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AHR-dependent genes and response to MTX therapy in rheumatoid arthritis patients

Methotrexate (MTX) is the first-line therapy for rheumatoid arthritis. Nevertheless, MTX resistance is quite a common issue in clinical practice. There are some premises that aryl hydrocarbon receptor (AhR) gene battery may take part in MTX metabolism. In the present retrospective study, we analyzed...

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Autores principales: Wajda, Anna, Walczuk, Ewa, Stypińska, Barbara, Lach, Jakub, Yermakovich, Danat, Sivitskaya, Larysa, Romanowska-Próchnicka, Katarzyna, Wysocki, Tomasz, Jarończyk, Małgorzata, Paradowska-Gorycka, Agnieszka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455325/
https://www.ncbi.nlm.nih.gov/pubmed/34302046
http://dx.doi.org/10.1038/s41397-021-00238-4
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author Wajda, Anna
Walczuk, Ewa
Stypińska, Barbara
Lach, Jakub
Yermakovich, Danat
Sivitskaya, Larysa
Romanowska-Próchnicka, Katarzyna
Wysocki, Tomasz
Jarończyk, Małgorzata
Paradowska-Gorycka, Agnieszka
author_facet Wajda, Anna
Walczuk, Ewa
Stypińska, Barbara
Lach, Jakub
Yermakovich, Danat
Sivitskaya, Larysa
Romanowska-Próchnicka, Katarzyna
Wysocki, Tomasz
Jarończyk, Małgorzata
Paradowska-Gorycka, Agnieszka
author_sort Wajda, Anna
collection PubMed
description Methotrexate (MTX) is the first-line therapy for rheumatoid arthritis. Nevertheless, MTX resistance is quite a common issue in clinical practice. There are some premises that aryl hydrocarbon receptor (AhR) gene battery may take part in MTX metabolism. In the present retrospective study, we analyzed genes expression of AHR genes battery associated with MTX metabolism in whole blood of RA patients with good and poor response to MTX treatment. Additionally, sequencing, genotyping and bioinformatics analysis of AHR repressor gene (AHRR) c.565C > G (rs2292596) and c.1933G > C (rs34453673) have been performed. Theoretically, both changes may have an impact on H3K36me3 and H3K27me3. Evolutionary analysis revealed that rs2292596 may be possibly damaging. Allele G in rs2292596 and DAS28 seems to be associated with a higher risk of poor response to MTX treatment in RA. RA patients with poor response to MTX treatment revealed upregulated AhR and SLC19A1 mRNA level. Treatment with IL-6 inhibitor may be helpful to overcome the low-dose MTX resistance. Analysis of gene expression revealed possible another cause of poor response to MTX treatment which is different from that observed in the case of acute lymphoblastic leukemia.
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spelling pubmed-84553252021-10-07 AHR-dependent genes and response to MTX therapy in rheumatoid arthritis patients Wajda, Anna Walczuk, Ewa Stypińska, Barbara Lach, Jakub Yermakovich, Danat Sivitskaya, Larysa Romanowska-Próchnicka, Katarzyna Wysocki, Tomasz Jarończyk, Małgorzata Paradowska-Gorycka, Agnieszka Pharmacogenomics J Article Methotrexate (MTX) is the first-line therapy for rheumatoid arthritis. Nevertheless, MTX resistance is quite a common issue in clinical practice. There are some premises that aryl hydrocarbon receptor (AhR) gene battery may take part in MTX metabolism. In the present retrospective study, we analyzed genes expression of AHR genes battery associated with MTX metabolism in whole blood of RA patients with good and poor response to MTX treatment. Additionally, sequencing, genotyping and bioinformatics analysis of AHR repressor gene (AHRR) c.565C > G (rs2292596) and c.1933G > C (rs34453673) have been performed. Theoretically, both changes may have an impact on H3K36me3 and H3K27me3. Evolutionary analysis revealed that rs2292596 may be possibly damaging. Allele G in rs2292596 and DAS28 seems to be associated with a higher risk of poor response to MTX treatment in RA. RA patients with poor response to MTX treatment revealed upregulated AhR and SLC19A1 mRNA level. Treatment with IL-6 inhibitor may be helpful to overcome the low-dose MTX resistance. Analysis of gene expression revealed possible another cause of poor response to MTX treatment which is different from that observed in the case of acute lymphoblastic leukemia. Nature Publishing Group UK 2021-07-23 2021 /pmc/articles/PMC8455325/ /pubmed/34302046 http://dx.doi.org/10.1038/s41397-021-00238-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wajda, Anna
Walczuk, Ewa
Stypińska, Barbara
Lach, Jakub
Yermakovich, Danat
Sivitskaya, Larysa
Romanowska-Próchnicka, Katarzyna
Wysocki, Tomasz
Jarończyk, Małgorzata
Paradowska-Gorycka, Agnieszka
AHR-dependent genes and response to MTX therapy in rheumatoid arthritis patients
title AHR-dependent genes and response to MTX therapy in rheumatoid arthritis patients
title_full AHR-dependent genes and response to MTX therapy in rheumatoid arthritis patients
title_fullStr AHR-dependent genes and response to MTX therapy in rheumatoid arthritis patients
title_full_unstemmed AHR-dependent genes and response to MTX therapy in rheumatoid arthritis patients
title_short AHR-dependent genes and response to MTX therapy in rheumatoid arthritis patients
title_sort ahr-dependent genes and response to mtx therapy in rheumatoid arthritis patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455325/
https://www.ncbi.nlm.nih.gov/pubmed/34302046
http://dx.doi.org/10.1038/s41397-021-00238-4
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