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High-Risk Rhabdomyosarcomas Feature a Convergent Cell State

  • Holly J Whitfield
  • , Nathaniel D Anderson
  • , Christina Burke
  • , Marian J Groot Koerkamp
  • , Conor Parks
  • , Toochi Ogbonnah
  • , Yvette Wood
  • , Alice Piapi
  • , Emilia Robertson
  • , Eleanor Watt
  • , Abigail White
  • , Solange De Noon
  • , Jonathan Kennedy
  • , Rajvi Nagrecha
  • , Michael T Meister
  • , Ewa Aladowicz
  • , Yang Kee Stella Man
  • , Virginia Laspidea
  • , Mi K Trinh
  • , Angus Hodder
  • Tarryn Porter, John E Lawrence, Elizabeth Tuck, Trung Nguyen, Anna Kelsey, Adrienne M Flanagan, Richard Hewitt, Naima Smeulders, Olga Slater, J Ciaran Hutchinson, Neil Sebire, Janet M Shipley, Jarno Drost, Karin Straathof, Sam Behjati

Onderzoeksoutput: Bijdrage aan tijdschriftArtikelpeer review

Samenvatting

Somatic mutations often predict survival in childhood cancers, as exemplified in rhabdomyosarcoma, where FOXO1 gene fusion status is a key prognostic feature. Here, we examined single-cell transcriptomics and discovered that cancer cells of lethal disease converge on a common cell state with a shared transcriptional landscape, irrespective of fusion status. Nuclear transcriptomics, chromatin accessibility, spatial transcriptomics, perturbation studies, and previously published data sets validated the overarching high-risk cell state. The convergent cell state only partially overlapped with transcriptional effects of the FOXO1 fusion and unexpectedly exhibited neural features. Overall, these findings delineate a cell state of high-risk rhabdomyosarcoma cells that transcends conventional molecular and histological boundaries, suggesting an overarching disease phenotype that could transform target discovery and inform clinical practice.

Originele taal-2Engels
TijdschriftCancer Research
DOI's
StatusE-publicatie vóór gedrukte publicatie - 14 jul 2026

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