<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu A</submitter><funding>Shenzhen Second People’s Hospital</funding><pagination>487-500</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9367658</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(1)</volume><pubmed_abstract>White adipose tissue wasting plays a critical role in the development and progression of cancer cachexia. However, the mechanism behind the loss of adipose tissue remains ill-defined. In this study, we found that cancer cell-derived exosomes highly expressed miR-425-3p. Administration of cancer cell-derived exosomes significantly inhibited proliferation and differentiation of human preadipocytes-viscereal (HPA-v) cells. In mature adipocytes, cancer cell-derived exosomes activated cAMP/PKA signalling and lipophagy, leading to adipocyte lipolysis and browning of white adipocytes. These exosomes-induced alterations were almost abolished by endocytosis inhibitor cytochalasin D (CytoD) and antagomiR-425-3p, or reproduced by miR-425-3p mimics. In addition, bioinformatics analysis and luciferase </pubmed_abstract><journal>Adipocyte</journal><pubmed_title>Cancer cell-derived exosomal miR-425-3p induces white adipocyte atrophy.</pubmed_title><pmcid>PMC9367658</pmcid><funding_grant_id>2019060014</funding_grant_id><pubmed_authors>Pan W</pubmed_authors><pubmed_authors>Zhuang S</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Liu A</pubmed_authors><pubmed_authors>Tang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cancer cell-derived exosomal miR-425-3p induces white adipocyte atrophy.</name><description>White adipose tissue wasting plays a critical role in the development and progression of cancer cachexia. However, the mechanism behind the loss of adipose tissue remains ill-defined. In this study, we found that cancer cell-derived exosomes highly expressed miR-425-3p. Administration of cancer cell-derived exosomes significantly inhibited proliferation and differentiation of human preadipocytes-viscereal (HPA-v) cells. In mature adipocytes, cancer cell-derived exosomes activated cAMP/PKA signalling and lipophagy, leading to adipocyte lipolysis and browning of white adipocytes. These exosomes-induced alterations were almost abolished by endocytosis inhibitor cytochalasin D (CytoD) and antagomiR-425-3p, or reproduced by miR-425-3p mimics. In addition, bioinformatics analysis and luciferase </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-18T18:08:53.534Z</modification><creation>2025-04-07T05:43:13.405Z</creation></dates><accession>S-EPMC9367658</accession><cross_references><pubmed>35941833</pubmed><doi>10.1080/21623945.2022.2108558</doi></cross_references></HashMap>