Title of article :
Assessment of Cannabinoids Agonist and Antagonist in Invasion Potential of K562 Cancer Cells
Author/Authors :
Gholizadeh, Fatemeh Department of Toxicology and Pharmacology - Faculty of Pharmacy and Poisoning Research Center - Tehran University of Medical Sciences, Tehran, Iran , Ghahremani, Mohammad Hossein Department of Toxicology and Pharmacology - Faculty of Pharmacy and Poisoning Research Center - Tehran University of Medical Sciences, Tehran, Iran , Aliebrahimi, Shima Department of Cellular and Molecular Biology - School of Biology - College of Science - University of Tehran, Tehran, Iran , Shadboorestan, Amir Department of Toxicology and Pharmacology - Faculty of Pharmacy and Poisoning Research Center - Tehran University of Medical Sciences, Tehran, Iran , Ostad, Nasser Department of Toxicology and Pharmacology - Faculty of Pharmacy and Poisoning Research Center - Tehran University of Medical Sciences, Tehran, Iran
Pages :
6
From page :
153
To page :
158
Abstract :
BBackground: The prominent hallmark of malignancies is the metastatic spread of cancer cells. Recent studies have reported that the nature of invasive cells could be changed after this phenomenon, causing chemotherapy resistance. It has been demonstrated that the up-regulated expression of matrix metalloproteinase (MMP) 2/MMP-9, as a metastasis biomarker, can fortify the metastatic potential of leukemia. Furthermore, investigations have confirmed the inhibitory effect of cannabinoid and endocannabinoid on the proliferation of cancer cells in vitro and in vivo. Methods: In the present study, the inhibitory effect of WIN 55212-2 a CB1/CB2 receptor agonist) and AM251 (a selective CB1 receptor antagonist) on K562 cells, as a chronic myelogenous leukemia (CML) model, was evaluated using MTT and invasion assay. Expressions of MMP-2 and MMP-9 were then assessed by Western blot analysis. Results: The data obtained from MTT assay showed that WIN 55212-2 could attenuate cell proliferation; however, AM251 was less effective in this regard. Our results showed that WIN 55212-2 considerably reduced cancer cell invasiveness, while AM251 exhibited a converse effect. Moreover, CB1 activation resulted in decreased expression of MMP-2 and MMP-9. Conclusion: Our findings clarifies that CB1 receptors are responsible for anti-invasive effects in the K562 cell line.
Keywords :
WIN 55212-2 , Matrix metalloproteinases , Leukemia , Cannabinoid receptor , AM251
Journal title :
Iranian Biomedical Journal(IBJ)
Serial Year :
2019
Record number :
2497811
Link To Document :
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