Alveolar rhabdomyosarcoma (ARMS) is an aggressive soft tissue sarcoma typically driven by the oncofusion protein PAX3::FOXO1 (P3F). Despite ARMS tumor histology and transcriptome resembling skeletal muscle, these tumors arise in areas devoid of skeletal muscle, indicating that non-myogenic cells can give rise to ARMS. Our lab demonstrated that endothelial progenitors are a cell of origin for rhabdomyosarcoma. Here we provide a protocol for generating iPSC-derived alveolar rhabdomyosarcoma cells (iARMS) during endothelial directed differentiation through enforced expression of P3F. This model allows for dissection of how P3F mediates transformation of endothelial progenitors into aggressive myogenic tumors.
Generation of an iPSC-derived alveolar rhabdomyosarcoma cell line during directed endothelial differentiation.
阅读:3
作者:Larsen Randolph K 4th, Searcy Madeline B, Stevens Bradley T, Gadek Katherine E, Zhang Yang, Abraham Brian J, Hatley Mark E
| 期刊: | Stem Cell Research | 影响因子: | 0.700 |
| 时间: | 2025 | 起止号: | 2025 Dec;89:103871 |
| doi: | 10.1016/j.scr.2025.103871 | ||
特别声明
1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。
2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。
3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。
4、投稿及合作请联系:info@biocloudy.com。
