Department of Neurosurgery, AP-HP, Hopital Beaujon, Clichy, France.
Oncogene. 2013 Sep 5;32(36):4264-72. doi: 10.1038/onc.2012.436. Epub 2012 Oct 8.
Aggressive variants of meningiomas (WHO grade II and III) represent up to 30% of those tumors that are among the most common primary central nervous system tumors in adults. Currently, there is no effective treatment for grade-II and -III meningiomas, the main treatment remaining surgical excision. Genetic studies have highlighted two main events associated with meningioma progression: an increase of chromosomal instability in tumors with NF2 inactivation and homozygous deletions or point mutations of the CDKN2AB locus. In this study we demonstrated that in mice, in addition to bi-allelic Nf2 inactivation, homozygous and heterozygous Adenovirus Cre-mediated Cdkn2ab deletions lead to increased meningioma frequency (72% and 50%, respectively) with a shorter latency (3.5 and 7.8 months, respectively) compared with control cohorts and induce grade II/III meningioma progression with an incidence of 34% and 28%, respectively. Moreover, Cdkn2ab inactivation in arachnoidal cells was associated with decreased senescence compared with Nf2(-/-) and wild-type arachnoidal cells in vitro. We have established three mouse meningioma cell lines and generated a syngenic orthotopic meningioma mouse model with 50-100% grade-II/III meningiomas after reimplantation. Comparative genomic hybridization of four meningiomas from Cdkn2ab homozygous mice and three cell cultures revealed the absence of unbalanced chromosomal segments in tumors and several chromosome imbalances in cell cultures. In addition, we were able to detect meningiomas by using bioluminescence and to evaluate tumor vascular permeability by dynamic magnetic resonance imaging. These results show that Nf2 and Cdkn2ab cooperate to promote meningioma progression in mice. The short latency of tumor development and the ability to derive grade II/III meningioma cell cultures are key aspects of this model to promote its use in pre-clinical drug testing.
侵袭性脑膜瘤(WHO 分级 II 和 III)占成人中枢神经系统最常见原发性肿瘤的 30%。目前,对于 II 级和 III 级脑膜瘤没有有效的治疗方法,主要的治疗方法仍然是手术切除。遗传研究强调了与脑膜瘤进展相关的两个主要事件:NF2 失活的肿瘤中染色体不稳定性增加和 CDKN2AB 基因座的纯合缺失或点突变。在这项研究中,我们证明了在小鼠中,除了双等位基因 Nf2 失活外,腺病毒 Cre 介导的 Cdkn2ab 缺失的纯合和杂合也会导致脑膜瘤发生率增加(分别为 72%和 50%),潜伏期更短(分别为 3.5 和 7.8 个月),与对照组相比,并分别诱导 34%和 28%的 II/III 级脑膜瘤进展。此外,与 Nf2(-/-)和野生型脑膜细胞相比,蛛网膜细胞中的 Cdkn2ab 失活与体外衰老减少相关。我们建立了三种小鼠脑膜瘤细胞系,并在重新植入后建立了具有 50-100% II/III 级脑膜瘤的同基因原位脑膜瘤小鼠模型。对 4 例 Cdkn2ab 纯合小鼠脑膜瘤和 3 种细胞培养物的比较基因组杂交显示,肿瘤中不存在不平衡染色体片段,而细胞培养物中存在多个染色体不平衡。此外,我们能够通过生物发光检测到脑膜瘤,并通过动态磁共振成像评估肿瘤血管通透性。这些结果表明,Nf2 和 Cdkn2ab 合作促进了小鼠脑膜瘤的进展。肿瘤发展的潜伏期短,并且能够获得 II 级和 III 级脑膜瘤细胞培养物,这是该模型的关键方面,有助于在临床前药物测试中使用该模型。