2018
DOI: 10.1016/j.tice.2018.05.011
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Foxc1 promotes the proliferation of fibroblast-like synoviocytes in rheumatoid arthritis via PI3K/AKT signalling pathway

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Cited by 17 publications
(9 citation statements)
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“…POU domain-related TFs function in the cell cycle regulation of immunoglobulins and are involved in viral infection (16). Regulators in the FOX family are well-known regulators of cell proliferation, e.g., FOXC1 increases the proliferation of fibroblast-like synoviocytes in autoimmune diseases (17). In contrast, activities of the tumor suppressor protein p53, ETS-related proteins, and immune-related TFs (including STAT3, SMAD4, and macrophage migration inhibitory factor) were negatively correlated with the MRSS ( Figure 3A).…”
Section: (Supplemental Figures 3 and 4 And Supplementalmentioning
confidence: 99%
“…POU domain-related TFs function in the cell cycle regulation of immunoglobulins and are involved in viral infection (16). Regulators in the FOX family are well-known regulators of cell proliferation, e.g., FOXC1 increases the proliferation of fibroblast-like synoviocytes in autoimmune diseases (17). In contrast, activities of the tumor suppressor protein p53, ETS-related proteins, and immune-related TFs (including STAT3, SMAD4, and macrophage migration inhibitory factor) were negatively correlated with the MRSS ( Figure 3A).…”
Section: (Supplemental Figures 3 and 4 And Supplementalmentioning
confidence: 99%
“…The present findings seem to be consistent with other research that found that FGFR is activated in the process of wound healing 25 . Intriguingly, published papers have established that foxc1 can promote the proliferation of fibroblast-like synoviocytes in rheumatoid arthritis via the PI3K/AKT signalling pathway 35 .…”
Section: ■ Discussionmentioning
confidence: 99%
“…Mizoguchi et al. ( 59 ) identify seven different fibroblast surface protein phenotypes and classified them into three subsets according to the expression of podoplanin (PDPN) ( 60 , 61 ), cadherin-11 (CDH11) ( 46 , 62 ), THY1 (also known as CD90) ( 63 ) and CD34 ( 64 ) by integrating transcriptomic data. they found that different subsets of fibroblasts play different roles in joint inflammation and bone destruction.…”
Section: Scrna-seq Of Synovial Fibroblastsmentioning
confidence: 99%