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Chen L, Tweddle DA. p53, SKP2, and DKK3 as MYCN Target Genes and Their Potential Therapeutic Significance. Front Oncol. 2012;2:173doi: 10.3389/fonc.2012.00173.
Chen, L., & Tweddle, D. A. (2012). p53, SKP2, and DKK3 as MYCN Target Genes and Their Potential Therapeutic Significance. Frontiers in oncology, 2173. https://doi.org/10.3389/fonc.2012.00173
Chen, Lindi, and Tweddle, Deborah A. "p53, SKP2, and DKK3 as MYCN Target Genes and Their Potential Therapeutic Significance." Frontiers in oncology vol. 2 (2012): 173. doi: https://doi.org/10.3389/fonc.2012.00173
Chen L, Tweddle DA. p53, SKP2, and DKK3 as MYCN Target Genes and Their Potential Therapeutic Significance. Front Oncol. 2012 Nov 28;2:173. doi: 10.3389/fonc.2012.00173. eCollection 2012. PMID: 23226679; PMCID: PMC3508619.
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Front Oncol. 2012 Nov 28;2:173. doi: 10.3389/fonc.2012.00173. eCollection 2012.

p53, SKP2, and DKK3 as MYCN Target Genes and Their Potential Therapeutic Significance.

Frontiers in oncology

Lindi Chen, Deborah A Tweddle

Affiliations

  1. Newcastle Cancer Centre, Northern Institute for Cancer Research, Newcastle University Newcastle, UK.

PMID: 23226679 PMCID: PMC3508619 DOI: 10.3389/fonc.2012.00173

Abstract

Neuroblastoma is the most common extra-cranial solid tumor of childhood. Despite significant advances, it currently still remains one of the most difficult childhood cancers to cure, with less than 40% of patients with high-risk disease being long-term survivors. MYCN is a proto-oncogene implicated to be directly involved in neuroblastoma development. Amplification of MYCN is associated with rapid tumor progression and poor prognosis. Novel therapeutic strategies which can improve the survival rates whilst reducing the toxicity in these patients are therefore required. Here we discuss genes regulated by MYCN in neuroblastoma, with particular reference to p53, SKP2, and DKK3 and strategies that may be employed to target them.

Keywords: DKK3; MDM2-p53 antagonists; MYCN; SKP2; neuroblastoma; p53

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