MiR-382 targets GOLM1 to inhibit metastasis of hepatocellular carcinoma and its down- regulation predicts a poor survival

被引:3
|
作者
Zhang, Shukun [1 ]
Ge, Wenmin [1 ]
Zou, Gangyong [1 ]
Yu, Lin [1 ]
Zhu, Yongcun [1 ]
Li, Qiujing [1 ]
Zhang, Yujie [1 ]
Wang, Zhanli [3 ]
Xu, Tao [2 ]
机构
[1] Weihai Municipal Hosp, Dept Pathol, Weihai, Shandong, Peoples R China
[2] Shandong Univ, Shandong Prov Hosp, Dept Gen Surg, 324 Jingwu Rd, Jinan 250021, Shandong, Peoples R China
[3] Weihai Municipal Hosp, Dept Stomatol, Weihai, Shandong, Peoples R China
来源
AMERICAN JOURNAL OF CANCER RESEARCH | 2018年 / 8卷 / 01期
关键词
HCC; miR-382; migration; invasion; prognosis; HCC; SUPPRESSES; CANCER; EXPRESSION; PROGNOSIS; INVASION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Accumulating evidences have illuminated that an amount of microRNAs are involved in human diseases including hepatocellular carcinoma (HCC). In this study, we found that the expression of miR-382 in HCC tissues was down-regulated compared with the non-cancerous tissues. Over-expression of miR-382 could significantly inhibit the migration and invasion of HCC cells in vitro and in vivo. Bioinformatic algorithms and luciferase reporter assays suggested that Golgi Membrane Protein 1 (GOLM1) was a direct target of miR-382. Interestingly, we found the down-regulation of GOLM1 in HCC cells could rescue these cells from miR-382-mediated suppression of migration and invasion. Our findings might demonstrate that miR-382 inhibited the metastasis of HCC by targeting GOLM1. Furthermore, cox proportional hazards analyses suggested that low expression of miR-382 was an independent prognostic factor for the HCC patients. In conclusion, our results highlighted that miR-382, a novel prognostic factor, target GOLM1 to inhibit metastasis of hepatocellular carcinoma.
引用
收藏
页码:120 / 131
页数:12
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