Molecular genetics of meningiomas: Building the roadmap towards personalized therapy

被引:18
作者
Peyre, M. [1 ,2 ,3 ]
Kalamarides, M. [1 ,2 ,3 ]
机构
[1] Hop La Pitie Salpetriere, AP HP, Serv Neurochirurg, 47-83 Blvd Hop, F-75013 Paris, France
[2] Inst Cerveau & Moelle Epiniere, Inserm, UMR S975, F-75013 Paris, France
[3] Univ Paris 6 Pierre & Marie Curie, F-75013 Paris, France
关键词
Meningioma; NF2; AKT1; SMO; TERT; Mouse model; Proteus syndrome; GROWTH-FACTOR RECEPTORS; TUMOR-SUPPRESSOR; MALIGNANT PROGRESSION; MITOGENIC SIGNALS; HTERT-PROTEIN; NF2; GENE; EXPRESSION; ACTIVATION; AKT1; MUTATIONS;
D O I
10.1016/j.neuchi.2014.06.007
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
New advances have recently been made in the field of molecular genetics and mouse modeling of meningiomas, opening new perspectives for future treatments. Recent genome-wide genotyping and exome sequencing studies have confirmed the pivotal role of NF2 in meningioma tumorigenesis, concerning roughly half of the tumors, and unraveled new mutations in non-NF2 meningiomas concerning AKT1, SMO, KLF4 and TRAF7. The molecular mechanisms underlying tumorigenesis of high histological grades have been progressively deciphered with the recent discovery of TERT promoter mutations in progressing tumors. A better understanding of the genetics and clinical behavior of high-grade meningiomas is mandatory in order to better design future clinical trials. New genetically engineered mouse models of benign and histologically aggressive meningioma represent a substantial resource for the establishment of relevant pre-clinical trials. By studying the mechanisms underlying these new tumorigenesis pathways and the corresponding mouse models, we should be able to offer personalized chemotherapy to patients with surgery- and radiation-refractory meningiomas in the near future. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:22 / 28
页数:7
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