<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ryniawec JM</submitter><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><pagination>676</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8946944</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(3)</volume><pubmed_abstract>The microenvironment of solid tumors is dynamic and frequently contains pockets of low oxygen levels (hypoxia) surrounded by oxygenated tissue. Indeed, a compromised vasculature is a hallmark of the tumor microenvironment, creating both spatial gradients and temporal variability in oxygen availability. Notably, hypoxia associates with increased metastasis and poor survival in patients. Therefore, to aid therapeutic decisions and better understand hypoxia's role in cancer progression, it is critical to identify endogenous biomarkers of hypoxia to spatially phenotype oncogenic lesions in human tissue, whether precancerous, benign, or malignant. Here, we characterize the glucose transporter GLUT3/SLC2A3 as a biomarker of hypoxic prostate epithelial cells and prostate tumors. Transcriptomic an</pubmed_abstract><journal>Diagnostics (Basel, Switzerland)</journal><pubmed_title>GLUT3/SLC2A3 Is an Endogenous Marker of Hypoxia in Prostate Cancer Cell Lines and Patient-Derived Xenograft Tumors.</pubmed_title><pmcid>PMC8946944</pmcid><funding_grant_id>R01CA242226, P30 CA23074</funding_grant_id><funding_grant_id>R01 CA242226</funding_grant_id><pubmed_authors>Loertscher E</pubmed_authors><pubmed_authors>de Oliveira Pessoa D</pubmed_authors><pubmed_authors>Rogers GC</pubmed_authors><pubmed_authors>Warfel NA</pubmed_authors><pubmed_authors>Coope MR</pubmed_authors><pubmed_authors>Ryniawec JM</pubmed_authors><pubmed_authors>Cress AE</pubmed_authors><pubmed_authors>Padi M</pubmed_authors><pubmed_authors>Bageerathan V</pubmed_authors></additional><is_claimable>false</is_claimable><name>GLUT3/SLC2A3 Is an Endogenous Marker of Hypoxia in Prostate Cancer Cell Lines and Patient-Derived Xenograft Tumors.</name><description>The microenvironment of solid tumors is dynamic and frequently contains pockets of low oxygen levels (hypoxia) surrounded by oxygenated tissue. Indeed, a compromised vasculature is a hallmark of the tumor microenvironment, creating both spatial gradients and temporal variability in oxygen availability. Notably, hypoxia associates with increased metastasis and poor survival in patients. Therefore, to aid therapeutic decisions and better understand hypoxia's role in cancer progression, it is critical to identify endogenous biomarkers of hypoxia to spatially phenotype oncogenic lesions in human tissue, whether precancerous, benign, or malignant. Here, we characterize the glucose transporter GLUT3/SLC2A3 as a biomarker of hypoxic prostate epithelial cells and prostate tumors. Transcriptomic an</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2026-04-08T17:46:30.439Z</modification><creation>2025-02-19T01:53:23.604Z</creation></dates><accession>S-EPMC8946944</accession><cross_references><pubmed>35328229</pubmed><doi>10.3390/diagnostics12030676</doi></cross_references></HashMap>