Establishment and characterization of NCC-DFSP5-C1: a novel patient-derived dermatofibrosarcoma protuberans cell line

被引:1
作者
Ono, Takuya [1 ,2 ]
Noguchi, Rei [1 ]
Osaki, Julia [1 ]
Akiyama, Taro [1 ,6 ]
Adachi, Yuki [1 ]
Kojima, Naoki [3 ]
Toda, Yu [4 ]
Fukushima, Suguru [4 ]
Yoshimatsu, Yuki [5 ]
Yoshida, Akihiko [3 ]
Kawai, Akira [4 ]
Kondo, Tadashi [1 ]
机构
[1] Natl Canc Ctr, Res Inst, Div Rare Canc Res, 5-1-1 Tsukiji,Chuo Ku, Tokyo 1040045, Japan
[2] Nagasaki Univ, Grad Sch Biomed Sci, 1-12-4 Sakamoto, Nagasaki 8528523, Japan
[3] Natl Canc Ctr, Dept Diagnost Pathol, 5-1-1 Tsukiji,Chuo Ku, Tokyo 1040045, Japan
[4] Natl Canc Ctr, Dept Musculoskeletal Oncol & Rehabil Med, 5-1-1 Tsukiji,Chuo Ku, Tokyo 1040045, Japan
[5] Tochigi Canc Ctr, Dept Patient Derived Canc Model, 4-9-13 Yohnan, Utsunomiya, Tochigi 3200834, Japan
[6] Chiba Univ, Grad Sch Med, Dept Orthopaed Surg, 1-8-1 Inohana,Chuo Ku, Chiba 2608670, Japan
关键词
Sarcoma; Dermatofibrosarcoma protuberans; Patient-derived cancer model; Patient-derived cell line; Fusion gene; FUSION; IMATINIB; EPIDEMIOLOGY; RECURRENCE; PROTEIN;
D O I
10.1007/s13577-024-01030-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dermatofibrosarcoma protuberans (DFSP) is the most prevalent dermal sarcoma, characterized by the presence of the fusion of the collagen type I alpha 1 (COL1A1) gene with the platelet-derived growth factor beta chain (PDGFB) gene. Although PDGF receptor inhibitor imatinib mesylate was approved for the treating patients with unresectable or metastatic DFSP, disease progression was shown in 9.2% of the patients. Therefore, developing novel therapeutic strategies is crucial for improving the prognosis of DFSP. Patient-derived cell lines play a vital role in preclinical studies; however, only a limited number of DFSP cell lines are currently available in public cell banks. Here, we successfully established a novel DFSP cell line (NCC-DFSP5-C1) using surgically resected tumor tissue from a patient with DFSP. NCC-DFSP5-C1 cells were confirmed to carry the COL1A1-PDGFB translocation and maintain the same mutation as the original tumor tissue. They exhibited consistent growth, formed spheroids, and were invasive. By screening a drug library using NCC-DFSP5-C1 and four previously established DFSP cell lines, we identified anti-cancer drugs that inhibit DFSP cell proliferation. Our observations suggest that the NCC-DFSP5-C1 cell line holds promise as a valuable tool for conducting fundamental and preclinical studies for DFSP.
引用
收藏
页码:854 / 864
页数:11
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