Coordinated silencing of MYC-mediated miR-29 by HDAC3 and EZH2 as a therapeutic target of histone modification in aggressive B-Cell lymphomas. Academic Article uri icon

Overview

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.

publication date

  • October 16, 2012

Research

keywords

  • Histone Deacetylases
  • Histones
  • Lymphoma, B-Cell
  • MicroRNAs
  • Polycomb Repressive Complex 2
  • Proto-Oncogene Proteins c-myc

Identity

PubMed Central ID

  • PMC3973134

Scopus Document Identifier

  • 84867606040

Digital Object Identifier (DOI)

  • 10.1016/j.ccr.2012.09.003

PubMed ID

  • 23079660

Additional Document Info

volume

  • 22

issue

  • 4