Reciprocal effects between microRNA-140-5p and ADAM10 suppress migration and invasion of human tongue cancer cells

被引:74
作者
Kai, Yang [1 ,2 ]
Peng, Wang [1 ,2 ]
Ling, Wu [1 ,2 ]
Hao Jiebing [3 ]
Zhuan, Bian [1 ,2 ]
机构
[1] Wuhan Univ, Sch & Hosp Stomatol, State Key Lab Breeding Base Basic Sci Stomatol, Wuhan 430079, Peoples R China
[2] Wuhan Univ, Sch & Hosp Stomatol, Key Lab Oral Biomed Minist Educ, Wuhan 430079, Peoples R China
[3] Second Char Hosp Henan Prov, Jiaozuo 454000, Peoples R China
基金
中国国家自然科学基金;
关键词
MicroRNA; Tongue squamous cell carcinoma; ADAM10; ERBB4; RECEPTOR TYROSINE KINASE; EXPRESSION; CARCINOMA; HISTONE-DEACETYLASE-7; TRANSLATION; ERBB4/HER4; CLEAVAGE; COMPLEX; TARGETS; MOUSE;
D O I
10.1016/j.bbrc.2014.02.032
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
ADAM10, overexpressed in tongue squamous cell carcinoma (TSCC), has been well documented for its role in tumor progression and metastasis. In the present study, we evaluated the inhibition effect of microRNAs (miRNAs) on the TSCC and identified that miR-140-5p could directly targets ADAM10 and inhibits the invasion and migration of TSCC cells. LAMC1, HDAC7 and PAX6, clustered into migration-related genes, were validated to be direct targets of miR-140-5p, while IGF1R and PSEN1 were not responsible to the regulation. Most intriguingly, ERBB4 was upregulated by miR-140-5p even though the interaction between ERBB4 3'UTR and miR-140-5p existed simultaneously. Meanwhile, ADAM10 is involved in the "positive" regulation of ERBB4 and negative regulation of PAX6 by miR-140-5p. Taken together, our results suggest that miR-140-5p play a role in TSCC cell migration and invasion, and two brand new relationships between miRNA and its targets emerged: (1) ADAM10 is not just a direct target of miR-140-5p, the repressed ADAM10 also helps to enhance the effect of miR-140-5p to other target genes: ERBB4 and PAX6; (2) ERBB4 is "positively" regulated by miR-140-5p. (C) 2014 Published by Elsevier Inc.
引用
收藏
页码:308 / 314
页数:7
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