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STAT5-Dependent CyclinD1 and Bcl-xL Expression in Bcr-Abl-Transformed Cells

机译:Bcr-Abl转化细胞中STAT5依赖性CyclinD1和Bcl-xL表达

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摘要

Signal transducers and activators of transcription (STATs) are a family of transcription factors that were originally identified as mediators of cytokine-induced gene expression. We and others have recently shown that STAT5 also plays a major role in cellular transformation by the Bcr-Abl oncogene. Here we show that the antiapoptotic bcl-xL gene product and the cell cycle regulator cyclin D1 are targets of STAT5 in Bcr-Abl-transformed cells.In the CML cell line K562 and in BaF3 cells ectopically expressing Bcr-Abl,both the cyclin D1 and bcl-x promoters are highly active.The activity of these promoters can bve strongly repressed by cotransfection of a dominant negative (DN) mutant of STAT5.Moreover,the cyclin D1 and bcl-x promoters contain STAT binding sites to which STAT5 constitutively binds in Bcr-Abl transformed cells.These results suggest that STAT5 contributes to transformation by Bcr-Abl by induction of cyclin D1 and bcl-xL expression.
机译:信号转导子和转录激活子(STATs)是转录因子家族,最初被确定为细胞因子诱导的基因表达的介质。我们和其他人最近表明,STAT5在Bcr-Abl癌基因的细胞转化中也起着重要作用。在这里,我们显示抗凋亡的bcl-xL基因产物和细胞周期调节细胞周期蛋白D1是Bcr-Abl转化细胞中STAT5的靶标。在CML细胞系K562和异位表达Bcr-Abl的BaF3细胞中,细胞周期蛋白D1 STAT5显性负(DN)突变体的共转染可强烈抑制这些启动子的活性。此外,cyclin D1和bcl-x启动子包含STAT5与STAT5组成性结合的位点。这些结果表明STAT5通过诱导细胞周期蛋白D1和bcl-xL表达而促进了Bcr-Abl的转化。

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