<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang C</submitter><funding>Shanghai Municipal Health Commission</funding><funding>National Natural Science Foundation of China</funding><pagination>94</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12942165</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(2)</volume><pubmed_abstract>&lt;h4>Background/objectives&lt;/h4>Aberrant metabolism in tumors exacerbates the immunosuppressive tumor microenvironment. The immunosuppressive metabolite kynurenine inhibits the activation of effector T cells. Current antitumor drugs targeting kynurenine focus on small molecule inhibitors, which exhibit suboptimal efficacy in suppressing kynurenine generation owing to the diversity of kynurenine synthesis pathways. In contrast, kynureninase (KYNase) can directly metabolize kynurenine regardless of the production source. However, its delivery is hindered by short blood-circulation half-life and poor tumor accumulation. Additionally, photodynamic therapy (PDT) has been reported to synergize with immunotherapy, suggesting a potential combinatorial photodynamic immunometabolic cancer therapy with</pubmed_abstract><journal>Journal of functional biomaterials</journal><pubmed_title>Self-Assembled Nanoparticles with Kynureninase-Fc Fusion Protein and Pheophorbide A for Photodynamic Immunometabolic Cancer Therapy.</pubmed_title><pmcid>PMC12942165</pmcid><funding_grant_id>2022XD045</funding_grant_id><funding_grant_id>82471857 and 91859110</funding_grant_id><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Lu W</pubmed_authors><pubmed_authors>Lin H</pubmed_authors><pubmed_authors>Yang A</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Self-Assembled Nanoparticles with Kynureninase-Fc Fusion Protein and Pheophorbide A for Photodynamic Immunometabolic Cancer Therapy.</name><description>&lt;h4>Background/objectives&lt;/h4>Aberrant metabolism in tumors exacerbates the immunosuppressive tumor microenvironment. The immunosuppressive metabolite kynurenine inhibits the activation of effector T cells. Current antitumor drugs targeting kynurenine focus on small molecule inhibitors, which exhibit suboptimal efficacy in suppressing kynurenine generation owing to the diversity of kynurenine synthesis pathways. In contrast, kynureninase (KYNase) can directly metabolize kynurenine regardless of the production source. However, its delivery is hindered by short blood-circulation half-life and poor tumor accumulation. Additionally, photodynamic therapy (PDT) has been reported to synergize with immunotherapy, suggesting a potential combinatorial photodynamic immunometabolic cancer therapy with</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-11T03:10:56.289Z</modification><creation>2026-07-11T03:09:07.686Z</creation></dates><accession>S-EPMC12942165</accession><cross_references><pubmed>41745555</pubmed><doi>10.3390/jfb17020094</doi></cross_references></HashMap>