<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Podolski-Renic A</submitter><funding>Science Fund of the Republic of Serbia</funding><pagination>189</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11859366</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(2)</volume><pubmed_abstract>&lt;b>Background/Objectives&lt;/b>: This study explores the potential of LB-100 (a protein phosphatase 2A-PP2A inhibitor) combined with adavosertib (a WEE1 kinase inhibitor) and doxorubicin (DOX), to overcome multidrug resistance (MDR) in cancer cells and enhance treatment efficacy. &lt;b>Methods&lt;/b>: We evaluated LB-100 combinations with adavosertib and DOX in patient-derived glioblastoma and non-small cell lung carcinoma cells (NSCLCs) using a real-time cell analyzer. Effectiveness was also assessed through immunofluorescence assay, and interactions were analyzed via SynergyFinder+. We also examined P-glycoprotein (P-gp) expression and drug resistance genes' expression in MDR glioblastoma and NSCLCs after LB-100 treatment, as well as LB-100 sensitizing effect on DOX and DOX accumulation. &lt;b>Resul</pubmed_abstract><journal>Pharmaceutics</journal><pubmed_title>LB-100 Enhances Drugs Efficacy Through Inhibition of P-Glycoprotein Expression in Multidrug-Resistant Glioblastoma and Non-Small Cell Lung Carcinoma Cellular Models.</pubmed_title><pmcid>PMC11859366</pmcid><funding_grant_id>#7739737</funding_grant_id><pubmed_authors>Podolski-Renic A</pubmed_authors><pubmed_authors>Jovanovic Stojanov S</pubmed_authors><pubmed_authors>Grozdanic M</pubmed_authors><pubmed_authors>Pesic M</pubmed_authors><pubmed_authors>Dragoj M</pubmed_authors><pubmed_authors>Lupsic E</pubmed_authors><pubmed_authors>Nikolic I</pubmed_authors><pubmed_authors>Dinic J</pubmed_authors><pubmed_authors>Chigriai M</pubmed_authors></additional><is_claimable>false</is_claimable><name>LB-100 Enhances Drugs Efficacy Through Inhibition of P-Glycoprotein Expression in Multidrug-Resistant Glioblastoma and Non-Small Cell Lung Carcinoma Cellular Models.</name><description>&lt;b>Background/Objectives&lt;/b>: This study explores the potential of LB-100 (a protein phosphatase 2A-PP2A inhibitor) combined with adavosertib (a WEE1 kinase inhibitor) and doxorubicin (DOX), to overcome multidrug resistance (MDR) in cancer cells and enhance treatment efficacy. &lt;b>Methods&lt;/b>: We evaluated LB-100 combinations with adavosertib and DOX in patient-derived glioblastoma and non-small cell lung carcinoma cells (NSCLCs) using a real-time cell analyzer. Effectiveness was also assessed through immunofluorescence assay, and interactions were analyzed via SynergyFinder+. We also examined P-glycoprotein (P-gp) expression and drug resistance genes' expression in MDR glioblastoma and NSCLCs after LB-100 treatment, as well as LB-100 sensitizing effect on DOX and DOX accumulation. &lt;b>Resul</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2025-04-22T18:57:50.951Z</modification><creation>2025-04-06T02:38:05.428Z</creation></dates><accession>S-EPMC11859366</accession><cross_references><pubmed>40006556</pubmed><doi>10.3390/pharmaceutics17020189</doi></cross_references></HashMap>