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Differences in expression of genes related to drug resistance and miRNAs regulating their expression in skin fibroblasts exposed to adalimumab and cyclosporine A

INTRODUCTION: Adalimumab and cyclosporine A are drugs used in moderate to severe forms of psoriasis. Despite the molecular orientation of the drugs, there is a loss of adequate cell sensitivity to the anti-cytokine therapy. AIM: To determine the changes in the gene expression profile associated with...

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Autores principales: Grabarek, Beniamin, Schweizer, Piotr, Adwent, Iwona, Wcisło-Dziadecka, Dominika, Krzaczyński, Jakub, Kruszniewska-Rajs, Celina, Gola, Joanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9880787/
https://www.ncbi.nlm.nih.gov/pubmed/36751547
http://dx.doi.org/10.5114/ada.2019.91506
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author Grabarek, Beniamin
Schweizer, Piotr
Adwent, Iwona
Wcisło-Dziadecka, Dominika
Krzaczyński, Jakub
Kruszniewska-Rajs, Celina
Gola, Joanna
author_facet Grabarek, Beniamin
Schweizer, Piotr
Adwent, Iwona
Wcisło-Dziadecka, Dominika
Krzaczyński, Jakub
Kruszniewska-Rajs, Celina
Gola, Joanna
author_sort Grabarek, Beniamin
collection PubMed
description INTRODUCTION: Adalimumab and cyclosporine A are drugs used in moderate to severe forms of psoriasis. Despite the molecular orientation of the drugs, there is a loss of adequate cell sensitivity to the anti-cytokine therapy. AIM: To determine the changes in the gene expression profile associated with drug resistance in the culture of normal human dermal fibroblasts (NHDF) exposed to adalimumab or cyclosporine A compared to the controls. MATERIAL AND METHODS: NHDF was exposed to adalimumab/cyclosporine A for 2, 8, 24 h compared to the control culture. Molecular analysis was performed using mRNA and miRNA microarray techniques. The obtained results were analysed using PL – Grid infrastructure (p < 0.05). RESULTS: Of the 22277 ID mRNA, 47 are associated with drug resistance, of which the change in expression of 17 mRNA ID is statistically significant (p < 0.05). The greatest change in transcriptional activity (FC ≥ 1.3) was observed for GLO1, SLC10A3, TUFT1, STATH, ABCB1, AGTR1. Expression of these genes can be regulated by miR-199a-5p, miR-1231, miR-34a, miR-3188, and miR-106a (except AGTR1). CONCLUSIONS: The analysis of changes in the expression of mRNA and miRNA related to drug resistance gives the possibility of monitoring the effectiveness of anti-cytokine therapy.
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spelling pubmed-98807872023-02-06 Differences in expression of genes related to drug resistance and miRNAs regulating their expression in skin fibroblasts exposed to adalimumab and cyclosporine A Grabarek, Beniamin Schweizer, Piotr Adwent, Iwona Wcisło-Dziadecka, Dominika Krzaczyński, Jakub Kruszniewska-Rajs, Celina Gola, Joanna Postepy Dermatol Alergol Original Paper INTRODUCTION: Adalimumab and cyclosporine A are drugs used in moderate to severe forms of psoriasis. Despite the molecular orientation of the drugs, there is a loss of adequate cell sensitivity to the anti-cytokine therapy. AIM: To determine the changes in the gene expression profile associated with drug resistance in the culture of normal human dermal fibroblasts (NHDF) exposed to adalimumab or cyclosporine A compared to the controls. MATERIAL AND METHODS: NHDF was exposed to adalimumab/cyclosporine A for 2, 8, 24 h compared to the control culture. Molecular analysis was performed using mRNA and miRNA microarray techniques. The obtained results were analysed using PL – Grid infrastructure (p < 0.05). RESULTS: Of the 22277 ID mRNA, 47 are associated with drug resistance, of which the change in expression of 17 mRNA ID is statistically significant (p < 0.05). The greatest change in transcriptional activity (FC ≥ 1.3) was observed for GLO1, SLC10A3, TUFT1, STATH, ABCB1, AGTR1. Expression of these genes can be regulated by miR-199a-5p, miR-1231, miR-34a, miR-3188, and miR-106a (except AGTR1). CONCLUSIONS: The analysis of changes in the expression of mRNA and miRNA related to drug resistance gives the possibility of monitoring the effectiveness of anti-cytokine therapy. Termedia Publishing House 2020-02-19 2021-04 /pmc/articles/PMC9880787/ /pubmed/36751547 http://dx.doi.org/10.5114/ada.2019.91506 Text en Copyright © 2022 Termedia https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0). License (http://creativecommons.org/licenses/by-nc-sa/4.0/ (https://creativecommons.org/licenses/by-nc-sa/4.0/) )
spellingShingle Original Paper
Grabarek, Beniamin
Schweizer, Piotr
Adwent, Iwona
Wcisło-Dziadecka, Dominika
Krzaczyński, Jakub
Kruszniewska-Rajs, Celina
Gola, Joanna
Differences in expression of genes related to drug resistance and miRNAs regulating their expression in skin fibroblasts exposed to adalimumab and cyclosporine A
title Differences in expression of genes related to drug resistance and miRNAs regulating their expression in skin fibroblasts exposed to adalimumab and cyclosporine A
title_full Differences in expression of genes related to drug resistance and miRNAs regulating their expression in skin fibroblasts exposed to adalimumab and cyclosporine A
title_fullStr Differences in expression of genes related to drug resistance and miRNAs regulating their expression in skin fibroblasts exposed to adalimumab and cyclosporine A
title_full_unstemmed Differences in expression of genes related to drug resistance and miRNAs regulating their expression in skin fibroblasts exposed to adalimumab and cyclosporine A
title_short Differences in expression of genes related to drug resistance and miRNAs regulating their expression in skin fibroblasts exposed to adalimumab and cyclosporine A
title_sort differences in expression of genes related to drug resistance and mirnas regulating their expression in skin fibroblasts exposed to adalimumab and cyclosporine a
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9880787/
https://www.ncbi.nlm.nih.gov/pubmed/36751547
http://dx.doi.org/10.5114/ada.2019.91506
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