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AHR 依赖性基因与类风湿关节炎患者对 MTX 治疗的反应。

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

机构信息

Department of Molecular Biology, National Institute of Geriatrics, Rheumatology and Rehabilitation, Warsaw, Poland.

Biobank Lab, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland.

出版信息

Pharmacogenomics J. 2021 Oct;21(5):608-621. doi: 10.1038/s41397-021-00238-4. Epub 2021 Jul 23.

Abstract

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.

摘要

甲氨蝶呤(MTX)是治疗类风湿关节炎的一线药物。然而,MTX 耐药在临床实践中是一个相当常见的问题。有一些前提假设认为芳香烃受体(AhR)基因电池可能参与 MTX 代谢。在本回顾性研究中,我们分析了 MTX 代谢相关的 AHR 基因电池在对 MTX 治疗反应良好和不良的 RA 患者全血中的基因表达。此外,还对 AHR 抑制剂基因(AHRR)c.565C> G(rs2292596)和 c.1933G> C(rs34453673)进行了测序、基因分型和生物信息学分析。理论上,这两种变化都可能对 H3K36me3 和 H3K27me3 产生影响。进化分析表明 rs2292596 可能具有潜在的破坏性。rs2292596 中的 G 等位基因和 DAS28 似乎与 RA 患者对 MTX 治疗反应不良的风险增加有关。对 MTX 治疗反应不良的 RA 患者表现出 AhR 和 SLC19A1 mRNA 水平上调。使用 IL-6 抑制剂治疗可能有助于克服低剂量 MTX 耐药。基因表达分析揭示了 MTX 治疗反应不良的另一个可能原因,与急性淋巴细胞白血病观察到的原因不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b830/8455325/edc6edd853e5/41397_2021_238_Fig1_HTML.jpg

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