Reduced miR-125a-5p expression is associated with gastric carcinogenesis through the targeting of E2F3

被引:48
|
作者
Xu, Yanjun [1 ]
Huang, Zhenxia [2 ,3 ]
Liu, Yueli [2 ,3 ]
机构
[1] Zhejiang Canc Hosp, Dept Chemotherapy, Hangzhou 310022, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Med, Dept Cell Biol, Hangzhou 310058, Zhejiang, Peoples R China
[3] Zhejiang Univ, Sch Med, Program Mol Cell Biol, Hangzhou 310058, Zhejiang, Peoples R China
关键词
miR-125a-5p; E2F3; gastric cancer; proliferation; migration; invasion; LUNG-CANCER; HEPATOCELLULAR-CARCINOMA; TRANSCRIPTION FACTOR; CELL-PROLIFERATION; BLADDER-CANCER; TUMOR-GROWTH; MICRORNA; OVEREXPRESSION; MIR-21; AMPLIFICATION;
D O I
10.3892/mmr.2014.2567
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Emerging evidence suggests that altered expression of microRNAs (miRNAs) is involved in cancer progression. However, the role of miR-125a-5p in gastric carcinogenesis remains unknown. Quantitative real-time PCR analysis revealed that the expression of miR-125a-5p was significantly decreased in >80% of gastric cancer tissues compared with their adjacent non-tumor tissues, and was markedly reduced in similar to 95% of intestinal-type gastric cancer tissues. The downregulated miR-125a-5p was significantly associated with gastric cancer metastasis. Ectopic expression of miR-125a-5p substantially inhibited the proliferation, migration and invasion activities of gastric cancer cells. Furthermore, forced expression of miR-125a-5p repressed the activity of a luciferase reporter carrying the 3'-untranslated (3'-UTR) region of E2F3, which was eliminated by mutation of the predicted miR-125a-binding site, indicating that E2F3 may be a potential target gene of miR-125a-5p. These data suggest that by targeting E2F3, miR-125a-5p may be important as a potential tumor suppressor gene in gastric carcinogenesis.
引用
收藏
页码:2601 / 2608
页数:8
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