<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Sheng Wang</submitter><species>Mus Musculus</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0018765000</full_dataset_link><submitter_email>shengwang@tju.edu.cn</submitter_email><submitter_affiliation>Tianjin University</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol></additional><is_claimable>false</is_claimable><name>Proteomic profiling of senescent tumor cell membrane</name><description>Senescent tumor cells exhibit intrinsically enhanced immunogenicity and can spontaneously generate tumor neoantigens. This endows their cell membrane with considerable potential as a versatile drug delivery platform and a reservoir of tumor-specific antigens for cancer immunotherapy and vaccine development. To explore the immune potential of senescent tumor cells, 4T1 breast cancer cells were subjected to a senescence inducer, doxorubicin to establish a stable senescent model. To systematically dissect the functional disparities between tumor cell membrane and senescent tumor cell membrane, label-free quantitative membrane proteomic analysis was performed on these two types of membrane vesicles.</description><dates><publication>Mon Aug 03 00:00:00 GMT+01:00 2026</publication></dates><accession>PXD082107</accession><cross_references><TAXONOMY>10090</TAXONOMY></cross_references></HashMap>