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Assessment of Cannabinoids Agonist and Antagonist in Invasion Potential of K562 Cancer Cells

BACKGROUND: 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 met...

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Autores principales: Gholizadeh, Fatemeh, Ghahremani, Mohammad Hossein, Aliebrahimi, Shima, Shadboorestan, Amir, Ostad, Seyed Nasser
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pasteur Institute of Iran 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707105/
https://www.ncbi.nlm.nih.gov/pubmed/29883990
http://dx.doi.org/10.29252/.23.2.153
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author Gholizadeh, Fatemeh
Ghahremani, Mohammad Hossein
Aliebrahimi, Shima
Shadboorestan, Amir
Ostad, Seyed Nasser
author_facet Gholizadeh, Fatemeh
Ghahremani, Mohammad Hossein
Aliebrahimi, Shima
Shadboorestan, Amir
Ostad, Seyed Nasser
author_sort Gholizadeh, Fatemeh
collection PubMed
description BACKGROUND: 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.
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spelling pubmed-67071052019-08-29 Assessment of Cannabinoids Agonist and Antagonist in Invasion Potential of K562 Cancer Cells Gholizadeh, Fatemeh Ghahremani, Mohammad Hossein Aliebrahimi, Shima Shadboorestan, Amir Ostad, Seyed Nasser Iran Biomed J Full Length BACKGROUND: 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. Pasteur Institute of Iran 2019-03 /pmc/articles/PMC6707105/ /pubmed/29883990 http://dx.doi.org/10.29252/.23.2.153 Text en © Iranian Biomedical Journal This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Length
Gholizadeh, Fatemeh
Ghahremani, Mohammad Hossein
Aliebrahimi, Shima
Shadboorestan, Amir
Ostad, Seyed Nasser
Assessment of Cannabinoids Agonist and Antagonist in Invasion Potential of K562 Cancer Cells
title Assessment of Cannabinoids Agonist and Antagonist in Invasion Potential of K562 Cancer Cells
title_full Assessment of Cannabinoids Agonist and Antagonist in Invasion Potential of K562 Cancer Cells
title_fullStr Assessment of Cannabinoids Agonist and Antagonist in Invasion Potential of K562 Cancer Cells
title_full_unstemmed Assessment of Cannabinoids Agonist and Antagonist in Invasion Potential of K562 Cancer Cells
title_short Assessment of Cannabinoids Agonist and Antagonist in Invasion Potential of K562 Cancer Cells
title_sort assessment of cannabinoids agonist and antagonist in invasion potential of k562 cancer cells
topic Full Length
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707105/
https://www.ncbi.nlm.nih.gov/pubmed/29883990
http://dx.doi.org/10.29252/.23.2.153
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