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Astrocyte Elevated Gene 1 Interacts with Acetyltransferase p300 and c-Jun To Promote Tumor Aggressiveness

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机构: [a]Key Laboratory of Tropical Disease Control (Sun Yat-sen University), Chinese Ministry of Education Guangzhou, Guangdong 510080, China [b]Department of Microbiology, Zhongshan School of Medicine, Guangzhou, Guangdong 510080, China [c]Department of Endocrinology and Diabetes Center, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong 510080, China [d]Department of Immunobiology, Jinan University, Guangzhou, Guangdong 510632, China [e]Department of Experimental Research, Cancer Center, Guangzhou, Guangdong 510080, China [f]Department of Biochemistry, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, Guangdong 510080, China
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关键词: E1A binding protein p300 (p300) acetylation astrocyte elevated gene 1 (AEG-1) c-Jun transcription factor glioma

摘要:
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.

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出版当年[2017]版:
大类 | 2 区 生物
小类 | 2 区 生化与分子生物学 3 区 细胞生物学
最新[2023]版:
大类 | 2 区 生物学
小类 | 3 区 生化与分子生物学 3 区 细胞生物学
第一作者:
第一作者机构: [a]Key Laboratory of Tropical Disease Control (Sun Yat-sen University), Chinese Ministry of Education Guangzhou, Guangdong 510080, China [b]Department of Microbiology, Zhongshan School of Medicine, Guangzhou, Guangdong 510080, China
通讯作者:
通讯机构: [a]Key Laboratory of Tropical Disease Control (Sun Yat-sen University), Chinese Ministry of Education Guangzhou, Guangdong 510080, China [b]Department of Microbiology, Zhongshan School of Medicine, Guangzhou, Guangdong 510080, China [f]Department of Biochemistry, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, Guangdong 510080, China [*1]Sun Yat-sen University Zhongshan School of Medicine, 15 Zhongshan Road II, Guangzhou, Guangdong 510080, China. [*2]Sun Yat-sen University Zhongshan School of Medicine, 74 Zhongshan Road II, Guangzhou, Guangdong 510080, China.
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