MiR-124 represses vasculogenic mimicry and cell motility by targeting amotL1 in cervical cancer cells

被引:114
作者
Wan, Hai-Ying [1 ,2 ]
Li, Qin-Qin [1 ,2 ]
Zhang, Yan [1 ,2 ]
Tian, Wei [1 ,2 ]
Li, Ya-Nan [3 ]
Liu, Min [1 ,2 ]
Li, Xin [1 ,2 ]
Tang, Hua [1 ,2 ]
机构
[1] Tianjin Med Univ, Tianjin Life Sci Res Ctr, Tianjin 300070, Peoples R China
[2] Tianjin Med Univ, Sch Basic Med Sci, Tianjin 300070, Peoples R China
[3] Tianjin Med Univ, Dept Lab Anim Sci & Technol, Tianjin 300070, Peoples R China
基金
中国国家自然科学基金;
关键词
miR-124; AmotL1; Cervical cancer cells; Vasculogenic mimicry; EMT; DOWN-REGULATION; FAMILY PROTEINS; PROLIFERATION; ANGIOGENESIS; MIGRATION; METASTASIS; CARCINOMA; GROWTH; CONTRIBUTES; JUNCTIONS;
D O I
10.1016/j.canlet.2014.09.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
miRNAs have extensive functions in differentiation, metabolism, programmed cell death, and tumor metastasis by post-transcriptional regulation. Vasculogenic mimicry is an important pathway in tumor metastasis. Many factors can regulate vasculogenic mimicry, including miRNAs. In previous studies, miR-124 was found to repress proliferation and metastasis in different types of cancers, but whether it functions in cervical cancer remained unknown. Here, we demonstrate that miR-124 can repress vasculogenic mimicry, migration and invasion in HeLa and C33A cells in vitro. Furthermore, we reveal that the effect of miR-124 on vasculogenic mimicry, migration and invasion results from its interaction with AmotL1. MiR-124 regulates AmotL1 negatively by targeting its 3'untranslated region (3'UTR). We found that miR-124 can repress the EMT process. Together, these results improve our understanding of the function of miR-124 in tumor metastasis and will help to provide new potential target sites for cervical cancer treatment. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:148 / 158
页数:11
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