<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Houweling M</submitter><funding>Brain Tumour Charity</funding><funding>The Brain Tumour Charity</funding><funding>KWF Kankerbestrijding</funding><pagination>297-305</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11798055</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>149(1)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Glioblastoma (GBM) is an incurable cancer type. New therapeutic options are investigated, including targeting the mitogen-activated protein kinase (MAPK) pathway using MEK inhibitors as radio-sensitizers. In this study, we investigated whether MEK inhibition via PD0325901 leads to radio-sensitization in experimental in vitro and in vivo models of GBM.&lt;h4>Materials and methods&lt;/h4>In vitro, GBM8 multicellular spheroids were irradiated with 3 fractions of 2 Gy, during 5 consecutive days of incubation with either PD0325901 or MEK-162. In vivo, we combined PD0325901 with radiotherapy in the GBM8 orthotopic mouse model, tumor growth was measured weekly by bioluminescence imaging and overall survival and toxicity were assessed.&lt;h4>Results&lt;/h4>Regrowth and viability of sphero</pubmed_abstract><journal>Journal of cancer research and clinical oncology</journal><pubmed_title>Radio-sensitizing effect of MEK inhibition in glioblastoma in vitro and in vivo.</pubmed_title><pmcid>PMC11798055</pmcid><funding_grant_id>488097</funding_grant_id><funding_grant_id>KWF 4874</funding_grant_id><funding_grant_id>GN-000429</funding_grant_id><funding_grant_id>11038</funding_grant_id><pubmed_authors>Heukelom S</pubmed_authors><pubmed_authors>Westerman BA</pubmed_authors><pubmed_authors>Wurdinger T</pubmed_authors><pubmed_authors>Noske D</pubmed_authors><pubmed_authors>Houweling M</pubmed_authors><pubmed_authors>Verheul H</pubmed_authors><pubmed_authors>Abdul UK</pubmed_authors><pubmed_authors>Lagerweij T</pubmed_authors><pubmed_authors>Brahm C</pubmed_authors><pubmed_authors>Koken PW</pubmed_authors><pubmed_authors>Sminia P</pubmed_authors><pubmed_authors>Honeywell R</pubmed_authors><pubmed_authors>Peters GJ</pubmed_authors><pubmed_authors>Wedekind LE</pubmed_authors></additional><is_claimable>false</is_claimable><name>Radio-sensitizing effect of MEK inhibition in glioblastoma in vitro and in vivo.</name><description>&lt;h4>Introduction&lt;/h4>Glioblastoma (GBM) is an incurable cancer type. New therapeutic options are investigated, including targeting the mitogen-activated protein kinase (MAPK) pathway using MEK inhibitors as radio-sensitizers. In this study, we investigated whether MEK inhibition via PD0325901 leads to radio-sensitization in experimental in vitro and in vivo models of GBM.&lt;h4>Materials and methods&lt;/h4>In vitro, GBM8 multicellular spheroids were irradiated with 3 fractions of 2 Gy, during 5 consecutive days of incubation with either PD0325901 or MEK-162. In vivo, we combined PD0325901 with radiotherapy in the GBM8 orthotopic mouse model, tumor growth was measured weekly by bioluminescence imaging and overall survival and toxicity were assessed.&lt;h4>Results&lt;/h4>Regrowth and viability of sphero</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2026-03-27T15:50:09.482Z</modification><creation>2025-08-27T03:06:40.443Z</creation></dates><accession>S-EPMC11798055</accession><cross_references><pubmed>36451044</pubmed><doi>10.1007/s00432-022-04483-3</doi></cross_references></HashMap>