<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Becker AMD</submitter><funding>European Research Council</funding><funding>Dutch Research Council (NWO)</funding><pagination>101048</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12454896</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(9)</volume><pubmed_abstract>Dendritic cells (DCs) are professional antigen-presenting cells endowed with the capacity to initiate strong antitumor immune responses. This function is critical for effective DC-based immunotherapies but is often hampered by tumor-derived immunosuppressive factors, as is observed for CD14&lt;sup>+&lt;/sup>CD163&lt;sup>+&lt;/sup> tumor-induced DC3s (ti-DC3s). ti-DC3s are increased in cancer patients where they display an immunosuppressive phenotype, accompanied by weak antigen-specific CD8 T cell-activating capacities. While tumor-derived interleukin-6, macrophage colony-stimulating factor, and prostaglandin E2 have been identified as factors inducing the transition from DC2s to ti-DC3s, a comprehensive unbiased profiling of the resulting changes in secretome and proteome has not been reported. Here,</pubmed_abstract><journal>Molecular &amp; cellular proteomics : MCP</journal><pubmed_title>Proteome and Secretome Profiling of the Melanoma-Induced Transition Toward Immune Incompetent Dendritic Cells Reveals Enhanced IDO1, Cathepsin, and Legumain Activity.</pubmed_title><pmcid>PMC12454896</pmcid><funding_grant_id>024.002.009</funding_grant_id><funding_grant_id>679921</funding_grant_id><pubmed_authors>Ignacio BJ</pubmed_authors><pubmed_authors>Ziegler AR</pubmed_authors><pubmed_authors>Verdoes M</pubmed_authors><pubmed_authors>Ramos-Tomillero I</pubmed_authors><pubmed_authors>Bonger KM</pubmed_authors><pubmed_authors>de Vries IJM</pubmed_authors><pubmed_authors>van Dalen FJ</pubmed_authors><pubmed_authors>Edgington-Mitchell LE</pubmed_authors><pubmed_authors>Becker AMD</pubmed_authors><pubmed_authors>Vermeulen M</pubmed_authors><pubmed_authors>Dijkstra JJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Proteome and Secretome Profiling of the Melanoma-Induced Transition Toward Immune Incompetent Dendritic Cells Reveals Enhanced IDO1, Cathepsin, and Legumain Activity.</name><description>Dendritic cells (DCs) are professional antigen-presenting cells endowed with the capacity to initiate strong antitumor immune responses. This function is critical for effective DC-based immunotherapies but is often hampered by tumor-derived immunosuppressive factors, as is observed for CD14&lt;sup>+&lt;/sup>CD163&lt;sup>+&lt;/sup> tumor-induced DC3s (ti-DC3s). ti-DC3s are increased in cancer patients where they display an immunosuppressive phenotype, accompanied by weak antigen-specific CD8 T cell-activating capacities. While tumor-derived interleukin-6, macrophage colony-stimulating factor, and prostaglandin E2 have been identified as factors inducing the transition from DC2s to ti-DC3s, a comprehensive unbiased profiling of the resulting changes in secretome and proteome has not been reported. Here,</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-06-03T19:54:13.909Z</modification><creation>2026-05-01T03:10:47.16Z</creation></dates><accession>S-EPMC12454896</accession><cross_references><pubmed>40789452</pubmed><doi>10.1016/j.mcpro.2025.101048</doi></cross_references></HashMap>