2020
DOI: 10.1530/ec-20-0045
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Microarray profile of B cells from Graves’ disease patients reveals biomarkers of proliferation

Abstract: B lymphocytes are the source of autoantibodies against the thyroid-stimulating hormone receptor (TSHR) in Graves’ disease (GD). Characterization of autoimmune B-cell expression profiles might enable a better understanding of GD pathogenesis. To reveal this, the expression levels of long noncoding RNAs (lncRNAs) and mRNAs (genes) in purified B cells from patients with newly diagnosed GD and healthy individuals were compared using microarrays, which elucidated 604 differentially expressed lncRNAs (DE-lncRNAs) an… Show more

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Cited by 7 publications
(4 citation statements)
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“…B cells play an important role in autoimmune diseases, not only by producing antibodies to participate in autoimmune reactions but also by secreting cytokines and chemokines to recruit T cells (Luu, et al 2014). In addition, some marker proteins were expressed during the maturation of B cells, and were used to identify different subtypes; the dysfunction of B cells led to changes in autoimmune tolerance (Jiang, et al 2020;Kang, et al 2021).…”
Section: Discussionmentioning
confidence: 99%
“…B cells play an important role in autoimmune diseases, not only by producing antibodies to participate in autoimmune reactions but also by secreting cytokines and chemokines to recruit T cells (Luu, et al 2014). In addition, some marker proteins were expressed during the maturation of B cells, and were used to identify different subtypes; the dysfunction of B cells led to changes in autoimmune tolerance (Jiang, et al 2020;Kang, et al 2021).…”
Section: Discussionmentioning
confidence: 99%
“…Yin et al performed a lncRNA microarray to identify AK021954, AB075506, and HMlincRNA1474 levels that were dysregulated in GD CD4 + T cells and might serve as novel biomarkers of GD [ 16 ]. Jiang et al found that n335641, n337845, and TCONS_00022357-XLOC_010919 may participate in the proliferation and survival of B cells in GD [ 21 ]. Yao et al focused on relapsed GD patients and found that three downregulated lncRNAs (NONHSAT093153.2, NONHSAT118924.2, and NONHSAT209004.1) were closely related to the recurrence of GD [ 15 ].…”
Section: Discussionmentioning
confidence: 99%
“…With the advancement in the depth and quality of transcriptome sequencing, an increasing number of distinguishably expressed lncRNAs has been illustrated in various disease. Several researches implicated lncRNAs in the development of various diseases, however, there are only scant data related to GD ( 27 , 28 , 29 ). In this study, we aimed to explore lncRNA and mRNA expression in GD CD4+T cells to provide new insight into the pathogenesis of GD.…”
Section: Discussionmentioning
confidence: 99%