| Literature DB >> 34383271 |
Yuki Yoshimatsu1, Rei Noguchi1, Ryuto Tsuchiya1, Yooksil Sin1, Takuya Ono1, Jun Sugaya2, Shintaro Iwata2, Akihiko Yoshida3, Akira Kawai2, Tadashi Kondo4.
Abstract
Myxofibrosarcoma (MFS) is an aggressive sarcoma with a highly complex karyotype. Complete resection is the only curative treatment for MFS because it is refractory to chemotherapy. To improve clinical outcomes, it is critical to develop novel treatments for MFS. Although patient-derived cell lines play a key role in cancer research, only 12 MFS cell lines have been reported to date, and considering the diversity of the disease, more cell lines need to be established. Hence, in the present study, we established a novel MFS cell line, NCC-MFS4-C1, using a surgically resected tumor tissue from a patient with MFS. NCC-MFS4-C1 cells exhibited copy number alterations similar to those of the original tumors and showed constant proliferation, spheroid formation, and aggressive invasion. By screening a drug library, we found that actinomycin D, bortezomib, docetaxel, eribulin, and romidepsin significantly reduced the proliferation of NCC-MFS4-C1 cells. Therefore, the NCC-MFS4-C1 cell line may be a useful resource for researching MFS.Entities:
Keywords: Drug screening; Myxofibrosarcoma; Patient-derived cancer model; Patient-derived cell line; Sarcoma
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Year: 2021 PMID: 34383271 DOI: 10.1007/s13577-021-00589-x
Source DB: PubMed Journal: Hum Cell ISSN: 0914-7470 Impact factor: 4.174