<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Theodoraki MN</submitter><funding>Deutsche Forschungsgemeinschaft</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>NIH</funding><pagination>1747732</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7153843</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(1)</volume><pubmed_abstract>The molecular cargo of tumor-cell-derived exosomes (TEX) mimics that of parental tumor cells. Thus, TEX could potentially serve as noninvasive biomarkers of cancer progression. However, separation of TEX from non-TEX in patients' plasma requires tumor antigen-specific detection reagents. CD44v3 has been of interest as a potential biomarker of disease progression in HNSCC, because its overexpression in tumor cells associates with poor outcome. Here, CD44v3+ TEX immunocaptured from plasma of 44 HNSCC patients and 7 healthy donors (HDs) were evaluated as potential biomarkers of disease activity and stage. Exosomes were isolated from plasma of by size exclusion chromatography. Using anti-CD44v3 or anti-CD3 mAbs on beads, CD44v3+ TEX CD3(-)TEX-enriched exosomes were immunocaptured from supernat</pubmed_abstract><journal>Oncoimmunology</journal><pubmed_title>CD44v3 protein-carrying tumor-derived exosomes in HNSCC patients' plasma as potential noninvasive biomarkers of disease activity.</pubmed_title><pmcid>PMC7153843</pmcid><funding_grant_id>RO-1CA 168628</funding_grant_id><funding_grant_id>R01 CA168628</funding_grant_id><funding_grant_id>research fellowship # TH 2172/1-1</funding_grant_id><funding_grant_id>R21-C205644</funding_grant_id><pubmed_authors>Theodoraki MN</pubmed_authors><pubmed_authors>Whiteside TL</pubmed_authors><pubmed_authors>Matsumoto A</pubmed_authors><pubmed_authors>Hoffmann TK</pubmed_authors><pubmed_authors>Beccard I</pubmed_authors></additional><is_claimable>false</is_claimable><name>CD44v3 protein-carrying tumor-derived exosomes in HNSCC patients' plasma as potential noninvasive biomarkers of disease activity.</name><description>The molecular cargo of tumor-cell-derived exosomes (TEX) mimics that of parental tumor cells. Thus, TEX could potentially serve as noninvasive biomarkers of cancer progression. However, separation of TEX from non-TEX in patients' plasma requires tumor antigen-specific detection reagents. CD44v3 has been of interest as a potential biomarker of disease progression in HNSCC, because its overexpression in tumor cells associates with poor outcome. Here, CD44v3+ TEX immunocaptured from plasma of 44 HNSCC patients and 7 healthy donors (HDs) were evaluated as potential biomarkers of disease activity and stage. Exosomes were isolated from plasma of by size exclusion chromatography. Using anti-CD44v3 or anti-CD3 mAbs on beads, CD44v3+ TEX CD3(-)TEX-enriched exosomes were immunocaptured from supernat</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2025-04-22T08:39:49.507Z</modification><creation>2020-05-22T18:03:02Z</creation></dates><accession>S-EPMC7153843</accession><cross_references><pubmed>32313730</pubmed><doi>10.1080/2162402X.2020.1747732</doi></cross_references></HashMap>