Polycomb-mediated loss of miR-31 activates NIK-dependent NF-κB pathway in adult T cell leukemia and other cancers

Cancer Cell. 2012 Jan 17;21(1):121-35. doi: 10.1016/j.ccr.2011.12.015.

Abstract

Constitutive NF-κB activation has causative roles in adult T cell leukemia (ATL) caused by HTLV-1 and other cancers. Here, we report a pathway involving Polycomb-mediated miRNA silencing and NF-κB activation. We determine the miRNA signatures and reveal miR-31 loss in primary ATL cells. MiR-31 negatively regulates the noncanonical NF-κB pathway by targeting NF-κB inducing kinase (NIK). Loss of miR-31 therefore triggers oncogenic signaling. In ATL cells, miR-31 level is epigenetically regulated, and aberrant upregulation of Polycomb proteins contribute to miR-31 downregulation in an epigenetic fashion, leading to activation of NF-κB and apoptosis resistance. Furthermore, this emerging circuit operates in other cancers and receptor-initiated NF-κB cascade. Our findings provide a perspective involving the epigenetic program, inflammatory responses, and oncogenic signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Epigenesis, Genetic
  • Gene Expression Profiling
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Leukemia-Lymphoma, Adult T-Cell / genetics*
  • Leukemia-Lymphoma, Adult T-Cell / metabolism
  • MicroRNAs / genetics*
  • NF-kappa B / genetics
  • NF-kappa B / metabolism*
  • NF-kappaB-Inducing Kinase
  • Oligonucleotide Array Sequence Analysis
  • Polycomb-Group Proteins
  • Protein Serine-Threonine Kinases / metabolism
  • Protein Serine-Threonine Kinases / physiology*
  • Repressor Proteins / genetics*
  • Repressor Proteins / metabolism
  • Repressor Proteins / physiology
  • Signal Transduction
  • T-Lymphocytes / metabolism
  • T-Lymphocytes / pathology*

Substances

  • MIRN31 microRNA, human
  • MicroRNAs
  • NF-kappa B
  • Polycomb-Group Proteins
  • Repressor Proteins
  • Protein Serine-Threonine Kinases

Associated data

  • GEO/GSE31629
  • GEO/GSE33602
  • GEO/GSE33615