| Literature DB >> 30737712 |
Fusako Kito1, Rieko Oyama1, Marimu Sakumoto1, Kumiko Shiozawa2, Zhiwei Qiao2, Shunichi Toki3, Akihiko Yoshida4, Akira Kawai3, Tadashi Kondo5,6.
Abstract
Myxofibrosarcoma (MFS) is an aggressive sarcoma that requires novel therapeutic approaches to improve its clinical outcome. Cell lines are a valuable tool for pre-clinical research; however, there is a lack of patient-derived cell lines of MFS available from public cell banks. This study aimed to develop a patient-derived cell line of MFS. A cell line designated NCC-MFS1-C1 was established from the primary tumor tissue of an 82-year-old male patient with MFS. The short tandem repeat pattern of NCC-MFS1-C1 cells was identical to that of the original tumor, but distinct from that of any other cell lines in public cell banks. NCC-MFS1-C1 cells were maintained as a monolayer culture for over 20 passages in 19 months; the cells exhibited spindle-like morphology, continuous growth, and ability for spheroid formation and invasion. Genomic assay showed that NCC-MFS1-C1 cells had gain and loss of genetic loci. Proteomic profiling revealed that the original tumor and the derived NCC-MFS1-C1 cells had similar, but distinct protein expression patterns. Screening of anti-cancer drugs in NCC-MFS1-C1 cells identified five candidate drugs for MFS. In conclusion, we established a novel MFS cell line, NCC-MFS1-C1, which could be used to study tumor development and effects of anti-cancer drugs.Entities:
Keywords: Cell line; Drug screening; Myxofibrosarcoma; Proteomics
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Year: 2019 PMID: 30737712 DOI: 10.1007/s13577-018-00233-1
Source DB: PubMed Journal: Hum Cell ISSN: 0914-7470 Impact factor: 4.174