Transglutaminase 2 expression is increased as a function of malignancy grade and negatively regulates cell growth in meningioma

PLoS One. 2014 Sep 23;9(9):e108228. doi: 10.1371/journal.pone.0108228. eCollection 2014.

Abstract

Most meningiomas are benign, but some clinical-aggressive tumors exhibit brain invasion and cannot be resected without significant complications. To identify molecular markers for these clinically-aggressive meningiomas, we performed microarray analyses on 24 primary cultures from 21 meningiomas and 3 arachnoid membranes. Using this approach, increased transglutaminase 2 (TGM2) expression was observed, which was subsequently validated in an independent set of 82 meningiomas by immunohistochemistry. Importantly, the TGM2 expression level was associated with increasing WHO malignancy grade as well as meningioma recurrence. Inhibition of TGM2 function by siRNA or cystamine induced meningioma cell death, which was associated with reduced AKT phosphorylation and caspase-3 activation. Collectively, these findings suggest that TGM2 expression increases as a function of malignancy grade and tumor recurrence and that inhibition of TGM2 reduces meningioma cell growth.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Caspase 3 / metabolism
  • Cell Death / physiology
  • GTP-Binding Proteins / genetics
  • GTP-Binding Proteins / metabolism*
  • Humans
  • Meningeal Neoplasms / enzymology*
  • Meningeal Neoplasms / pathology
  • Meningioma / enzymology*
  • Meningioma / pathology
  • Neoplasm Grading
  • Protein Glutamine gamma Glutamyltransferase 2
  • Proto-Oncogene Proteins c-akt / metabolism
  • Transglutaminases / genetics
  • Transglutaminases / metabolism*

Substances

  • TGM2 protein, human
  • Protein Glutamine gamma Glutamyltransferase 2
  • Transglutaminases
  • Proto-Oncogene Proteins c-akt
  • Caspase 3
  • GTP-Binding Proteins

Grants and funding

This work was supported by the National Science Council Taiwan (NSC 100-2314-B-182A-015-MY3 to Y.H.; NSC 100-2321-B-182A-001- to T.Y.) and the Chang Gung Medical Foundation Taiwan (grant number CMRPG392052 to Y.H.; CMRPG392201 to T.Y.). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.