MicroRNA-326 functions as a tumor suppressor in colorectal cancer by targeting the nin one binding protein

被引:66
|
作者
Wu, Lei [1 ,2 ]
Hui, Hui [3 ]
Wang, Li-Juan [4 ]
Wang, Hao [1 ,2 ]
Liu, Qiu-Fang [2 ]
Han, Su-Xia [1 ]
机构
[1] Xi An Jiao Tong Univ, Coll Med, Affiliated Hosp 1, Dept Radiotherapy, Xian 710061, Shaanxi, Peoples R China
[2] Shaanxi Prov Tumor Hosp, Ctr Radiotherapy, Xian 710068, Shaanxi, Peoples R China
[3] Shaanxi Prov Tumor Hosp, Ctr Gynecol Oncol, Xian 710068, Shaanxi, Peoples R China
[4] Xi An Jiao Tong Univ, Coll Med, Affiliated Hosp 1, Dept Oncol, Xian 710061, Shaanxi, Peoples R China
关键词
miR-326; nin one binding protein; proliferation; prognosis; colorectal cancer; CELL-CYCLE; NOB1; SUPPRESSES; DOWN-REGULATION; IN-VITRO; PROLIFERATION; GROWTH; RNA; EXPRESSION; PROGNOSIS; MIGRATION;
D O I
10.3892/or.2015.3840
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Accumulating evidence has demonstrated that microRNAs (miRNAs) are involved in multiple processes in cancer development and progression. miR-326 has been identified as a tumor suppressor miRNA in several types of human cancer. However, the specific function of miR-326 and its target the nin one binding protein (NOB1) in colorectal carcinoma (CRC) remains unclear. In the present study, we found that miR-326 inhibited cell proliferation, migration and invasion, and induced cell apoptosis and cell cycle arrest of CRC cells by directly targeting NOB1. Furthermore, the upregulation of miR-326 in CRC cells was revealed to be associated with a feedback loop involving downregulation of the NOB1, which mimics the phenotype induced by miR-326. Importantly, we found that the CRC patients with high expression of miR-326 or low expression of NOB1 tend to obtain a better prognosis. Thus, for the first time, we provide convincing evidence that downregulation of miR-326 inhibited tumor proliferation and tumor metastasis by directly targeting NOB1 in CRC. NOB1 and miR-326 could be potential therapeutic targets for CRC.
引用
收藏
页码:2309 / 2318
页数:10
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