| Literature DB >> 28923398 |
Li-Na Sun1, Zheng Zhi1, Liang-Yan Chen1, Qun Zhou1, Xiu-Ming Li1, Wen-Juan Gan2, Shu Chen3, Meng Yang3, Yao Liu1, Tong Shen1, Yong Xu4, Jian-Ming Li5.
Abstract
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 SIRT1 suppressed CRC metastasis in vitro and in vivo as a negative regulator for miR-15b-5p transcription. Mechanistically, SIRT1 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. SIRT1 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 SIRT1/miR-15b-5p/ACOX1 axis in CRC metastasis and suggested a potential target for metastatic CRC therapy.Entities:
Keywords: Cancer metastasis; Colorectal cancer; Fatty-acid oxidation; SIRT1; microRNA
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Year: 2017 PMID: 28923398 DOI: 10.1016/j.canlet.2017.09.001
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679