<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>19(7)</volume><submitter>Raymond D</submitter><pubmed_abstract>With current imaging, discriminating tumor progression from treatment effect following immunotherapy or oncolytic virotherapy of glioblastoma (GBM) is challenging. A blood based diagnostic biomarker would therefore be helpful. Axl is a receptor tyrosine kinase that is highly expressed by many cancers including GBM. Axl expression is regulated through enzymatic cleavage of its extracellular domain. The resulting fragment can be detected in serum as soluble Axl (sAxl). sAxl levels can distinguish patients with melanoma, hepatocellular carcinoma, and pancreatic ductal adenocarcinoma from healthy controls. This is a pilot study to determine if sAxl is a candidate biomarker for GBM. The sAxl levels in the serum of 40 healthy volunteers and 20 GBM patients were determined using an enzyme-linked </pubmed_abstract><journal>PloS one</journal><pagination>e0301739</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11226040</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Evaluating soluble Axl as a biomarker for glioblastoma: A pilot study.</pubmed_title><pmcid>PMC11226040</pmcid><pubmed_authors>Zwernik S</pubmed_authors><pubmed_authors>Kassam A</pubmed_authors><pubmed_authors>Fukui M</pubmed_authors><pubmed_authors>Akhtar P</pubmed_authors><pubmed_authors>Raymond D</pubmed_authors><pubmed_authors>Rovin R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Evaluating soluble Axl as a biomarker for glioblastoma: A pilot study.</name><description>With current imaging, discriminating tumor progression from treatment effect following immunotherapy or oncolytic virotherapy of glioblastoma (GBM) is challenging. A blood based diagnostic biomarker would therefore be helpful. Axl is a receptor tyrosine kinase that is highly expressed by many cancers including GBM. Axl expression is regulated through enzymatic cleavage of its extracellular domain. The resulting fragment can be detected in serum as soluble Axl (sAxl). sAxl levels can distinguish patients with melanoma, hepatocellular carcinoma, and pancreatic ductal adenocarcinoma from healthy controls. This is a pilot study to determine if sAxl is a candidate biomarker for GBM. The sAxl levels in the serum of 40 healthy volunteers and 20 GBM patients were determined using an enzyme-linked </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2025-04-04T23:54:50.038Z</modification><creation>2025-04-04T23:54:50.038Z</creation></dates><accession>S-EPMC11226040</accession><cross_references><pubmed>38968207</pubmed><doi>10.1371/journal.pone.0301739</doi></cross_references></HashMap>