TY - JOUR
T1 - Astrocyte elevated gene 1 interacts with acetyltransferase p300 and c-Jun to promote tumor aggressiveness
AU - Liu, Liping
AU - Guan, Hongyu
AU - Li, Yun
AU - Ying, Zhe
AU - Wu, Jueheng
AU - Zhu, Xun
AU - Song, Libing
AU - Li, Jun
AU - Li, Mengfeng
N1 - Publisher Copyright:
© 2017 American Society for Microbiology.
PY - 2017
Y1 - 2017
N2 - 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.
AB - 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.
KW - Acetylation
KW - Astrocyte elevated gene 1 (AEG-1)
KW - C-jun transcription factor
KW - E1A binding protein p300 (p300)
KW - Glioma
UR - http://www.scopus.com/inward/record.url?scp=85013866891&partnerID=8YFLogxK
U2 - 10.1128/MCB.00456-16
DO - 10.1128/MCB.00456-16
M3 - Article
C2 - 27956703
AN - SCOPUS:85013866891
SN - 0270-7306
VL - 37
JO - Molecular and Cellular Biology
JF - Molecular and Cellular Biology
IS - 5
M1 - e00456-16
ER -