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建立并鉴定 NCC-MFS6-C1:一种新型黏液纤维肉瘤的患者来源细胞系。

Establishment and characterization of NCC-MFS6-C1: a novel patient-derived cell line of myxofibrosarcoma.

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 Diagnosis Pathology, National Cancer Center Hospital, 5-1-1 Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.

出版信息

Hum Cell. 2022 Nov;35(6):1993-2001. doi: 10.1007/s13577-022-00749-7. Epub 2022 Aug 10.

Abstract

Myxofibrosarcoma (MFS) is a rare and aggressive mesenchymal malignancy characterized by complex karyotypes with heterogeneous clinical features. The standard treatment for primary MFS is curative resection; however, the utility of systemic chemotherapy and radiotherapy has not been established. Although patient-derived cancer cell lines are a key bioresource for developing novel therapies, the number of MFS cell lines available from public cell banks is limited by the rarity of the disease, and large-scale drug screening has not yet been performed. To address this issue, we aimed to establish and characterize a novel MFS cell line. We successfully established a cell line, NCC-MFS6-C1, which harbors genetic abnormalities common in MFS and exhibits aggressive phenotypes such as continuous growth, spheroid formation, and invasion in tissue culture conditions. We performed drug screening using NCC-MFS6-C1 along with five MFS cell lines established in our laboratory and clarified the response spectrum of 214 existing anticancer agents. We found that two anticancer agents, gemcitabine and romidepsin, showed considerable antiproliferative effects, and these observations were concordant with the findings of our previous report, in which these agents attenuated the proliferation of five previously reported MFS cell lines. We conclude that NCC-MFS6-C1 is a useful resource for studying MFS.

摘要

黏液纤维肉瘤(MFS)是一种罕见且侵袭性的间叶性恶性肿瘤,其特征为具有复杂核型和异质性临床特征。原发性 MFS 的标准治疗方法是治愈性切除;然而,系统化疗和放疗的效用尚未确定。虽然患者来源的癌细胞系是开发新疗法的关键生物资源,但由于疾病的罕见性,公共细胞库中可获得的 MFS 细胞系数量有限,并且尚未进行大规模的药物筛选。为了解决这个问题,我们旨在建立和表征一种新型的 MFS 细胞系。我们成功建立了一个细胞系,NCC-MFS6-C1,它具有 MFS 中常见的遗传异常,并表现出在组织培养条件下连续生长、球体形成和侵袭等侵袭性表型。我们使用 NCC-MFS6-C1 与我们实验室建立的五株 MFS 细胞系一起进行了药物筛选,并阐明了 214 种现有抗癌药物的反应谱。我们发现两种抗癌药物,吉西他滨和罗米地辛,表现出相当大的抗增殖作用,这些观察结果与我们之前的报告一致,在该报告中,这些药物减弱了之前报告的五株 MFS 细胞系的增殖。我们得出结论,NCC-MFS6-C1 是研究 MFS 的有用资源。

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