miR-92b suppresses growth and invasion of esophageal cancer Eca109 cells by regulating EZH2 gene expression
10.3872/j.issn.1007-385x.2018.02.002
- VernacularTitle:miR-92b通过调控EZH2基因的表达抑制食管癌细胞Eca109的增殖和 侵袭
- Author:
LIU Fei
1
;
MENG Lingjiao
1
;
LIU Shina
1
;
GU Lina
1
;
LI Juan
1
;
ZHANG Jiandong
1
;
WU Yunyan
1
;
SANG Meixiang
1
Author Information
1. Research Center, the Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, Hebei, China
- Publication Type:Journal Article
- Keywords:
esophageal carcinoma(EC);
miR-92b;
enhancer of zeste homolog 2（ E Z H 2 ) gene;
proliferation;
invasion;
migration
- From:
Chinese Journal of Cancer Biotherapy
2018;25(2):118-124
- CountryChina
- Language:Chinese
-
Abstract:
[Abstract] Objective: To investigate the regulating effects of miR-92b on the expression of EZH2 (enhancer of zeste homolog 2) gene and the proliferation and invasion abilities of esophageal cancer (EC) cells. Methods: Fifteen cases of esophageal cancer tissues that preserved in the research center of the Fourth HospitalAffiliated to Heibei Medical University from January 2016 to January 2017 were selected for this study. The bioinformatics tool was used to predict the possible miRNAs that might target EZH2. The mimics of predicted miRNAs were transfected into human esophageal carcinoma cell lines Eca109, respectively. Then the regulation effect of miRNAs on EZH2 gene expression was validated by real-time PCR, Western blotting and dual luciferase reporter experiment. In the meanwhile, EZH2 over-expression plasmids were co-transfected into esophageal carcinoma Eca109 cells, and the effects of miRNAs and EZH2 expression changes on the proliferation, apoptosis , invasion and migration of esophageal carcinoma cells were detected by CCK-8 method, Flow Cytometry, Transwell Invasion and migration assay, respectively. Results: Bioinformatics analysis showed that miR-92b, let7a and miR-25 could combine with potential binding sites at 3’-terminal non-translation region of EZH2 gene. Real-time PCR results showed that only miR-92b was able to regulate the expression of EZH2, and miR-92b was negatively correlated to EZH2 in esophageal cancer (P<0.01). Compared with mimic-NC, the expression of EZH2 mRNA, protein and luciferase activity in Eca109 cells after miR-92b mimic transfection was significantly down-regulated (both P<0.01). However, miR-92b mimic transfection had no effect on the apoptosis of Eca109 cells. Moreover, the proliferation, invasion and migration of Eca109 cells were significantly inhibited after transfection with miR-92b-mimic (P<0.01). In addition, after co-transfection with EZH2 over-expression plasmids, the effects of miR-92b-mimic on the proliferation, invasion and migration of Eca109 cells were significantly weakened (P<0.01). Conclusion: miR-92b can inhibit the proliferation,invasionandmigrationofesophagealcarcinomacells,anditsmechanismmayberelatedtoitstargetregulationofEZH2.
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- Full text:20180202.pdf
