<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shah VM</submitter><funding>Brenden-Colson Center for Pancreatic Care</funding><funding>Brenden-Colson Center Foundation and Oregon State University College of Pharmacy</funding><funding>NCI NIH HHS</funding><pagination>2651</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10747591</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(12)</volume><pubmed_abstract>Pancreatic cancer remains a formidable challenge due to limited treatment options and its aggressive nature. In recent years, the naturally occurring anticancer compound juglone has emerged as a potential therapeutic candidate, showing promising results in inhibiting tumor growth and inducing cancer cell apoptosis. However, concerns over its toxicity have hampered juglone's clinical application. To address this issue, we have explored the use of polymeric micelles as a delivery system for juglone in pancreatic cancer treatment. These micelles, formulated using Poloxamer 407 and D-α-Tocopherol polyethylene glycol 1000 succinate, offer an innovative solution to enhance juglone's therapeutic potential while minimizing toxicity. In-vitro studies have demonstrated that micelle-formulated juglon</pubmed_abstract><journal>Pharmaceutics</journal><pubmed_title>Micelle-Formulated Juglone Effectively Targets Pancreatic Cancer and Remodels the Tumor Microenvironment.</pubmed_title><pmcid>PMC10747591</pmcid><funding_grant_id>P30 CA069533</funding_grant_id><funding_grant_id>U01 CA224012</funding_grant_id><funding_grant_id>U01CA224012</funding_grant_id><funding_grant_id>DoD PA210068</funding_grant_id><funding_grant_id>R01 CA186241</funding_grant_id><pubmed_authors>Brody JR</pubmed_authors><pubmed_authors>Pelz C</pubmed_authors><pubmed_authors>Al-Fatease A</pubmed_authors><pubmed_authors>Smith A</pubmed_authors><pubmed_authors>Tsuda M</pubmed_authors><pubmed_authors>MacPherson K</pubmed_authors><pubmed_authors>Chin K</pubmed_authors><pubmed_authors>Yardimci GG</pubmed_authors><pubmed_authors>Krieger M</pubmed_authors><pubmed_authors>Sheppard BC</pubmed_authors><pubmed_authors>Daniel CJ</pubmed_authors><pubmed_authors>Rizvi S</pubmed_authors><pubmed_authors>Alani AW</pubmed_authors><pubmed_authors>Eng J</pubmed_authors><pubmed_authors>Shah VM</pubmed_authors><pubmed_authors>Sears RC</pubmed_authors><pubmed_authors>Langer EM</pubmed_authors><pubmed_authors>Munks MW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Micelle-Formulated Juglone Effectively Targets Pancreatic Cancer and Remodels the Tumor Microenvironment.</name><description>Pancreatic cancer remains a formidable challenge due to limited treatment options and its aggressive nature. In recent years, the naturally occurring anticancer compound juglone has emerged as a potential therapeutic candidate, showing promising results in inhibiting tumor growth and inducing cancer cell apoptosis. However, concerns over its toxicity have hampered juglone's clinical application. To address this issue, we have explored the use of polymeric micelles as a delivery system for juglone in pancreatic cancer treatment. These micelles, formulated using Poloxamer 407 and D-α-Tocopherol polyethylene glycol 1000 succinate, offer an innovative solution to enhance juglone's therapeutic potential while minimizing toxicity. In-vitro studies have demonstrated that micelle-formulated juglon</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2026-04-08T14:46:27.693Z</modification><creation>2025-04-19T14:34:24.943Z</creation></dates><accession>S-EPMC10747591</accession><cross_references><pubmed>38139993</pubmed><doi>10.3390/pharmaceutics15122651</doi></cross_references></HashMap>