| Literature DB >> 24739462 |
Min Yan1, Yan Zhang2, Bin He1, Jin Xiang3, Zi-feng Wang3, Fei-meng Zheng3, Jie Xu3, Ming-yuan Chen3, Yu-liang Zhu4, Hai-jun Wen3, Xiang-bo Wan5, Cai-feng Yue3, Na Yang3, Wei Zhang3, Jia-liang Zhang3, Jing Wang3, Yang Wang6, Lian-hong Li6, Yi-xin Zeng3, Eric W-F Lam7, Mien-Chie Hung8, Quentin Liu9.
Abstract
Lack of cellular differentiation is a key feature of nasopharyngeal carcinoma (NPC), but it also presents as a unique opportunity for intervention by differentiation therapy. Here using RNA-seq profiling analysis and functional assays, we demonstrate that reduced IKKα expression is responsible for the undifferentiated phenotype of NPC. Conversely, overexpression of IKKα induces differentiation and reduces tumorigenicity of NPC cells without activating NF-κB signalling. Importantly, we describe a mechanism whereby EZH2 directs IKKα transcriptional repression via H3K27 histone methylation on the IKKα promoter. The differentiation agent, retinoic acid, increases IKKα expression by suppressing EZH2-mediated H3K27 histone methylation, resulting in enhanced differentiation of NPC cells. In agreement, an inverse correlation between IKKα (low) and EZH2 (high) expression is associated with a lack of differentiation in NPC patient samples. Collectively, these findings demonstrate a role for IKKα in NPC differentiation and reveal an epigenetic mechanism for IKKα regulation, unveiling a new avenue for differentiation therapy.Entities:
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Year: 2014 PMID: 24739462 DOI: 10.1038/ncomms4661
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919