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Updated: Mar 29, 2026

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Wnt5a, Ryk and Ror2 expression in glioblastoma subgroups
Yuil Kim1, Mineui Hong1, In-Gu Do1
1Department of Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Wnt5a signaling, involving Ryk and Ror2 receptors, is present in glioblastoma but doesn't impact prognosis. Beta-catenin showed a shorter survival in glioblastoma with oligodendroglioma component.
Area of Science:
- Neuro-oncology
- Molecular Biology
- Cancer Signaling
Background:
- Wnt5a, a non-canonical Wnt ligand, exhibits context-dependent roles in neoplasms.
- Previous studies indicate increased Wnt5a expression and Ryk-mediated invasion in glioblastomas.
Purpose of the Study:
- To investigate the expression of Wnt5a, its receptors Ryk and Ror2, and β-catenin in glioblastoma.
- To analyze associations with clinicopathological/molecular variables and prognosis.
Main Methods:
- Protein expression analysis of Wnt5a, Ryk, Ror2, and β-catenin in 186 glioblastoma cases.
- Statistical analysis of correlations with clinicopathological and molecular data.
- Prognostic impact assessment.
Main Results:
- Wnt5a, Ryk, and Ror2 were expressed in all glioblastoma cases.
- Ryk and Ror2 expression correlated with Wnt5a expression.
- No prognostic impact of Wnt5a, Ryk, or Ror2 was observed; β-catenin correlated with shorter progression-free survival in the GBMO subgroup.
Conclusions:
- Findings support Ryk-mediated Wnt5a effects in glioblastoma.
- Suggests a potential role for Ror2 in Wnt5a signaling pathways within glioblastoma.
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