Department of Pathology and Pathophysiology, Medical College of Soochow University, Soochow University, Suzhou 215123, People's Republic of China.
First Affiliated Hospital of Soochow University, Soochow University, Suzhou 215123, People's Republic of China.
Cancer Lett. 2017 Nov 28;409:104-115. doi: 10.1016/j.canlet.2017.09.001. Epub 2017 Sep 18.
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.
III 类去乙酰化酶 SIRT1(沉默调节蛋白 1)是 SIRT 家族蛋白的成员,在包括结直肠癌(CRC)在内的多种癌症中发挥关键作用。在这里,我们报告 SIRT1 作为 miR-15b-5p 转录的负调节剂,在体外和体内抑制 CRC 转移。在机制上,SIRT1 通过去乙酰化 AP-1 来损害 AP-1 对 miR-15b-5p 反式激活的调节作用。重要的是,酰基辅酶 A 氧化酶 1(ACOX1),脂肪酸氧化(FAO)途径的关键酶,被发现是 miR-15b-5p 的直接靶标。在 CRC 细胞和异种移植物中,SIRT1 的表达与 ACOX1 的表达呈正相关。此外,ACOX1 的过表达减弱了 miR-15b-5p 过表达增强 CRC 细胞迁移和侵袭的作用。总之,我们的研究证明了 SIRT1/miR-15b-5p/ACOX1 轴在 CRC 转移中的功能作用,并为转移性 CRC 的治疗提供了一个潜在的靶点。