| Literature DB >> 27956703 |
Liping Liu1,2, Hongyu Guan3, Yun Li4, Zhe Ying1,2, Jueheng Wu1, Xun Zhu1,2, Libing Song5, Jun Li6,7, Mengfeng Li6,2.
Abstract
Astrocyte elevated gene 1 (AEG-1) is an oncoprotein that strongly promotes the development and progression of cancers. However, the detailed underlying mechanisms through which AEG-1 enhances tumor development and progression remain to be determined. In this study, we identified c-Jun and p300 to be novel interacting partners of AEG-1 in gliomas. AEG-1 promoted c-Jun transcriptional activity by interacting with the c-Jun/p300 complex and inducing c-Jun acetylation. Furthermore, the AEG-1/c-Jun/p300 complex was found to bind the promoter of c-Jun downstream targeted genes, consequently establishing an acetylated chromatin state that favors transcriptional activation. Importantly, AEG-1/p300-mediated c-Jun acetylation resulted in the development of a more aggressive malignant phenotype in gliomas through a drastic increase in glioma cell proliferation and angiogenesis in vitro and in vivo Consistently, the AEG-1 expression levels in clinical glioma specimens correlated with the status of c-Jun activation. Taken together, our results suggest that AEG-1 mediates a novel epigenetic mechanism that enhances c-Jun transcriptional activity to induce glioma progression and that AEG-1 might be a novel, potential target for the treatment of gliomas.Entities:
Keywords: E1A binding protein p300 (p300); acetylation; astrocyte elevated gene 1 (AEG-1); c-Jun transcription factor; glioma
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Year: 2017 PMID: 27956703 PMCID: PMC5311247 DOI: 10.1128/MCB.00456-16
Source DB: PubMed Journal: Mol Cell Biol ISSN: 0270-7306 Impact factor: 4.272