Galang C K, García-Ramírez J, Solski P A, Westwick J K, Der C J, Neznanov N N, Oshima R G, Hauser C A
La Jolla Cancer Research Foundation, La Jolla, California, 92037-1063, USA.
J Biol Chem. 1996 Apr 5;271(14):7992-8. doi: 10.1074/jbc.271.14.7992.
Overexpression of Neu (ErbB-2/HER2) is found in approximately 20% of breast tumors. Activation of Neu by a point mutation (NeuT) causes constitutive tyrosine kinase activity of this transmembrane receptor and transforming activity in fibroblasts. To identify downstream targets of Neu, we have analyzed the ability of Neu to activate gene expression. Expression of NeuT, but not normal Neu, caused transcriptional activation of Ets, AP-1, or NF-kappaB-dependent reporter genes. Dominant inhibitory Ras or Raf mutants blocked the Neu-mediated transcriptional activation, confirming that Ras signaling pathways were required for this activation. Analysis with Ets2 mutants indicated that activation of Ets2 transcriptional activity mediated by NeuT or oncogenic Ras required phosphorylation of the same Ets2 residue, threonine 72. Cotransfection of dominant inhibitory Ets2 mutants specifically blocked NeuT-mediated activation of Ets-dependent reporter genes. Furthermore, in focus formation assays using NIH 3T3 cells, the transforming activity of NeuT was inhibited 5-fold when NeuT was cotransfected with a dominant negative Ets2 mutant. However, parallel colony formation assays showed that the Ets2 dominant negative mutant did not inhibit the growth of normal cells. Together, these data show that NeuT activates a variety of transcription factor families via the Ras signaling pathway and that Ets activation is required for NeuT-mediated cellular transformation. Thus, downstream targets of Neu, including Ets transcription factors, may be useful points for therapeutic intervention in Neu/ErbB-2-associated cancers.
在大约20%的乳腺肿瘤中发现Neu(ErbB-2/HER2)过表达。Neu通过点突变(NeuT)激活后会导致该跨膜受体的组成型酪氨酸激酶活性以及在成纤维细胞中的转化活性。为了鉴定Neu的下游靶点,我们分析了Neu激活基因表达的能力。NeuT而非正常Neu的表达导致Ets、AP-1或NF-κB依赖性报告基因的转录激活。显性抑制性Ras或Raf突变体阻断了Neu介导的转录激活,证实这种激活需要Ras信号通路。用Ets2突变体分析表明,NeuT或致癌性Ras介导的Ets2转录活性激活需要相同的Ets2残基苏氨酸72磷酸化。显性抑制性Ets2突变体的共转染特异性地阻断了NeuT介导的Ets依赖性报告基因的激活。此外,在使用NIH 3T3细胞的焦点形成试验中,当NeuT与显性负性Ets2突变体共转染时,NeuT的转化活性被抑制了5倍。然而,平行的集落形成试验表明,Ets2显性负性突变体并不抑制正常细胞的生长。总之,这些数据表明NeuT通过Ras信号通路激活多种转录因子家族,并且Ets激活是NeuT介导的细胞转化所必需的。因此,Neu的下游靶点,包括Ets转录因子,可能是Neu/ErbB-2相关癌症治疗干预的有用靶点。