c-Myb down-regulation is associated with human colon cell differentiation, apoptosis, and decreased Bcl-2 expression

Cancer Res. 1998 Nov 15;58(22):5168-75.

Abstract

c-myb is expressed in human and murine colonic mucosa and elevated expression occurs in premalignant adenomatous polyps and carcinomas. c-Myb is required for colon cell proliferation, and there is evidence of c-myb down-regulation during differentiation. Recently, c-myb has been implicated in hematopoietic cell survival via regulation of bcl-2 gene expression. However, c-myb expression during terminal differentiation and apoptosis in the colonic crypt has not been examined. The experiments in this study examine the spatial and temporal expression of c-Myb protein in vivo using human colonic crypt sections and in vitro in human colon tumor cell lines undergoing butyrate-induced differentiation and apoptosis. Electron microscopy, together with molecular and biochemical analysis, was used to define the differentiation status of the cells. Results demonstrate a decrease in c-Myb expression during the commitment of cells to differentiation and apoptosis. Decreased levels of c-Myb are accompanied by a decrease in Bcl-2. These data suggest that the transcription factor c-Myb has a role in regulating the balance between proliferation, differentiation, and apoptosis in the colonic crypt. Furthermore, elevated c-Myb levels in colon tumor cells may lead to persistent bcl-2 expression, thus protecting tumor cells from programmed cell death.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaline Phosphatase / metabolism
  • Apoptosis / genetics*
  • Butyrates / pharmacology
  • Cell Differentiation / genetics*
  • Colon / cytology*
  • Colon / drug effects
  • Colon / metabolism*
  • Colon / ultrastructure
  • Colonic Neoplasms / metabolism*
  • Colonic Neoplasms / pathology
  • DNA Fragmentation
  • Down-Regulation
  • Enzyme Induction
  • Gene Amplification
  • Genes, bcl-2
  • Humans
  • Oncogenes*
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / metabolism*
  • Tumor Cells, Cultured / drug effects

Substances

  • Butyrates
  • Proto-Oncogene Proteins c-bcl-2
  • Alkaline Phosphatase