{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Jun Y"],"funding":["SNUBH Research Fund","Korea Health Industry Development Institute","Korea government","Korean Health Industry Development Institute","National Research Foundation of Korea"],"pagination":["543-555"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9359730"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["82(4)"],"pubmed_abstract":["Alternatively spliced RNA isoforms are a hallmark of tumors, but their nature, prevalence, and clinical implications in gastric cancer have not been comprehensively characterized. We systematically profiled the splicing landscape of 83 gastric tumors and matched normal mucosa, identifying and experimentally validating eight splicing events that can classify all gastric cancers into three subtypes: epithelial-splicing (EpiS), mesenchymal-splicing (MesS), and hybrid-splicing. These subtypes were associated with distinct molecular signatures and epithelial-mesenchymal transition markers. Subtype-specific splicing events were enriched in motifs for splicing factors RBM24 and ESRP1, which were upregulated in MesS and EpiS tumors, respectively. A simple classifier based only on RNA levels of RBM"],"journal":["Cancer research"],"pubmed_title":["Comprehensive Analysis of Alternative Splicing in Gastric Cancer Identifies Epithelial-Mesenchymal Transition Subtypes Associated with Survival."],"pmcid":["PMC9359730"],"funding_grant_id":["NRF-2020R1C1C1009225","HI13C2148","NRF-2015K1A4A3047851","HI14C1277","13-2021-0015"],"pubmed_authors":["Lee S","Lee C","Lee WP","Jun Y","Kim JI","Suh YS","Lee J","Anczukow O","Yang HK","Park S"],"additional_accession":[]},"is_claimable":false,"name":"Comprehensive Analysis of Alternative Splicing in Gastric Cancer Identifies Epithelial-Mesenchymal Transition Subtypes Associated with Survival.","description":"Alternatively spliced RNA isoforms are a hallmark of tumors, but their nature, prevalence, and clinical implications in gastric cancer have not been comprehensively characterized. We systematically profiled the splicing landscape of 83 gastric tumors and matched normal mucosa, identifying and experimentally validating eight splicing events that can classify all gastric cancers into three subtypes: epithelial-splicing (EpiS), mesenchymal-splicing (MesS), and hybrid-splicing. These subtypes were associated with distinct molecular signatures and epithelial-mesenchymal transition markers. Subtype-specific splicing events were enriched in motifs for splicing factors RBM24 and ESRP1, which were upregulated in MesS and EpiS tumors, respectively. A simple classifier based only on RNA levels of RBM","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Feb","modification":"2026-07-14T16:59:25.666Z","creation":"2025-04-04T21:03:49.626Z"},"accession":"S-EPMC9359730","cross_references":{"pubmed":["34903603"],"doi":["10.1158/0008-5472.CAN-21-2117"]}}