Nuclear beta-catenin accumulation associates with epithelial morphogenesis in craniopharyngiomas

Acta Neuropathol. 2007 May;113(5):585-90. doi: 10.1007/s00401-006-0184-3. Epub 2007 Jan 13.

Abstract

Activation of the Wnt/wingless signalling cascade is a key mechanism in developmental morphogenesis, whereas aberrant nuclear accumulation of beta-catenin in adult tissues seems to be associated with neoplastic transformation and tumour progression. Adamantinomatous craniopharyngiomas carry activating mutations in exon 3 of the beta-catenin gene, which results in a distinct pattern of nuclear beta-catenin accumulation in up to 95% of respective tumour specimens. To better characterise the impact of nuclear beta-catenin aggregation in these neoplasms, we systematically examined epithelial differentiation and cell cycle-associated molecules in accumulating compared to non-accumulating tumour cell clusters using a cohort of 65 adamantinomatous craniopharyngiomas. Monoclonal antibodies directed against cytokeratins 5/6 (CK5/6) were utilised to differentiate squamous from simple epithelium, the latter being identified by immunoreactivity for cytokeratins 8 and 18 (CK8/CK18). Intriguingly, nuclear beta-catenin accumulation in whorl-like tumour cell clusters was always associated with a distinct CK8 and CK18 immunoreactivity, whereas surrounding non-accumulating tumour cells showed exclusively squamous differentiation indicated by CK5/6 expression. In addition, a low proliferation activity combined with an increased expression of p21(WAF1/CIP1), a key control protein of the cell cycle, was observed in beta-catenin accumulating cells. Our data support an impact of nuclear beta-catenin on different cytoarchitectural and epithelial differentiation patterns in adamantinomatous craniopharyngiomas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Cell Differentiation
  • Cell Nucleus / metabolism
  • Cell Nucleus / pathology
  • Child
  • Child, Preschool
  • Craniopharyngioma / metabolism*
  • Craniopharyngioma / pathology*
  • Cyclin-Dependent Kinase Inhibitor p21 / metabolism
  • Epithelium / growth & development*
  • Epithelium / pathology
  • Female
  • Gene Expression Regulation, Neoplastic / physiology
  • Humans
  • Keratin-18 / metabolism
  • Keratin-8 / metabolism
  • Male
  • Middle Aged
  • Morphogenesis / physiology*
  • beta Catenin / metabolism*

Substances

  • CTNNB1 protein, human
  • Cyclin-Dependent Kinase Inhibitor p21
  • Keratin-18
  • Keratin-8
  • beta Catenin