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ΔNp63, a Target of DEC1 and Histone Deacetylase 2, Modulates the Efficacy of Histone Deacetylase Inhibitors in Growth Suppression and Keratinocyte Differentiation
被引:29
作者:
Qian, Yingjuan
[1
]
Jung, Yong-Sam
[1
]
Chen, Xinbin
[1
]
机构:
[1] Univ Calif Davis, Comparat Oncol Lab, Davis, CA 95616 USA
基金:
美国国家卫生研究院;
关键词:
CELL-CYCLE ARREST;
P53;
FAMILY;
TRANSCRIPTION FACTOR;
PROXIMAL PROMOTER;
CANCER CELLS;
C-TERMINUS;
E-BOX;
P63;
EXPRESSION;
STRA13;
D O I:
10.1074/jbc.M110.207241
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The p63 gene, a member of the p53 family, is expressed as TA and Delta N isoforms. Delta Np63 is the predominant isoform expressed in cells of epithelial origin and frequently overexpressed in cancers. However, what regulates p63 expression is uncertain. Here, we showed that Delta Np63 is regulated by the transcription factor DEC1, a p53 family target. We also showed that the ability of DEC1 to regulate Delta Np63 is enhanced by histone deacetylase (HDAC) inhibitors or knockdown of histone deacetylase 2 (HDAC2). Consistent with this, we found that DEC1 and HDAC2 physically interact and knockdown of HDAC2 leads to increased binding of DEC1 to the Delta Np63 promoter. Interestingly, we found that growth suppression induced by HDAC inhibitors is attenuated by ectopic expression of DEC1 in a Delta Np63-dependent manner. In addition, we showed that ectopic expression of DEC1 inhibits, whereas knockdown of DEC1 promotes, keratinocyte differentiation via modulating Delta Np63 expression. Finally, we showed that DEC1 cooperates with HDAC inhibitors to further decrease keratinocyte differentiation. Together, we conclude that Delta Np63 is a novel target of DEC1 and HDAC2 and modulates the efficacy of HDAC inhibitors in growth suppression and keratinocyte differentiation.
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页码:12033 / 12041
页数:9
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