Division of Rare Cancer Research, National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
The Department of Orthopaedic Surgery, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba-shi, 260-0856, Japan.
Hum Cell. 2022 Sep;35(5):1621-1629. doi: 10.1007/s13577-022-00724-2. Epub 2022 Jun 2.
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.
骨巨细胞瘤(GCTB)是一种罕见的中度恶性骨肿瘤,具有很强的局部浸润能力,其遗传特征是 H3-3A 基因突变。标准治疗是根治性手术肿瘤切除。GCTB 手术后既有局部复发,也有肺部转移,尚未建立有效的系统化疗。因此,有必要开发针对 GCTB 的新型化疗药物。虽然患者来源的肿瘤细胞系是临床前研究的有力工具,但迄今为止仅报道了 15 种 GCTB 细胞系,且仅有 4 种可公开获得。因此,本研究旨在建立和鉴定一种新的 GCTB 细胞系,用于 GCTB 的临床前研究。在此,我们描述了从 GCTB 患者的原发性肿瘤组织中建立的细胞系 NCC-GCTB5-C1。NCC-GCTB5-C1 显示 H3-3A 基因突变,这是 GCTB 的典型特征;因此,它具有用于体外研究的有用特性。我们使用 NCC-GCTB5-C1 以及四种 GCTB 细胞系对 214 种抗肿瘤药物进行了最大规模的综合筛选分析。罗米地辛(组蛋白去乙酰化酶抑制剂)、喜树碱和放线菌素 D(拓扑异构酶抑制剂)显示出显著的抗肿瘤作用,提示这些抗肿瘤药物可能是 GCTB 治疗的潜在候选药物。因此,NCC-GCTB5-C1 细胞系可能有助于阐明 GCTB 的发病机制和开发新的 GCTB 治疗方法。