Role of Stat3alpha in mutant EGFR signaling in Glioma
Project Number5R01CA099931-05
Former Number1R01CA095466-01
Contact PI/Project LeaderSCHAEFER, TIMOTHY S
Awardee OrganizationMESO SCALE DIAGNOSTICS, LLC
Description
Abstract Text
DESCRIPTION: (provided by applicant)
Glioblastoma multiforme (GBM) are highly vascularized tumors of the brain. One
of the most frequently observed genetic alterations in GBM is the rearrangement
of the epidermal growth factor receptor (EGFR). This mutation EGFRvIII, the
result of exons 2-8, results in a receptor that no longer binds ligand and is
constitutively activated. The expression of this receptor results in the
activation of a number of signaling pathways and confers an increase in the
proliferative capacity and tumorigenicity of cells expressing the receptor.
Signal transducers and activators of transcription (Stat) proteins are a family
of latent transcription factors normally activated by numerous cytokines and
growth factors. One member of the family, Stat3, has been implicated in
aberrant cell proliferation and constitutively activated Stat3cx has been seen
in several types of neoplastic cells and solid tumors. In experiments designed
to explore Stat3 signaling in human brain tumors, we have found that Stat3a is
constitutively activated in low- and high-grade glioma (compared to normal
brain tissue). In other preliminary experiments, we have demonstrated a direct
interaction between Stat3a and EGFRvIII in extracts from cells that express
both proteins. The expression of EGFRvIII leads to the activation of Stat3a
with a concomitant increase in Stat3a-mediated transcription and this
activation required serine phosphorylation on serine residue 727 indicating a
convergence of more than one signaling event in Stat3a activation by EG FRvIII.
In experiments described here, we propose to determine the role of Stat3a in
the growth properties imparted by EGFRvIII expression both in vitro and in vivo
using EGFRvIII derived mutants that cannot activate Stat3a and by the use of
dominant-negative Stat3a molecules to directly block Stat3cx mediated
signaling. The in vitro studies will be performed using cultured glioma cells
that express EGFRvIII while the In vivo experiments will be performed using a
novel intracranial induction system developed in our laboratory.
Public Health Relevance Statement
Data not available.
NIH Spending Category
No NIH Spending Category available.
Project Terms
angiogenesisapoptosisathymic mousebiological signal transductioncell linecell proliferationepidermal growth factorgene induction /repressionglioblastoma multiformegrowth factor receptorsmolecular cloningneoplastic growthpoint mutationprotein structure functionreceptor bindingreceptor expressionsite directed mutagenesisterminal nick end labelingtranscription factortransfectionxenotransplantation
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