Focal adhesion kinase and p53 synergistically decrease neuroblastoma cell survival

Academic Article

Abstract

  • © 2015 Elsevier Inc. Neuroblastoma is the most common extracranial solid tumor of childhood and is responsible for over 15% of pediatric cancer deaths. Focal adhesion kinase (FAK) is a nonreceptor tyrosine kinase that is important in many facets of neuroblastoma tumor development and progression. The p53 oncogene, although wild type in most neuroblastomas, lacks significant function as a tumor suppressor in these tumors. Recent reports have found that FAK and p53 interact in some tumor types. We have hypothesized FAK and p53 coordinately control each other's expression and also interact in neuroblastoma. In the present study, we showed that not only do FAK and p53 interact but each one controls the expression of the other. In addition, we also examined the effects of FAK inhibition combined with p53 activation in neuroblastoma and showed that these two, in combination, had a synergistic effect on neuroblastoma cell survival. The findings from this present study help to further our understanding of the regulation of neuroblastoma tumorigenesis and may provide novel therapeutic strategies and targets for neuroblastoma and other pediatric solid tumors.
  • Published In

    Digital Object Identifier (doi)

    Author List

  • Gillory LA; Stewart JE; Megison ML; Waters AM; Beierle EA
  • Start Page

  • 339
  • End Page

  • 349
  • Volume

  • 196
  • Issue

  • 2