<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>24(12)</volume><submitter>Chen X</submitter><pubmed_abstract>Nasopharyngeal carcinoma (NPC) represents a malignant tumor linked to Epstein-Barr virus (EBV) that is characterized by distinctive, clinically relevant biological features. As protein N-glycosylation plays critical roles in cancer progression, we applied quantitative glycoproteomics to characterize NPC-specific glycosylation patterns. Using label-free proteomics and intact N-glycoproteomics, we analyzed 17 NPC tissues and 7 normal mucosal epithelia. Integrated analysis with PET/CT imaging and bioinformatics revealed correlations among differentially expressed glycoproteins, glycosyltransferases, and immunophenotypes. Functional validation demonstrated that MANEA, an enzyme linked to high-mannose glycosylation, influences NPC cell proliferation and migration. Furthermore, MANEA likely modu</pubmed_abstract><journal>Journal of proteome research</journal><pagination>6272-6284</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12687360</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Proteomics Combined with N-Glycoproteomics to Explore the Pathogenesis of Nasopharyngeal Carcinoma.</pubmed_title><pmcid>PMC12687360</pmcid><pubmed_authors>Lin Q</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Ling H</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Zhou Y</pubmed_authors><pubmed_authors>Wu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Proteomics Combined with N-Glycoproteomics to Explore the Pathogenesis of Nasopharyngeal Carcinoma.</name><description>Nasopharyngeal carcinoma (NPC) represents a malignant tumor linked to Epstein-Barr virus (EBV) that is characterized by distinctive, clinically relevant biological features. As protein N-glycosylation plays critical roles in cancer progression, we applied quantitative glycoproteomics to characterize NPC-specific glycosylation patterns. Using label-free proteomics and intact N-glycoproteomics, we analyzed 17 NPC tissues and 7 normal mucosal epithelia. Integrated analysis with PET/CT imaging and bioinformatics revealed correlations among differentially expressed glycoproteins, glycosyltransferases, and immunophenotypes. Functional validation demonstrated that MANEA, an enzyme linked to high-mannose glycosylation, influences NPC cell proliferation and migration. Furthermore, MANEA likely modu</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-05T23:43:20.676Z</modification><creation>2026-05-23T03:13:36.987Z</creation></dates><accession>S-EPMC12687360</accession><cross_references><pubmed>41269767</pubmed><doi>10.1021/acs.jproteome.5c00793</doi></cross_references></HashMap>