<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(2)</volume><submitter>Geng L</submitter><pubmed_abstract>Ferroptosis (FPT), a novel form of programmed cell death, is characterized by overwhelming iron/reactive oxygen species (ROS)-dependent accumulation of lipid peroxidation (LPO). However, the insufficiency of endogenous iron and ROS level limited the FPT therapeutic efficacy to a large extent. To overcome this obstacle, the bromodomain-containing protein 4 (BRD&lt;sub>4&lt;/sub>)-inhibitor (+)-JQ1 (JQ1) and iron-supplement ferric ammonium citrate (FAC)-loaded gold nanorods (GNRs) are encapsulated into the zeolitic imidazolate framework-8 (ZIF-8) to form matchbox-like GNRs@JF/ZIF-8 for the amplified FPT therapy. The existence of matchbox (ZIF-8) is stable in physiologically neutral conditions but degradable in acidic environment, which could prevent the loaded agents from prematurely reacting. Mor</pubmed_abstract><journal>Acta pharmaceutica Sinica. B</journal><pagination>863-878</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9979193</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Iron-based and BRD&lt;sub>4&lt;/sub>-downregulated strategy for amplified ferroptosis based on pH-sensitive/NIR-II-boosted nano-matchbox.</pubmed_title><pmcid>PMC9979193</pmcid><pubmed_authors>Jing H</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Liang X</pubmed_authors><pubmed_authors>Geng L</pubmed_authors><pubmed_authors>Lu T</pubmed_authors><pubmed_authors>Zhou Y</pubmed_authors><pubmed_authors>Li N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Iron-based and BRD&lt;sub>4&lt;/sub>-downregulated strategy for amplified ferroptosis based on pH-sensitive/NIR-II-boosted nano-matchbox.</name><description>Ferroptosis (FPT), a novel form of programmed cell death, is characterized by overwhelming iron/reactive oxygen species (ROS)-dependent accumulation of lipid peroxidation (LPO). However, the insufficiency of endogenous iron and ROS level limited the FPT therapeutic efficacy to a large extent. To overcome this obstacle, the bromodomain-containing protein 4 (BRD&lt;sub>4&lt;/sub>)-inhibitor (+)-JQ1 (JQ1) and iron-supplement ferric ammonium citrate (FAC)-loaded gold nanorods (GNRs) are encapsulated into the zeolitic imidazolate framework-8 (ZIF-8) to form matchbox-like GNRs@JF/ZIF-8 for the amplified FPT therapy. The existence of matchbox (ZIF-8) is stable in physiologically neutral conditions but degradable in acidic environment, which could prevent the loaded agents from prematurely reacting. Mor</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-05-29T22:03:29.973Z</modification><creation>2024-11-09T06:04:23.079Z</creation></dates><accession>S-EPMC9979193</accession><cross_references><pubmed>36873167</pubmed><doi>10.1016/j.apsb.2022.05.011</doi></cross_references></HashMap>