<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(1)</volume><submitter>Romani C</submitter><pubmed_abstract>Adenoid cystic carcinoma (ACC) of salivary gland is a slowly growing tumor showing a propensity for delayed recurrence, with decreased survival rates. The identification of poor prognosis patients may help in defining molecular-based targeted strategies in this rare disease orphan of new treatments. Through a gene expression microarray-based approach followed by GSE functional analysis the expression profile of 46 primary untreated ACC samples and of ACC (h-TERT) tumor cells was analyzed. Patients who experienced early relapse showed enrichment in proliferation-related gene sets, including the G2-M checkpoint, E2F and myc targets, and in gene sets related to IFN signaling and aberrant proteostasis (FDR &lt; 0.1), indicating increased mitotic and transcriptional activity in aggressive ACC. Sim</pubmed_abstract><journal>Scientific reports</journal><pagination>1809</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9889376</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Functional profiles of curatively treated adenoid cystic carcinoma unveil prognostic features and potentially targetable pathways.</pubmed_title><pmcid>PMC9889376</pmcid><pubmed_authors>Bossi P</pubmed_authors><pubmed_authors>Bozzola A</pubmed_authors><pubmed_authors>Bignotti E</pubmed_authors><pubmed_authors>Bugatti M</pubmed_authors><pubmed_authors>Lombardi D</pubmed_authors><pubmed_authors>Ravaggi A</pubmed_authors><pubmed_authors>Ardighieri L</pubmed_authors><pubmed_authors>Romani C</pubmed_authors><pubmed_authors>Lorini L</pubmed_authors><pubmed_authors>Battocchio S</pubmed_authors><pubmed_authors>Ravanelli M</pubmed_authors><pubmed_authors>Gurizzan C</pubmed_authors><pubmed_authors>Calza S</pubmed_authors><pubmed_authors>Tomasoni M</pubmed_authors><pubmed_authors>Tomasini D</pubmed_authors><pubmed_authors>Mattavelli D</pubmed_authors><pubmed_authors>Piazza C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Functional profiles of curatively treated adenoid cystic carcinoma unveil prognostic features and potentially targetable pathways.</name><description>Adenoid cystic carcinoma (ACC) of salivary gland is a slowly growing tumor showing a propensity for delayed recurrence, with decreased survival rates. The identification of poor prognosis patients may help in defining molecular-based targeted strategies in this rare disease orphan of new treatments. Through a gene expression microarray-based approach followed by GSE functional analysis the expression profile of 46 primary untreated ACC samples and of ACC (h-TERT) tumor cells was analyzed. Patients who experienced early relapse showed enrichment in proliferation-related gene sets, including the G2-M checkpoint, E2F and myc targets, and in gene sets related to IFN signaling and aberrant proteostasis (FDR &lt; 0.1), indicating increased mitotic and transcriptional activity in aggressive ACC. Sim</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-06T19:15:08.718Z</modification><creation>2025-04-06T19:15:08.718Z</creation></dates><accession>S-EPMC9889376</accession><cross_references><pubmed>36720951</pubmed><doi>10.1038/s41598-023-28901-9</doi></cross_references></HashMap>