| Literature DB >> 35653034 |
Taro Akiyama1,2, Yuki Yoshimatsu1,3, Rei Noguchi1, Yooksil Sin1, Ryuto Tsuchiya1,2, Takuya Ono1, Suguru Fukushima4, Yu Toda4, Naoki Kojima5, Akihiko Yoshida5, Seji Ohtori2, Akira Kawai4, Tadashi Kondo6.
Abstract
Giant cell tumor of bone (GCTB), is a rare intermediate malignant bone tumor with high local infiltrative ability, and is genetically characterized by mutation in the H3-3A gene. Standard treatment is curative surgical tumor resection. GCTB demonstrates both local recurrence and pulmonary metastasis after surgical treatment, and effective systematic chemotherapy is yet to be established. Therefore, development of novel chemotherapies for GCTB is necessary. Although patient-derived tumor cell lines are potent tools for preclinical research, 15 GCTB cell lines have been reported to date, and only four are publicly available. Thus, this study aimed to establish and characterize a novel GCTB cell line for preclinical studies on GCTB. Herein, we described the establishment of a cell line, NCC-GCTB5-C1, from the primary tumor tissue of a patient with GCTB. NCC-GCTB5-C1 was shown to harbor a mutation in the H3-3A gene, which is typical of GCTB; thus, it has useful properties for in vitro studies. We conducted the largest integrated screening analysis of 214 antitumor agents using NCC-GCTB5-C1 along with four GCTB cell lines. Romidepsin (a histone deacetylase inhibitor), camptothecin, and actinomycin D (topoisomerase inhibitors) demonstrated remarkable antitumor effects, suggesting that these antitumor agents are potential therapeutic candidates for GCTB treatment. Therefore, the NCC-GCTB5-C1 cell line could potentially contribute to the elucidation of GCTB pathogenesis and the development of novel GCTB treatments.Entities:
Keywords: Antitumor drug screening; Cell lines; Giant cell tumor of bone; Preclinical model
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Year: 2022 PMID: 35653034 DOI: 10.1007/s13577-022-00724-2
Source DB: PubMed Journal: Hum Cell ISSN: 0914-7470 Impact factor: 4.374