<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE327nnn/GSE327216/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Homo sapiens</species><gds_type>Non-coding RNA profiling by array</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE327216</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Circulating miR-22 predicts TACE response and targets WEE1 in hepatocellular carcinoma</name><description>Transarterial Chemoembolization (TACE) is the standard therapy for intermediate-stage liver cancer, yet high failure rates and a lack of early biomarkers remain significant challenges. Our study shows that circulating miR-22 levels increase significantly within 48 hours in TACE non-responders, providing a much faster alternative to traditional imaging for identifying treatment failure. Mechanistically, we identified the G2/M checkpoint kinase WEE1 as a direct functional target of miR-22. The miR-22/WEE1 axis has been identified as both a reliable predictor of outcomes and a potential target for personalized therapeutic interventions.</description><dates><publication>2026/05/06</publication></dates><accession>GSE327216</accession><cross_references><GSM>GSM9651393</GSM><GSM>GSM9651392</GSM><GSM>GSM9651391</GSM><GSM>GSM9651390</GSM><GSM>GSM9651397</GSM><GSM>GSM9651386</GSM><GSM>GSM9651396</GSM><GSM>GSM9651395</GSM><GSM>GSM9651394</GSM><GSM>GSM9651400</GSM><GSM>GSM9651389</GSM><GSM>GSM9651399</GSM><GSM>GSM9651388</GSM><GSM>GSM9651398</GSM><GSM>GSM9651387</GSM><GPL>15018</GPL><GSE>327216</GSE><taxon>Homo sapiens</taxon><PMID>[42041589]</PMID></cross_references></HashMap>