Iranian
Biomedical Journal
Volume 27, Issue 4 (7-2023)
IBJ 2023, 27(4): 167-172 |
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Akrami H, Gholami H, Fattahi M R, Zeraatiannejad M. Effect of miR-4270 Suppression on Migration in Hepatocellular Carcinoma Cell Line (HepG2). IBJ 2023; 27 (4) :167-172
URL: http://ibj.pasteur.ac.ir/article-1-3923-en.html
URL: http://ibj.pasteur.ac.ir/article-1-3923-en.html
1- Gastroenterohepatology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran , hassan_akrami@yahoo.com
2- Gastroenterohepatology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran
2- Gastroenterohepatology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran
Abstract:
Background: Liver transplantation and surgical resection are two major strategies for treatment of hepatocellular carcinoma (HCC) patients. One approach to treating HCC is the suppression of metastasis to other tissues. Herein, we aimed to study the effect of miR-4270 inhibitor on migration of HepG2 cells as well as activity of matrix metalloproteinase (MMP) these cells in order to find a strategy to suppress metastasis in future.
Methods: HepG2 cells were treated with 0, 10, 20, 30, 40, 50, 60, 70, 80, and 90 nM of miR-4270 inhibitor, and then the cell viability was measured by trypan blue staining. Afterwards, cell migration and MMP activity of HepG2 cells were assessed by wound healing assay and zymography, respectively. The MMP gene expression was determined by real-time reverse transcription polymerase chain reaction.
Results: Results showed that miR-4270 inhibitor decreased the cell viability of HepG2 cells in a concentration-dependent manner. Also, inhibition of the miR-4270 reduced invasion, MMP activity, and expression of MMP genes in HepG2 cells, respectively.
Conclusion: Our findings suggest that miR-4270 inhibitor decreases in vitro migration, which could help find a new approach for HCC therapy patients.
Methods: HepG2 cells were treated with 0, 10, 20, 30, 40, 50, 60, 70, 80, and 90 nM of miR-4270 inhibitor, and then the cell viability was measured by trypan blue staining. Afterwards, cell migration and MMP activity of HepG2 cells were assessed by wound healing assay and zymography, respectively. The MMP gene expression was determined by real-time reverse transcription polymerase chain reaction.
Results: Results showed that miR-4270 inhibitor decreased the cell viability of HepG2 cells in a concentration-dependent manner. Also, inhibition of the miR-4270 reduced invasion, MMP activity, and expression of MMP genes in HepG2 cells, respectively.
Conclusion: Our findings suggest that miR-4270 inhibitor decreases in vitro migration, which could help find a new approach for HCC therapy patients.
Type of Study: Full Length/Original Article |
Subject:
Cancer Biology
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