» Articles » PMID: 23591193

The Role of the WNT/β-catenin Pathway in Central Nervous System Primitive Neuroectodermal Tumours (CNS PNETs)

Overview
Journal Br J Cancer
Specialty Oncology
Date 2013 Apr 18
PMID 23591193
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Central nervous system primitive neuroectodermal tumours (CNS PNETs) are embryonal tumours occurring predominantly in children. Current lack of knowledge regarding their underlying biology hinders development of more effective treatments. We previously identified WNT/β-catenin pathway activation in one-third of CNS PNETs, which was potentially linked to a better prognosis. In this study, we have extended our cohort, achieving a statistically significant correlation with prognosis. We additionally investigated the biological effects of WNT/β-catenin pathway activation in tumour pathogenesis.

Methods: A total of 42 primary and 8 recurrent CNS PNETs were analysed for WNT/β-catenin pathway status using β-catenin immunohistochemistry. Genomic copy number and mRNA expression data were analysed to identify a molecular profile linked to WNT/β-catenin pathway activation.

Results: Pathway activation was seen in 26% of CNS PNETs and was significantly associated with longer overall survival. Genes displaying a significant difference in expression levels, between tumours with and without WNT/β-catenin pathway activation, included several involved in normal CNS development suggesting aberrant pathway activation may be disrupting this process.

Conclusion: We have identified WNT/β-catenin pathway status as a marker, which could potentially be used to stratify disease risk for patients with CNS PNET. Gene expression data suggest pathway activation is disrupting normal differentiation in the CNS.

Citing Articles

Meta-analysis identifies key genes and pathways implicated in Benzo[a]pyrene exposure response.

Zhu M, Hwang J, Xu C Chemosphere. 2024; 364:143121.

PMID: 39154768 PMC: 11424241. DOI: 10.1016/j.chemosphere.2024.143121.


Pan-caner analysis identifies PSMA7 as a targets for amplification at 20q13.33 in tumorigenesis.

Sheng G, Li F, Jin W, Wang K Sci Rep. 2024; 14(1):3034.

PMID: 38321088 PMC: 10847487. DOI: 10.1038/s41598-024-53585-0.


Retinoic acid induces differentiation in neuroblastoma via ROR1 by modulating retinoic acid response elements.

Illendula A, Fultang N, Peethambaran B Oncol Rep. 2020; 44(3):1013-1024.

PMID: 32705280 PMC: 7388440. DOI: 10.3892/or.2020.7681.


Transcriptional co-expression regulatory network analysis for Snail and Slug identifies , an inflammatory cytokine receptor, to be preferentially expressed in ST-EPN- and PF-EPN-A molecular subgroups of intracranial ependymomas.

Malgulwar P, Sharma V, Tomar A, Verma C, Nambirajan A, Singh M Oncotarget. 2018; 9(84):35480-35492.

PMID: 30464804 PMC: 6231457. DOI: 10.18632/oncotarget.26211.


Integrated bioinformatic analysis unveils significant genes and pathways in the pathogenesis of supratentorial primitive neuroectodermal tumor.

Wang G, Li L, Liu B, Han X, Wang C, Wang J Onco Targets Ther. 2018; 11:1849-1859.

PMID: 29670360 PMC: 5894672. DOI: 10.2147/OTT.S148776.


References
1.
Perala N, Immonen T, Sariola H . The expression of plexins during mouse embryogenesis. Gene Expr Patterns. 2005; 5(3):355-62. DOI: 10.1016/j.modgep.2004.10.001. View

2.
Miller S, Rogers H, Lyon P, Rand V, Adamowicz-Brice M, Clifford S . Genome-wide molecular characterization of central nervous system primitive neuroectodermal tumor and pineoblastoma. Neuro Oncol. 2011; 13(8):866-79. PMC: 3145471. DOI: 10.1093/neuonc/nor070. View

3.
Ellison D, Kocak M, Dalton J, Megahed H, Lusher M, Ryan S . Definition of disease-risk stratification groups in childhood medulloblastoma using combined clinical, pathologic, and molecular variables. J Clin Oncol. 2010; 29(11):1400-7. PMC: 3525837. DOI: 10.1200/JCO.2010.30.2810. View

4.
Ellison D, Onilude O, Lindsey J, Lusher M, Weston C, Taylor R . beta-Catenin status predicts a favorable outcome in childhood medulloblastoma: the United Kingdom Children's Cancer Study Group Brain Tumour Committee. J Clin Oncol. 2005; 23(31):7951-7. DOI: 10.1200/JCO.2005.01.5479. View

5.
Pfaffl M . A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 2001; 29(9):e45. PMC: 55695. DOI: 10.1093/nar/29.9.e45. View