Wnt and BMP signals control intestinal adenoma cell fates

Int J Cancer. 2012 Nov 15;131(10):2242-52. doi: 10.1002/ijc.27500. Epub 2012 Mar 28.


Cellular hierarchies and signals that govern stemness and differentiation of intestinal adenoma cells are not well defined. In this study, we used organotypic culture to investigate the impact of β-catenin and BMP signals in cells that form intestinal adenoma in the mouse. We found that activation of β-catenin signaling by loss of APC or transgenic induction of oncogenic mutant β-catenin (Ctnnb1(mut) ) initiates the conversion of untransformed intestinal cells to tumor cells. These tumor cells display cancer stem cell (CSC) traits such as increased expression of the CSC markers Cd133 and Cd44, a high capacity for self-renewal and unlimited proliferative potential. Subsequent inactivation of transgenic Ctnnb1(mut) results in the reversion of tumor cells to normal intestinal stem cells, which immediately reinstall the cellular hierarchy of the normal intestinal epithelium. Our data demonstrate that oncogenic activation of β-catenin signaling initiates the early steps of intestinal cellular transformation in the absence of irreversible genetic or epigenetic changes. Interestingly, we found that tumor cells in culture and in adenoma produce BMP4, which counteracts CSC-like traits by initiating irreversible cellular differentiation and loss of self-renewal capacity. We conclude that the opposition of stemness-maintaining oncogenic β-catenin signals and autocrine differentiating BMP signals within the adenoma cell provides a rationale for the formation of cellular hierarchies in intestinal adenoma and may serve to limit adenoma growth.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoma / genetics
  • Adenoma / metabolism*
  • Animals
  • Bone Morphogenetic Proteins / genetics
  • Bone Morphogenetic Proteins / metabolism*
  • Cell Differentiation / genetics
  • Gene Expression Regulation, Neoplastic
  • Intestinal Mucosa / metabolism*
  • Intestines / pathology*
  • Mice
  • Mice, Transgenic
  • Mutation
  • Neoplastic Stem Cells / cytology
  • Neoplastic Stem Cells / metabolism
  • Signal Transduction*
  • Spheroids, Cellular
  • Tumor Cells, Cultured
  • Wnt Proteins / metabolism*
  • beta Catenin / genetics
  • beta Catenin / metabolism


  • Bone Morphogenetic Proteins
  • Wnt Proteins
  • beta Catenin