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Bone marrow mesenchymal stem cell-derived exosomal miR-206 inhibits osteosarcoma progression by targeting TRA2B
被引:95
|作者:
Zhang, Hongliang
[1
,2
]
Wang, Jun
[1
,2
]
Ren, Tingting
[1
,2
]
Huang, Yi
[1
,2
]
Liang, Xin
[1
,2
]
Yu, Yiyang
[1
,2
]
Wang, Wei
[1
,2
]
Niu, Jianfang
[1
,2
]
Guo, Wei
[1
,2
]
机构:
[1] Peking Univ Peoples Hosp, Musculoskeletal Tumor Ctr, 11 Xizhimen South St, Beijing 100044, Peoples R China
[2] Beijing Key Lab Musculoskeletal Tumor, Beijing, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
Bone tumor;
Extracellular vehicle;
MicroRNA;
Proliferation;
Pulmonary metastasis;
CANCER;
MICROENVIRONMENT;
COMMUNICATION;
PROLIFERATION;
MICRORNA-206;
MIGRATION;
GROWTH;
D O I:
10.1016/j.canlet.2020.07.008
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Osteosarcoma is the most common primary malignant bone tumor in young people. Recently, extracellular vesicles, especially exosomes, have been reported to play an increasingly important role in the development of many types of tumors. In this research, we found that overexpression of transformer 2 beta (TRA2B) was associated with tumor progression in osteosarcoma, and TRA2B was the target gene of miR-206, which was downregulated in osteosarcoma tissues. Furthermore, we observed that bone marrow mesenchymal stem cell (BMSC)-derived exosomes could carry and transport miR-206 to osteosarcoma cells. Both in vitro and in vivo results showed that BMSC-derived exosomal miR-206 could inhibit the proliferation, migration and invasion of osteosarcoma cells and induce their apoptosis. Taken together, our study demonstrates that BMSC-derived exosomal miR-206 can be transferred into osteosarcoma cells and inhibit tumor progression by targeting TRA2B, which provides new insight into the molecular mechanism of osteosarcoma and highlights the potential of miR-206 and TRA2B as new therapeutic targets.
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页码:54 / 65
页数:12
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