<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Campelo SN</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Irreversible electroporation (IRE) has been previously investigated in preclinical trials as a treatment for intracranial malignancies. Here, we investigate next generation high-frequency irreversible electroporation (H-FIRE), as both a monotherapy and a combinatorial therapy, for the treatment of malignant gliomas.&lt;h4>Methods&lt;/h4>Hydrogel tissue scaffolds and numerical modeling were used to inform &lt;i>in-vivo&lt;/i> H-FIRE pulsing parameters for our orthotopic tumor-bearing glioma model. Fischer rats were separated into five treatment cohorts including high-dose H-FIRE (1750V/cm), low-dose H-FIRE (600V/cm), combinatorial high-dose H-FIRE + liposomal doxorubicin, low-dose H-FIRE + liposomal doxorubicin, and standalone liposomal doxorubicin groups. Cohorts were compared again</pubmed_abstract><journal>Frontiers in oncology</journal><pagination>1171278</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10196182</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>High-frequency irreversible electroporation improves survival and immune cell infiltration in rodents with malignant gliomas.</pubmed_title><pmcid>PMC10196182</pmcid><pubmed_authors>Garcia J</pubmed_authors><pubmed_authors>Thomas SC</pubmed_authors><pubmed_authors>Saunier S</pubmed_authors><pubmed_authors>Verbridge SS</pubmed_authors><pubmed_authors>Rossmeisl JH</pubmed_authors><pubmed_authors>Lorenzo MF</pubmed_authors><pubmed_authors>Partridge B</pubmed_authors><pubmed_authors>Campelo SN</pubmed_authors><pubmed_authors>Hinckley J</pubmed_authors><pubmed_authors>Alinezhadbalalami N</pubmed_authors><pubmed_authors>Kani Y</pubmed_authors><pubmed_authors>Davalos RV</pubmed_authors></additional><is_claimable>false</is_claimable><name>High-frequency irreversible electroporation improves survival and immune cell infiltration in rodents with malignant gliomas.</name><description>&lt;h4>Background&lt;/h4>Irreversible electroporation (IRE) has been previously investigated in preclinical trials as a treatment for intracranial malignancies. Here, we investigate next generation high-frequency irreversible electroporation (H-FIRE), as both a monotherapy and a combinatorial therapy, for the treatment of malignant gliomas.&lt;h4>Methods&lt;/h4>Hydrogel tissue scaffolds and numerical modeling were used to inform &lt;i>in-vivo&lt;/i> H-FIRE pulsing parameters for our orthotopic tumor-bearing glioma model. Fischer rats were separated into five treatment cohorts including high-dose H-FIRE (1750V/cm), low-dose H-FIRE (600V/cm), combinatorial high-dose H-FIRE + liposomal doxorubicin, low-dose H-FIRE + liposomal doxorubicin, and standalone liposomal doxorubicin groups. Cohorts were compared again</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-26T21:25:44.165Z</modification><creation>2025-04-06T16:50:19.241Z</creation></dates><accession>S-EPMC10196182</accession><cross_references><pubmed>37213298</pubmed><doi>10.3389/fonc.2023.1171278</doi></cross_references></HashMap>