Multimodal single-cell analyses reveal distinct fusion-regulated transcriptional programs in Ewing sarcoma

Ewing sarcoma (EwS) is a fusion-driven malignancy, peaking in adolescence. Although EwS tumors are driven uniquely by EWS::FLI1 and related fusions, patient outcomes vary greatly. If and how tumor plasticity of EWS::FLI1-regulated transcriptional signatures contributes to disease progression is not known. To address this, we utilized a single-cell co-assay of RNA and chromatin accessibility (ATAC) sequencing to identify gene regulatory networks in EwS. By comprehensively characterizing regulatory elements across cell lines, we identified multiple unique modules of gene regulation. Differential usage and prevalence of these modules was evident across cell lines, associated with distinct epigenetic and transcriptomic signatures, and in specific cases, modifiable by exogenous TGF-β. When we examined primary EwS patient tumors, we observed these same regulatory modules were variably enriched both across and within tumors, highlighting the existence of intratumoral heterogeneity in gene regulatory networks. Our findings demonstrate that multiple, co-existing transcriptional programs shape the phenotypic diversity of EwS and suggest that the balance between these networks may have important implications for clinical outcomes and targeted therapy development.

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Publication Details

Journal
eLife
Published
2026-11-11
DOI
https://doi.org/10.7554/elife.109124.3
Primary Topic
Sarcoma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00

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article

Multimodal single-cell analyses reveal distinct fusion-regulated transcriptional programs in Ewing sarcoma

Anand G. Patel, Emma D. Wrenn, Scott N. Furlan, April Ann Apfelbaum et al.
1 links
eLife
Sarcoma Diagnosis and Treatment
article

Multimodal single-cell analyses reveal distinct fusion-regulated transcriptional programs in Ewing sarcoma

Anand G. Patel, Emma D. Wrenn, Scott N. Furlan, April Ann Apfelbaum, Michael A. Dyer, Elizabeth R. Lawlor, Rula Green Gladden, Jay F. Sarthy, Sami B. Kanaan, Zev N. Kronenberg, Shruti S. Bhise, Olivia G. Waltner, Roger Volden, Mark A Mendoza
article en

Abstract

Ewing sarcoma (EwS) is a fusion-driven malignancy, peaking in adolescence. Although EwS tumors are driven uniquely by EWS::FLI1 and related fusions, patient outcomes vary greatly. If and how tumor plasticity of EWS::FLI1-regulated transcriptional signatures contributes to disease progression is not known. To address this, we utilized a single-cell co-assay of RNA and chromatin accessibility (ATAC) sequencing to identify gene regulatory networks in EwS. By comprehensively characterizing regulatory elements across cell lines, we identified multiple unique modules of gene regulation. Differential usage and prevalence of these modules was evident across cell lines, associated with distinct epigenetic and transcriptomic signatures, and in specific cases, modifiable by exogenous TGF-β. When we examined primary EwS patient tumors, we observed these same regulatory modules were variably enriched both across and within tumors, highlighting the existence of intratumoral heterogeneity in gene regulatory networks. Our findings demonstrate that multiple, co-existing transcriptional programs shape the phenotypic diversity of EwS and suggest that the balance between these networks may have important implications for clinical outcomes and targeted therapy development.

eLifeVol. 14
St. Jude Children's Research Hospital (US), University of Washington (US), Fred Hutch Cancer Center (US), Seattle Children's Research Institute (US), Pacific Biosciences (United States) (US)
Fred Hutchinson Cancer Research Center, University of Washington, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, National Institutes of Health, National Cancer Institute, National Institute of General Medical Sciences
Good health and well-being
Sarcoma Diagnosis and Treatment
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