Establishment and characterization of a new highly metastatic human osteosarcoma cell line derived from Saos2

被引:0
作者
Du, Lin [1 ,2 ]
Fan, Qiming [1 ]
Tu, Bing [1 ]
Yan, Wei [1 ]
Tang, Tingting [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Key Lab Orthoped Implants, Dept Orthoped Surg, Sch Med,Shanghai Peoples Hosp 9, Shanghai 200011, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 1, Shanghai 200080, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2014年 / 7卷 / 06期
基金
中国国家自然科学基金;
关键词
Animal model; osteosarcoma; metastasis; microarray; MESENCHYMAL STEM-CELLS; MURINE OSTEOSARCOMA; OSTEOGENIC-SARCOMA; GENE-EXPRESSION; MOUSE MODEL; NUDE-MICE; GROWTH; CANCER; INHIBITION; SUPPRESSOR;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteosarcoma is the most common primary malignancy of bone in adolescents and young adults. There is a shortage of tumorigenic and highly metastatic human osteosarcoma cell lines that can be used for metastasis study. Here we establish and characterize a highly metastatic human osteosarcoma cell line that is derived from Saos2 cell line based on bioluminescence. The occasional pulmonary metastatic cells developed from Saos2 were isolated, harvested, characterized and named Saos2-l. The parental Saos2 and Saos2-l cells were further characterized both in vitro and in vivo. Results showed that Saos2-l cells demonstrated increased cell adhesion, migration and invasion compared to the parental Saos2 cells. Conversely, Saos2-l cells grew at a slightly slower rate than that of the parental cells. When injected into nude mice, Saos2-l cells had a greater increase in developing pulmonary metastases compared to the parental Saos2 cells. Further transcriptional profiling analysis revealed that some gene expression were up-regulated or down-regulated in the highly metastatic Saos2-l cells, indicating possible influencing factors of metastasis. Thus, we have established and characterized a highly metastatic human osteosarcoma cell line that should serve as a valuable tool for future investigations on the pathogenesis, metastasis and potential treatments of human osteosarcoma.
引用
收藏
页码:2871 / 2882
页数:12
相关论文
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