Nuclear translocation of β-catenin is essential for glioma cell survival

J Neuroimmune Pharmacol. 2012 Dec;7(4):892-903. doi: 10.1007/s11481-012-9354-3. Epub 2012 Mar 15.


Identification of molecular pathways that are essential for cancer cell survival is vital for understanding the underlying biology, as well as to design effective cancer therapeutics. β-catenin, a multifunctional oncogenic protein, participates in cell development. Its multifaceted functions primarily lie to the subcellular distribution. The present study demonstrated that β-catenin accumulated in the nucleus to a greater extent in high-grade gliomas compared with low-grade gliomas. In addition, nuclear localization correlated with a worse prognosis for patients, as determined by immunohistochemical analysis of 74 glioma samples. Nuclear expression of β-catenin was down-regulated in LN229 and U87 glioma cells by a small molecule inhibitor of β-catenin/TCF4 signaling, demonstrating strongly inhibited β-catenin/TCF4 transcriptional activity and STAT3 luciferase activity, as well as decreased mRNA and protein levels of nuclear β-catenin, TCF4, EGFR, AKT1, AKT2 and STAT3. Furthermore, repressed nuclear translocation of β-catenin resulted in inhibition of proliferation and invasiveness, and also induced apoptosis of glioma cells. Similar results were also observed in vivo; intratumoral injection of such small molecule inhibitor downregulated expression of nuclear β-catenin, TCF4, and components of the EGFR pathway, and also delayed tumor growth in nude mice harboring subcutaneous U87 xenografts. Results from the present study provided evidence that nuclear accumulation of β-catenin participated in malignant progression of gliomas and implicated poor prognosis, highlighting it as a potential therapeutic target for gliomas.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Blotting, Western
  • Cell Cycle / drug effects
  • Cell Line, Tumor
  • Cell Nucleus / genetics*
  • Cell Survival / genetics
  • Cell Survival / physiology
  • Colony-Forming Units Assay
  • Fluorescent Antibody Technique
  • Glioma / genetics*
  • Humans
  • Immunohistochemistry
  • Luciferases / genetics
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Polymerase Chain Reaction
  • Sulfonamides / pharmacology
  • Translocation, Genetic / physiology*
  • Xenograft Model Antitumor Assays
  • beta Catenin / antagonists & inhibitors
  • beta Catenin / genetics*
  • beta Catenin / physiology*


  • FH535
  • Sulfonamides
  • beta Catenin
  • Luciferases