Establishment and characterization of NCC-MFS3-C1: a novel patient-derived cell line of myxofibrosarcoma
Establishment and characterization of NCC-MFS3-C1: a novel patient-derived cell line of myxofibrosarcoma
复制标题
NCC-MFS3-C1 的建立和表征:一种新型的患者来源的粘液纤维肉瘤细胞系
DOI:
10.1007/s13577-021-00548-6
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发表时间:
2021
期刊:
影响因子:
4.3
通讯作者:
Kondo Tadashi
中科院分区:
文献类型:
--
作者:
Tsuchiya Ryuto;Yoshimatsu Yuki;Noguchi Rei;Sin Yooksil;Ono Takuya;Sei Akane;Takeshita Fumitaka;Sugaya Jun;Iwata Shintaro;Yoshida Akihiko;Ohtori Seiji;Kawai Akira;Kondo Tadashi
Myxofibrosarcoma (MFS) is one of the most aggressive sarcomas with highly complex karyotypes and genomic profiles. Although a complete resection is required in the treatment of MFS, it is often not achieved due to its strong invasive nature. Additionally, MFS is refractory to conventional chemotherapy, leading to poor prognosis. Therefore, it is necessary to develop novel treatment modalities for MFS. Patient-derived cell lines are important tools in basic research and preclinical studies. However, only 10 MFS cell lines have been reported to date. Furthermore, among these cell lines, merely two MFS cell lines are publicly available. Hence, we established a novel MFS cell line named NCC-MFS3-C1, using a surgically resected tumor specimen from a patient with MFS. NCC-MFS3-C1 cells had copy number alterations corresponding to the original tumor. NCC-MFS3-C1 cells demonstrate constant proliferation, spheroid formation, and aggressive invasion. In drug screening tests, the proteasome inhibitor bortezomib and the histone deacetylase inhibitor romidepsin demonstrated significant antiproliferative effects on NCC-MFS3-C1 cells. Thus, the NCC-MFS3-C1 cell line is a useful tool in both basic and preclinical studies for MFS.