MiR-145 functions as a tumor suppressor targeting NUAK1 in human intrahepatic cholangiocarcinoma

被引:34
|
作者
Xiong, Xinkui [1 ,2 ]
Sun, Daoyi [1 ,2 ]
Chai, Hao [1 ,2 ]
Shan, Wengang [1 ,2 ]
Yu, Yue [2 ]
Pu, Liyong [1 ,2 ]
Cheng, Feng [1 ,2 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Liver Transplantat Ctr, Nanjing 210029, Jiangsu, Peoples R China
[2] Minist Publ Hlth, Key Lab Living Donor Liver Transplantat, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
MiR-145; NUAK1; Intrahepatic cholangiocarcinoma; AKT; Matrix metalloproteinase protein; CELL LUNG-CANCER; GASTRIC-CANCER; MICRORNA-145; DOWNSTREAM; EXPRESSION; SURVIVAL; INVASION; MATRIX; ARK5; PROGRESSION;
D O I
10.1016/j.bbrc.2015.08.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The dysregulation of micro (mi)RNAs is associated with cancer development. The miRNA miR-145 is downregulated in intrahepatic cholangiocarcinoma (ICC); however, its precise role in tumor progression has not yet been elucidated. Novel (nua) kinase family (NUAK)1 functions as an oncogene in various cancers and is a putative target of miR-145 regulation. In this study, we investigated the regulation of NUAK1 by miR-145 in ICC. We found that miR-145 level was significantly decreased in ICC tissue and cell lines, which corresponded with an increase in NUAK1 expression. NUAK1 was found to be a direct target of miR-145 regulation. The overexpression of miR-145 in ICC cell lines inhibited proliferation, growth, and invasion by suppressing NUAK1 expression, which was associated with a decrease in Akt signaling and matrix metalloproteinase protein expression. Similar results were observed by inhibiting NUAK1 expression. These results demonstrate that miR-145 can prevent ICC progression by targeting NUAK1 and its downstream effectors, and can therefore be useful for clinical diagnosis and targeted therapy of ICC. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:262 / 269
页数:8
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