miR-20b Regulates Expression of Proteinase-Activated Receptor-1 (PAR-1) Thrombin Receptor in Melanoma Cells

Saleiban et al., Pigment Cell Melanoma Res. (2014) - PMID: 24405508

Product(s) used in this publication:  Custom Peptide Synthesis


The proteinase-activated receptor 1 (PAR-1) plays a central role in melanoma progression and its expression level is believed to correlate with the degree of cancer invasiveness. Here, we show that PAR-1 is post-transcriptionally regulated by miR-20b microRNA in human melanoma cells. PAR-1 was found to be expressed in metastatic melanoma cells but was barely detectable in primary melanoma. By transducing primary melanoma cells with a lentivirus containing a 3'-UTR construct of PAR-1 mRNA, we could show that endogenous melanoma microRNAs interacted with PAR-1 3'-UTR and silenced a fused luciferase reporter. Transfection of an inhibitor against miR-20b into primary melanoma cells reversed this process. Finally, transfection of miR-20b mimic into metastatic melanoma cells caused downregulation of the luciferase reporter. We conclude that miR-20b regulates expression of melanoma PAR-1 receptor, which may explain the differential expression of PAR-1 observed in human melanoma.

© 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.


gene expression regulation; melanoma; metastasis; microRNAs; proteinase-activated receptor-1

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