Altered expression of MicroRNA in synovial fibroblasts and synovial tissue in rheumatoid arthritis.
By J. Stańczyk, D. L. Pedrioli, F. Brentano, O. Sánchez-Pernaute, C. Kolling, R. Gay, Michael Detmar, S. Gay, D. Kyburz. Arthritis & Rheumatism, 2008
910 citations recorded by the source corpus.
Subfields: Cancer Research, Rheumatology
View Paper: https://www.semanticscholar.org/paper/0ab968e37d1462f792f7e266e884705e0f69258a
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Citations in the corpus
- miR-155 gene: a typical multifunctional microRNA. (2009, background): “In summary, miR-155 might function as a protective miRNA that locally down-regulates the expression of certain MMPs, thus controlling tissue damage due to inflammation [27].”
- microRNA as Biomarkers and Diagnostics (2016, background): “Altered expression of miRNAs in the synovial tissue and synovial fibroblasts of patients with rheumatoid arthritis has been reported, and increased expression levels of miRNA miR-155 and miR-146a were found in rheumatoid arthritis (Stanczyk et al., 2008).”
- MicroRNA: Biogenesis, Function and Role in Cancer (2010, background): “It is predicted that miRNA account for 15% of the human genome and regulate at least 30% of protein-coding genes [4-8].”
- MicroRNA-155 promotes autoimmune inflammation by enhancing inflammatory T cell development (2010, background): “Elevated expression of miR-155 has been observed in brain lesions from multiple sclerosis (MS) patients (Junker et al., 2009) and in synovial samples from patients with rheumatoid arthritis (RA) (Stanczyk et al., 2008).”
- The Role of MicroRNAs in Human Diseases (2010, background): “Specifically, increased miR-155 and miR-146a expression in RA synovial fibroblasts have been in comparison to those patients with Osteoarth-ritis (OA) (155) .”
- Upregulated miR-146a expression in peripheral blood mononuclear cells from rheumatoid arthritis patients (2008, background): “Stanczyk and coworkers [27] reported a fourfold increase in miR-146a expression and a twofold increase in miR-155 expression in RA synovial fibroblasts compared with osteoarthritis synovial fibroblasts.”