Ontology highlight
ABSTRACT: Background
Dispersal of glioblastoma (GBM) cells leads to recurrence and poor prognosis. Accordingly, molecular pathways involved in dispersal are potential therapeutic targets. The mitogen activated protein kinase/extracellular signal regulated kinase (MAPK/ERK) pathway is commonly dysregulated in GBM, and targeting this pathway with MEK inhibitors has proven effective in controlling tumor growth. Since this pathway also regulates ECM remodeling and actin organization - processes crucial to cell adhesion, substrate attachment, and cell motility - the aim of this study was to determine whether inhibiting this pathway could also impede dispersal.Methods
A variety of methods were used to quantify the effects of the MEK inhibitor, PD0325901, on potential regulators of dispersa
SUBMITTER: Shannon S
PROVIDER: S-EPMC5303286 | biostudies-literature | 2017 Feb
REPOSITORIES: biostudies-literature