Abstract
Neuroblastoma, the most common extracranial solid tumor of childhood, is thought to originate from undifferentiated neural crest cells. Amplification of the MYC family member, MYCN, is found in ∼25% of cases and correlates with high-risk disease and poor prognosis. Currently, amplification of MYCN remains the best-characterized genetic marker of risk in neuroblastoma. This article reviews roles for MYCN in neuroblastoma and highlights recent identification of other driver mutations. Strategies to target MYCN at the level of protein stability and transcription are also reviewed.
Citation impact
642
total citations
- FWCI
- —
- Percentile
- —
- References
- 211
Citations per year
Authors
2Topics & keywords
Topics
Keywords
- Neuroblastoma
- Medicine
- Neurosurgery
- Neurology
- Pediatric Neurology
- General surgery
- Pediatrics
- Surgery
UN Sustainable Development Goals
- No poverty
No related works found for this paper.