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. 2022 Jan 5;12:788535. doi: 10.3389/fendo.2021.788535

Table 1.

Non-coding RNAs in the pathogenesis of GO.

Noncoding-RNAs Samples/cells Expression change Function Effects in GO References
miR-146a Plasma Downregulation Promote the differentiation of Th17 cell Pro-inflammatory (62)
CD4+ T Downregulation Increase Th1 response Pro-inflammatory (63, 64)
Orbital tissue Upregulation Increase the IL-6 level Exacerbate GO (69)
Orbital tissue Upregulation Decreases FN, collagen Iα, and α -SMA Inhibit fibrosis process (72, 73)
miR-183 and miR-96 CD4+ T Upregulation Contribute to the activation of CD4+ T cells Pro-inflammatory (66)
miR-21-5P Orbital tissue Upregulation Promote collagen Iα and total collagen production Promote fibrogenesis (76)
miR-146a and miR-155 Orbital tissue Upregulation Reducing the expression of PTEN and ZNRF3 Promote proliferation (70)
m iR-27a and miR-27b Orbital tissue Downregulation Cause the adipogenic differentiation of OFs Promote adipogenesis (79)
m iR-130a Orbital tissue Upregulation Enhance lipid accumulation Fatty tissue accumulation (78)
circRNA_14940 Orbital tissue Upregulation Regulate the Wnt signaling pathway, ECM receptor interaction and PIK3-AKT signaling pathway Participate in the pathogenesis of GO (80)