<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE324nnn/GSE324393/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE324393</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Polygonum aviculare L. and Its Active Compound Myricetin Inhibit Rheumatoid Arthritis by Targeting Yes</name><description>Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by synovial inflammation and joint destruction. In RA, fibroblast-like synoviocytes (FLS) acquire a pathogenic phenotype in response to inflammatory cytokines, promoting synovial inflammation and tissue destruction. Thus, targeting pathological FLS activation has emerged as a promising therapeutic strategy. Herein, we aimed to identify novel plant-derived candidates capable of suppressing synovial inflammation. Screening of 327 plants identified Polygonum aviculare L. (PA) as a potent inhibitor of IL-17-mediated synovial inflammation. PA attenuated IL-17-, TNF-α-, and IL-1β-mediated pathological responses in RA patient-derived FLS (RA-FLS) and alleviated clinical symptoms and histopathological changes in an animal model. Transcriptomic analysis revealed that PA reversed IL-17-induced gene expression and suppressed inflammation-related pathways, with NF-κB emerging as a central regulatory axis. UHPLC-based compound profiling combined with AI-driven bioactivity prediction identified myricetin as an active compound of PA with anti-inflammatory and NF-κB inhibitory activity. Myricetin exerted anti-RA effects in RA-FLS, and both PA and myricetin attenuated synovial inflammation in a 3D synovium-like micromass culture system. PA and myricetin targeted Yes and inhibited its activity, with subsequent suppression of SHP-2 phosphorylation and downstream signaling pathways. Notably, myricetin directly bound to the ATP-binding site of Yes. These findings demonstrate that PA and myricetin inhibit pathogenic responses through the Yes–SHP-2 signaling axis and highlight their potential as plant-derived therapeutic candidates for RA.</description><dates><publication>2026/06/10</publication></dates><accession>GSE324393</accession><cross_references><GSM>GSM9574954</GSM><GSM>GSM9574955</GSM><GSM>GSM9574960</GSM><GSM>GSM9574961</GSM><GSM>GSM9574962</GSM><GSM>GSM9574956</GSM><GSM>GSM9574957</GSM><GSM>GSM9574958</GSM><GSM>GSM9574959</GSM><GPL>24676</GPL><GSE>324393</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>