐明,但很明显ISG15具有调节多种细胞和生理功能的能力。与这一观点一致的是,在人类肿瘤和肿瘤细胞系中已发现ISG15途径的改变。在此,我们综述了ISG15作为内源性肿瘤抑制因子发挥作用的证据,当它在恶性细胞中失调时,可能会被颠覆从而促进肿瘤发生。