Author
Listed:
- Kyle S. Smith
(St Jude Children’s Research Hospital)
- Laure Bihannic
(St Jude Children’s Research Hospital)
- Brian L. Gudenas
(St Jude Children’s Research Hospital)
- Parthiv Haldipur
(Seattle Children’s Research Institute)
- Ran Tao
(St Jude Children’s Research Hospital)
- Qingsong Gao
(St Jude Children’s Research Hospital
St Jude Children’s Research Hospital)
- Yiran Li
(St Jude Children’s Research Hospital)
- Kimberly A. Aldinger
(Seattle Children’s Research Institute)
- Igor Y. Iskusnykh
(University of Tennessee)
- Victor V. Chizhikov
(University of Tennessee)
- Matthew Scoggins
(St Jude Children’s Research Hospital)
- Silu Zhang
(St Jude Children’s Research Hospital)
- Angela Edwards
(St Jude Children’s Research Hospital)
- Mei Deng
(University of Washington)
- Ian A. Glass
(University of Washington)
- Lynne M. Overman
(Newcastle University)
- Jake Millman
(Seattle Children’s Research Institute)
- Alexandria H. Sjoboen
(Seattle Children’s Research Institute)
- Jennifer Hadley
(St Jude Children’s Research Hospital)
- Joseph Golser
(Seattle Children’s Research Institute)
- Kshitij Mankad
(Great Ormond Street Hospital for Children)
- Heather Sheppard
(St Jude Children’s Research Hospital)
- Arzu Onar-Thomas
(St Jude Children’s Research Hospital)
- Amar Gajjar
(St Jude Children’s Research Hospital)
- Giles W. Robinson
(St Jude Children’s Research Hospital)
- Volker Hovestadt
(Dana Farber Cancer Institute)
- Brent A. Orr
(St Jude Children’s Research Hospital)
- Zoltán Patay
(St Jude Children’s Research Hospital)
- Kathleen J. Millen
(Seattle Children’s Research Institute)
- Paul A. Northcott
(St Jude Children’s Research Hospital)
Abstract
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.
Suggested Citation
Kyle S. Smith & Laure Bihannic & Brian L. Gudenas & Parthiv Haldipur & Ran Tao & Qingsong Gao & Yiran Li & Kimberly A. Aldinger & Igor Y. Iskusnykh & Victor V. Chizhikov & Matthew Scoggins & Silu Zhan, 2022.
"Unified rhombic lip origins of group 3 and group 4 medulloblastoma,"
Nature, Nature, vol. 609(7929), pages 1012-1020, September.
Handle:
RePEc:nat:nature:v:609:y:2022:i:7929:d:10.1038_s41586-022-05208-9
DOI: 10.1038/s41586-022-05208-9
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