Establishment and characterization of NCC-DFSP3-C1: a novel patient-derived dermatofibrosarcoma protuberans cell line

被引:0
|
作者
Yuki Yoshimatsu
Rei Noguchi
Ryuto Tsuchiya
Akane Sei
Makoto Nakagawa
Akihiko Yoshida
Akira Kawai
Tadashi Kondo
机构
[1] National Cancer Center Research Institute,Division of Rare Cancer Research
[2] Chiba University,Department of Orthopaedic Surgery, Graduate School of Medicine
[3] National Cancer Center Hospital,Department of Musculoskeletal Oncology
[4] National Cancer Center Hospital,Department of Diagnostic Pathology
来源
Human Cell | 2020年 / 33卷
关键词
Sarcoma; Dermatofibrosarcoma protuberans; Patient-derived cancer model; Patient-derived cell line; Fusion gene;
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学科分类号
摘要
Dermatofibrosarcoma protuberans (DFSP) is the most common dermal sarcoma; it is characterized by the presence of the COL1A1–PDGFB translocation, which causes the constitutive activation of the platelet-derived growth factor β (PDGFB) signaling pathway. DFSP frequently exhibits local recurrence and is refractory to conventional chemotherapy. Therefore, a novel therapeutic strategy is required for improving the prognosis of DFSP. Although patient-derived cell lines are important tools for pre-clinical studies, currently, only a few such cell lines are available for DFSP in cell banks. Here, we report the establishment of a novel DFSP cell line. Using a surgically resected metastatic tumor tissue from a patient with DFSP, we established a cell line called NCC-DFSP3-C1. The NCC-DFSP3-C1 cells had a COL1A1–PDGFB translocation and retained the same copy number aberrations as the original tumor tissue. NCC-DFSP3-C1 cells exhibited constant growth, spheroid formation, and invasive ability. By screening a drug library, we identified anti-cancer agents with inhibitory effects on the proliferation of NCC-DFSP3-C1 cells; these anti-cancer agents included proteasomal, histone deacetylase, and kinase inhibitors. We concluded that the NCC-DFSP3-C1 cell line may serve as a useful tool for performing basic and pre-clinical studies on DFSP.
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页码:894 / 903
页数:9
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