小RNA
基因敲除
生物标志物
癌症
癌症研究
转移
体内
抑制器
细胞生长
生物
实时聚合酶链反应
癌变
医学
细胞培养
基因
遗传学
作者
Hai Guo,Jinxia Fan,Xiaofeng Zhao,Xiaozhong Yang,Jie He,Lingling Huang,Yuanyuan Zhang
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2019-02-01
卷期号:443: 179-188
被引量:27
标识
DOI:10.1016/j.canlet.2018.11.021
摘要
An integrated study was conducted to identify the potential prognosis biomarker of the gastric cancer. The study analyzed the expression level of microRNAs (miRNAs) and clinical follow-up information of gastric cancer patients. miR-371-3p was determined as a promising biomarker for the prognosis of GCs among the 74 dysregulated miRNAs examined. The qRT-PCR analysis of the expression of miR-371-3p in 121 GC tumors confirmed its overexpression and correlation with aggravation of the GC patients. The in vitro functional assays demonstrated that overexpression of miR-371-3p promoted proliferation, colony formation, migration and invasion of the GC cells, whereas miR-371-3p depletion led to the opposite. The findings were further confirmed by the in vivo knockdown of miR-371-3p experiment: the depletion of miR-371-3p inhibited tumor growth and metastasis. Based on the results of the bioinformatics analysis and bioassays, TOB1 was found to be the direct target of miR-371-3p, functioning as a tumor suppressor in GC cells. TOB1 was prerequisite for miR-371-3p to promote cell proliferation and migration. In conclusion, the results suggest that miR-371-3p is a potential prognosis biomarker and therapeutic target for GC.
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