Roles of the NF-kappaB Pathway in Glioblastoma Stem Cells and Chordoma Public Deposited

Downloadable Content

Download PDF
Alternate title
  • Roles of the NF-κB Pathway in Glioblastoma Stem Cells and Chordoma
Last Modified
  • March 20, 2019
  • Rinkenbaugh, Amanda
    • Affiliation: School of Medicine, Department of Pathology and Laboratory Medicine
  • The NF-κB pathway consists of a family of five transcription factors: RelA/p65, RelB, c-Rel, p100/p52, and p105/p50. Originally discovered for its involvement in inflammation and immune signaling, aberrant constitutive NF-κB activation is seen in many tumor types. NF-κB-dependent target gene regulation mediates several hallmarks of cancer, including survival, suppression of apoptosis, and invasion. This work examines NF-κB signaling in both glioblastoma and chordoma samples. In the first project, NF-κB is found to mediate cancer stem cell maintenance in glioblastoma explants. Both genetic and pharmacological NF-κB inhibition impair neurosphere formation at limiting dilutions. Use of an ex vivo brain slice co-culture model confirmed the in vitro findings, providing a novel platform for drug testing in glioblastoma studies that bridges the gap between cell culture and intracranial animal models. In the second project, NF-κB regulates proliferation and invasion of chordoma cell lines. Due to the rarity of chordomas, these tumors have not been well- characterized at a molecular level. These results provide some of the early evidence for NF- κB activation, potentially through regulation of IL-6, IL-8, and MMP9. Both of these studies suggest that IKK/NF-κB inhibition could provide therapeutic benefit in glioblastoma and chordoma, affecting multiple phenotypes that drive the poor prognosis of these tumors.
Date of publication
Resource type
Rights statement
  • In Copyright
  • Deshmukh, Mohanish
  • Baldwin, Albert
  • Miller, C. Ryan
  • Vaziri, Cyrus
  • Coleman, William
  • Doctor of Philosophy
Degree granting institution
  • University of North Carolina at Chapel Hill Graduate School
Graduation year
  • 2016

This work has no parents.