MiR-199a/b-5p inhibits hepatocellular carcinoma progression by post-transcriptionally suppressing ROCK1

被引:47
|
作者
Zhan, Yangyang [1 ,2 ]
Zheng, NanXin [3 ]
Teng, Fei [3 ]
Bao, Leilei [1 ,2 ,4 ]
Liu, Fang [3 ]
Zhang, Mingjian [1 ,2 ]
Guo, Meng [1 ,2 ,3 ]
Guo, Wenyuan [3 ]
Ding, Guoshan [3 ]
Wang, Quanxing [1 ,2 ]
机构
[1] Second Mil Med Univ, Inst Immunol, Shanghai 200433, Peoples R China
[2] Second Mil Med Univ, Natl Key Lab Med Immunol, Shanghai 200433, Peoples R China
[3] Second Mil Med Univ, Changzheng Hosp, Dept Liver Surg & Organ Transplantat, Shanghai 200003, Peoples R China
[4] 411 Hosp PLA, Dept Pharm, Shanghai 200080, Peoples R China
基金
中国国家自然科学基金;
关键词
miRNA; hepatocellular carcinoma; miR-199a/b-5p; metastasis; ROCK1; TUMOR-SUPPRESSOR; MICRORNA DEREGULATION; EXPRESSION; ADHESION; KINASE; ROLES; DIFFERENTIATION; PROLIFERATION; EPIDEMIOLOGY; MECHANISMS;
D O I
10.18632/oncotarget.18052
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this study, we explored the actions of miR-199a/b-5p during hepatocellular carcinoma (HCC) progression and its potential target genes. Through heatmap miRNA expression analysis of 15 matched HCC tumor and adjacent non-tumor liver tissues from the TCGA database, we detected 19 mRNAs that were upregulated and 13 that were downregulated specifically in HCC. Among these, miR-199 family members were downregulated in HCC tumors and cell lines, as compared to controls. Low miR-199a/b-5p expression was also associated with poor overall survival of HCC patients. miR199a/b-5p overexpression in HCC cell lines inhibited cell proliferation, migration and invasion, both in vitro and in vivo. In addition, miR199-a/b-5p post-transcriptionally suppressed Rho-associated coiled-coil kinase 1 (ROCK1). This in turn led to inhibition of ROCK1/MLC and PI3K/Akt signaling, which is necessary for HCC proliferation and metastasis. These results indicate that miR-199a/b acts as tumor suppressors in HCC and represent promising therapeutic targets.
引用
收藏
页码:67169 / 67180
页数:12
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