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建立并鉴定 NCC-DDLPS3-C1:一种新型去分化脂肪肉瘤的患者来源细胞系。

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

机构信息

Division of Rare Cancer Research, National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.

Department of Orthopaedic Surgery, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 260-8670, Japan.

出版信息

Hum Cell. 2021 May;34(3):1008-1018. doi: 10.1007/s13577-021-00515-1. Epub 2021 Mar 6.

DOI:10.1007/s13577-021-00515-1
PMID:33677797
Abstract

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.

摘要

去分化脂肪肉瘤(DDLPS)是一种高度恶性的脂肪肉瘤亚型,其特征是 MDM2 和 CDK4(12q14-15)的扩增。它是由分化良好的脂肪肉瘤去分化引起的。DDLPS 对常规化疗具有抗性;因此,手术切除是主要的治疗方式。然而,由于其位置较深,完全切除 DDLPS 较为困难,这导致预后不良。因此,需要新的系统化疗来改善临床结果。患者来源的细胞系是开发新型化疗的重要工具。然而,公共细胞库中没有 DDLPS 细胞系。在这项研究中,我们使用一位 DDLPS 患者的手术切除标本建立了一种新型的 DDLPS 细胞系,NCC-DDLPS3-C1。NCC-DDLPS3-C1 细胞保留了 MDM2 和 CDK4 的特征性基因扩增。此外,与原始肿瘤一致,还观察到其他与 DDLPS 预后不良相关的基因扩增和缺失。这些细胞还表现出快速的细胞增殖、侵袭能力、球体形成能力和在裸鼠中的致瘤能力。此外,药物筛选测试显示蛋白酶体抑制剂和 HDAC 抑制剂具有显著的抗增殖作用。因此,NCC-DDLPS3-C1 细胞系应该是开发 DDLPS 新型化疗的有用工具。

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