Establishment and characterization of NCC-GCTB1-C1:a novel patient-derived cancer cell line of giant cell tumor of bone

被引:11
|
作者
Noguchi, Rei [1 ]
Yoshimatsu, Yuki [1 ]
Ono, Takuya [1 ]
Sei, Akane [1 ]
Hirabayashi, Kaoru [2 ]
Ozawa, Iwao [3 ]
Kikuta, Kazutaka [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] Tochigi Canc Ctr, Div Diagnost Pathol, 4-9-13 Yohnan, Utsunomiya, Tochigi 3200834, Japan
[3] Tochigi Canc Ctr, Div Hepatobiliary Pancreat Surg, 4-9-13 Yohnan, Utsunomiya, Tochigi 3200834, Japan
[4] Tochigi Canc Ctr, Div Musculoskeletal Oncol & Orthopaed Surg, 4-9-13 Yohnan, Utsunomiya, Tochigi 3200834, Japan
关键词
Giant cell tumor of bone; Cell line; Anticancer drug screen; NCC-GCTB1-C1; GCTB in vitro model; ANTIANGIOGENIC THERAPY; H3F3A; MUTATIONS; CHROMATIN;
D O I
10.1007/s13577-020-00415-w
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Giant cell tumor of bone (GCTB) is a rare osteolytic bone tumor, accounting for approximately 5% of all primary bone tumors. GCTB is characterized by unique giant cells. It is also characterized by recurrent mutations in the histone tail of the histone variant H3.3,H3F3A, on chromosome 1, therapeutic implications of which have not been established yet. There are few effective standardized treatments for GCTB, and a novel therapy has long been required. Patient-derived cancer cells have facilitated the understanding of mechanisms underlying the etiology and progression of multiple cancers. Thus far, only 10 GCTB cell lines have been reported, and none of them are publicly available. The aim of this study was to develop an accessible patient-derived cell line of GCTB, which could be used as a screening tool for drug development. Here, we describe the establishment of a cell line, designated NCC-GCTB1-C1, from the primary tumor tissue of a male patient with GCTB on the right distal radius. NCC-GCTB1-C1 cells were maintained as a monolayer culture for over 23 passages for 7 months. These cells exhibited continuous growth, as well as spheroid formation and invasive ability. Using an oncology agent screen, we tested the effect of anticancer drugs on the proliferation of NCC-GCTB1-C1 cells. The cells displayed a remarkable response to romidepsin and vincristine. Thus, we established a novel GCTB cell line, NCC-GCTB1-C1, which could be a useful tool for studying GCTB tumorigenesis and the efficacy of anticancer drugs.
引用
收藏
页码:1321 / 1328
页数:8
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