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

Cell Physiol Biochem. 2017;44(5):1882-1895. doi: 10.1159/000485877. Epub 2017 Dec 8.

Abstract

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.

Keywords: Annexin A3; Colorectal cancer; EMT; Invasion; MiR-495; P53.

MeSH terms

  • Annexin A3 / antagonists & inhibitors
  • Annexin A3 / genetics
  • Annexin A3 / metabolism*
  • Antagomirs / metabolism
  • Cadherins / genetics
  • Cadherins / metabolism
  • Cell Line, Tumor
  • Cell Movement
  • Colorectal Neoplasms / metabolism
  • Colorectal Neoplasms / pathology*
  • Down-Regulation
  • Epithelial-Mesenchymal Transition*
  • Female
  • HCT116 Cells
  • Humans
  • Male
  • Matrix Metalloproteinase 2 / analysis
  • Matrix Metalloproteinase 7 / analysis
  • MicroRNAs / antagonists & inhibitors
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Middle Aged
  • RNA Interference
  • Snail Family Transcription Factors / genetics
  • Snail Family Transcription Factors / metabolism
  • Tissue Inhibitor of Metalloproteinase-1 / analysis
  • Tumor Suppressor Protein p53 / antagonists & inhibitors
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism*
  • Up-Regulation
  • Vimentin / genetics
  • Vimentin / metabolism
  • Zinc Finger E-box-Binding Homeobox 1 / genetics
  • Zinc Finger E-box-Binding Homeobox 1 / metabolism

Substances

  • Antagomirs
  • Cadherins
  • MIRN495 microRNA, human
  • MicroRNAs
  • Snail Family Transcription Factors
  • TIMP1 protein, human
  • TP53 protein, human
  • Tissue Inhibitor of Metalloproteinase-1
  • Tumor Suppressor Protein p53
  • Vimentin
  • Zinc Finger E-box-Binding Homeobox 1
  • Annexin A3
  • Matrix Metalloproteinase 7
  • Matrix Metalloproteinase 2