| Literature DB >> 35947340 |
Yuki Yoshimatsu1, Rei Noguchi1, Yooksil Sin1, Ryuto Tsuchiya1, Takuya Ono1, Taro Akiyama1, Chiaki Sato2, Eisuke Kobayashi2, Naoki Kojima3, Akihiko Yoshida3, Akira Kawai2, Tadashi Kondo4.
Abstract
Myxofibrosarcoma (MFS) is a rare and aggressive mesenchymal malignancy characterized by complex karyotypes with heterogeneous clinical features. The standard treatment for primary MFS is curative resection; however, the utility of systemic chemotherapy and radiotherapy has not been established. Although patient-derived cancer cell lines are a key bioresource for developing novel therapies, the number of MFS cell lines available from public cell banks is limited by the rarity of the disease, and large-scale drug screening has not yet been performed. To address this issue, we aimed to establish and characterize a novel MFS cell line. We successfully established a cell line, NCC-MFS6-C1, which harbors genetic abnormalities common in MFS and exhibits aggressive phenotypes such as continuous growth, spheroid formation, and invasion in tissue culture conditions. We performed drug screening using NCC-MFS6-C1 along with five MFS cell lines established in our laboratory and clarified the response spectrum of 214 existing anticancer agents. We found that two anticancer agents, gemcitabine and romidepsin, showed considerable antiproliferative effects, and these observations were concordant with the findings of our previous report, in which these agents attenuated the proliferation of five previously reported MFS cell lines. We conclude that NCC-MFS6-C1 is a useful resource for studying MFS.Entities:
Keywords: Drug screening; Myxofibrosarcoma; Patient-derived cancer cell line; Spheroid
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Year: 2022 PMID: 35947340 DOI: 10.1007/s13577-022-00749-7
Source DB: PubMed Journal: Hum Cell ISSN: 0914-7470 Impact factor: 4.374