<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kroon J</submitter><funding>NanoNextNL Drug Delivery programme 03D.01</funding><funding>the Netherlands Organisation</funding><funding>European Research Council</funding><funding>Dutch Cancer Society</funding><funding>PRONET</funding><pagination>815-24</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5006873</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>75(8)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The inflammatory tumor microenvironment, and more specifically the tumor-associated macrophages, plays an essential role in the development and progression of prostate cancer towards metastatic bone disease. Tumors are often characterized by a leaky vasculature, which - combined with the prolonged circulation kinetics of liposomes - leads to efficient tumor localization of these drug carriers, via the so-called enhanced permeability and retention (EPR) -effect. In this study, we evaluated the utility of targeted, liposomal drug delivery of the glucocorticoid dexamethasone in a model of prostate cancer bone metastases.&lt;h4>Methods&lt;/h4>Tumor-bearing Balb-c nu/nu mice were treated intravenously with 0.2-1.0-5.0 mg/kg/week free- and liposomal DEX for 3-4 weeks and tumor growt</pubmed_abstract><journal>The Prostate</journal><pubmed_title>Liposomal delivery of dexamethasone attenuates prostate cancer bone metastatic tumor growth in vivo.</pubmed_title><pmcid>PMC5006873</pmcid><funding_grant_id>UL-2011-4030</funding_grant_id><funding_grant_id>309494</funding_grant_id><funding_grant_id>916.131.10</funding_grant_id><funding_grant_id>309494:NeoNaNo</funding_grant_id><pubmed_authors>van Bloois L</pubmed_authors><pubmed_authors>Cheung H</pubmed_authors><pubmed_authors>van der Horst G</pubmed_authors><pubmed_authors>Buijs JT</pubmed_authors><pubmed_authors>Pelger RC</pubmed_authors><pubmed_authors>Storm G</pubmed_authors><pubmed_authors>Metselaar JM</pubmed_authors><pubmed_authors>Lammers T</pubmed_authors><pubmed_authors>van der Pluijm G</pubmed_authors><pubmed_authors>van der Mark M</pubmed_authors><pubmed_authors>Kroon J</pubmed_authors><pubmed_authors>Rizzo LY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Liposomal delivery of dexamethasone attenuates prostate cancer bone metastatic tumor growth in vivo.</name><description>&lt;h4>Background&lt;/h4>The inflammatory tumor microenvironment, and more specifically the tumor-associated macrophages, plays an essential role in the development and progression of prostate cancer towards metastatic bone disease. Tumors are often characterized by a leaky vasculature, which - combined with the prolonged circulation kinetics of liposomes - leads to efficient tumor localization of these drug carriers, via the so-called enhanced permeability and retention (EPR) -effect. In this study, we evaluated the utility of targeted, liposomal drug delivery of the glucocorticoid dexamethasone in a model of prostate cancer bone metastases.&lt;h4>Methods&lt;/h4>Tumor-bearing Balb-c nu/nu mice were treated intravenously with 0.2-1.0-5.0 mg/kg/week free- and liposomal DEX for 3-4 weeks and tumor growt</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Jun</publication><modification>2026-03-16T15:57:56.242Z</modification><creation>2025-08-28T03:08:55.153Z</creation></dates><accession>S-EPMC5006873</accession><cross_references><pubmed>25663076</pubmed><doi>10.1002/pros.22963</doi></cross_references></HashMap>