| Literature DB >> 33611700 |
Ryuto Tsuchiya1,2, Yuki Yoshimatsu1, Rei Noguchi1, Takuya Ono1, Akane Sei1, Fumitaka Takeshita3, Jun Sugaya4, Shintaro Iwata4, Akihiko Yoshida5, Seiji Ohtori2, Akira Kawai4, Tadashi Kondo6.
Abstract
Synovial sarcoma (SS) is defined as a monomorphic blue spindle cell sarcoma showing variable epithelial differentiation, and is characterized by a specific fusion gene, SS18-SSX. Although SS is rare, it accounts for approximately 8% of all soft tissue sarcomas, which occupies a significant proportion of soft tissue tumors. The prognosis of SS is unfavorable, with 5-year survival rate of 50-60%, and only a few anti-cancer agents are recommended for its treatment. Thus, we need to urgently establish novel treatment methods. Patient-derived cell lines are essential tools in basic research and pre-clinical studies. However, there are only 4 publicly available SS cell lines. Therefore, we established a novel SS cell line, NCC-SS4-C1, using surgically resected tumor tissues of a patient with SS. The cell line maintained the characteristic fusion gene, SS18-SSX1, and copy number alteration, in concordance with the original tumor. The cells also exhibited moderate cell proliferation, invasion ability, and spheroid formation ability. Moreover, a drug-screening test using 4 SS cell lines, including NCC-SS4-C1, demonstrated the significant anti-proliferative effects of ALK and HDAC inhibitors. Thus, we concluded that the NCC-SS4-C1 cell line is a useful tool for basic and pre-clinical studies of SS.Entities:
Keywords: Drug screening; Patient-derived cancer model; Patient-derived cell line; Sarcoma; Synovial sarcoma
Year: 2021 PMID: 33611700 DOI: 10.1007/s13577-021-00509-z
Source DB: PubMed Journal: Hum Cell ISSN: 0914-7470 Impact factor: 4.174