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.

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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