Suero-Abreu Giselle A, Praveen Raju G, Aristizábal Orlando, Volkova Eugenia, Wojcinski Alexandre, Houston Edward J, Pham Diane, Szulc Kamila U, Colon Daniel, Joyner Alexandra L, Turnbull Daniel H
Skirball Institute of Biomolecular Medicine and Department of Radiology, NYU School of Medicine, New York, NY, USA.
Developmental Biology Department, Memorial Sloan-Kettering Cancer Center, New York, NY, USA; Department of Pediatrics, Weill Cornell Medical College, New York, NY, USA.
Neoplasia. 2014 Dec;16(12):993-1006. doi: 10.1016/j.neo.2014.10.001.
Mouse models have increased our understanding of the pathogenesis of medulloblastoma (MB), the most common malignant pediatric brain tumor that often forms in the cerebellum. A major goal of ongoing research is to better understand the early stages of tumorigenesis and to establish the genetic and environmental changes that underlie MB initiation and growth. However, studies of MB progression in mouse models are difficult due to the heterogeneity of tumor onset times and growth patterns and the lack of clinical symptoms at early stages. Magnetic resonance imaging (MRI) is critical for noninvasive, longitudinal, three-dimensional (3D) brain tumor imaging in the clinic but is limited in resolution and sensitivity for imaging early MBs in mice. In this study, high-resolution (100 μm in 2 hours) and high-throughput (150 μm in 15 minutes) manganese-enhanced MRI (MEMRI) protocols were optimized for early detection and monitoring of MBs in a Patched-1 (Ptch1) conditional knockout (CKO) model. The high tissue contrast obtained with MEMRI revealed detailed cerebellar morphology and enabled detection of MBs over a wide range of stages including pretumoral lesions as early as 2 to 3 weeks postnatal with volumes close to 0.1 mm(3). Furthermore, longitudinal MEMRI allowed noninvasive monitoring of tumors and demonstrated that lesions within and between individuals have different tumorigenic potentials. 3D volumetric studies allowed quantitative analysis of MB tumor morphology and growth rates in individual Ptch1-CKO mice. These results show that MEMRI provides a powerful method for early in vivo detection and longitudinal imaging of MB progression in the mouse brain.
小鼠模型增进了我们对髓母细胞瘤(MB)发病机制的理解,髓母细胞瘤是最常见的小儿恶性脑肿瘤,常形成于小脑。当前研究的一个主要目标是更好地理解肿瘤发生的早期阶段,并确定MB起始和生长背后的基因和环境变化。然而,由于肿瘤发病时间和生长模式的异质性以及早期缺乏临床症状,在小鼠模型中研究MB进展很困难。磁共振成像(MRI)在临床上对于脑肿瘤的非侵入性、纵向、三维(3D)成像至关重要,但在对小鼠早期MB成像时,其分辨率和灵敏度有限。在本研究中,针对Patched-1(Ptch1)条件性敲除(CKO)模型中MB的早期检测和监测,优化了高分辨率(2小时内达到100μm)和高通量(15分钟内达到150μm)的锰增强MRI(MEMRI)方案。通过MEMRI获得的高组织对比度揭示了详细的小脑形态,并能够在广泛的阶段检测到MB,包括早在出生后2至3周体积接近0.1mm³的肿瘤前病变。此外,纵向MEMRI允许对肿瘤进行非侵入性监测,并表明个体内部和个体之间的病变具有不同的致瘤潜力。3D体积研究允许对单个Ptch1-CKO小鼠的MB肿瘤形态和生长速率进行定量分析。这些结果表明,MEMRI为小鼠脑中MB进展的早期体内检测和纵向成像提供了一种强大的方法。