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长期随访期间难治性脑膜瘤中FOXM1表达的改变及巨噬细胞极化

Alteration of FOXM1 expression and macrophage polarization in refractory meningiomas during long-term follow-up.

作者信息

Takei Jun, Tanaka Toshihide, Teshigawara Akihiko, Tochigi Satoru, Hasegawa Yuzuru, Murayama Yuichi

机构信息

Department of Neurosurgery, Jikei University School of Medicine Kashiwa Hospital, Chiba, Japan.

Department of Neurosurgery, Jikei University School of Medicine, Tokyo, Japan.

出版信息

Transl Cancer Res. 2021 Jan;10(1):553-566. doi: 10.21037/tcr-20-1896.

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.

摘要

I级脑膜瘤的恶性进展且潜伏期较长的情况较为罕见。我们经历了I级脑膜瘤通过多次手术转变为具有难治性和复发性的II/III级脑膜瘤。本研究纳入了3例非典型/间变性脑膜瘤患者,他们在初次手术切除I级(脑膜皮型)脑膜瘤后,未进行辅助放疗,经历了长时间的复发。所有病例(病例1、2和3)初始肿瘤的组织学检查结果显示为脑膜皮型脑膜瘤,MIB-1阳性细胞分别为1%、5%和0.1%。令人惊讶的是,磁共振成像(MRI)分别在初次手术后2年、12年和12年检测到复发肿瘤。病例1在第三次复发后为非典型脑膜瘤,病例2和3分别在第二次和第三次复发后为间变性脑膜瘤。病例2的患者接受了辅助放疗。在病例2中,肿瘤在颅内复发,并检测到远处转移至肺部,伴有大量胸腔积液。为了研究从良性脑膜瘤向恶性脑膜瘤恶性进展的发病机制,使用所有3例患者初始肿瘤和复发肿瘤的手术标本,通过免疫组织化学比较了CD163/CD68的表达,并通过逆转录聚合酶链反应(RT-PCR)比较了FOXM1 mRNA的表达。与匹配的初始肿瘤相比,复发肿瘤中CD163/CD68阳性率和FOXM1 mRNA表达增加。即使在复发的I级脑膜瘤中也诱导了CD163和FOXM1的表达水平,这表明巨噬细胞极化和促有丝分裂转录因子可能与脑膜瘤的临床行为相关,并可作为恶性进展的预测标志物。即使I级脑膜瘤已完全切除,仔细的长期随访对于脑膜瘤恶性进展的早期诊断也很重要。对于复发性和恶性脑膜瘤,期望开发包括放疗和新型分子靶向治疗在内的多学科方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caee/8797451/397abc946aea/tcr-10-01-553-f1.jpg

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