MicroRNA-98 and microRNA-214 post-transcriptionally regulate enhancer of zeste homolog 2 and inhibit migration and invasion in human esophageal squamous cell carcinoma
- Equal contributors
1 Institute of Cardiothoracic Surgery, Changhai Hospital, 168, Changhai Rd., Shanghai, P. R. China
2 Department of Cardiothoracic Surgery, Changhai Hospital, Shanghai, P.R. China
3 Department of Pathology, Changhai Hospital, Second Military Medical University, Shanghai, P.R. China
4 Department of Cardiothoracic Surgery, Fuzhou General Hospital of Nanjing Command, PLA., Fujian, P.R. China
5 Department of Pathology, Fuzhou General Hospital of Nanjing Command, PLA, Fujian, P.R. China
Molecular Cancer 2012, 11:51 doi:10.1186/1476-4598-11-51Published: 6 August 2012
The enhancer of zeste homolog 2 (EZH2) was found to be overexpressed and associated with tumor metastasis in esophageal squamous cell carcinoma (ESCC). On the other hand, it was reported that miR-26a, miR-98, miR-101, miR-124, miR-138 and miR-214 could inhibit the expression of EZH2 in some tumors. However, the role of miRNAs in the regulation of EZH2 expression in human ESCC has not been documented. The aim of this study was to determine the role of these miRNAs in the regulation of tumor metastasis via EZH2 overexpression in human ESCC.
Methods and results
The expression of these miRNAs and EZH2 mRNA were examined by qPCR and the expression of EZH2 protein was detected by western blot. The role of these miRNAs in migration and invasion was studied in ESCC cell line (Eca109) transfected with miRNA mimics or cotransfected with miRNA mimics and pcDNA-EZH2 plasmid (without the 3’-UTR of EZH2). Through clinical investigation, we found that miR-98 and miR-214 expression was significantly lower in ESCC tissues than in matched normal tissues, and the expression level of miR-98 and miR-214 was inversely correlated to EZH2 protein expression and the clinical features such as pathological grade, tumor stage and lymph node metastasis in ESCC. In Eca109 cells, overexpression of miR-98 and miR-214 significantly inhibited the migration and invasion of ESCC cells, which was reversed by transfection of EZH2.
These findings suggest that decreased expression of miR-98 and miR-214 might promote metastasis of human ESCC by inducing accumulation of EZH2 protein.