| Literature DB >> 35655041 |
Yuki Yoshimatsu1, Rei Noguchi1, Yooksil Sin1, Ryuto Tsuchiya1, Takuya Ono1, Taro Akiyama1, Jun Sugaya2, Naoki Kojima1,3,2, Akihiko Yoshida3, Akira Kawai2, Tadashi Kondo4.
Abstract
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.Entities:
Keywords: Drug screening; Patient-derived cancer model; Patient-derived cell line; Sarcoma; Synovial sarcoma
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Year: 2022 PMID: 35655041 DOI: 10.1007/s13577-022-00721-5
Source DB: PubMed Journal: Hum Cell ISSN: 0914-7470 Impact factor: 4.174