<HashMap><database>JPOST Repository</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Mzid>https://storage.jpostdb.org/JPST003851/files/FTGcleTOT.mzid</Mzid><Mzid>https://storage.jpostdb.org/JPST003851/files/FTGcleTTt.mzid</Mzid><Mgf>https://storage.jpostdb.org/JPST003851/files/FTGcleTTt.mgf</Mgf><Mgf>https://storage.jpostdb.org/JPST003851/files/FTGcleTOT.mgf</Mgf><Other>https://storage.jpostdb.org/JPST003851/files/20250603%20NEW.7z</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Proteomics</omics_type><submitter>Sheng-Hui Lan</submitter><species>Homo Sapiens (human)</species><full_dataset_link>https://repository.jpostdb.org/entry/JPST003851</full_dataset_link><submitter_affiliation>National Yang Ming Chiao Tung University</submitter_affiliation><sample_protocol></sample_protocol><repository>jPOST</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Outer membrane proteins of autophagosomes isolated from EGF-treated MDA-MB-231 cells</name><description>In this study, we investigated how EGFR activation via EGF treatment reprograms metabolic pathways in triple-negative breast cancer (TNBC) cells by modulating autophagic secretion. Proteomic profiling was performed on isolated autophagosomes from EGF-treated MDA-MB-231 cells to identify outermembrane-associated proteins. These data provide insights into how secretory autophagy contributes to tumor metabolic remodeling.</description><dates><publication>Wed Jun 17 00:00:00 BST 2026</publication></dates><accession>PXD064652</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>