Long non-coding RNA HOXA11-AS functions as a competing endogenous RNA to regulate ROCK1 expression by sponging miR-124-3p in osteosarcoma

被引:74
作者
Cui, Mingxing [1 ]
Wang, Jingyu [1 ]
Li, Qingjiang [1 ]
Zhang, Junlei [1 ]
Jia, Jinling [1 ]
Zhan, Xinli [2 ]
机构
[1] Xinxiang Med Univ, Affiliated Hosp 1, Dept Orthopaed, Weihui 453100, Henan, Peoples R China
[2] Guangxi Med Univ, Affiliated Hosp 1, Dept Orthopaed, Nanning 530021, Guangxi, Peoples R China
关键词
Osteosarcoma; Long non-coding RNAs; HOXA11-AS; MiR-124-3p; ROCK1; BLADDER-CANCER CELLS; PROLIFERATION; EPIDEMIOLOGY; PROGRESSION; METASTASIS; INVASION; END;
D O I
10.1016/j.biopha.2017.05.081
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Long non-coding RNAs (lncRNAs) have been strongly associated with various types of cancer. this study was to explore the critical role of lncRNA HOXA11-AS in osteosarcoma (OS) progression. Briefly, we should that the expression of HOXA11-AS was upregulated in OS tissues and cell lines. The high expression of HOXA11-AS was associated with advanced clinical stage, distant metastasis and poor overall survival of OS. In addition, We found that HOXA11-AS silencing suppressed OS cells proliferation, invasion and induced cell arrest in G0/G1 phase. Furthermore, our data showed that HOXA11-AS acts as an endogenous sponge by directly binding miR-124-3p, and decreasing the expression of miR-124-3p. Moreover, we found that HOXA11-AS may regulate tumor progression by affecting miR-124-3p targets, and ROCK1 expression. To conclude, our study helps to elucidate the effectiveness of HOXA11-AS promotion on OS cell proliferation and metastasis. A better understanding of interaction mechanism between HOXA11-AS-miR-124-3p-ROCK1 signaling axis may be a step forward in the development of new therapeutic strategies for the treatment of OS. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:437 / 444
页数:8
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