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

被引:72
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
相关论文
共 46 条
[1]  
[Anonymous], ONCOTARGET
[2]   Increased nuclear NAD biosynthesis and SIRT1 activation prevent axonal degeneration [J].
Araki, T ;
Sasaki, Y ;
Milbrandt, J .
SCIENCE, 2004, 305 (5686) :1010-1013
[3]   Activation of Sirt1 decreases adipocyte formation during osteoblast differentiation of mesenchymal stem cells [J].
Bäckesjö, CM ;
Li, Y ;
Lindgren, U ;
Haldosén, LA .
JOURNAL OF BONE AND MINERAL RESEARCH, 2006, 21 (07) :993-1002
[4]   Estrogen receptor α and the activating protein-1 complex cooperate during insulin-like growth factor-I-induced transcriptional activation of the pS2/TFF1 gene [J].
Baron, Sylvain ;
Escande, Aurelie ;
Alberola, Geraldine ;
Bystricky, Kerstin ;
Balaguer, Patrick ;
Richard-Foy, Helene .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (16) :11732-11741
[5]   Calorie restriction, SIRT1 and metabolism: Understanding longevity [J].
Bordone, L ;
Guarente, L .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (04) :298-305
[6]  
Brown Miguel, 2013, Frontiers in Genetics, V4, P145, DOI 10.3389/fgene.2013.00145
[7]   Sirt1 Is Required for Resveratrol-Mediated Chemopreventive Effects in Colorectal Cancer Cells [J].
Buhrmann, Constanze ;
Shayan, Parviz ;
Popper, Bastian ;
Goel, Ajay ;
Shakibaei, Mehdi .
NUTRIENTS, 2016, 8 (03)
[8]   Increase in activity during calorie restriction requires Sirt1 [J].
Chen, D ;
Steele, AD ;
Lindquist, S ;
Guarente, L .
SCIENCE, 2005, 310 (5754) :1641-1641
[9]   Hydroquinone-induced malignant transformation of TK6 cells by facilitating SIRT1-mediated p53 degradation and up-regulating KRAS [J].
Chen, Yuting ;
Chen, Jiajia ;
Yun, Lin ;
Xu, Longmei ;
Liu, Jiaxian ;
Xu, Yongchun ;
Yang, Hui ;
Liang, Hairong ;
Tang, Huanwen .
TOXICOLOGY LETTERS, 2016, 259 :133-142
[10]   SIRT1 promotes epithelial-mesenchymal transition and metastasis in colorectal cancer by regulating Fra-1 expression [J].
Cheng, Feifei ;
Su, Li ;
Yao, Chao ;
Liu, Limei ;
Shen, Junjie ;
Liu, Chungang ;
Chen, Xuejiao ;
Luo, Yongli ;
Jiang, Lupin ;
Shan, Juanjuan ;
Chen, Jun ;
Zhu, Wei ;
Shao, Jimin ;
Qian, Cheng .
CANCER LETTERS, 2016, 375 (02) :274-283