Literature DB >> 15500943

E1AF, an ets-oncogene family transcription factor.

Masanobu Shindoh1, Fumihiro Higashino, Takao Kohgo.   

Abstract

E1AF is an ets-oncogene family transcription factor. E1AF was shown to upregulate multiple matrix metalloproteinase (MMP) genes and contribute to the malignant phenotype of cancer cells by inducing invasive and metastatic activities. E1AF is upregulated by hepatocyte growth factor (HGF) stimulation, which indicates that E1AF would participate in cell motility by HGF/scatter factor. On the other hand, E1AF upregulates p21waf1/cip1 to induce cell cycle arrest when cells are exposed to stress. EWS/ETS fusions are frequently observed in Ewing's sarcoma, and we have revealed that EWS/ETS chimeric protein activates telomerase activity by upregulating hTERT. However, substitution ets binding site (EBS) mutants did not affect the responsiveness to EWS/E1AF. DNA-IP assay showed that the complexes contained EWS/E1AF bound to the hTERT promoter, which suggested that EWS/ETS functions as a co-activator for TERT transcription. Our findings that EWS/ETS acts as a transcriptional co-factor may imply that the transcription pathway is regulated by the interaction of transcription factors.

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Year:  2004        PMID: 15500943     DOI: 10.1016/j.canlet.2004.07.020

Source DB:  PubMed          Journal:  Cancer Lett        ISSN: 0304-3835            Impact factor:   8.679


  9 in total

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4.  Functional interaction of E1AF and Sp1 in glioma invasion.

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Journal:  Mol Cell Biol       Date:  2007-10-15       Impact factor: 4.272

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6.  Cellular repressor of E1A-stimulated genes attenuates cardiac hypertrophy and fibrosis.

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Journal:  J Cell Mol Med       Date:  2008-12-24       Impact factor: 5.310

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Journal:  Oncotarget       Date:  2016-07-26

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  9 in total

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