<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>29(1)</volume><submitter>Xue P</submitter><pubmed_abstract>Exosomal microRNAs (miRNAs) have been implicated in the development and progression of a variety of tumors; however, whether they contribute to medulloblastoma (MB) tumorigenesis remains to be elucidated. To address this, we first characterized the miRNA profiles of circulating exosomes by miRNA sequencing to identify miRNAs differentially expressed between children with MB and healthy controls. Then, we conducted in vitro and in vivo functional assays with the identified miRNAs and their predicted targets. We found that, compared with healthy controls, 35 miRNAs were upregulated and 5 downregulated in exosomes isolated from the plasma of MB patients. We further found that the expression of miR-101-3p and miR-423-5p was significantly higher in plasma exosomes from MB patients than in healt</pubmed_abstract><journal>Cell death and differentiation</journal><pagination>82-95</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8738741</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Exosomal miR-101-3p and miR-423-5p inhibit medulloblastoma tumorigenesis through targeting FOXP4 and EZH2.</pubmed_title><pmcid>PMC8738741</pmcid><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Huang S</pubmed_authors><pubmed_authors>Yang L</pubmed_authors><pubmed_authors>Xue P</pubmed_authors><pubmed_authors>Fu J</pubmed_authors><pubmed_authors>Han X</pubmed_authors><pubmed_authors>Xiao W</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Zhou Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Exosomal miR-101-3p and miR-423-5p inhibit medulloblastoma tumorigenesis through targeting FOXP4 and EZH2.</name><description>Exosomal microRNAs (miRNAs) have been implicated in the development and progression of a variety of tumors; however, whether they contribute to medulloblastoma (MB) tumorigenesis remains to be elucidated. To address this, we first characterized the miRNA profiles of circulating exosomes by miRNA sequencing to identify miRNAs differentially expressed between children with MB and healthy controls. Then, we conducted in vitro and in vivo functional assays with the identified miRNAs and their predicted targets. We found that, compared with healthy controls, 35 miRNAs were upregulated and 5 downregulated in exosomes isolated from the plasma of MB patients. We further found that the expression of miR-101-3p and miR-423-5p was significantly higher in plasma exosomes from MB patients than in healt</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2026-06-06T22:11:59.558Z</modification><creation>2025-04-19T18:09:52.561Z</creation></dates><accession>S-EPMC8738741</accession><cross_references><pubmed>34294888</pubmed><doi>10.1038/s41418-021-00838-4</doi></cross_references></HashMap>