整合空间和遗传谱系追踪揭示Group3和Group4髓母细胞瘤复发背后的细胞状态可塑性

Recent studies place Group 3/4 medulloblastomas (G3/4 MBs) within the rhombic lip (RL)-derived glutamatergic lineage, indicating that a stalled differentiation program underlies their malignant evolution. However, it remains unclear whether these tumors retain the plasticity to transition within this lineage framework, and how their cellular states are reshaped in response to therapy. To address these questions, we constructed a single-cell multiomics atlas of G3/4 MBs using 84 tumor specimens from 38 patients, including 7 longitudinally matched cases collected through the University of California, San Francisco Brain Tumor Center (UCSF BTC) and the Children's Brain Tumor Network (CBTN). From these samples, we generated single-nucleus transcriptomic and chromatin accessibility profiles from 57 frozen samples, and spatial transcriptomic profiles from 27 FFPE samples using Visium and Xenium. We also incorporated single-cell lineage-tracing data from intracranial xenografts derived from two G3 MB cell lines. Genetic lineage tracing integrating static barcodes with endogenous mutations demonstrated that xenografts recapitulate the developmental cell-type composition of treatment-naive primary human MBs, with barcode-defined individual clones maintaining highly similar and stable cell-type fractions. Comparison of matched primary and recurrent clinical tumors revealed no substantial differences in developmental composition. Despite this stability, phylogenetic analysis uncovered markedly increased plasticity in recurrent tumors, driven by dedifferentiation transitions from unipolar brush cell-like states to RL progenitor-like states. Tumor regions exhibiting high plasticity were spatially clustered and corresponded to structurally disorganized areas. Our work establishes cell-state plasticity as a defining feature of recurrent G3/4 MBs, providing a mechanistic framework for understanding recurrence following therapy.