miR612 is associated with esophageal squamous cell carcinoma development and metastasis, mediated through TP53

被引:11
作者
Zhou, Ping [1 ]
Dong, He [1 ]
He, Shuqian [1 ]
Fang, Lei [1 ]
Jiang, Nan [2 ]
Sun, Qing [1 ]
机构
[1] Shandong Univ, Dept Pathol, Qianfoshan Hosp, 16766 Jingshi Rd, Jinan 250014, Shandong, Peoples R China
[2] Shandong Univ, Sch Med, Dept Pathol, Jinan 250014, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
esophageal squamous cell carcinoma; microRNA-612; TP53; lymph node metastasis; GENOME-WIDE ASSOCIATION; SUSCEPTIBILITY LOCI; MIR-612; SUPPRESSES; GENE-EXPRESSION; DOWN-REGULATION; CANCER; MICRORNA; PROFILES; P53; SURVIVAL;
D O I
10.3892/mmr.2017.6808
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) serve an important role in the regulation of gene expression. In the present study, differential expressions of miRNAs were compared between esophageal squamous cell carcinoma (ESCC) tissues and normal esophageal tissues. In combination with miRNA target prediction databases, a significantly increased expression of miR-612 was discovered in ESCC. The relationship between miR-612 and TP53 gene expression and their roles in ESCC invasion and metastasis was further studied by reverse transcription-quantitative polymerase chain reaction and western blotting in EC109 cells and cancer tissues. The EC109 cell invasion and migration were significantly reduced after miR-612 expression was inhibited. The levels of wild type TP53 protein and mRNA were lower in ESCC tissues compared to the normal esophageal epithelium. In addition, the mRNA and protein expression levels were reported as downregulated further in tumors with metastasis than in tumors without. In conclusion, miR-612 is identified as associated with ESCC development and metastasis, likely through the regulation of TP53 expression, which could be a potential therapeutic target.
引用
收藏
页码:1855 / 1863
页数:9
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