Fan Jing-Yi, Fan Ya-Jie, Wang Xiang-Ling, Xie Hong, Gao Hui-Jie, Zhang Yi, Liu Min, Tang Hua
Tianjin Life Science Research Center and Department of Pathogen Biology, School of Basic Medical Sciences, Tianjin Medical University, China.
FEBS Lett. 2017 Jan;591(1):118-128. doi: 10.1002/1873-3468.12502. Epub 2016 Dec 20.
Dysregulation of microRNAs (miRNAs) can contribute to tumorigenesis in cancers. In this study, we found that miR-429 was downregulated in cervical cancer (CC) tissues and suppressed cell viability and proliferation while promoting apoptosis in CC cells. IKKβ was a novel target gene of miR-429 and ectopic expression of IKKβ abrogated the phenotypes induced by miR-429. When IKKβ was downregulated by miR-429, nuclear factor κB (NF-κB) pathway activation, interleukin-6 (IL-6), and interferon-β (IFN-β) production were decreased in CC cells. These findings indicate that miR-429 is involved in regulation of the NF-κB pathway by targeting IKKβ and functions as a tumor suppressor in cervical carcinogenesis.
微小RNA(miRNA)失调可促进癌症的肿瘤发生。在本研究中,我们发现miR-429在宫颈癌(CC)组织中表达下调,它可抑制CC细胞的活力和增殖,同时促进细胞凋亡。IKKβ是miR-429的一个新靶基因,IKKβ的异位表达消除了miR-429诱导的表型。当IKKβ被miR-429下调时,CC细胞中核因子κB(NF-κB)通路的激活、白细胞介素-6(IL-6)和干扰素-β(IFN-β)的产生均减少。这些发现表明,miR-429通过靶向IKKβ参与NF-κB通路的调控,并在宫颈癌发生过程中发挥肿瘤抑制作用。