RETRACTED: miR-622 suppresses tumor formation by directly targeting VEGFA in papillary thyroid carcinoma (Retracted Article)

被引:26
|
作者
Wang, Renjie [1 ]
Ma, Qingjie [1 ]
Ji, Linlin [1 ]
Yao, Yue [1 ]
Ma, Mengshi [1 ]
Wen, Qiang [1 ]
机构
[1] Jilin Univ, China Japan Union Hosp, Dept Nucl Med, 126 Xiantai St, Changchun 13033, Jilin, Peoples R China
来源
ONCOTARGETS AND THERAPY | 2018年 / 11卷
基金
中国国家自然科学基金;
关键词
thyroid cancer; miR-622; VEGFA; proliferation; invasion; ENDOTHELIAL GROWTH-FACTOR; MICRORNAS; INVASION; METASTASIS; PROLIFERATION; MIGRATION;
D O I
10.2147/OTT.S156810
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: MicroRNAs (miRNAs) were reportedly to play crucial roles in papillary thyroid carcinoma (PTC) tumorigenesis and development. Therefore, the discovery of miRNAs may provide a new and powerful tool for diagnosis and treatment of PTC. Purpose: The aim of this study was to investigate the biological function and underlying mechanism of miR-622 in PTC. Materials and methods: The expression levels of miR-622 in PTC patient tissues and cell lines were determined by quantitative RT-PCR (qRT-PCR). The biological function including cell proliferation, colony formation, migration and invasion, as well as underling mechanism of miR-622 in PTC, were also evaluated by a series of in vitro and in vivo experiments. Results: miR-622 expression level was significantly downregulated in PTC tissues and cell lines. Decreased miR-622 expression was associated with advanced clinical stage and lymph node metastasis (P<0.01). The overexpression of miR-622 in TPC-1 cells inhibited cell proliferation, migration and invasion in vitro, as well as suppress tumor growth in vivo. Moreover, we also demonstrated that miR-622 specifically targeted the 3'-UTR regions of vascular endothelial growth factor A (VEGFA) and inhibited its expression both mRNA level and protein levels. Overexpression of VEGFA reversed miR-622-mediated inhibition effect on cell proliferation, migration and invasion in thyroid cancer cells. More importantly, VEGFA expression was significantly increased and inversely correlated with the levels of miR-622 in PTC tissues. Conclusion: These results show that miR-622 acts as a tumor suppressor in thyroid cancer, at least in part, via targeting VEGFA, and suggest that miR-622 may serves as a potential target for treatment of thyroid cancer patients.
引用
收藏
页码:1501 / 1509
页数:9
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