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Inhibitory Effect of Coadministration of Silibinin and Cpg-Odn2006 on Metastatic Characteristics (Mmp-2 and Tlr-9) of Hepatocarcinoma Cell Line



Rezaei A1 ; Saadat F2 ; Safavifar F3 ; Berahmeh A4 ; Khorramizadeh MR5, 6
Authors
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Authors Affiliations
  1. 1. School of Biology, Institute of Biological Sciences, Damghan University, Damghan, Iran
  2. 2. Department of Immunology, Faculty of Medicine, Guilan University of Medical Sciences, Rasht, Iran
  3. 3. Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Pathobiology, Faculty of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Biosensor Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Biothechnology Research Center, Tehran University of Medical Sciences, Tehran, Iran

Source: Journal of Mazandaran University of Medical Sciences Published:2019

Abstract

Background and purpose: Hepatocellular carcinoma (HCC) is a most common liver malignancy and Toll-like receptor-9 (TLR9) is essential for CpG DNA-induced immune responses. The aim of this study was to assess the anti-metastatic effects of combined administration of silibinin and CpG-ODN2006 on human hepatocellular carcinoma HepG-2 cell line model. Materials and methods: Inhibitory effects of various concentrations of silibinin and CpG-ODN2006 on HepG-2 cells growth and detection of best dosages for simultaneous usage were assessed by Methylthiazolyldiphenyl-tetrazolium bromide (MTT) method. Expression levels of Matrix Metalloproteinase-2 (MMP2) and TLR9 genes were analyzed by real-time PCR. Gelatin zymography was used to determine the activity of MMP2. Results: Inhibitory effect of coadministration of silibinin (100 μM) and CpG-ODN2006 (100 nM) on HepG-2 cells growth was significant (P<0.05). Real-Time PCR showed no significant differences in cycle threshold of the genes expression analyses (P>0.05). Conclusion: Low dose CpG administration efficiently customized silibinin impact on hepatic cancer. Low doses of the drugs and activating immune mechnasims are definitely preferred, therefore, the co-adminstration of these drugs provide a clear vision for the future of combination therapy. © 2019, Mazandaran University of Medical Sciences. All rights reserved.
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