LncRNA FEZF1-AS1 enhances epithelial-mesenchymal transition (EMT) through suppressing E-cadherin and regulating WNT pathway in non-small cell lung cancer (NSCLC).

作者: Rong He , Fei hu Zhang , Ning Shen

DOI: 10.1016/J.BIOPHA.2017.08.057

关键词:

摘要: Abstract Objective Recent discoveries verify that long non-coding RNAs (lncRNAs) are important functional regulators involved in non-small cell lung cancer (NSCLC) progression. However, RNA FEZF1-AS1 was not been investigated NSCLC so for. Methods We applied the quantitative real time polymerase chain reaction (qRT-PCR) assays to detect expression of lncRNA tissues and adjacent normal tissues. Cell proliferation invasion capacities were evaluated by MTT, colony formation, assays. Chromatin immunoprecipitation (ChIP) (RIP) methods demonstrated association between E-cadherin. The relative protein levels analyzed western blot analysis. Results LncRNA significantly up-regulated compared with Higher associated lymph node metastasis, poor differentiation grade advanced TNM stage. In vitro, we revealed down-regulation inhibited NSCLC. Moreover, suppressed epithelial-mesenchymal transition (EMT) process increasing E-cadherin ZO-1, whereas, decreasing Slug, Twist Vimentin cells. Furthermore, could epigenetically repress via binding LSD1 EZH2 also knockdown Wnt/β-catenin signaling Conclusion These results function as a tumor promoting regulator NSCLC, which may provide target treatment

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