Romeo Giovanna, Fiorucci Gianna, Chiantore Maria V, Percario Zulema A, Vannucchi Serena, Affabris Elisabetta
Laboratory of Virology, Istituto Superiore di Sanità, Rome, Italy.
J Interferon Cytokine Res. 2002 Jan;22(1):39-47. doi: 10.1089/107999002753452647.
Numerous evidence has demonstrated the involvement in growth control of interferon (IFN) regulatory factor-1 (IRF-1), which shows tumor suppressor activity. IRF-1 is a well-studied member of the IRF transcription factors that reveals functional diversity in the regulation of cellular response by activating expression of a diverse set of target genes, depending on the cell type and on the specific stimuli. IRF-1 gene rearrangements may be a crucial point in the pathogenesis of some cancer types. Furthermore, different aspects of the tumor suppressor function of IRF-1 may be explained, at least in part, by the observations that IRF-1 is a regulator of cell cycle and apoptosis and that its inactivation accelerates cell transformation. Studies on gene knockout mice contributed greatly to the clarification of these multiple IRF-1 functions. We summarize our current knowledge of the antigrowth effect of IRF-1, focusing also on a more general involvement of IRF-1 in mediating negative regulation of cell growth induced by numerous cytokines and other biologic response modifiers.
大量证据表明,干扰素(IFN)调节因子-1(IRF-1)参与生长控制,具有肿瘤抑制活性。IRF-1是IRF转录因子中一个研究充分的成员,它通过激活多种靶基因的表达来调节细胞反应,表现出功能多样性,这取决于细胞类型和特定刺激。IRF-1基因重排可能是某些癌症类型发病机制中的一个关键点。此外,IRF-1肿瘤抑制功能的不同方面至少可以部分地通过以下观察结果来解释:IRF-1是细胞周期和细胞凋亡的调节因子,其失活会加速细胞转化。对基因敲除小鼠的研究极大地有助于阐明IRF-1的这些多种功能。我们总结了目前关于IRF-1抗生长作用的知识,同时也关注IRF-1在介导多种细胞因子和其他生物反应调节剂诱导的细胞生长负调控中的更广泛作用。