肉瘤
生物
基因
小儿癌症
核糖核酸
癌症研究
原发性肿瘤
疾病
癌症
遗传学
转移
病理
医学
作者
Andrew Goodspeed,Avery Bodlak,Alexis B. Duffy,Sarah Nelson-Taylor,Naoki Oike,Timothy Porfilio,Ryota Shirai,Deandra Walker,Amy Treece,Jennifer O. Black,Nathan Donaldson,Carrye Cost,Tim Garrington,Brian Greffe,Sandra Luna‐Fineman,Jenna Demedis,Jessica Lake,Etienne Danis,Michael R. Verneris,Daniel L. Adams
标识
DOI:10.1101/2024.01.18.576251
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI