Knockdown of long non-coding RNA TP73-AS1 inhibits osteosarcoma cell proliferation and invasion through sponging miR-142

被引:30
|
作者
Yang, Guangling [1 ]
Song, Ruipeng [1 ]
Wang, Limin [1 ]
Wu, Xuejian [1 ]
机构
[1] Zhengzhou Univ, Dept Orthoped, Affiliated Hosp 1, East 1 Jianshe Rd, Zhengzhou 450052, Henan, Peoples R China
关键词
Osteosarcoma; TP73-AS1; miR-142; Rac1; EPITHELIAL-MESENCHYMAL TRANSITION; HEPATOCELLULAR-CARCINOMA; HUMAN CANCERS; LUNG-CANCER; RAC1; METASTASIS; APOPTOSIS; LNCRNA; OVEREXPRESSION; EXPRESSION;
D O I
10.1016/j.biopha.2018.04.146
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 RNA P73 antisense RNA 1 T (lncRNA TP73-AS1) has been shown to involve in the progression of numerous tumors. Nevertheless, the expression as well as the functional mechanisms of TP73-AS1 in osteosarcoma (OS) are still largely unknown. This study aimed to explore the roles and underlying mechanism of TP73-AS1 in OS progression. In thye present study, TP73-AS1 expression was significantly increased in OS tissues and cell lines. High TP73-AS1 expression was associated with poor overall survival of OS patients. TP73-AS1 knockdown suppressed OS cells proliferation and invasion in vitro as well as tumor growth in vivo. Furthermore, we identified that miR-142 could act as a direct target for TP73-AS1 and miR-142 inhibition reversed the suppression of OS cells proliferation and invasion induced by TP73-AS1 knockdown. In addition, we showed that TP73-AS1 could function as a sponge of miR-142 to positively regulate Rac1 in OS cells. Thus, our data suggested that TP73-AS1 served as an oncogenic lncRNA in OS progression, and could be regarded as an efficient therapeutic target in the treatment of OS.
引用
收藏
页码:1238 / 1245
页数:8
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