小RNA
转移
基因敲除
癌症研究
生物
Oncomir公司
体内
癌症
细胞培养
基因
遗传学
作者
Jianlin Ma,Yun Zhan,Zhipeng Xu,Yi Li,Aiping Luo,Fang Ding,Xiufeng Cao,Hongyan Chen,Zhihua Liu
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2017-04-10
卷期号:398: 37-45
被引量:67
标识
DOI:10.1016/j.canlet.2017.04.006
摘要
Esophageal squamous cell carcinoma (ESCC) is one of the most common digestive tumors in Asia. Recent researches demonstrate that miRNAs are involved in the development of ESCC. In this study, we identified a miRNA cluster, termed miR-99b/let-7e/miR-125a as pro-metastasis oncomir. Overexpression of this miRNA cluster promoted ESCC cell migration and invasion in vitro and induced an experimental metastasis in vivo. ZEB1 was discovered to bind to the promoter region of miR-99b/let-7e/miR-125a cluster and regulate the expression of miRNAs at transcriptional level. Knockdown of ZEB1 resulted in a decrease of both mature and primary miRNAs. Further research revealed AT-rich interaction domain 3A (ARID3A) as a direct target of miR-99b/let-7e/miR-125a cluster. Reduced ARID3A phenocopied miR-99b/let-7e/miR-125a overexpression, and elevated ARID3A counteracted the pro-metastasis effect of miR-99b/let-7e/miR-125a. Moreover, ARID3A was downregulated by ZEB1 in a miR-99b/let-7e/miR-125a dependent manner. Collectively, our study sheds light on the essential role of miR-99b/let-7e/miR-125a cluster in tumor metastasis.
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