<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Escude Martinez de Castilla P</submitter><funding>Fondation ARC pour la Recherche sur le Cancer</funding><funding>Agence Nationale de la Recherche</funding><funding>Horizon 2020</funding><funding>Fondation pour la Recherche Médicale</funding><funding>HORIZON EUROPE Marie Sklodowska-Curie Actions</funding><pagination>e2500605</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12447046</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(24)</volume><pubmed_abstract>Prostate cancer (PCa) ranks as the fifth leading cause of cancer-related deaths among men worldwide. In 10-20% of the cases, PCa progresses to an incurable, castration-resistant stage. Castration-resistant PCa cells often overexpress prostate-specific membrane antigen (PSMA), a membrane protein that may serve as their Achilles' heel. Over the past decades, RNA-based therapeutics have emerged as promising treatments for a vast array of diseases, including cancer. In this study, with the ultimate goal of developing a targeted therapy for PCa, lipid nanoparticles (LNPs) are decorated with an anti-PSMA nanobody using click chemistry with a PEG-lipid. Direct stochastic optical reconstruction microscopy (dSTORM) and cluster analysis confirm the presence of at least one nanobody on the surface of</pubmed_abstract><journal>Advanced healthcare materials</journal><pubmed_title>Nanobody-Decorated Lipid Nanoparticles for Enhanced mRNA Delivery to Tumors In Vivo.</pubmed_title><pmcid>PMC12447046</pmcid><funding_grant_id>ANR-20-CE18-0026-0</funding_grant_id><funding_grant_id>ANR‐20‐CE18‐0026‐0</funding_grant_id><funding_grant_id>860303</funding_grant_id><funding_grant_id>825828</funding_grant_id><funding_grant_id>ARCDOC42022010004513</funding_grant_id><funding_grant_id>PGA1 RF20190208474</funding_grant_id><funding_grant_id>AJE20160635884</funding_grant_id><pubmed_authors>Escude Martinez de Castilla P</pubmed_authors><pubmed_authors>van Niel G</pubmed_authors><pubmed_authors>van Weerden WM</pubmed_authors><pubmed_authors>van Royen ME</pubmed_authors><pubmed_authors>Kooijmans SAA</pubmed_authors><pubmed_authors>Fens MH</pubmed_authors><pubmed_authors>Rietveld J</pubmed_authors><pubmed_authors>Schiffelers RM</pubmed_authors><pubmed_authors>Jenster G</pubmed_authors><pubmed_authors>Verdi V</pubmed_authors><pubmed_authors>van Kempen S</pubmed_authors><pubmed_authors>Vader P</pubmed_authors><pubmed_authors>Koekman AC</pubmed_authors><pubmed_authors>Yang Q</pubmed_authors><pubmed_authors>Estape Senti M</pubmed_authors><pubmed_authors>de Voogt W</pubmed_authors><pubmed_authors>van Merris J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Nanobody-Decorated Lipid Nanoparticles for Enhanced mRNA Delivery to Tumors In Vivo.</name><description>Prostate cancer (PCa) ranks as the fifth leading cause of cancer-related deaths among men worldwide. In 10-20% of the cases, PCa progresses to an incurable, castration-resistant stage. Castration-resistant PCa cells often overexpress prostate-specific membrane antigen (PSMA), a membrane protein that may serve as their Achilles' heel. Over the past decades, RNA-based therapeutics have emerged as promising treatments for a vast array of diseases, including cancer. In this study, with the ultimate goal of developing a targeted therapy for PCa, lipid nanoparticles (LNPs) are decorated with an anti-PSMA nanobody using click chemistry with a PEG-lipid. Direct stochastic optical reconstruction microscopy (dSTORM) and cluster analysis confirm the presence of at least one nanobody on the surface of</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T14:39:08.019Z</modification><creation>2026-05-29T03:05:30.508Z</creation></dates><accession>S-EPMC12447046</accession><cross_references><pubmed>40613352</pubmed><doi>10.1002/adhm.202500605</doi></cross_references></HashMap>