<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sun L</submitter><funding>Natural Science Foundation of Tianjin Municipal Science and Technology Commission</funding><funding>National Natural Science Foundation of China</funding><funding>Tianjin Research Innovation Project for Postgraduate Students for support</funding><pagination>e2104051</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8787384</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(3)</volume><pubmed_abstract>Toll-like receptor (TLR) activation in macrophages plays a critical role in the pathogenesis of acute lung injury (ALI). While TLR inhibition is a promising strategy to control the overwhelming inflammation in ALI, there still lacks effective TLR inhibitors for clinical uses to date. A unique class of peptide-coated gold nanoparticles (GNPs) is previously discovered, which effectively inhibited TLR signaling and protected mice from lipopolysaccharide (LPS)-induced ALI. To fast translate such a discovery into potential clinical applicable nanotherapeutics, herein an elegant strategy of "nano-enabled drug repurposing" with "nano-targeting" is introduced to empower the existing drugs for new uses. Combining transcriptome sequencing with Connectivity Map analysis, it is identified that the pro</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Nano-Enabled Reposition of Proton Pump Inhibitors for TLR Inhibition: Toward A New Targeted Nanotherapy for Acute Lung Injury.</pubmed_title><pmcid>PMC8787384</pmcid><funding_grant_id>81971549</funding_grant_id><funding_grant_id>81770070</funding_grant_id><funding_grant_id>20JCYBJC00040</funding_grant_id><funding_grant_id>2020YJSB136</funding_grant_id><pubmed_authors>Sun L</pubmed_authors><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Yang H</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Ma A</pubmed_authors><pubmed_authors>Wang R</pubmed_authors><pubmed_authors>Fung SY</pubmed_authors><pubmed_authors>Saferali A</pubmed_authors><pubmed_authors>Ma H</pubmed_authors><pubmed_authors>Gao W</pubmed_authors><pubmed_authors>Gong J</pubmed_authors><pubmed_authors>Turvey SE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Nano-Enabled Reposition of Proton Pump Inhibitors for TLR Inhibition: Toward A New Targeted Nanotherapy for Acute Lung Injury.</name><description>Toll-like receptor (TLR) activation in macrophages plays a critical role in the pathogenesis of acute lung injury (ALI). While TLR inhibition is a promising strategy to control the overwhelming inflammation in ALI, there still lacks effective TLR inhibitors for clinical uses to date. A unique class of peptide-coated gold nanoparticles (GNPs) is previously discovered, which effectively inhibited TLR signaling and protected mice from lipopolysaccharide (LPS)-induced ALI. To fast translate such a discovery into potential clinical applicable nanotherapeutics, herein an elegant strategy of "nano-enabled drug repurposing" with "nano-targeting" is introduced to empower the existing drugs for new uses. Combining transcriptome sequencing with Connectivity Map analysis, it is identified that the pro</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2026-05-09T04:28:56.372Z</modification><creation>2022-02-11T15:46:41.64Z</creation></dates><accession>S-EPMC8787384</accession><cross_references><pubmed>34816630</pubmed><doi>10.1002/advs.202104051</doi></cross_references></HashMap>