<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Moran J</submitter><funding>MSc Translational Oncology</funding><funding>Deans Research Initiative Award</funding><funding>Trinity College Dublin</funding><pagination>360</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9959685</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(2)</volume><pubmed_abstract>Glioblastoma multiforme (GBM) is the most common adult primary brain malignancy, with dismal survival rates of ~14.6 months. The current standard-of-care consists of surgical resection and chemoradiotherapy, however the treatment response is limited by factors such as tumour heterogeneity, treatment resistance, the blood-brain barrier, and immunosuppression. Several immunotherapies have undergone clinical development for GBM but demonstrated inadequate efficacy, yet future combinatorial approaches are likely to hold more promise. Olaparib is FDA-approved for BRCA-mutated advanced ovarian and breast cancer, and clinical studies have revealed its utility as a safe and efficacious radio- and chemo-sensitiser in GBM. The ability of Olaparib to enhance natural killer (NK) cell-mediated response</pubmed_abstract><journal>Pharmaceutics</journal><pubmed_title>Investigating the Effects of Olaparib on the Susceptibility of Glioblastoma Multiforme Tumour Cells to Natural Killer Cell-Mediated Responses.</pubmed_title><pmcid>PMC9959685</pmcid><funding_grant_id>N/A</funding_grant_id><pubmed_authors>Dev KK</pubmed_authors><pubmed_authors>Marion C</pubmed_authors><pubmed_authors>Conroy MJ</pubmed_authors><pubmed_authors>Keenan E</pubmed_authors><pubmed_authors>O'Sullivan J</pubmed_authors><pubmed_authors>Kane LE</pubmed_authors><pubmed_authors>Moran J</pubmed_authors><pubmed_authors>Mylod E</pubmed_authors><pubmed_authors>Mekhaeil M</pubmed_authors><pubmed_authors>Lysaght J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Investigating the Effects of Olaparib on the Susceptibility of Glioblastoma Multiforme Tumour Cells to Natural Killer Cell-Mediated Responses.</name><description>Glioblastoma multiforme (GBM) is the most common adult primary brain malignancy, with dismal survival rates of ~14.6 months. The current standard-of-care consists of surgical resection and chemoradiotherapy, however the treatment response is limited by factors such as tumour heterogeneity, treatment resistance, the blood-brain barrier, and immunosuppression. Several immunotherapies have undergone clinical development for GBM but demonstrated inadequate efficacy, yet future combinatorial approaches are likely to hold more promise. Olaparib is FDA-approved for BRCA-mutated advanced ovarian and breast cancer, and clinical studies have revealed its utility as a safe and efficacious radio- and chemo-sensitiser in GBM. The ability of Olaparib to enhance natural killer (NK) cell-mediated response</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2026-04-08T14:36:30.091Z</modification><creation>2024-11-20T08:07:05.855Z</creation></dates><accession>S-EPMC9959685</accession><cross_references><pubmed>36839682</pubmed><doi>10.3390/pharmaceutics15020360</doi></cross_references></HashMap>