<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Dahong Zhang</submitter><species>Homo Sapiens</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0016917000</full_dataset_link><submitter_email>Zhangdahong666@163.com</submitter_email><submitter_affiliation>Zhejiang Provincial People's Hospital</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Identification of the direct molecular target of sanguinarine in bladder cancer cells</name><description>Sanguinarine possesses anticancer, antioxidant activities; however, its direct target(s) and mechanism of action have long remained unclear, limiting its translational and clinical application. Here, we employed limited proteolysis-coupled mass spectrometry (LiP-MS) to identify its direct target(s) in the T24 bladder cancer cell line, thereby providing a theoretical basis for further clinical development.</description><dates><publication>Fri May 01 00:00:00 BST 2026</publication></dates><accession>PXD078043</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>