| Literature DB >> 26718215 |
Yongsheng Zhang1, Lu Han2, Jian Pang3, Yang Wang3, Fan Feng4, Qiyu Jiang5.
Abstract
The microRNA miR-452 has been shown to function as a tumor suppressor. However, the cellular mechanism and potential application of miR-452-mediated cancer suppression remain great unknown. This study aims to identify how miR-452 acts in regulating non-small cell lung cancer (NSCLC) proliferation and metastasis. Expression of miR-452 via adenoviral (Ad) vector inhibits the proliferation, invasion, and migration of NSCLC cells A549 or H460. Our data also shows that miR-452 down-regulates the expression of Bmi-1 as well as pro-survival or anti-apoptosis regulators Survivin, cIAP-1, and cIAP-2. By such gene interference, miR-452 modulates NSCLC cell epithelial-mesenchymal transition (EMT) and further disrupts their migration and invasion. Moreover, miR-452 blocks the activation of PI3K/AKT pathway, which is also required for EMT process. These data reveal that miR-452 treatment could be a novel target or strategy for NSCLC treatment.Entities:
Keywords: Bmi-1; EMT; Metastasis; NSCLC; PI3K/AKT signaling pathway; miR-452
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Year: 2015 PMID: 26718215 DOI: 10.1007/s13277-015-4725-z
Source DB: PubMed Journal: Tumour Biol ISSN: 1010-4283