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Effects of Methadone on the Toll-like Receptor 4 Expression in Human Non-Small Cell Lung Carcinoma A549 Cell Line Using In-silico and In vitro Techniques

BACKGROUND: In this study, the effects of methadone and naloxone on the expression of toll-like receptor 4 (TLR4) gene have been evaluated in human non-small cell lung carcinoma A549 cell line migration using in-silico and in vitro techniques. MATERIALS AND METHODS: Lung cancer A549 cell cultures we...

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Autores principales: Vaseghi, Golnaz, Rashidi, Nastaran, Zare, Nasrin, Ghasemi, Fahimeh, Pourhadi, Marjan, Rafiee, Laleh, Javanmard, Shaghayegh Haghjooy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9926039/
https://www.ncbi.nlm.nih.gov/pubmed/36798925
http://dx.doi.org/10.4103/abr.abr_97_21
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author Vaseghi, Golnaz
Rashidi, Nastaran
Zare, Nasrin
Ghasemi, Fahimeh
Pourhadi, Marjan
Rafiee, Laleh
Javanmard, Shaghayegh Haghjooy
author_facet Vaseghi, Golnaz
Rashidi, Nastaran
Zare, Nasrin
Ghasemi, Fahimeh
Pourhadi, Marjan
Rafiee, Laleh
Javanmard, Shaghayegh Haghjooy
author_sort Vaseghi, Golnaz
collection PubMed
description BACKGROUND: In this study, the effects of methadone and naloxone on the expression of toll-like receptor 4 (TLR4) gene have been evaluated in human non-small cell lung carcinoma A549 cell line migration using in-silico and in vitro techniques. MATERIALS AND METHODS: Lung cancer A549 cell cultures were stimulated for 24 h with methadone (5, 10, and 20 μM) and naloxone (20 and 40 μM) concentrations. The level of TLR4 expression was determined by the quantitative real-time polymerase chain reaction. Migration of the A549 cells was investigated after a 4-h incubation period with methadone using the Boyden Chamber assay. RESULTS: Migration rate of the A549 cells treated with 5 (P < 0.05) and 20 (P < 0.01) μM methadone was, respectively, increased and decreased with 20 μM naloxone (P < 0.05). Furthermore, the TLR4 expression was enhanced with 5 (P < 0.05) and 20 (P < 0.01) μM methadone and decreased with 20 (P < 0.05) and 40 μM naloxone (P < 0.01). In addition, in silico docking analysis revealed docking of methadone to MD-2 and TLR4. CONCLUSION: According to the present DATA, methadone affects the TLR4 expression. It may however cause adverse consequences by increasing the TLR4 expression. Therefore, the useful analgesic properties of methadone should be separated from the unwanted TLR4-mediated side effects.
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spelling pubmed-99260392023-02-15 Effects of Methadone on the Toll-like Receptor 4 Expression in Human Non-Small Cell Lung Carcinoma A549 Cell Line Using In-silico and In vitro Techniques Vaseghi, Golnaz Rashidi, Nastaran Zare, Nasrin Ghasemi, Fahimeh Pourhadi, Marjan Rafiee, Laleh Javanmard, Shaghayegh Haghjooy Adv Biomed Res Original Article BACKGROUND: In this study, the effects of methadone and naloxone on the expression of toll-like receptor 4 (TLR4) gene have been evaluated in human non-small cell lung carcinoma A549 cell line migration using in-silico and in vitro techniques. MATERIALS AND METHODS: Lung cancer A549 cell cultures were stimulated for 24 h with methadone (5, 10, and 20 μM) and naloxone (20 and 40 μM) concentrations. The level of TLR4 expression was determined by the quantitative real-time polymerase chain reaction. Migration of the A549 cells was investigated after a 4-h incubation period with methadone using the Boyden Chamber assay. RESULTS: Migration rate of the A549 cells treated with 5 (P < 0.05) and 20 (P < 0.01) μM methadone was, respectively, increased and decreased with 20 μM naloxone (P < 0.05). Furthermore, the TLR4 expression was enhanced with 5 (P < 0.05) and 20 (P < 0.01) μM methadone and decreased with 20 (P < 0.05) and 40 μM naloxone (P < 0.01). In addition, in silico docking analysis revealed docking of methadone to MD-2 and TLR4. CONCLUSION: According to the present DATA, methadone affects the TLR4 expression. It may however cause adverse consequences by increasing the TLR4 expression. Therefore, the useful analgesic properties of methadone should be separated from the unwanted TLR4-mediated side effects. Wolters Kluwer - Medknow 2022-12-26 /pmc/articles/PMC9926039/ /pubmed/36798925 http://dx.doi.org/10.4103/abr.abr_97_21 Text en Copyright: © 2022 Advanced Biomedical Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Vaseghi, Golnaz
Rashidi, Nastaran
Zare, Nasrin
Ghasemi, Fahimeh
Pourhadi, Marjan
Rafiee, Laleh
Javanmard, Shaghayegh Haghjooy
Effects of Methadone on the Toll-like Receptor 4 Expression in Human Non-Small Cell Lung Carcinoma A549 Cell Line Using In-silico and In vitro Techniques
title Effects of Methadone on the Toll-like Receptor 4 Expression in Human Non-Small Cell Lung Carcinoma A549 Cell Line Using In-silico and In vitro Techniques
title_full Effects of Methadone on the Toll-like Receptor 4 Expression in Human Non-Small Cell Lung Carcinoma A549 Cell Line Using In-silico and In vitro Techniques
title_fullStr Effects of Methadone on the Toll-like Receptor 4 Expression in Human Non-Small Cell Lung Carcinoma A549 Cell Line Using In-silico and In vitro Techniques
title_full_unstemmed Effects of Methadone on the Toll-like Receptor 4 Expression in Human Non-Small Cell Lung Carcinoma A549 Cell Line Using In-silico and In vitro Techniques
title_short Effects of Methadone on the Toll-like Receptor 4 Expression in Human Non-Small Cell Lung Carcinoma A549 Cell Line Using In-silico and In vitro Techniques
title_sort effects of methadone on the toll-like receptor 4 expression in human non-small cell lung carcinoma a549 cell line using in-silico and in vitro techniques
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9926039/
https://www.ncbi.nlm.nih.gov/pubmed/36798925
http://dx.doi.org/10.4103/abr.abr_97_21
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