Molecular determinants of glioma cell migration and invasion

Abstract

Object. Migration and invasion are important prerequisites for the infiltrative and destructive growth patterns of malignant gliomas. Infiltrative growth prevents complete tumor resection and causes significant neurological morbidity and mortality. Methods. The authors assessed the expression of matrix metalloproteinases (MMPs) at messenger RNA and protein levels, MMP-2 and MMP-9 activities, and expression levels of a panel of anti- and proapoptotic proteins of the BCL-2 family. They then correlated their findings with α V β 3 integrin expression and the migratory and invasive potentials in 12 human malignant glioma cell lines. Multiple MMPs were expressed by most cell lines. The levels of MMP-2 and MMP-3 and the activities of MMP-2 and MMP-9 correlated with tumor cell invasion. Migration and invasion were also correlated. Although the expression levels of α V β 3 integrin did not predict migration or invasion, a neutralizing α V β 3 integrin antibody inhibited migration and invasion selectively in cell lines that contained a high level of α V β 3 integrin expression, thus indicating the important role of α V β 3 integrin for migration and invasion in this subset of cell lines. An expression pattern of BCL-2 family proteins that favor resistance to apoptosis was associated with enhanced migration, invasion, and MMP activity. Wild-type p53 cell lines migrated farther than mutant p53 cell lines. Conclusions. Activities of MMP-2 and MMP-9 are the best predictors of glioma cell invasion. The α V β 3 integrin mediates migration and invasion in a subset of glioma cell lines, but these processes do not depend on α V β 3 integrin expression. Antiapoptotic BCL-2 family protein expression is a predictor of efficient migration and invasion.