Malignant progression to anaplastic meningioma: Neuropathology, molecular pathology, and experimental models

被引:25
|
作者
Cimino, Patrick J. [1 ]
机构
[1] Univ Washington, Div Neuropathol, Dept Pathol, Seattle, WA 98104 USA
关键词
Meningioma; Anaplastic meningioma; Malignant progression; Neuropathology; TUMOR-SUPPRESSOR GENE; SPORADIC MENINGIOMA; IMMUNOHISTOCHEMICAL DETECTION; PROGESTERONE-RECEPTORS; TELOMERASE ACTIVITY; GENOMIC ANALYSIS; PHASE-II; NF2; GENE; EXPRESSION; MUTATIONS;
D O I
10.1016/j.yexmp.2015.08.007
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Meningioma is a common adult intracranial tumor, and while several cases are considered benign, a subset is malignant with biologically aggressive behavior and is refractory to current treatment strategies of combined surgery and radiotherapy. Anaplastic meningiomas are quite aggressive and correspond to a World Health Organization (WHO) Grade III tumor. This highly aggressive phenotype mandates the need for more efficacious therapies. Designing rational therapies for treatment will have its foundation in the biologic understanding of involved genes and molecular pathways in these types of tumors. Anaplastic meningiomas (WHO Grade III) can arise from malignant transformation of lower grade (WHO Grade I/II) tumors, however there is an incomplete understanding of specific genetic drivers of malignant transformation in these tumors. Here, the current understanding of anaplastic meningiomas is reviewed in the context of human neuropathologic specimens and small animal models. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:354 / 359
页数:6
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