bioRxiv · 10.1101/2024.01.18.576251
Single cell RNA-sequencing of Ewing sarcoma tumors demonstrates transcriptional heterogeneity and clonal evolution.
Abstract
Ewing sarcoma is the second most common bone cancer in children, accounting for 2% of pediatric cancer diagnoses. Patients who present with metastatic disease at the time of diagnosis have a dismal prognosis, compared to the >70% 5-year survival of those with localized disease. Here, we utilized single cell RNA-sequencing to characterize the transcriptional landscape of primary Ewing sarcoma tumors and surrounding tumor microenvironment (TME). Copy-number analysis identified subclonal evolution within patients prior to treatment. Primary tumor samples demonstrate a heterogenous transcriptional landscape with several conserved gene expression programs, including those composed of genes related to proliferation and EWS targets. Single cell RNA-sequencing and immunofluorescence of circulating tumor cells at the time of diagnosis identified TSPAN8 as a novel therapeutic target.
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Goodspeed, A., Bodlak, A., Nelson-Taylor, S., Oike, N., Shirai, R., Walker, D., Porfilio, T. E., Treece, A., Black, J. O., Donaldson, N., Cost, C., Garrington, T., Greffe, B., Luna-Fineman, S., Demedis, J., Lake, J. A., Danis, E., Verneris, M. R., Hayashi, M.. 2024-01-20. Single cell RNA-sequencing of Ewing sarcoma tumors demonstrates transcriptional heterogeneity and clonal evolution.. https://doi.org/10.1101/2024.01.18.576251
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