Emori Makoto, Nakahashi Naoya, Takasawa Akira, Murata Kenji, Murahashi Yasutaka, Shimizu Junya, Tsukahara Tomohide, Sugita Shintaro, Takada Kohichi, Hasegawa Tadashi, Osanai Makoto, Iba Kosuke
Department of Orthopedic Surgery, Sapporo Medical University School of Medicine, West 16, South 1, Chuo- Ku, Sapporo, 060-8543, Japan.
Departments of Pathology, Sapporo Medical University School of Medicine, West 16, South 1, Chuo- Ku, Sapporo, 060-8543, Japan.
Hum Cell. 2023 Nov;36(6):2195-2203. doi: 10.1007/s13577-023-00944-0. Epub 2023 Jul 15.
Dedifferentiated chondrosarcoma (DDCS) is a high-grade subtype with a bi-morphic histological appearance of a conventional chondrosarcoma component and it can abruptly transition to a high-grade non-cartilaginous sarcoma. To better understand the biological features of DDCSs and to help develop new therapies, a novel DDCS cell line, SMU-DDCS, was established. Tissue from an open biopsy of a tumor resected from a 75-year-old patient was subjected to primary culture. The cell line was established and authenticated by assessing DNA microsatellite short tandem repeats. The cells maintained in monolayer cultures exhibited constant growth, spheroid formation, and high invasive capacity. Out of the four mice inoculated with SMU-DDCS cells, tumors developed in three mice after 2 weeks. R132C mutation was found in the IDH1 but not the IDH2 genomic DNA sequence of SMU-DDCS cells. SMU-DDCS cells exhibited low chemosensitivity to doxorubicin, methotrexate, and cisplatin. This SMU-DDCS cell line harboring an IDH1 mutation will be a useful tool for investigating DDCS development and for evaluating novel therapeutic agents against it.
去分化软骨肉瘤(DDCS)是一种高级别亚型,具有传统软骨肉瘤成分的双相组织学表现,并且可突然转变为高级别非软骨肉瘤。为了更好地了解DDCS的生物学特性并帮助开发新的治疗方法,建立了一种新的DDCS细胞系SMU-DDCS。对一名75岁患者切除肿瘤的开放活检组织进行原代培养。通过评估DNA微卫星短串联重复序列建立并鉴定了该细胞系。单层培养的细胞表现出持续生长、球体形成和高侵袭能力。在接种SMU-DDCS细胞的四只小鼠中,三只小鼠在2周后长出肿瘤。在SMU-DDCS细胞的IDH1基因而非IDH2基因组DNA序列中发现了R132C突变。SMU-DDCS细胞对阿霉素、甲氨蝶呤和顺铂表现出低化学敏感性。这种携带IDH1突变的SMU-DDCS细胞系将成为研究DDCS发生发展以及评估针对它的新型治疗药物的有用工具。