<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhou Y</submitter><funding>National Natural Science Foundation of China</funding><pagination>e2300994</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11468986</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(27)</volume><pubmed_abstract>Ferroptosis as programmed cell death received considerable attention in cancer research. Recently, studies have associated ferroptosis with photodynamic therapy (PDT) because PDT promotes glutathione (GSH) deletion, glutathione peroxidase 4 (GPX4) degradation, and lipid peroxide accumulation. However, PDT-induced ferroptosis may be potentially prevented by ferroptosis suppressor protein 1 (FSP1). To address this limitation, herein, a novel strategy is developed to trigger ferroptosis by PDT and FSP1 inhibition. For enhancement of this strategy, a photoresponsive nanocomplex, self-assembled by BODIPY-modified poly(amidoamine) (BMP), is utilized to stably encapsulate the inhibitor of FSP1 (iFSP1) and chlorin e6 (Ce6). The nanosystem promotes intracellular delivery, penetration, and accumulat</pubmed_abstract><journal>Advanced healthcare materials</journal><pubmed_title>Photo-Enhanced Synergistic Induction of Ferroptosis for Anti-Cancer Immunotherapy.</pubmed_title><pmcid>PMC11468986</pmcid><funding_grant_id>82222903</funding_grant_id><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Kang W</pubmed_authors><pubmed_authors>Chen K</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Xu A</pubmed_authors><pubmed_authors>Lin WK</pubmed_authors><pubmed_authors>Yang R</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Zhou Y</pubmed_authors><pubmed_authors>Cheng Y</pubmed_authors><pubmed_authors>Jin L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Photo-Enhanced Synergistic Induction of Ferroptosis for Anti-Cancer Immunotherapy.</name><description>Ferroptosis as programmed cell death received considerable attention in cancer research. Recently, studies have associated ferroptosis with photodynamic therapy (PDT) because PDT promotes glutathione (GSH) deletion, glutathione peroxidase 4 (GPX4) degradation, and lipid peroxide accumulation. However, PDT-induced ferroptosis may be potentially prevented by ferroptosis suppressor protein 1 (FSP1). To address this limitation, herein, a novel strategy is developed to trigger ferroptosis by PDT and FSP1 inhibition. For enhancement of this strategy, a photoresponsive nanocomplex, self-assembled by BODIPY-modified poly(amidoamine) (BMP), is utilized to stably encapsulate the inhibitor of FSP1 (iFSP1) and chlorin e6 (Ce6). The nanosystem promotes intracellular delivery, penetration, and accumulat</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Oct</publication><modification>2026-06-08T06:23:36.432Z</modification><creation>2025-04-04T00:35:31.774Z</creation></dates><accession>S-EPMC11468986</accession><cross_references><pubmed>37432874</pubmed><doi>10.1002/adhm.202300994</doi></cross_references></HashMap>