SIRT1 suppresses colorectal cancer metastasis by transcriptional repression of miR-15b-5p

被引:68
|
作者
Sun, Li-Na [1 ]
Zhi, Zheng [1 ]
Chen, Liang-Yan [1 ]
Zhou, Qun [1 ]
Li, Xiu-Ming [1 ]
Gan, Wen-Juan [2 ]
Chen, Shu [3 ]
Yang, Meng [3 ]
Liu, Yao [1 ]
Shen, Tong [1 ]
Xu, Yong [4 ]
Li, Jian-Ming [1 ]
机构
[1] Soochow Univ, Med Coll, Dept Pathol & Pathophysiol, Suzhou 215123, Peoples R China
[2] Soochow Univ, Affiliated Hosp 1, Suzhou 215123, Peoples R China
[3] Soochow Univ, Med Coll, Dept Clin Med, Suzhou 215123, Peoples R China
[4] Nanjing Med Univ, Dept Pathophysiol, Nanjing 210029, Jiangsu, Peoples R China
基金
中国博士后科学基金; 国家重点研发计划;
关键词
SIRT1; microRNA; Colorectal cancer; Fatty-acid oxidation; Cancer metastasis; CALORIE RESTRICTION; RECEPTOR-ALPHA; EXPRESSION; ACTIVATION; GROWTH; STEATOHEPATITIS; PROLIFERATION; METABOLISM; MICRORNA; PHOSPHORYLATION;
D O I
10.1016/j.canlet.2017.09.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The class III deacetylase sirtuin 1 (SIRT1), a member of the sirtuin family proteins, plays a key role in many types of cancers including colorectal cancer (CRC). Here we report that SIRTI suppressed CRC metastasis in vitro and in vivo as a negative regulator for miR-15b-5p transcription. Mechanistically, SIRTI impaired regulatory effects of activator protein (AP-1) on miR-15b-5p trans-activation through deacetylation of AP-1. Importantly, acyl-CoA oxidase 1 (ACOX1), a key enzyme of the fatty acid oxidation (FAO) pathway, was found as a direct target for miR-15b-5p. SIRTI expression was positively correlated with ACOX1 expression in CRC cells and in xenografts. Moreover, ACOX1 overexpression attenuated the augmentation of migration and invasion of CRC cells by miR-15b-5p overexpression. In conclusion, our study demonstrated a functional role of the SIRTI/miR-15b-5p/ACOXI axis in CRC metastasis and suggested a potential target for metastatic CRC therapy. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:104 / 115
页数:12
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