| Literature DB >> 23079660 |
Xinwei Zhang1,2, Xiaohong Zhao1, Warren Fiskus3, Jianhong Lin4, Tint Lwin1, Rekha Rao3, Yizhuo Zhang2, John C Chan5, Kai Fu5, Victor E Marquez6, Selina Chen-Kiang7, Lynn C Moscinski1, Edward Seto1, William S Dalton1, Kenneth L Wright1, Eduardo Sotomayor1, Kapil Bhalla3, Jianguo Tao1.
Abstract
We investigated the transcriptional and epigenetic repression of miR-29 by MYC, HDAC3, and EZH2 in mantle cell lymphoma and other MYC-associated lymphomas. We demonstrate that miR-29 is repressed by MYC through a corepressor complex with HDAC3 and EZH2. MYC contributes to EZH2 upregulation via repression of the EZH2 targeting miR-26a, and EZH2 induces MYC via inhibition of the MYC targeting miR-494 to create positive feedback. Combined inhibition of HDAC3 and EZH2 cooperatively disrupted the MYC-EZH2-miR-29 axis, resulting in restoration of miR-29 expression, downregulation of miR-29-targeted genes, and lymphoma growth suppression in vitro and in vivo. These findings define a MYC-mediated miRNA repression mechanism, shed light on MYC lymphomagenesis mechanisms, and reveal promising therapeutic targets for aggressive B-cell malignancies.Entities:
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Year: 2012 PMID: 23079660 PMCID: PMC3973134 DOI: 10.1016/j.ccr.2012.09.003
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743