Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Department of Biochemistry and Molecular Genetics, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Cell. 2024 Jan 18;187(2):446-463.e16. doi: 10.1016/j.cell.2023.12.013.
Treatment failure for the lethal brain tumor glioblastoma (GBM) is attributed to intratumoral heterogeneity and tumor evolution. We utilized 3D neuronavigation during surgical resection to acquire samples representing the whole tumor mapped by 3D spatial coordinates. Integrative tissue and single-cell analysis revealed sources of genomic, epigenomic, and microenvironmental intratumoral heterogeneity and their spatial patterning. By distinguishing tumor-wide molecular features from those with regional specificity, we inferred GBM evolutionary trajectories from neurodevelopmental lineage origins and initiating events such as chromothripsis to emergence of genetic subclones and spatially restricted activation of differential tumor and microenvironmental programs in the core, periphery, and contrast-enhancing regions. Our work depicts GBM evolution and heterogeneity from a 3D whole-tumor perspective, highlights potential therapeutic targets that might circumvent heterogeneity-related failures, and establishes an interactive platform enabling 360° visualization and analysis of 3D spatial patterns for user-selected genes, programs, and other features across whole GBM tumors.
治疗致命性脑肿瘤胶质母细胞瘤(GBM)的失败归因于肿瘤内异质性和肿瘤进化。我们在手术切除过程中利用 3D 神经导航获取样本,这些样本代表了通过 3D 空间坐标映射的整个肿瘤。综合组织和单细胞分析揭示了基因组、表观基因组和肿瘤内微环境异质性的来源及其空间模式。通过区分全肿瘤的分子特征和具有区域特异性的特征,我们从神经发育谱系起源和起始事件(如染色体重排)推断出 GBM 进化轨迹,以及遗传亚克隆的出现以及在核心、周边和对比增强区域中差异肿瘤和微环境程序的空间受限激活。我们的工作从 3D 全肿瘤的角度描绘了 GBM 的进化和异质性,突出了可能规避与异质性相关失败的潜在治疗靶点,并建立了一个交互式平台,使用户能够选择基因、程序和其他特征,对整个 GBM 肿瘤进行 360°可视化和分析。