LncRNA expression signatures of twist-induced epithelial-to-mesenchymal transition in MCF10A cells.

Abstract The epithelial-to-mesenchymal transient (EMT) is associated with tumor metastasis. Twist is one of the key transcription factors for EMT and relates to tumor cell migration. Long non-coding RNAs (lncRNAs) have recently emerged as important regulatory molecules involved in a broad range of biological processes and complicated diseases. However, it is unknown whether a signal network and lncRNAs are involved in Twist-induced EMT program. Taking MCF10A/Twist as a model, more than 99 lncRNAs and 3164 genes are regulated in the Twist-induced EMT process using lncRNA-array and cDNA micro-array. We establish a downstream signal network associated with EMT induced by Twist using bioinformatic analysis (Gene Ontology, pathway analysis) and experimental data. A set of multiple canonical signal pathways (such as WNT, MAPK, JAK/STAT, TGF-β, mTOR, Hedgehog and P53 signaling pathways) and several lncRNAs [such as lncRNA (chr6, 26124411–26139312, +), lncRNA (chr1, 41944445–41949874, −), lncRNA (chr17, 44833874–44834830, +)] are altered in MCF10A/Twist cells. More interestingly, lncRNA (chr17, 44833874–44834830, +), lncRNA (chr17, 21142183–21156578, −), lncRNA (chr6, 26124411–26139312, +) and lncRNA (chr19, 438420–2083745, −) may be involved in regulation or activation of WNT signaling pathway in the Twist-induced EMT process. These findings first determine that Twist contributes to invasion and metastasis by inducing wide-ranging transcriptional and functional changes of lncRNAs and signal pathways in our study.