Dipotassium Glycyrrhizinate on Melanoma Cell Line: Inhibition of Cerebral Metastases Formation by Targeting NF-kB Genes-Mediating MicroRNA-4443 and MicroRNA-3620-Dipotassium Glycyrrhizinate Effect on Melanoma.

Glycyrrhizic acid (GA), a natural compound isolated from licorice ( Glycyrrhiza glabra ), has exhibited anti-inflammatory and anti-tumor effects in vitro. Dipotassium glycyrrhizinate (DPG), a dipotassium salt of GA, also has shown an anti-tumor effect on glioblastoma cell lines, U87MG and T98G. The study investigated the DPG effects in the melanoma cell line (SK-MEL-28). MTT assay demonstrated that the viability of the cells was significantly decreased in a time- and dose-dependent manner after DPG (IC 50 = 36 mM; 24 h). DNA fragmentation suggested that DPG (IC 50 ) induced cellular apoptosis, which was confirmed by a significant number of TUNEL-positive cells ( p -value = 0.048) and by PARP-1 [0.55 vs. 1.02 arbitrary units (AUs), p -value = 0.001], BAX (1.91 vs. 1.05 AUs, p -value = 0.09), and BCL-2 (0.51 vs. 1.07 AUs, p -value = 0.0018) mRNA compared to control cells. The proliferation and wound-healing assays showed an anti-proliferative effect on DPG-IC 50 -treated cells, also indicating an inhibitory effect on cell migration ( p -values < 0.001). Moreover, it was observed that DPG promoted a 100% reduction in melanospheres formation ( p -value = 0.008). Our previous microRNAs (miRs) global analysis has revealed that DPG might increase miR-4443 and miR-3620 expression levels. Thus, qPCR showed that after DPG treatment, SK-MEL-28 cells presented significantly high miR-4443 (1.77 vs. 1.04 AUs, p -value = 0.02) and miR-3620 (2.30 vs. 1.00 AUs, p -value = 0.01) expression compared to control cells, which are predicted to target the NF-kB , CD209 and TNC genes, respectively. Both genes are responsible for cell attachment and migration, and qPCR revealed significantly decreased CD209 (1.01 vs. 0.54 AUs, p -value = 0.018) and TNC (1.00 vs. 0.31 AUs, p -value = 2.38 × 10 -6 ) mRNA expression levels after DPG compared to untreated cells. Furthermore, the migration of SK-MEL-28 cells stimulated by 12-O-tetradecanoylphorbol-13-acetate (TPA) was attenuated by adding DPG by wound-healing assay (48 h: p -value = 0.004; 72 h: p -value = 7.0 × 10 -4 ). In addition, the MMP-9 expression level was inhibited by DPG in melanoma cells stimulated by TPA and compared to TPA-treated cells (3.56 vs. 0.99 AUs, p -value = 0.0016) after 24 h of treatment. Our results suggested that DPG has an apoptotic, anti-proliferative, and anti-migratory effect on SK-MEL-28 cells. DPG was also able to inhibit cancer stem-like cells that may cause cerebral tumor formation.