Division of Rare Cancer Research, National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Department of Musculoskeletal Oncology and Rehabilitation Medicine, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Hum Cell. 2024 Nov;37(6):1734-1741. doi: 10.1007/s13577-024-01122-6. Epub 2024 Aug 23.
Synovial sarcoma (SS) is identified as a sarcoma with monomorphic blue spindle cells that display variable epithelial differentiation and is characterized by the SS18::SSX fusion gene. SS accounts for approximately 5-10% of all soft tissue sarcomas, making it a relatively common type within this group of tumors. Since SS is generally sensitive to chemotherapy, the standard treatment for SS includes extensive surgical resection, complemented by neoadjuvant chemotherapy with several approved anticancer drugs. However, in advanced and metastatic cases, the efficacy of these drugs is limited, resulting in poor prognoses. This underscores the need for innovative therapeutic strategies. Patient-derived cancer cell lines are essential tools for basic and preclinical research, yet only four SS cell lines are publicly available. To facilitate the studies of SS, we have developed a novel SS cell line, named NCC-SS6-C1, derived from surgically excised tumor tissue of an SS patient. NCC-SS6-C1 cells preserve the SS18::SSX1 fusion gene, consistent with the genetic characteristics of the original tumor. The cells exhibit continuous proliferation, invasiveness, and the ability to form spheroids. Additionally, we confirmed that this cell line was useful for evaluating the efficacy of anticancer drugs. Our results suggest that NCC-SS6-C1 is a useful tool for basic and pre-clinical studies of SS.
滑膜肉瘤(SS)是一种具有单相蓝色梭形细胞的肉瘤,表现出可变的上皮分化,其特征在于 SS18::SSX 融合基因。SS 约占所有软组织肉瘤的 5-10%,在这类肿瘤中相对常见。由于 SS 通常对化疗敏感,SS 的标准治疗包括广泛的手术切除,并辅以几种批准的抗癌药物进行新辅助化疗。然而,在晚期和转移性病例中,这些药物的疗效有限,导致预后不良。这突显了需要创新的治疗策略。患者来源的癌细胞系是基础和临床前研究的重要工具,但仅有四种 SS 细胞系可供公开使用。为了促进 SS 的研究,我们从 SS 患者手术切除的肿瘤组织中开发了一种新型 SS 细胞系,命名为 NCC-SS6-C1。NCC-SS6-C1 细胞保留了 SS18::SSX1 融合基因,与原始肿瘤的遗传特征一致。这些细胞表现出连续的增殖、侵袭性和形成球体的能力。此外,我们证实该细胞系可用于评估抗癌药物的疗效。我们的结果表明,NCC-SS6-C1 是 SS 的基础和临床前研究的有用工具。