<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Relier S</submitter><funding>Ligue Contre le Cancer</funding><funding>Cancerop?le Grand Sud Ouest</funding><funding>Des ?toiles dans la Mer</funding><funding>Institut National Du Cancer</funding><funding>Institut du Cancer de Montpellier</funding><funding>Association pour la Recherche sur les Tumeurs C?r?brales</funding><funding>European Regional Development Fund</funding><funding>R?gion Occitanie Pyr?n?es-M?diterran?e</funding><funding>Centre Hospitalier R?gional Universitaire de Montpellier</funding><pagination>11967-11972</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9453740</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>94(35)</volume><pubmed_abstract>One of the main challenges in cancer management relates to the discovery of reliable biomarkers, which could guide decision-making and predict treatment outcome. In particular, the rise and democratization of high-throughput molecular profiling technologies bolstered the discovery of "biomarker signatures" that could maximize the prediction performance. Such an approach was largely employed from diverse OMICs data (i.e., genomics, transcriptomics, proteomics, metabolomics) but not from epitranscriptomics, which encompasses more than 100 biochemical modifications driving the post-transcriptional fate of RNA: stability, splicing, storage, and translation. We and others have studied chemical marks in isolation and associated them with cancer evolution, adaptation, as well as the response to c</pubmed_abstract><journal>Analytical chemistry</journal><pubmed_title>Multivariate Analysis of RNA Chemistry Marks Uncovers Epitranscriptomics-Based Biomarker Signature for Adult Diffuse Glioma Diagnostics.</pubmed_title><pmcid>PMC9453740</pmcid><funding_grant_id>2020-116</funding_grant_id><funding_grant_id>INCa-DGOS-Inserm 6045</funding_grant_id><pubmed_authors>Fontaine D</pubmed_authors><pubmed_authors>Burel Vandenbos F</pubmed_authors><pubmed_authors>Relier S</pubmed_authors><pubmed_authors>David A</pubmed_authors><pubmed_authors>Amalric A</pubmed_authors><pubmed_authors>Duffau H</pubmed_authors><pubmed_authors>Attina A</pubmed_authors><pubmed_authors>Hirtz C</pubmed_authors><pubmed_authors>Koumare IB</pubmed_authors><pubmed_authors>Rivals E</pubmed_authors><pubmed_authors>Hugnot JP</pubmed_authors><pubmed_authors>Baroncini M</pubmed_authors><pubmed_authors>Bauchet L</pubmed_authors><pubmed_authors>Rigau V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multivariate Analysis of RNA Chemistry Marks Uncovers Epitranscriptomics-Based Biomarker Signature for Adult Diffuse Glioma Diagnostics.</name><description>One of the main challenges in cancer management relates to the discovery of reliable biomarkers, which could guide decision-making and predict treatment outcome. In particular, the rise and democratization of high-throughput molecular profiling technologies bolstered the discovery of "biomarker signatures" that could maximize the prediction performance. Such an approach was largely employed from diverse OMICs data (i.e., genomics, transcriptomics, proteomics, metabolomics) but not from epitranscriptomics, which encompasses more than 100 biochemical modifications driving the post-transcriptional fate of RNA: stability, splicing, storage, and translation. We and others have studied chemical marks in isolation and associated them with cancer evolution, adaptation, as well as the response to c</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-18T15:35:08.893Z</modification><creation>2025-04-07T02:20:31.593Z</creation></dates><accession>S-EPMC9453740</accession><cross_references><pubmed>35998076</pubmed><doi>10.1021/acs.analchem.2c01526</doi></cross_references></HashMap>