Upregulation of miR-598 promotes cell proliferation and cell cycle progression in human colorectal carcinoma by suppressing INPP5E expression

被引:18
|
作者
Li, Kun-Ping [1 ]
Fang, Yong-Ping [1 ]
Liao, Jin-Qi [1 ]
Duan, Jin-Dong [1 ]
Feng, Li-Guang [1 ]
Luo, Xiao-Zai [1 ]
Liang, Zhi-Jian [1 ]
机构
[1] Huizhou First Hosp, Dept Gen Surg, 20 San Xin Nan Rd, Huizhou 516000, Guangdong, Peoples R China
关键词
miR-598; colorectal cancer; 72 kDa inositol polyphosphate-5-phosphatase; cell proliferation; cell cycle; CANCER CELLS; METASTASIS; INVASION;
D O I
10.3892/mmr.2017.8207
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Colorectal cancer (CRC) is one of the most common types of cancer worldwide. Recently, microRNAs (miRs) have been considered as novel therapeutic targets for the treatment of cancer. miR-598 is a poorly investigated miR. The underlying mechanism of miR-598 in CRC cells remains to be elucidated. In the present study, miR-598 was demonstrated to be significantly upregulated in CRC tissue by analyzing data from The Cancer Genome Atlas and the Gene Expression Omnibus. The results of a polymerase chain reaction demonstrated that miR-598 expression was significantly upregulated in CRC tissues and cells. Gain of function and loss of function assays demonstrated that miR-598 significantly promoted cell proliferation and cell cycle progression. miR-598 was demonstrated to modulate cell functions by regulating 72 kDa inositol polyphosphate-5-phosphatase (INPP5E). In addition, knockdown of INPP5E counteracted the growth arrest caused by an miR-598-inhibitor. In conclusion, the present study demonstrated that miR-598 contributed to cell proliferation and cell cycle progression in CRC by targeting INPP5E.
引用
收藏
页码:2991 / 2997
页数:7
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