Unified rhombic lip origins of group 3 and group 4 medulloblastoma

髓母细胞瘤 生物 小脑 表型 神经科学 遗传学 基因
作者
Kyle Smith,Laure Bihannic,Brian Gudenas,Parthiv Haldipur,Ran Tao,Qingsong Gao,Yiran Li,Kimberly A. Aldinger,Igor Y. Iskusnykh,Victor V. Chizhikov,Matthew Scoggins,Silu Zhang,Angela Edwards,Mei Deng,Ian A. Glass,Lynne M. Overman,Jake Millman,Alexandria H. Sjoboen,Jennifer Hadley,Joseph Golser,Kshitij Mankad,Heather Sheppard,Arzu Onar‐Thomas,Amar Gajjar,Giles Robinson,Volker Hovestadt,Brent A. Orr,Zoltán Patay,Kathleen J. Millen,Paul A. Northcott
出处
期刊:Nature [Springer Nature]
卷期号:609 (7929): 1012-1020 被引量:88
标识
DOI:10.1038/s41586-022-05208-9
摘要

Medulloblastoma, a malignant childhood cerebellar tumour, segregates molecularly into biologically distinct subgroups, suggesting that a personalized approach to therapy would be beneficial1. Mouse modelling and cross-species genomics have provided increasing evidence of discrete, subgroup-specific developmental origins2. However, the anatomical and cellular complexity of developing human tissues3—particularly within the rhombic lip germinal zone, which produces all glutamatergic neuronal lineages before internalization into the cerebellar nodulus—makes it difficult to validate previous inferences that were derived from studies in mice. Here we use multi-omics to resolve the origins of medulloblastoma subgroups in the developing human cerebellum. Molecular signatures encoded within a human rhombic-lip-derived lineage trajectory aligned with photoreceptor and unipolar brush cell expression profiles that are maintained in group 3 and group 4 medulloblastoma, suggesting a convergent basis. A systematic diagnostic-imaging review of a prospective institutional cohort localized the putative anatomical origins of group 3 and group 4 tumours to the nodulus. Our results connect the molecular and phenotypic features of clinically challenging medulloblastoma subgroups to their unified beginnings in the rhombic lip in the early stages of human development.

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