The MiR-495/Annexin A3/P53 Axis Inhibits the Invasion and EMT of Colorectal Cancer Cells

被引:32
|
作者
Bai, Zhigang [1 ]
Wang, Jin [1 ]
Wang, Tingting [1 ]
Li, Yuan [1 ]
Zhao, Xiaomu [1 ]
Wu, Guocong [1 ]
Yang, Yingchi [1 ]
Deng, Wei [1 ]
Zhang, Zhongtao [1 ]
机构
[1] Capital Med Univ, Beijing Friendship Hosp, Dept Gen Surg, Beijing Key Lab Canc Invas & Metastasis Res,Natl, Beijing, Peoples R China
关键词
Colorectal cancer; MiR-495; Annexin A3; P53; Invasion; EMT; EPITHELIAL-MESENCHYMAL TRANSITION; ANNEXIN A3; TUMOR PROGRESSION; EXPRESSION; METASTASIS; MIGRATION; STATISTICS; SUPPRESSOR; GROWTH; ACTS;
D O I
10.1159/000485877
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background/Aims: More and more reports have shown that the dysregulation of miRNAs can contribute to the progression and metastasis of human cancers. Many studies have shown that the down-regulation of the miR-495 level occurs in a variety of cancers, including colorectal cancer (CRC). However, the precise molecular mechanisms of miR-495 in CRC have not been well clarified. In the current study, we investigated the biological functions and molecular mechanisms of miR-495 in CRC cell lines. Methods: qRT-PCR was used to determine the level of miR-495 in CRC cell lines and tissues. A miR-495 mimic and inhibitor were transfected into CRC cells, and the effects of miR-495 on the invasion and EMT were explored by qRT-PCR as well as transwell and Western blot assays. Meanwhile, luciferase assays were performed to validate Annexin A3 as a miR-495 target in CRC cells. Results: In our study, we found that miR-495 is down-regulated in CRC tissues and cell lines. Moreover, the low level of miR-495 was associated with increased expression of Annexin A3 in CRC tissues and cell lines. The invasion and EMT of CRC cells were suppressed by the overexpression of miR-495. However, the down-regulation of miR-495 promoted the invasion and EMT of CRC cells. Bioinformatics analysis predicted that Annexin A3 was a potential target gene of miR-495. Next, the luciferase reporter assay confirmed that miR-495 could directly target Annexin A3. Consistent with the effect of miR-495, the down-regulation of Annexin A3 by siRNA inhibited the invasion and EMT of CRC cells through the up-regulation of p53. The introduction of Annexin A3 in CRC cells partially blocked the effects of the miR-495 mimic. Conclusion: The introduction of miR-495 directly targeted Annexin A3 to inhibit the invasion and EMT of CRC cells by up-regulating p53, and the down-regulation of Annexin A3 was essential for inhibiting the invasion and EMT of CRC cells by overexpressing miR-495. Overall, the re-activation of the miR-495/Annexin A3/p53 axis may represent a new strategy for overcoming metastasis of CRC. (C) 2017 The Author(s) Published by S. Karger AG, Basel
引用
收藏
页码:1882 / 1895
页数:14
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