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Volume 16, Issue 5 (Sep-Oct 2022)
mljgoums 2022, 16(5): 37-42 |
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zeinali P, saghaeian M, Asadi J, Jafari S M. High Dose of 3, 7-Dimethyl-1-Propargylxanthine Induces Cell Death in YM-1 and KYSE30 Cancer Cell Lines. mljgoums 2022; 16 (5) :37-42
URL: http://mlj.goums.ac.ir/article-1-1496-en.html
URL: http://mlj.goums.ac.ir/article-1-1496-en.html
1- Department of Biochemistry and Biophysics, School of Medicine, Golestan University of Medical Sciences, Gorgan, Iran
2- Metabolic Disorders Research Center, Golestan University of Medical Sciences, Gorgan, Iran
3- Metabolic Disorders Research Center, Golestan University if Medical Sciences, Gorgan, Iran
4- Metabolic Disorders Research Center, Golestan University if Medical Sciences, Gorgan, Iran , s.meh.jafari@goums.ac.ir
2- Metabolic Disorders Research Center, Golestan University of Medical Sciences, Gorgan, Iran
3- Metabolic Disorders Research Center, Golestan University if Medical Sciences, Gorgan, Iran
4- Metabolic Disorders Research Center, Golestan University if Medical Sciences, Gorgan, Iran , s.meh.jafari@goums.ac.ir
Abstract: (1127 Views)
Background and objectives: Activation of adenosine A2a receptor has been shown to induce the growth and metastasis of cancer cells. The role of this receptor in esophageal cancer has not yet been determined. The present study aimed to investigate effects of an adenosine A2a receptor antagonist (3, 7-dimethyl-1-propargylxanthine) on growth of esophageal cancer cells.
Methods: Real-time polymerase chain reaction was performed to evaluate mRNA expression of the A2a adenosine receptor in KYSE-30 and YM-1 esophageal cancer cell lines. Effects of the antagonist on viability of the cells were evaluated by MTT assay.
Results: At low concentrations, the antagonist had no effect on cell viability. However, at concentrations ≥200 μM, the antagonist significantly reduced viability of both cell lines (p<0.05).
Conclusion: The results of this study indicate that the adenosine A2a receptor antagonist exerts inhibitory effects on KYSE30 and YM-1 cancer cells in a dose-dependent manner. Therefore, the use of this antagonist can be exploited as a therapeutic target for the treatment of esophageal cancer.
Methods: Real-time polymerase chain reaction was performed to evaluate mRNA expression of the A2a adenosine receptor in KYSE-30 and YM-1 esophageal cancer cell lines. Effects of the antagonist on viability of the cells were evaluated by MTT assay.
Results: At low concentrations, the antagonist had no effect on cell viability. However, at concentrations ≥200 μM, the antagonist significantly reduced viability of both cell lines (p<0.05).
Conclusion: The results of this study indicate that the adenosine A2a receptor antagonist exerts inhibitory effects on KYSE30 and YM-1 cancer cells in a dose-dependent manner. Therefore, the use of this antagonist can be exploited as a therapeutic target for the treatment of esophageal cancer.
Research Article: Research Article |
Subject:
Biochemistry
Received: 2022/03/11 | Accepted: 2022/04/30 | Published: 2022/09/6 | ePublished: 2022/09/6
Received: 2022/03/11 | Accepted: 2022/04/30 | Published: 2022/09/6 | ePublished: 2022/09/6
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