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Alteration of FOXM1 expression and macrophage polarization in refractory meningiomas during long-term follow-up
Jun Takei1,2, Toshihide Tanaka1, Akihiko Teshigawara1
1Department of Neurosurgery, Jikei University School of Medicine Kashiwa Hospital, Chiba, Japan.
Abstract:
Malignant progression of grade I meningioma with a long latency period is rare. We experienced grade II/III meningiomas with refractoriness and recurrence from grade I meningiomas through multiple surgeries. Three patients with atypical/anaplastic meningioma experienced long-latent recurrence after initial surgery for grade I (meningothelial) meningioma without following adjuvant radiotherapy were included in the present study. Histological findings of the initial tumors in all cases (case 1, 2, and 3) revealed meningothelial meningioma with 1%, 5%, and 0.1% MIB-1 positive cells, respectively. Surprisingly, magnetic resonance imaging (MRI) detected a recurrent tumor 2, 12, and 12 years after the initial operation, respectively. Case 1 was atypical meningioma after third recurrence, and case 2 and 3 were anaplastic meningioma after second and third recurrence, respectively. The patient in case 2 received adjuvant radiotherapy. In case 2, the tumor recurred intracranial and distant metastasis to the lung with huge substantial pleural effusion was detected. To investigate the pathogenesis of malignant progression from benign to malignant meningioma, CD163/CD68 expression by immunohistochemically and FOXM1 mRNA expression by RT-PCR were compared using surgical specimens from initial and recurrent tumors in all three patients. The ratio of CD163/CD68 positivity and FOXM1 mRNA expression were increased in recurrent tumors compared with matched initial tumors. CD163 and FOXM1 expression levels were induced even in recurrent grade I meningioma, suggesting that macrophage polarization and pro-mitotic transcriptional factor might be associated with clinical behavior of meningioma and be useful as a prediction marker for malignant progression. Careful long-term follow-up is important for early diagnosis of malignant progression in meningiomas, even if grade I meningioma is completely resected. Development of a multidisciplinary approach including radiation and novel molecular targeted therapy is expected for recurrent and malignant meningiomas.
Insights
Malignant progression of benign meningioma is rare but can occur over long periods. Increased CD163/CD68 and FOXM1 expression in recurrent tumors suggests these markers may predict malignant transformation.
Area of Science:
- Neuro-oncology
- Pathology
- Molecular Biology
Background:
- Meningiomas are typically benign tumors, but malignant progression can occur.
- Long latency periods between initial diagnosis and malignant transformation are infrequently observed.
Observation:
- Three patients with initially diagnosed grade I meningioma developed recurrent atypical or anaplastic meningiomas after 2-12 years.
- Recurrent tumors showed increased expression of CD163/CD68 (macrophage markers) and FOXM1 (a pro-mitotic transcription factor) compared to initial tumors.
Findings:
- Elevated CD163/CD68 and FOXM1 expression levels were detected even in recurrent grade I meningiomas, indicating early molecular changes.
- These molecular changes suggest a role for macrophage polarization and FOXM1 in the malignant progression of meningiomas.
Implications:
- CD163, CD68, and FOXM1 may serve as predictive markers for meningioma malignant progression.
- Long-term surveillance is crucial for early detection of malignant transformation in meningiomas.
- Multidisciplinary approaches, including targeted therapies, are needed for managing recurrent and malignant meningiomas.
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