Establishment and characterization of NCC-SS5-C1: a novel patient-derived cell line of synovial sarcoma

Synovial sarcoma (SS) is a rare and aggressive mesenchymal malignancy driven by a unique chromosomal translocation that generates the expression of the SS18:SSX fusion protein. It occurs at almost any anatomical site and most commonly in young adults. The standard curative treatment for primary SS i...

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Veröffentlicht in:Human cell : official journal of Human Cell Research Society 2022-07, Vol.35 (4), p.1290-1297
Hauptverfasser: Yoshimatsu, Yuki, Noguchi, Rei, Sin, Yooksil, Tsuchiya, Ryuto, Ono, Takuya, Akiyama, Taro, Sugaya, Jun, Kojima, Naoki, Yoshida, Akihiko, Kawai, Akira, Kondo, Tadashi
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Sprache:eng
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Zusammenfassung:Synovial sarcoma (SS) is a rare and aggressive mesenchymal malignancy driven by a unique chromosomal translocation that generates the expression of the SS18:SSX fusion protein. It occurs at almost any anatomical site and most commonly in young adults. The standard curative treatment for primary SS is a wide surgical resection combined with radiotherapy and/or neoadjuvant chemotherapy. The prognosis of SS varies among patients, with the 5 years survival rate ranging from 50 to 60% in adults and 90% in children. Although patient-derived cell lines are a useful resource for the development of new therapies, only a few are available from public cell banks. Therefore, this study aimed to establish and characterize a novel SS cell line. We successfully established a novel cell line, NCC-SS5-C1, harboring an SS18-SSX1 fusion gene. NCC-SS5-C1 cells demonstrated constant growth and invasion ability. We performed integrative drug screening using eight SS cell lines, including NCC-SS5-C1 cells, and examined the response spectrum of existing anticancer agents. We conclude that NCC-SS5-C1 is a useful resource for studying SS.
ISSN:1749-0774
0914-7470
1749-0774
DOI:10.1007/s13577-022-00721-5