Overexpressing circular RNA hsa_circ_0002052 impairs osteosarcoma progression via inhibiting Wnt/β-catenin pathway by regulating miR-1205/APC2 axis

被引:98
作者
Wu, Zhen [1 ]
Shi, Wangping [2 ]
Jiang, Chendi [3 ]
机构
[1] Tongde Hosp Zhejiang Prov, Orthopaed Dept, Hangzhou 310012, Zhejiang, Peoples R China
[2] Hangzhou Hosp, Zhejiang Med & Hlth Grp, Dept Pharm, Hangzhou 310022, Zhejiang, Peoples R China
[3] Wenzhou Med Univ, Dingli Clin Inst, Dept Orthopaed Surg, 32 Dajian Lane, Wenzhou 325000, Zhejiang, Peoples R China
关键词
hsa_circ_0002052; Osteosarcoma; Progression; miR-1205; APC2; Wnt/beta-catenin; PROMOTES; PROLIFERATION; EXPRESSION; APOPTOSIS; INVASION; GROWTH;
D O I
10.1016/j.bbrc.2018.05.184
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Circular RNAs (circRNAs) are a novel class of noncoding RNAs, whose importance in cancer has been gradually acknowledged. However, the functions of circRNAs in tumorigenesis have not been fully understood. In the present study, we identified a novel circRNA hsa_circ_0002052 significantly down-regulated in osteosarcoma (OS) tissues and cell lines. Moreover, we found that hsa_circ_0002052 could act as a biomarker to indicate the prognosis of OS patients. Functionally, we showed that hsa_circ_0002052 overexpression significantly suppressed OS cell proliferation, migration and invasion while promoting apoptosis in vitro. Similarly, in vivo assay indicated that ectopic expression of hsa_circ_0002052 impaired OS cell growth. In terms of mechanism, we found that hsa_circ_0002052 inhibited miR-1205 while miR1205 targeted APC2, a negative regulator of Wnt/13-catenin signaling pathway. By releasing the inhibition of miR-1205 on APC2 expression, hsa_circ_0002052 suppressed the activation of Wnt/beta-catenin signaling pathway, leading to attenuated OS progression. Taken together, our study for the first time revealed a suppressive circRNA hsa_circ_0002052 involved in OS progression. Our study suggested hsa_circ_0002052/miR-1205/APC2/Wnt/beta-catenin axis might be a potential target for OS therapy. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:465 / 471
页数:7
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