<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(12)</volume><submitter>Wang J</submitter><pubmed_abstract>&lt;b>Rationale&lt;/b>: Rheumatoid arthritis (RA) is a prototype of inflammatory arthritis in which synovial fibroblasts (SFs) play key roles in cartilage and bone destruction through tumor-like proliferation, migration, invasion and inflammation. This study aimed to research forkhead box protein C1 (FoxC1) and microRNA (miR)-141-3p, which modulate pathological changes in the synovial membrane, to find possible strategies for treating RA. &lt;b>Methods&lt;/b>: FoxC1, β-catenin and miR-141-3p gene expression in synovial tissues and SFs was quantified by real-time PCR; FoxC1 and β-catenin protein levels were evaluated by immunohistochemistry, immunofluorescence, and Western blotting. We transiently transfected human SFs with FoxC1 and β-catenin overexpression and silencing vectors and assessed prolifera</pubmed_abstract><journal>Theranostics</journal><pagination>5412-5434</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7196314</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Identification of a novel microRNA-141-3p/Forkhead box C1/β-catenin axis associated with rheumatoid arthritis synovial fibroblast function in vivo and in vitro.</pubmed_title><pmcid>PMC7196314</pmcid><pubmed_authors>Lu M</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Gao M</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Gao W</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Chang J</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Yin L</pubmed_authors><pubmed_authors>Liu W</pubmed_authors><pubmed_authors>Yin Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification of a novel microRNA-141-3p/Forkhead box C1/β-catenin axis associated with rheumatoid arthritis synovial fibroblast function in vivo and in vitro.</name><description>&lt;b>Rationale&lt;/b>: Rheumatoid arthritis (RA) is a prototype of inflammatory arthritis in which synovial fibroblasts (SFs) play key roles in cartilage and bone destruction through tumor-like proliferation, migration, invasion and inflammation. This study aimed to research forkhead box protein C1 (FoxC1) and microRNA (miR)-141-3p, which modulate pathological changes in the synovial membrane, to find possible strategies for treating RA. &lt;b>Methods&lt;/b>: FoxC1, β-catenin and miR-141-3p gene expression in synovial tissues and SFs was quantified by real-time PCR; FoxC1 and β-catenin protein levels were evaluated by immunohistochemistry, immunofluorescence, and Western blotting. We transiently transfected human SFs with FoxC1 and β-catenin overexpression and silencing vectors and assessed prolifera</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2025-04-04T19:05:03.321Z</modification><creation>2020-05-22T19:27:07Z</creation></dates><accession>S-EPMC7196314</accession><cross_references><pubmed>32373221</pubmed><doi>10.7150/thno.45214</doi></cross_references></HashMap>