Establishment and characterization of NCC-DDLPS1-C1: a novel patient-derived cell line of dedifferentiated liposarcoma

被引:5
|
作者
Tsuchiya, Ryuto [1 ,2 ]
Yoshimatsu, Yuki [1 ]
Noguchi, Rei [1 ]
Sei, Akane [1 ]
Takeshita, Fumitaka [3 ]
Sugaya, Jun [4 ]
Fukushima, Suguru [4 ]
Yoshida, Akihiko [5 ]
Ohtori, Seiji [2 ]
Kawai, Akira [4 ]
Kondo, Tadashi [1 ]
机构
[1] Natl Canc Ctr, Div Rare Canc Res, Res Inst, Chuo Ku, 5-1-1 Tsukiji, Tokyo 1040045, Japan
[2] Chiba Univ, Dept Orthopaed Surg, Grad Sch Med, Chuo Ku, 1-8-1 Inohana, Chiba 2608670, Japan
[3] Natl Canc Ctr, Dept Translat Oncol, Fundamental Innovat Oncol Core Ctr, Res Inst,Chuo Ku, 5-1-1 Tsukiji, Tokyo 1040045, Japan
[4] Natl Canc Ctr, Dept Musculoskeletal Oncol, Chuo Ku, 5-1-1 Tsukiji, Tokyo 1040045, Japan
[5] Natl Canc Ctr, Dept Diagnost Pathol, Chuo Ku, 5-1-1 Tsukiji, Tokyo 1040045, Japan
关键词
Sarcoma; Dedifferentiated liposarcoma; Patient-derived cancer model; Patient-derived cell line; MALIGNANT FIBROUS HISTIOCYTOMAS; ADIPOCYTIC DIFFERENTIATION; AMPLIFICATION; MDM2; OVEREXPRESSION; BORTEZOMIB; PATHWAY;
D O I
10.1007/s13577-020-00436-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dedifferentiated liposarcoma (DDLPS) is one of the four subtypes of liposarcomas; it is characterized by the amplification of the 12q13-15 region, which includesMDM2andCDK4genes. DDLPS has an extremely high local recurrence rate and is refractory to chemotherapy and radiation, which leads to poor prognosis. Therefore, a novel therapeutic strategy should be urgently established for improving the prognosis of DDLPS. Although patient-derived cell lines are important tools for basic research, there are no DDLPS cell lines available from public cell banks. Here, we report the establishment of a novel DDLPS cell line. Using the surgically resected tumor tissue from a patient with DDLPS, we established a cell line and named it NCC-DDLPS1-C1. The NCC-DDLPS1-C1 cells contained 12q13-15, 1p32, and 1q23 amplicons and highly expressed MDM2 and CDK4 proteins. NCC-DDLPS-C1 cells exhibited constant growth, spheroid formation, aggressive invasion, and tumorigenesis in mice. By screening a drug library, we identified that the proteasome inhibitor, bortezomib, had inhibitory effects on the proliferation of NCC-DDLPS1-C1 cells. We concluded that the NCC-DDLPS1-C1 cell line may serve as a useful tool for basic and pre-clinical studies of DDLPS.
引用
收藏
页码:260 / 270
页数:11
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