The Role of EGFR-Met Interactions in the Pathogenesis of Glioblastoma and Resistance to Treatment

Title:The Role of EGFR-Met Interactions in the Pathogenesis of Glioblastoma and Resistance to Treatment

Volume: 17 Issue: 3

Author(s): Gao Guo, Ram N. Narayan, Lindsay Horton, Toral R. Patel and Amyn A. Habib

Affiliation:

Keywords: EGFR, Met, glioma, glioblastoma, GBM, targeted treatment, synergistic, antagonistic. EGFR wild type, EGFRvIII, EGFR mutants.

Abstract: Glioblastoma (GBM) is the most common primary malignant brain tumor in adults. It is a devastating and intractable disease with a poor outcome. Aberrant receptor tyrosine kinase signaling is a key driver in gliomagenesis and resistance to treatment. EGFR gene amplification and mutations are an important genetic alteration in GBM resulting in increased expression of EGFR wild type (EGFRwt) as well as mutant oncogenic forms of the EGFR. EGFRvIII is the most common oncogenic mutant in GBM and is usually co-expressed with EGFRwt. EGFRvIII does not bind ligand and is constitutively active. Recent studies have also highlighted a key role for Met in gliomagenesis and the EGFR and Met may act in concert to promote the malignant phenotype. Met is transactivated by EGFRvIII and plays a key role in EGFRvIII-mediated resistance to targeted treatment. HGF, a Met ligand, is highly expressed in GBM. HGF and Met create an important autocrine signaling loop that promotes GBM invasion. In addition, HGF/Met is able to induce EGFR activation, leading to enhanced activation of oncogenic signaling in GBM. In this review, we discuss the evidence for EGFR and Met interaction in GBM and discuss the mechanisms and biological consequences of transactivation between the two kinases. Additionally, we discuss the therapeutic potential of targeting both EGFR and Met signaling for the treatment of GBM.

Cite this article as:

Guo Gao, Narayan N. Ram, Horton Lindsay, Patel R. Toral and Habib A. Amyn, The Role of EGFR-Met Interactions in the Pathogenesis of Glioblastoma and Resistance to Treatment, Current Cancer Drug Targets 2017; 17 (3) . https://dx.doi.org/10.2174/1568009616666161215162515