lncRNA MELTF-AS1 facilitates osteosarcoma metastasis by modulating MMP14 expression

被引:18
作者
Ding, Lei [1 ]
Liu, Taiyuan [2 ,3 ]
Qu, Yuan [4 ]
Kang, Zhichen [1 ]
Guo, Lixin [1 ]
Zhang, Haina [1 ]
Jiang, Junjie [1 ]
Qu, Fuling [1 ]
Ge, Wanbao [4 ]
Zhang, Shanyong [4 ]
机构
[1] Second Hosp Jilin Univ, Dept Rehabil, Changchun 130000, Jilin, Peoples R China
[2] Second Hosp Jilin Univ, Dept Breast Surg, Changchun 130000, Jilin, Peoples R China
[3] Dalian Med Univ, Affiliated Hosp 2, Dept Breast Surg, Dalian 116023, Liaoning, Peoples R China
[4] Second Hosp Jilin Univ, Dept Spine Surg, Changchun 130000, Jilin, Peoples R China
来源
MOLECULAR THERAPY-NUCLEIC ACIDS | 2021年 / 26卷
基金
中国国家自然科学基金;
关键词
LONG NONCODING RNAS; CANCER; CERNA; PROGRESSION;
D O I
10.1016/j.omtn.2021.08.022
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
Osteosarcoma is a highly aggressive cancer common in children and adolescents. There is still a lack of effective treatments for metastatic or recurrent osteosarcoma. The role of long noncoding RNAs (lncRNAs) in osteosarcoma has gradually attracted attention. Here, we identified lncRNAs that were abnormally expressed in metastatic osteosarcoma through analyzing the sequencing data of osteosarcoma tissues and selected upregulated lncRNA MELTF-AS1 for detailed study. The qRT-PCR analysis showed that the expression of MELTF-AS1 was increased in osteosarcoma tissues and cells, and the high expression of MELTF-AS1 indicated a poor prognosis of osteosarcoma patients. The high expression of MELTFAS1 in osteosarcoma was partly due to the transcriptional activation of RREB1. The results of transwell assays, scratch wound healing assays, and the tail vein injection lung metastasis model demonstrated that knocking down MELTF-AS1 inhibited metastasis ability of osteosarcoma cells. Furthermore, the results of RNA pull-down assays, luciferase reporter assays, and MELTF-AS1 could regulate MMP14 expression through interaction with miR-485-5p. Our study suggested that MELTF-AS1 functioned as a pro-metastasis gene in osteosarcoma by upregulating MMP14 and that it could be a potential therapeutic and diagnostic target for osteosarcoma.
引用
收藏
页码:787 / 797
页数:11
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