<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Yubo Zhou</submitter><species>Homo Sapiens</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0018186000</full_dataset_link><submitter_email>ybzhou@simm.ac.cn</submitter_email><submitter_affiliation>Zhongshan Institute  for Drug Discovery</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Discovery of Selective and Potent BRPF1 Dege-reraders for the Treatment of Endocrine-sensitive Breast Cancer</name><description>ESR1 mutations and activation of growth factor signaling (e.g., PI3K-AKT) drive endocrine therapy resistance in breast cancer, largely limiting the success of breast cancer treatment. We reported a first-in-class, selective and potent BRPF1-targeted proteolysis-targeting chimera (PROTAC) B-8, and it downregulated H3K23ac and ER, causing cell cycle arrest and autophagic cell death.</description><dates><publication>Mon Jul 06 00:00:00 GMT+01:00 2026</publication></dates><accession>PXD080650</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>