A requirement for DICER to maintain full promoter CpG island hypermethylation in human cancer cells

Cancer Res. 2008 Apr 15;68(8):2570-5. doi: 10.1158/0008-5472.CAN-07-6405.

Abstract

Promoter hypermethylation is a prevalent phenomenon, found in virtually all cancer types studied thus far, and accounts for tumor suppressor gene silencing in the absence of genetic mutations. The mechanism behind the establishment and maintenance of such aberrant hypermethylation has been under intense study. Here, we have uncovered a link between aberrant gene silencing associated with promoter CpG island DNA methylation and the siRNA/miRNA processing enzyme, DICER, in human cancer cells. By comparing demethylated HCT116 colon cancer cells with HCT116 cells genetically rendered hypomorphic for DICER, we identified a group of epigenetically silenced genes that became reactivated in the absence of functional DICER. This reactivation is associated with a dramatic loss of localized promoter DNA hypermethylation. Thus, intact DICER is required to maintain full promoter DNA hypermethylation of select epigenetically silenced loci in human cancer cells.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Cell Line, Tumor
  • Colonic Neoplasms / genetics
  • Colonic Neoplasms / pathology
  • CpG Islands / genetics*
  • DNA Methylation*
  • DNA, Neoplasm / genetics
  • Gene Silencing*
  • Humans
  • Oligonucleotide Array Sequence Analysis
  • Promoter Regions, Genetic*
  • RNA, Neoplasm / genetics
  • RNA, Neoplasm / isolation & purification
  • Reverse Transcriptase Polymerase Chain Reaction
  • Ribonuclease III / genetics*
  • Ribonuclease III / metabolism

Substances

  • DNA, Neoplasm
  • RNA, Neoplasm
  • Ribonuclease III