MicroRNA-383-5p inhibits the proliferation and promotes the apoptosis of gastric cancer cells by targeting cancerous inhibitor of PP2A

被引:12
作者
Li, Xinxin [1 ]
Yuan, Jinpeng [1 ]
Cao, Qiangjian [1 ]
Xie, Aosi [1 ]
Chen, Juntian [1 ]
机构
[1] Shantou Univ Med Coll, Affiliated Hosp 1, Dept Gastrointestinal Surg, 57 Changping Rd, Shantou 515041, Guangdong, Peoples R China
关键词
microRNA-383-5p; gastric cancer; cancerous inhibitor of PP2A; DOWN-REGULATION; LUNG-CANCER; EXPRESSION; CIP2A; METASTASIS; INVASION; GROWTH; MIGRATION; PATHWAY;
D O I
10.3892/ijmm.2020.4603
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
The aberrant expression of microRNA (miRNAor miR)-383-5p has been found in numerous types of cancer. However, the function of miR-383-5p in gastric cancer (GC) remains elusive and requires further investigation. In the present study, the level of miR-383-5p and cancerous inhibitor of PP2A (CIP2A) in GC cell lines was determined by reverse transcription-quantitative PCR analysis. GC cell proliferation, apoptosis and cell cycle distribution were determined by the MTT assay and flow cytometry, respectively. The mRNA target of miR-383-5p was identified by dual luciferase activity assay. It was observed that the expression of miR-383-5p was lower and that of CIP2A was higher in GC cells compared with the GES-1 normal human gastric epithelial cell line. Transfectoin with miR-383-5p mimic significantly inhibited GC cell proliferation, while it promoted cell apoptosis and G(0)/G(1) arrest by targeting CIP2A. Taken together, the findings of the present study demonstrate that miR-383-5p inhibits GC cell proliferation and promotes apoptosis and G(0)/G(1) arrest by targeting CIP2A, indicating that targeting miR-383-5p may hold promise as a future therapeutic strategy for patients with GC.
引用
收藏
页码:397 / 405
页数:9
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