Department of Pathology and Molecular Pathology, University Hospital Zurich, Schmelzbergstrasse 12, 8006, Zurich, Switzerland.
Medical Faculty, University of Zurich, Zurich, Switzerland.
Hum Cell. 2024 Jan;37(1):356-363. doi: 10.1007/s13577-023-01001-6. Epub 2023 Nov 11.
Extraskeletal osteosarcoma (ESOS) is a rare malignant mesenchymal tumor that originates in the soft tissue. ESOS accounts for less than 1% of all soft tissue sarcomas and exhibits an aggressive behavior with a high propensity for local recurrence and distant metastasis. Despite advances in treatment, the prognosis for ESOS remains poor, with a five-year survival rate of less than 50% and 27% for metastatic patients. Ex vivo models derived from patient samples are critical tools for studying rare diseases with poor prognoses, such as ESOS, and identifying potential new treatment strategies. In this work, we established a novel ESOS ex vivo sarco-sphere model from a metastatic lesion to the dermis for research and functional testing purposes. The ex vivo cell model accurately recapitulated the native tumor, as evidenced by histomorphology and molecular profiles. Through a functional screening approach, we were able to identify novel individual anti-cancer drug sensitivities for different drugs such as romidepsin, miverbresib and to multiple kinase inhibitors. Overall, our new ESOS ex vivo cell model represents a valuable tool for investigating disease mechanisms and answering basic and translational research questions.
骨外骨肉瘤(ESOS)是一种罕见的恶性间叶组织肿瘤,起源于软组织。ESOS 占所有软组织肉瘤的比例不到 1%,表现出侵袭性行为,局部复发和远处转移的倾向很高。尽管治疗取得了进展,但 ESOS 的预后仍然不佳,五年生存率低于 50%,转移性患者为 27%。源自患者样本的体外模型是研究预后不良的罕见疾病(如 ESOS)和确定潜在新治疗策略的重要工具。在这项工作中,我们从皮肤转移的转移性病变建立了一种新的 ESOS 体外肉瘤球体模型,用于研究和功能测试。体外细胞模型通过组织形态学和分子谱准确地再现了原始肿瘤。通过功能筛选方法,我们能够鉴定出不同药物(如罗米地辛、米伏布瑞司和多种激酶抑制剂)的新的个体抗癌药物敏感性。总的来说,我们的新 ESOS 体外细胞模型是研究疾病机制和回答基础和转化研究问题的有价值的工具。