miR-489-3p promotes malignant progression of non-small cell lung cancer through the inactivation of Wnt/β-catenin signaling pathway via regulating USP48

Respiratory Research

Li Li¹  Xu Ran¹  Yi Liu¹  Shengrong Yang¹  Yunhe Li¹  Zhenghong Wang¹  Pei Zhang¹  Bing Zhu¹  Yujie Luo¹  Bing Wang¹ 

[1] Department of Thoracic and Cardiovascular Surgery, The Second Affiliated Hospital of Chongqing Medical University;

关键词: NSCLC;    miR-489-3p;    USP48;    Wnt/β-catenin signaling pathway;   

DOI  :  10.1186/s12931-022-01988-w

来源: DOAJ

【 摘 要 】

Abstract Background Non-small cell lung cancer (NSCLC) is the most prevalent form of lung cancer globally, with average age of cancer patients becoming younger gradually. It is of significance to gain a comprehensive understanding of molecular mechanism underlying NSCLC. Methods Quantitative polymerase chain reaction (qPCR) and western blot were applied to measure RNA and protein levels separately. Functional assays and western blot were performed to determine the effects of miR-489-3p and USP48 on cell growth, migration and epithelial-mesenchymal transition (EMT) in NSCLC. TOP/FOP flash luciferase reporter assay was carried out to detect the activity of Wnt pathway. Besides, qPCR, RNA pulldown and luciferase reporter assays were conducted to probe into the target gene of miR-489-3p. Immunoprecipitation-western blot (IP-western blot) analysis was implemented to assess the effect of USP48 on the ubiquitination of β-catenin. Results miR-489-3p hampers NSCLC cell proliferation, migration and EMT in vitro and NSCLC tumorigenesis and metastasis in vivo. Additionally, miR-489-3p inactivates Wnt/β-catenin signaling pathway and regulates USP48 to inhibit the ubiquitination of β-catenin. Moreover, USP48 propels the development of NSCLC cells. Conclusions The current study demonstrated that miR-489-3p promotes the malignant progression of NSCLC cells via targeting USP48, which might offer a new perspective into NSCLC treatment. Graphical abstract

【 授权许可】

Unknown