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Author Spotlight: Modeling Brain Tumors In Vivo Using Electroporation-Based Delivery of Plasmid DNA Representing Patient Mutation Signatures
Published on: June 23, 2023
Meningioma: current updates on genetics, classification, and mouse modeling
Frank Szulzewsky1, H Nayanga Thirimanne1, Eric C Holland1,2
1Human Biology Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Meningiomas, common brain tumors, can be aggressive. Genetic mutations, like NF2 loss, influence tumor behavior, driving research into new treatments and mouse models for better understanding.
Area of Science:
- Neuro-oncology
- Genetics
- Tumor Biology
Background:
- Meningiomas are the most common primary brain tumors in adults.
- While often benign and surgically curable, a subset exhibits aggressive behavior, invasion, and recurrence.
- Histopathological classification may not fully predict tumor aggressiveness or recurrence.
Purpose of the Study:
- To review recent advances in meningioma biology and classification.
- To highlight common genetic mutations and their impact on tumor behavior.
- To discuss novel genetically engineered mouse models for studying meningiomas.
Main Methods:
- Analysis of large-scale molecular data including whole exome/genome sequencing, DNA methylation sequencing, and RNA sequencing.
- Review of current literature on genetic aberrations in meningiomas.
- Examination of newly developed genetically engineered mouse models.
Main Results:
- NF2 loss is the most common genetic aberration, found in both low- and high-grade meningiomas.
- NF2-wildtype meningiomas frequently harbor mutations in TRAF7, KLF4, AKT1, PI3KCA, and SMO, and are often benign.
- New genetically engineered mouse models are emerging to study specific mutations.
Conclusions:
- Molecular data provides new insights into meningioma biology, risk factors, and prognostic subtypes.
- Understanding genetic aberrations is crucial for predicting and treating aggressive meningiomas.
- Genetically engineered mouse models offer promising tools for future research into meningioma pathogenesis and treatment.
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