<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22(9)</volume><submitter>Francis SM</submitter><pubmed_abstract>The high rates of recurrence and low median survival in many B-cell cancers highlight a need for new targeted therapeutic modalities. In dividing cells, eukaryotic translation initiation factor 5A (eIF5A) is hypusinated and involved in regulation of protein synthesis and proliferation, whereas the non-hypusinated form of eIF5A is a potent inducer of cell death in malignant cells. Here, we demonstrate the potential of modulating eIF5A expression as a novel approach to treating B-cell cancers. SNS01-T is a nonviral polyethylenimine-based nanoparticle, designed to induce apoptosis selectively in B-cell cancers by small interfering RNA-mediated suppression of hypusinated eIF5A and plasmid-based overexpression of a non-hypusinable eIF5A mutant. In this study, we show that SNS01-T is preferentia</pubmed_abstract><journal>Molecular therapy : the journal of the American Society of Gene Therapy</journal><pagination>1643-52</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4435495</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>SNS01-T modulation of eIF5A inhibits B-cell cancer progression and synergizes with bortezomib and lenalidomide.</pubmed_title><pmcid>PMC4435495</pmcid><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Dondero R</pubmed_authors><pubmed_authors>Thompson JE</pubmed_authors><pubmed_authors>Zheng Q</pubmed_authors><pubmed_authors>Tang T</pubmed_authors><pubmed_authors>Francis SM</pubmed_authors><pubmed_authors>Taylor CA</pubmed_authors></additional><is_claimable>false</is_claimable><name>SNS01-T modulation of eIF5A inhibits B-cell cancer progression and synergizes with bortezomib and lenalidomide.</name><description>The high rates of recurrence and low median survival in many B-cell cancers highlight a need for new targeted therapeutic modalities. In dividing cells, eukaryotic translation initiation factor 5A (eIF5A) is hypusinated and involved in regulation of protein synthesis and proliferation, whereas the non-hypusinated form of eIF5A is a potent inducer of cell death in malignant cells. Here, we demonstrate the potential of modulating eIF5A expression as a novel approach to treating B-cell cancers. SNS01-T is a nonviral polyethylenimine-based nanoparticle, designed to induce apoptosis selectively in B-cell cancers by small interfering RNA-mediated suppression of hypusinated eIF5A and plasmid-based overexpression of a non-hypusinable eIF5A mutant. In this study, we show that SNS01-T is preferentia</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Sep</publication><modification>2026-05-01T18:20:10.397Z</modification><creation>2019-03-27T01:51:47Z</creation></dates><accession>S-EPMC4435495</accession><cross_references><pubmed>24569836</pubmed><doi>10.1038/mt.2014.24</doi></cross_references></HashMap>