<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Kun Cao</submitter><species>Homo Sapiens</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0018260000</full_dataset_link><submitter_email>caokun@gdmu.edu.cn</submitter_email><submitter_affiliation>The First Dongguan Affiliated Hospital of Guangdong Medical University</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Proteomic profiling of LX-2 cells treated with TGF-beta and DOX versus TGF-beta alone</name><description>This project aims to investigate whether doxycycline (DOX) can attenuate TGF-β1-induced fibrotic activation in human hepatic stellate LX-2 cells. We performed quantitative proteomic analysis using LC-MS/MS to compare protein expression profiles between TGF-β1-treated and TGF-β1 plus DOX-treated groups. The results will reveal potential anti-fibrotic mechanisms of DOX and identify key proteins and pathways involved in the regulation of hepatic fibrosis.</description><dates><publication>Thu Jul 09 00:00:00 GMT+01:00 2026</publication></dates><accession>PXD080784</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>