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Authors Cai H, Chen X, Tang Y, Deng Y
Received 19 October 2016
Accepted for publication 18 December 2016
Published 28 February 2017 Volume 2017:10 Pages 1269—1278
DOI https://doi.org/10.2147/OTT.S125172
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Narasimha Reddy Parine
Peer reviewer comments 3
Editor who approved publication: Dr Jianmin Xu
Abstract: MicroRNAs (miRNAs), as key regulators of gene expression, are closely
related to tumor occurrence and progression. MiR-194 has been proved as a tumor
regulatory factor in various cancers; however, the biological function and
mechanism of action in colorectal cancer (CRC) have not been well explored. In
the present study, we found that miR-194 expression is upregulated in CRC
clinical specimens, while overexpression of miR-194 promotes cell migration and
invasion in CRC cell lines. Besides, miR-194 significantly influenced the
epithelial–mesenchymal transition (EMT) markers by downregulating E-cadherin
expression (P <0.01) and upregulating
vimentin and MMP-2 expression (P <0.001, P <0.05). Cell
migration is the cell movement related to actin cytoskeleton. In this study, we
found miR-194 increased cell polarization in SW480 cells. Moreover, zymography
assay showed that miR-194 significantly upregulated the gelatin-degrading
activity of MMP-2 (P <0.01).
Collectively, our findings suggest that miR-194 functions as a tumor promoter
in CRC, which may provide new insights for the study of CRC development and
metastasis.
Keywords: colorectal cancer, miR-194, epithelial
mesenchymal transition, migration, invasion