Circular RNA circ_0002137 regulated the progression of osteosarcoma through regulating miR-433-3p/ IGF1R axis

被引:13
|
作者
Zhang, Meng [1 ]
Yu, Guang-Yang [1 ]
Liu, Gang [1 ]
Liu, Wei-Dong [1 ]
机构
[1] Nanjing Med Univ, Dept Orthoped, Affiliated Huaian Peoples Hosp 1, 6 West Beijing Rd, Huaian 223001, Jiangsu, Peoples R China
关键词
circRNA; hsa_circ_0002137; IGF1R; miR‐ 433‐ 3p; osteosarcoma; WEB TOOL; EXPRESSION; SARCOMA; GROWTH; TUMORS; CIXUTUMUMAB; COMBINATION; METASTASIS; INHIBITOR; MIGRATION;
D O I
10.1111/jcmm.16166
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Current clinical treatment targeting osteosarcoma (OS) are limited for OS patients with pulmonary metastasis or relapse, which led to high mortality (70%-85%) for advanced osteosarcoma patients. Although ongoing efforts have been made to illustrate the mechanisms of tumorigenesis and progression in OS; however, it was far for us to learn a comprehensive molecular mechanism implies in OS development. In our study, we implicated a circRNA hsa_circ_0002137, which was higher expressed in osteosarcoma tumours compared with paracancerous tissue. The dysregulated expression pattern was also found in osteosarcoma cell lines. The role of circ_0002137 was explored via down- or up-regulated experiments. It was proved that down-regulation of circ_0002137 suppressed the progress of OS, including cell invasion, cell cycle and cell apoptosis. Furthermore, the correlation between circ_0002137 and miR-433-3p was predicted using bioinformatic tools and verified utilizing RNA pull-down assay and luciferase reporter assay. Interestingly, we found that the inhibitory effect of circ_0002137 on OS was dependent of insulin-like growth factor-1 receptor (IGF1R). In conclusion, it was demonstrated that circ_0002137 could restrain the progression of OS through regulating miR-433-3p/IGF1R axis, providing a comprehensive landscape of circ_0002137 in the generation and development of OS.
引用
收藏
页码:1806 / 1816
页数:11
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