<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang L</submitter><funding>National Natural Science Foundation of China</funding><pagination>26538-26548</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9083100</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(47)</volume><pubmed_abstract>Exposure to nanoparticles may lead to pneumoconiosis and lung cancer; however, whether patients suffering from pneumoconiosis also face a high risk of lung cancer has been under debate for decades. Recently, exosomes have been found to play critical roles in many diseases &lt;i>via&lt;/i> intercellular cargo transportation, which has provided a new insight into the mechanistic investigation of nanoparticle-induced respiratory disorders. Herein, we isolated exosomes from the venous blood of patients with pneumoconiosis and healthy controls and then, we profiled the expression signatures of exosomal miRNAs using high-throughput sequencing technology. A total of 14 aberrantly expressed miRNAs were identified and used to process target gene prediction and functional annotation. Specially, miR-125a a</pubmed_abstract><journal>RSC advances</journal><pubmed_title>Up-regulation of exosomal miR-125a in pneumoconiosis inhibits lung cancer development by suppressing expressions of EZH2 and hnRNPK.</pubmed_title><pmcid>PMC9083100</pmcid><funding_grant_id>81773404</funding_grant_id><funding_grant_id>81273039</funding_grant_id><funding_grant_id>81472954</funding_grant_id><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Guo W</pubmed_authors><pubmed_authors>Wang D</pubmed_authors><pubmed_authors>Duan S</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Hao C</pubmed_authors><pubmed_authors>Yao W</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Up-regulation of exosomal miR-125a in pneumoconiosis inhibits lung cancer development by suppressing expressions of EZH2 and hnRNPK.</name><description>Exposure to nanoparticles may lead to pneumoconiosis and lung cancer; however, whether patients suffering from pneumoconiosis also face a high risk of lung cancer has been under debate for decades. Recently, exosomes have been found to play critical roles in many diseases &lt;i>via&lt;/i> intercellular cargo transportation, which has provided a new insight into the mechanistic investigation of nanoparticle-induced respiratory disorders. Herein, we isolated exosomes from the venous blood of patients with pneumoconiosis and healthy controls and then, we profiled the expression signatures of exosomal miRNAs using high-throughput sequencing technology. A total of 14 aberrantly expressed miRNAs were identified and used to process target gene prediction and functional annotation. Specially, miR-125a a</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jul</publication><modification>2026-05-30T20:53:43.35Z</modification><creation>2025-04-04T10:01:41.701Z</creation></dates><accession>S-EPMC9083100</accession><cross_references><pubmed>35541090</pubmed><doi>10.1039/c8ra03081b</doi></cross_references></HashMap>