ADP-ribosylation factor-like protein 2;
apoptosis;
proliferation;
miR-214;
human colon cancer;
HEPATOCELLULAR-CARCINOMA;
CELL-PROLIFERATION;
GROWTH;
METASTASIS;
EXPRESSION;
ANGIOGENESIS;
CONTRIBUTES;
PROGRESSION;
APOPTOSIS;
D O I:
10.3892/ol.2014.2746
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
microRNAs (miRNAs/miRs) are a conserved class of endogenous, short non-coding RNAs that post-transcriptionally regulate the expression of genes involved in diverse cellular processes. miR-214 has been reported to be associated with several cancers, including human colon cancer. However, the function of miR-214 in colon cancer development is poorly understood. In the current study, miR-214 was demonstrated to be downregulated in colon cancer tissues compared with healthy colon tissues. Functional studies showed that miR-214 overexpression results in the inhibition of cell viability, colony formation and proliferation, and the induction of cell apoptosis. ADP-ribosylation factor-like protein 2 (ARL2) is predicted to be a target candidate of miR-214. A luciferase reporter assay, western blot analysis and quantitative polymerase chain reaction were performed, which revealed that miR-214 negatively regulates ARL2 expression by targeting its 3' untranslated region directly. In conclusion, the results of the present study revealed that miR-214 suppresses colon cancer cell growth via the suppression of ARL2, and indicated that miR-214 may present a significant potential therapeutic target for colon cancer.