Abstract 2247: SHP2 expression and function in different subtypes of glioblastoma

SHP2, a Src-homology 2 domain (SH2)-containing tyrosine phosphatase encoded by PTPN11, is a ubiquitously expressed cytoplasmic enzyme that regulates events downstream of several growth factor and cytokine receptors involved in survival, pro-migratory and differentiation signaling. In the normal developing nervous system, SHP2 is involved in neural stem cell self renewal. Dysregulation of SHP2 function has been implicated in tumorigenesis and characterized as an activated downstream regulator of oncogenes in gastric carcinoma, anaplastic large-cell lymphoma, breast cancer and glioblastoma. In the context of glioblastoma, we have shown that SHP2, and specifically its phosphatase activity, is directly involved in EGFRvIII-induced oncogenesis. Our present research aims at understanding the function of SHP2 within different glioma cell types as well as the four characterized subtypes of glioblastoma (GBM). Genomic analysis of SHP2 expression using the TCGA GBM cohort shows differential expression among the recently characterized subtypes of GBMs, with higher SHP2 mRNA expression in the classical subtype. Additionally, SHP2 is preferentially expressed in glioma stem cells versus differentiated cells isolated from the same patients. Furthermore, our current analysis shows that reduction of SHP2 expression in glioma stem cells affects the expression of genes linked to stemness. SHP2 PTPase function may therefore be a link between normal stem cell proliferation and gliomagenesis induced by EGFR/RTK activated signaling. Citation Format: Laura Roccograndi, Yingtao Bi, Ramana Davuluri, Nadia Dahmane, Donald M. O9Rourke. SHP2 expression and function in different subtypes of glioblastoma. [abstract]. In: Proceedings of the 106th Annual Meeting of the American Association for Cancer Research; 2015 Apr 18-22; Philadelphia, PA. Philadelphia (PA): AACR; Cancer Res 2015;75(15 Suppl):Abstract nr 2247. doi:10.1158/1538-7445.AM2015-2247