AHR-dependent genes and response to MTX therapy in rheumatoid arthritis patients.
Anna WajdaEwa WalczukBarbara StypińskaJakub LachDanat YermakovichLarysa SivitskayaKatarzyna Romanowska-PróchnickaTomasz WysockiMałgorzata JarończykAgnieszka Paradowska-GoryckaPublished in: The pharmacogenomics journal (2021)
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.
Keyphrases
- rheumatoid arthritis
- genome wide
- gene expression
- low dose
- disease activity
- acute lymphoblastic leukemia
- rheumatoid arthritis patients
- clinical practice
- single cell
- stem cells
- poor prognosis
- high dose
- combination therapy
- copy number
- mesenchymal stem cells
- replacement therapy
- interstitial lung disease
- ankylosing spondylitis
- binding protein
- idiopathic pulmonary fibrosis
- allogeneic hematopoietic stem cell transplantation
- genome wide analysis