A DNA-Methylated Sight on Autoimmune Inflammation Network across RA, pSS, and SLE

المؤلفون المشاركون

Xu, Jian
Liu, Shuang
Lei, Dongyun
Wang, Xingqiang
Ding, Jie
Tao, Li
Zhang, Fan
Peng, Jiangyun

المصدر

Journal of Immunology Research

العدد

المجلد 2018، العدد 2018 (31 ديسمبر/كانون الأول 2018)، ص ص. 1-13، 13ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2018-08-12

دولة النشر

مصر

عدد الصفحات

13

التخصصات الرئيسية

الأحياء

الملخص EN

Methylation variabilities of inflammatory cytokines play important roles in the development of systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), and primary Sjögren’s syndrome (pSS).

With heightened focus on personalized and precise medicine, it is necessary to compare and contrast the difference and similarity of cytokine methylation status between the 3 most classic autoimmune diseases (AIDs).

In this study, we integrated 5 Cytokine-Chips from genome-wide DNA methylation datasets of the 3 kind of AIDs, delta-beta value was calculated for intergroup difference, and comprehensive bioinformatics analyses of cytokine genes with aberrant methylations were performed.

125 shared differential methylation variabilities (DMVs) were identified.

There were 102 shared DMVs with similar methylation status; 3 hypomethylated differential methylation regions (DMRs) across the AIDs were found, and all 3 DMRs were hypomethylated.

DMRs (AZU1, LTBR, and RTEL1) were likely to serve as activator in the inflammatory process.

Particularly, AZU1 and LTBR with hypomethylated TSS and first exon located in the promoter regions were able to trigger inflammation signaling cascades and play critical roles in autoimmune tautology.

Moreover, functional epigenetic module (FEM) algorithm showed that different inflammatory networks are involved in different AIDs; 5 hotspots were identified as biologically plausible pathways in inducing or perpetuating of inflammation which are epigenetically deregulated in AIDs.

We concluded methylation variabilities among the same cytokines can greatly impact the perpetuation of inflammatory process or signal pathway of AIDs.

Differentiating the cytokine methylation status will serve as valuable resource for researchers alike to gain better understanding of the epigenetic mechanisms of the three AIDs.

Even more importantly, better understanding of cytokine methylation variability existing between the three classic AIDs will aid in identification of potential epigenetic biomarkers and therapeutic targets.

This trial is registered with ChiCTR-INR-16010290, a clinical trial for the treatment of rheumatoid arthritis with Warming yang and Smoothening Meridians.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Wang, Xingqiang& Lei, Dongyun& Ding, Jie& Liu, Shuang& Tao, Li& Zhang, Fan…[et al.]. 2018. A DNA-Methylated Sight on Autoimmune Inflammation Network across RA, pSS, and SLE. Journal of Immunology Research،Vol. 2018, no. 2018, pp.1-13.
https://search.emarefa.net/detail/BIM-1192320

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Wang, Xingqiang…[et al.]. A DNA-Methylated Sight on Autoimmune Inflammation Network across RA, pSS, and SLE. Journal of Immunology Research No. 2018 (2018), pp.1-13.
https://search.emarefa.net/detail/BIM-1192320

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Wang, Xingqiang& Lei, Dongyun& Ding, Jie& Liu, Shuang& Tao, Li& Zhang, Fan…[et al.]. A DNA-Methylated Sight on Autoimmune Inflammation Network across RA, pSS, and SLE. Journal of Immunology Research. 2018. Vol. 2018, no. 2018, pp.1-13.
https://search.emarefa.net/detail/BIM-1192320

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-1192320