Long non-coding RNA RP11-59H7.3 promotes cell proliferation and invasion matastasis in colorectal cancer by miR-139-5p/NOTCH1 axis

被引:0
作者
Zhu, Xiaojian [1 ,2 ,3 ]
Luo, Chen [1 ,2 ,3 ]
Bu, Fanqin [1 ,2 ,3 ]
Lin, Kang [1 ,2 ]
Zhu, Zhengming [1 ]
机构
[1] Nanchang Univ, Gastrointestinal Surg, Affiliated Hosp 2, Nanchang, Jiangxi, Peoples R China
[2] Nanchang Univ, Jiangxi Med Coll, Nanchang, Jiangxi, Peoples R China
[3] Jiangxi Prov Key Lab Mol Med, Nanchang, Jiangxi, Peoples R China
来源
AGING-US | 2020年 / 12卷 / 12期
基金
中国国家自然科学基金;
关键词
LncRNA; RP11-59H7.3; MiR-139-5p; NOTCH1; colorectal cancer; PROGRESSION; LNCRNA;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Increasing evidence suggests long non-coding RNAs (lncRNAs) are distinctively expressed in several cancers. However, the functions of these lncRNAs in cancer development remain unknown. In the current study, we report high expression of a novel lncRNA, RP11-59H7.3, and its association with prognosis in colorectal cancer (CRC) patients. Functional analyses of this lncRNA revealed its role in promoting proliferation and progression of the cell cycle, as well as enhancement of cell migration and invasion. Furthermore, our results revealed that knockdown of RP11-59H7.3 promoted cell apoptosis, with luciferase reporter assays showing that it directly binds to miR-139-5p. Knockdown of this lncRNA significantly reduced expression of NOTCH1, a direct target of miR-139-5p. Additionally, we show that suppression NOTCH1 by miR-139-5p could be partially rescued by overexpressing RP11-59H7.3. Analysis of the relationship between RP11-59H7.3 and miR-139-5p, in CRC tissues, showed a negative correlation while a positive association was observed between the RP11-59H7.3 expression and levels of NOTCH1. Taken together, these results demonstrated that the RP11-59H7.3/miR-139-5/NOTCH1 axis functions as a key regulator in CRC metastasis. RP11-59H7.3 represents a potential biomarker for CRC diagnosis and could be an important target for development of novel therapies to manage the disease.
引用
收藏
页码:11653 / 11666
页数:14
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