microRNA-214 functions as a tumor suppressor in human colon cancer via the suppression of ADP-ribosylation factor-like protein 2

被引:45
作者
Long, Li-Min [1 ]
He, Ben-Fu [2 ]
Huang, Guo-Qing [3 ]
Guo, Yong-Hong [1 ]
Liu, You-Shuo [1 ]
Huo, Ji-Rong [4 ]
机构
[1] Cent S Univ, Xiangya Hosp 2, Dept Geriatr, Changsha 410011, Hunan, Peoples R China
[2] Peoples Liberat Army, Hosp 421, Dept Oncol, Guangzhou 510318, Guangdong, Peoples R China
[3] Cent S Univ, Xiangya Hosp, Dept Emergency, Changsha 410008, Hunan, Peoples R China
[4] Cent S Univ, Xiangya Hosp 2, Dept Gastroenterol, Changsha 410011, Hunan, Peoples R China
关键词
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.
引用
收藏
页码:645 / 650
页数:6
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