A New Player in Neuroblastoma: YAP and Its Role in the Neuroblastoma Microenvironment

Jenny Shim1,2, Kelly C Goldsmith1,2,3

  • 1Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322, USA.

Cancers
|September 28, 2021
PubMed

Insights

Neuroblastoma, a common pediatric cancer, has poor outcomes for recurrent cases. This review explores the Yes-Associated Protein (YAP) and its role in the tumor microenvironment, offering potential therapeutic strategies.

Area of Science:

  • Pediatric Oncology
  • Cancer Biology
  • Tumor Microenvironment Research

Background:

  • Neuroblastoma is the most frequent pediatric solid tumor outside the skull, causing significant mortality.
  • Recurrent high-risk neuroblastomas have a dismal prognosis, with less than 5% achieving a second remission.
  • The tumor microenvironment (TME) is crucial for cancer progression and therapeutic resistance in neuroblastoma.

Purpose of the Study:

  • To review the role of the Yes-Associated Protein (YAP) in neuroblastoma.
  • To elucidate YAP's influence on the neuroblastoma tumor microenvironment (TME).
  • To discuss therapeutic strategies targeting YAP in neuroblastoma.

Main Methods:

  • Literature review focusing on YAP's function in cancer.
  • Analysis of YAP's interaction with the neuroblastoma TME.
  • Synthesis of current and prospective YAP-inhibiting therapies.

Main Results:

  • YAP, a key regulator in the Hippo pathway, impacts cancer proliferation, tumor initiation, and treatment response.
  • YAP signaling is implicated in modulating the neuroblastoma TME.
  • Evidence suggests YAP's involvement in neuroblastoma progression and therapy resistance.

Conclusions:

  • YAP is a significant factor in neuroblastoma development and its TME.
  • Targeting YAP presents a promising therapeutic avenue for neuroblastoma.
  • Further research into YAP inhibition could improve outcomes for high-risk neuroblastoma patients.