生物
车站3
转录因子
抄写(语言学)
癌症研究
转化(遗传学)
细胞培养
癌基因
细胞生物学
细胞凋亡
分子生物学
信号转导
细胞周期
遗传学
基因
哲学
语言学
作者
Jacqueline Bromberg,Melissa H Wrzeszczynska,Geeta Devgan,Yanxiang Zhao,Richard G. Pestell,Chris Albanese,James Darnell
出处
期刊:Cell
[Cell Press]
日期:1999-08-01
卷期号:98 (3): 295-303
被引量:2800
标识
DOI:10.1016/s0092-8674(00)81959-5
摘要
STATs are latent transcription factors that mediate cytokine- and growth factor–directed transcription. In many human cancers and transformed cell lines, Stat3 is persistently activated, and in cell culture, active Stat3 is either required for transformation, enhances transformation, or blocks apoptosis. We report that substitution of two cysteine residues within the C-terminal loop of the SH2 domain of Stat3 produces a molecule that dimerizes spontaneously, binds to DNA, and activates transcription. The Stat3-C molecule in immortalized fibroblasts causes cellular transformation scored by colony formation in soft agar and tumor formation in nude mice. Thus, the activated Stat3 molecule by itself can mediate cellular transformation and the experiments focus attention on the importance of constitutive Stat3 activation in human tumors.
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