<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Romer TB</submitter><funding>Kræftens Bekæmpelse</funding><funding>University of Copenhagen | Det Sundhedsvidenskabelige Fakultet, Københavns Universitet</funding><funding>The NEYE Foundation</funding><funding>Lundbeck Foundation</funding><pagination>1239-1250</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8548315</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>125(9)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Novel immunotherapies targeting cancer-associated truncated O-glycans Tn (GalNAcα-Ser/Thr) and STn (Neu5Acα2-6GalNacα-Ser/Thr) are promising strategies for cancer treatment. However, no comprehensive, antibody-based mapping of truncated O-glycans in tumours exist to guide drug development.&lt;h4>Methods&lt;/h4>We used monoclonal antibodies to map the expression of truncated O-glycans in >700 tissue cores representing healthy and tumour tissues originating from breast, colon, lung, pancreas, skin, CNS and mesenchymal tissue. Patient-derived xenografts were used to evaluate Tn expression upon tumour engraftment.&lt;h4>Results&lt;/h4>The Tn-antigen was highly expressed in breast (57%, n = 64), colorectal (51%, n = 140) and pancreatic (53%, n = 108) tumours, while STn was mainly observe</pubmed_abstract><journal>British journal of cancer</journal><pubmed_title>Mapping of truncated O-glycans in cancers of epithelial and non-epithelial origin.</pubmed_title><pmcid>PMC8548315</pmcid><funding_grant_id>313-2019-869</funding_grant_id><pubmed_authors>Groen A</pubmed_authors><pubmed_authors>Schnabel J</pubmed_authors><pubmed_authors>Wandall HH</pubmed_authors><pubmed_authors>Pedersen JW</pubmed_authors><pubmed_authors>Dabelsteen S</pubmed_authors><pubmed_authors>Romer TB</pubmed_authors><pubmed_authors>Aasted MKM</pubmed_authors><pubmed_authors>Tan E</pubmed_authors><pubmed_authors>Haue AD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mapping of truncated O-glycans in cancers of epithelial and non-epithelial origin.</name><description>&lt;h4>Background&lt;/h4>Novel immunotherapies targeting cancer-associated truncated O-glycans Tn (GalNAcα-Ser/Thr) and STn (Neu5Acα2-6GalNacα-Ser/Thr) are promising strategies for cancer treatment. However, no comprehensive, antibody-based mapping of truncated O-glycans in tumours exist to guide drug development.&lt;h4>Methods&lt;/h4>We used monoclonal antibodies to map the expression of truncated O-glycans in >700 tissue cores representing healthy and tumour tissues originating from breast, colon, lung, pancreas, skin, CNS and mesenchymal tissue. Patient-derived xenografts were used to evaluate Tn expression upon tumour engraftment.&lt;h4>Results&lt;/h4>The Tn-antigen was highly expressed in breast (57%, n = 64), colorectal (51%, n = 140) and pancreatic (53%, n = 108) tumours, while STn was mainly observe</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2025-04-22T05:38:37.109Z</modification><creation>2025-04-05T21:26:25.784Z</creation></dates><accession>S-EPMC8548315</accession><cross_references><pubmed>34526666</pubmed><doi>10.1038/s41416-021-01530-7</doi></cross_references></HashMap>