STAT3 is required for the gp130-mediated full activation of the c-myc gene

被引:343
作者
Kiuchi, N [1 ]
Nakajima, K [1 ]
Ichiba, M [1 ]
Fukada, T [1 ]
Narimatsu, M [1 ]
Mizuno, K [1 ]
Hibi, M [1 ]
Hirano, T [1 ]
机构
[1] Osaka Univ, Sch Med, Div Mol Oncol, Biomed Res Ctr, Suita, Osaka 5650871, Japan
关键词
signal transducer and activator of transcription 3 c-myc; promoter; interleukin; 6; gp130;
D O I
10.1084/jem.189.1.63
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The signal transducers and activators of transcription (STAT) family members have been implicated in regulating the growth, differentiation and death of normal and transformed cells in response to either extracellular stimuli, including cytokines and growth factors, or intracellular tyrosine kinases, c-myc expression is coordinately regulated by multiple signals in these diverse cellular responses. We show that STAT3 mostly mediates the rapid activation of the c-myc gene upon stimulation of the interleukin (IL)-6 receptor or gp130, a signal transducing subunit of the receptor complexes for the IL-6 cytokine family. STAT3 does so most likely by binding to cis-regulatory region(s) of the c-myc gene. We show that STAT3 binds to a region overlapping with the E2F site in the c-myc promoter and this site is critical for the c-myc gene promoter-driven transcriptional activation by IL-6 or gp130 signals. This is the first identification of the linkage between a member of the STAT family and the c-myc gene activation, and also explains how the IL-G family of cytokines is capable of inducing the expression of the c-myc gene.
引用
收藏
页码:63 / 73
页数:11
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