<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Choi WS</submitter><funding>Terry Fox Research Institute Prairie Cancer Research Consortium</funding><funding>Canadian Institutes of Health Research</funding><funding>CIHR</funding><pagination>3072-3086</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12916726</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(12)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Glioblastoma (GBM) is a deadly brain cancer with a dismal prognosis. There is evidence that infiltration and therapy resistance in GBM are driven by tumor microtubes (TMs), ultra-long membrane-enclosed protrusions that serve as intercellular communication channels. The aims of this study were to investigate the role of TMs and identify the molecular drivers involved in TM formation.&lt;h4>Methods&lt;/h4>We used patient-derived GBM neurosphere cultures that produce TMs to investigate TM dynamics, the proteins and pathways involved in TM formation, and the effect of targeting brain fatty acid-binding protein (FABP7) on mouse survival using an orthotopic model of GBM.&lt;h4>Results&lt;/h4>The radial glial cell marker, FABP7, is highly expressed in TMs. Like GAP43, FABP7 is critically i</pubmed_abstract><journal>Neuro-oncology</journal><pubmed_title>Glioblastoma tumor microtubes and brain fatty acid-binding protein: Path to directional infiltration.</pubmed_title><pmcid>PMC12916726</pmcid><funding_grant_id>190313</funding_grant_id><pubmed_authors>Yasmin L</pubmed_authors><pubmed_authors>Au K</pubmed_authors><pubmed_authors>Godbout R</pubmed_authors><pubmed_authors>Bukhari AB</pubmed_authors><pubmed_authors>Jeon P</pubmed_authors><pubmed_authors>Larocque MP</pubmed_authors><pubmed_authors>Peyton S</pubmed_authors><pubmed_authors>Garg M</pubmed_authors><pubmed_authors>Glubrecht DD</pubmed_authors><pubmed_authors>Sun X</pubmed_authors><pubmed_authors>van Landeghem FKH</pubmed_authors><pubmed_authors>Mak C</pubmed_authors><pubmed_authors>Goping IS</pubmed_authors><pubmed_authors>Githaka JM</pubmed_authors><pubmed_authors>Choi WS</pubmed_authors><pubmed_authors>McGinn D</pubmed_authors><pubmed_authors>Xu X</pubmed_authors><pubmed_authors>Liu RZ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Glioblastoma tumor microtubes and brain fatty acid-binding protein: Path to directional infiltration.</name><description>&lt;h4>Background&lt;/h4>Glioblastoma (GBM) is a deadly brain cancer with a dismal prognosis. There is evidence that infiltration and therapy resistance in GBM are driven by tumor microtubes (TMs), ultra-long membrane-enclosed protrusions that serve as intercellular communication channels. The aims of this study were to investigate the role of TMs and identify the molecular drivers involved in TM formation.&lt;h4>Methods&lt;/h4>We used patient-derived GBM neurosphere cultures that produce TMs to investigate TM dynamics, the proteins and pathways involved in TM formation, and the effect of targeting brain fatty acid-binding protein (FABP7) on mouse survival using an orthotopic model of GBM.&lt;h4>Results&lt;/h4>The radial glial cell marker, FABP7, is highly expressed in TMs. Like GAP43, FABP7 is critically i</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-07-16T10:07:42.623Z</modification><creation>2026-07-09T10:49:03.006Z</creation></dates><accession>S-EPMC12916726</accession><cross_references><pubmed>40891350</pubmed><doi>10.1093/neuonc/noaf200</doi></cross_references></HashMap>