<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(6)</volume><submitter>Li Y</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Arthritis is a degenerative joint disease influenced by various environmental factors, including exposure to Benzophenone-3 (BP3), a common UV filter. This study aims to elucidate the toxicological impact of BP3 on arthritis pathogenesis using network toxicology approaches.&lt;h4>Method&lt;/h4>We integrated data from the Comparative Toxicogenomics Database (CTD) and Gene Expression Omnibus (GEO) to identify differentially expressed BP3-related toxicological targets in osteoarthritis (OA). Enrichment analyses were conducted to determine the implicated biological processes, cellular components, and molecular functions. Further, the involvement of the PI3K-Akt signaling pathway was investigated, along with correlations with immune cell infiltration and immune-related pathways. Mo</pubmed_abstract><journal>Toxicology research</journal><pagination>tfae199</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11645663</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The impact of Benzophenone-3 on osteoarthritis pathogenesis: a network toxicology approach.</pubmed_title><pmcid>PMC11645663</pmcid><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Hu H</pubmed_authors><pubmed_authors>Liu P</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors></additional><is_claimable>false</is_claimable><name>The impact of Benzophenone-3 on osteoarthritis pathogenesis: a network toxicology approach.</name><description>&lt;h4>Background&lt;/h4>Arthritis is a degenerative joint disease influenced by various environmental factors, including exposure to Benzophenone-3 (BP3), a common UV filter. This study aims to elucidate the toxicological impact of BP3 on arthritis pathogenesis using network toxicology approaches.&lt;h4>Method&lt;/h4>We integrated data from the Comparative Toxicogenomics Database (CTD) and Gene Expression Omnibus (GEO) to identify differentially expressed BP3-related toxicological targets in osteoarthritis (OA). Enrichment analyses were conducted to determine the implicated biological processes, cellular components, and molecular functions. Further, the involvement of the PI3K-Akt signaling pathway was investigated, along with correlations with immune cell infiltration and immune-related pathways. Mo</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2026-06-06T14:35:07.217Z</modification><creation>2026-05-31T03:09:59.897Z</creation></dates><accession>S-EPMC11645663</accession><cross_references><pubmed>39677492</pubmed><doi>10.1093/toxres/tfae199</doi></cross_references></HashMap>