<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shi Y</submitter><funding>Guangdong Medical Science and Technology Research Fund Project</funding><funding>Guangzhou Health Science and Technology Project</funding><pagination>27613</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12307690</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(1)</volume><pubmed_abstract>Hepatocellular carcinoma (HCC) is frequently associated with Yeats-domain containing 2 (YEATS2) overexpression, which enhances tumor progression via the PI3K/AKT pathway. Our study delineates YEATS2's oncogenic functions in HCC and its potential as a prognostic and predictive biomarker. Through comprehensive in vitro and bioinformatics analyses, we reveal that YEATS2 promotes cell proliferation, invasion, and epithelial-mesenchymal transition (EMT). Additionally, YEATS2 modulates the tumor immune microenvironment and predicts response to immunotherapies and chemotherapies. YEATS2's serum stability suggests its utility as a non-invasive biomarker for personalized HCC treatment.</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>The value of acetylation reader YEATS2 in hepatocellular carcinoma management.</pubmed_title><pmcid>PMC12307690</pmcid><funding_grant_id>B2023049</funding_grant_id><funding_grant_id>A2023165</funding_grant_id><funding_grant_id>20251A011074</funding_grant_id><funding_grant_id>20251A011073</funding_grant_id><pubmed_authors>Huang S</pubmed_authors><pubmed_authors>Zhou Q</pubmed_authors><pubmed_authors>Xiao W</pubmed_authors><pubmed_authors>Jia H</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Kang J</pubmed_authors><pubmed_authors>Shi Y</pubmed_authors><pubmed_authors>Xiao Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>The value of acetylation reader YEATS2 in hepatocellular carcinoma management.</name><description>Hepatocellular carcinoma (HCC) is frequently associated with Yeats-domain containing 2 (YEATS2) overexpression, which enhances tumor progression via the PI3K/AKT pathway. Our study delineates YEATS2's oncogenic functions in HCC and its potential as a prognostic and predictive biomarker. Through comprehensive in vitro and bioinformatics analyses, we reveal that YEATS2 promotes cell proliferation, invasion, and epithelial-mesenchymal transition (EMT). Additionally, YEATS2 modulates the tumor immune microenvironment and predicts response to immunotherapies and chemotherapies. YEATS2's serum stability suggests its utility as a non-invasive biomarker for personalized HCC treatment.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2026-03-17T15:50:05.4Z</modification><creation>2025-08-17T03:06:20.353Z</creation></dates><accession>S-EPMC12307690</accession><cross_references><pubmed>40731114</pubmed><doi>10.1038/s41598-025-09945-5</doi></cross_references></HashMap>