| Literature DB >> 30942957 |
Xiaofeng Li1,2,3,4, Qiang Fu1,2,3,4, Hui Li2,4,5,6, Lei Zhu1,2,3,4, Wei Chen1,2,3,4, Tonglei Ruan7, Wengui Xu1,2,3,4, Xiaozhou Yu1,2,3,4.
Abstract
Lung cancer is a malignancy with one of the highest incidence rates, and it is the leading cause of cancer-related death. To gain further insights into the underlying mechanisms of tumor growth and metastasis, we investigated the role and expression of microRNAs in lung adenocarcinoma (LUAD). We discovered a significantly lower expression level of microRNA-520c-3p (miR-520c-3p) in LUAD tissues than in nontumor tissues. miR-520c-3p is known to regulate multiple biological functions and cellular behaviors. In this study, we show that AKT1 and AKT2 are key direct targets of miR-520c-3p, which are required for its biological roles in LUAD. Mechanistically, downregulation of miR-520c-3p in LUAD is due to DNA methylation of the miR-520c-3p promoter region. Conversely, the activity of the transcription factor Yin Yang 1 (YY1) results in the upregulation of miR-520c-3p. Taken together, our results reveal methylation/YY1/miR-520c-3p/AKT1/AKT2 as a molecular axis with a potent biological function and highlight miR-520c-3p as a novel potent tumor suppressor in LUAD.Entities:
Keywords: AKT; YY1; lung adenocarcinoma; methylation; microRNA
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Year: 2019 PMID: 30942957 DOI: 10.1111/febs.14835
Source DB: PubMed Journal: FEBS J ISSN: 1742-464X Impact factor: 5.542