{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Colangelo T"],"funding":["Associazione Italiana per la Ricerca sul Cancro","Italian Ministry of Health","Worldwide Cancer Research","Fondazione Pezcoller","Fondazione Umberto Veronesi"],"pagination":["226"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9773489"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["21(1)"],"pubmed_abstract":["T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive T-cell malignancy characterized by genotypically-defined and phenotypically divergent cell populations, governed by adaptive landscapes. Clonal expansions are associated to genetic and epigenetic events, and modulation of external stimuli that affect the hierarchical structure of subclones and support the dynamics of leukemic subsets. Recently, small extracellular vesicles (sEV) such as exosomes were also shown to play a role in leukemia. Here, by coupling miRNome, bulk and single cell transcriptome profiling, we found that T-ALL-secreted sEV contain NOTCH1-dependent microRNAs (EV-miRs), which control oncogenic pathways acting as autocrine stimuli and ultimately promoting the expansion/survival of highly proliferative cell subset"],"journal":["Molecular cancer"],"pubmed_title":["Extracellular vesicle microRNAs contribute to Notch signaling pathway in T-cell acute lymphoblastic leukemia."],"pmcid":["PMC9773489"],"funding_grant_id":["GR-2016-02363975","GR-2019-12370460","#19548","20-0318","IG-23070","IG-22827","#21010","GR-2016-02361287"],"pubmed_authors":["Tamiro F","Cuttano R","Rossi G","Panelli P","Bianchi F","Colangelo T","Giambra V","Palumbo O","Mazzarelli F","De Santis E","Melocchi V"],"additional_accession":[]},"is_claimable":false,"name":"Extracellular vesicle microRNAs contribute to Notch signaling pathway in T-cell acute lymphoblastic leukemia.","description":"T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive T-cell malignancy characterized by genotypically-defined and phenotypically divergent cell populations, governed by adaptive landscapes. Clonal expansions are associated to genetic and epigenetic events, and modulation of external stimuli that affect the hierarchical structure of subclones and support the dynamics of leukemic subsets. Recently, small extracellular vesicles (sEV) such as exosomes were also shown to play a role in leukemia. Here, by coupling miRNome, bulk and single cell transcriptome profiling, we found that T-ALL-secreted sEV contain NOTCH1-dependent microRNAs (EV-miRs), which control oncogenic pathways acting as autocrine stimuli and ultimately promoting the expansion/survival of highly proliferative cell subset","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Dec","modification":"2026-05-28T21:28:20.135Z","creation":"2025-02-19T03:24:42.891Z"},"accession":"S-EPMC9773489","cross_references":{"pubmed":["36550553"],"doi":["10.1186/s12943-022-01698-3"]}}