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Decoding the Role of DVL1 in Intracranial Meningioma
Anja Bukovac1,2, Katarina Dragičević3, Anja Kafka1,2
1Laboratory of Neurooncology, Croatian Institute for Brain Research, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.
Disruptions in the DVL1 gene are linked to meningioma progression. Nuclear DVL1 expression correlates with higher tumor grade and Wnt pathway activation, suggesting its potential as a biomarker.
Area of Science:
- Neuro-oncology
- Molecular biology
- Genetics
Background:
- The Wnt signaling pathway is implicated in meningioma progression.
- The precise role of DVL1, a key Wnt mediator, in meningioma remains unclear.
- Investigating DVL1's PDZ domain is crucial for understanding its interactions and function.
Purpose of the Study:
- To investigate the impact of DVL1 gene alterations on human intracranial meningioma progression.
- To analyze genetic alterations within the DVL1 PDZ domain.
- To assess the correlation between DVL1 expression and meningioma characteristics.
Main Methods:
- Genetic analysis for microsatellite instability and loss of heterozygosity.
- Sequencing of the DVL1 PDZ gene region to identify mutations.
- Immunohistochemistry to evaluate DVL1 and active β-catenin expression.
Main Results:
- Microsatellite instability (9.09%) and loss of heterozygosity (6.06%) were observed.
- Repetitive deletions and duplications in the DVL1 PDZ gene region were identified.
- Nuclear DVL1 expression significantly correlated with higher active β-catenin levels (p=0.029) and increased meningioma grade (p=0.030).
Conclusions:
- DVL1 gene alterations influence meningioma progression.
- Nuclear DVL1 expression serves as a potential biomarker for meningioma progression.
- DVL1 expression indicates Wnt signaling pathway activation in meningiomas.
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