Establishment and characterization of NCC-DDLPS3-C1: a novel patient-derived cell line of dedifferentiated liposarcoma

被引:7
|
作者
Tsuchiya, Ryuto [1 ,2 ]
Yoshimatsu, Yuki [1 ]
Noguchi, Rei [1 ]
Ono, Takuya [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, Res Inst, Div Rare Canc Res, Chuo Ku, 5-1-1 Tsukiji, Tokyo 1040045, Japan
[2] Chiba Univ, Grad Sch Med, Dept Orthopaed Surg, Chuo Ku, 1-8-1 Inohana, Chiba 2608670, Japan
[3] Natl Canc Ctr, Fundamental Innovat Oncol Core Ctr, Dept Translat Oncol, 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; Drug screening;
D O I
10.1007/s13577-021-00515-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dedifferentiated liposarcoma (DDLPS) is a highly malignant subtype of liposarcoma, with characteristic amplification of MDM2 and CDK4 (12q14-15). It is caused by the dedifferentiation of well-differentiated liposarcoma. DDLPS is refractory to conventional chemotherapy; thus, surgical resection is the primary treatment modality. However, complete resection of DDLPS is difficult because of its deep location, which results in poor prognosis. Therefore, novel systemic chemotherapy is required to improve the clinical outcome. Patient-derived cell lines are important tools in the development of novel chemotherapy. However, there are no DDLPS cell lines available from public cell banks. In this study, we established a novel DDLPS cell line, NCC-DDLPS3-C1, using a surgically resected specimen from a patient with DDLPS. NCC-DDLPS3-C1 cells retained the characteristic gene amplification of MDM2 and CDK4. In addition, other gene amplifications and losses related to the poor prognosis of DDLPS were also observed in concordance with the original tumor. The cells also exhibited rapid cell proliferation, aggressive invasion ability, spheroid formation ability, and tumorigenic ability in nude mice. Furthermore, a drug-screening test showed significant antiproliferative effects of proteasome inhibitors and HDAC inhibitors. Thus, the NCC-DDLPS3-C1 cell line should be a useful tool for the development of novel chemotherapy for DDLPS.
引用
收藏
页码:1008 / 1018
页数:11
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