*Result*: Multivariate Analysis of RNA Chemistry Marks Uncovers Epitranscriptomics-Based Biomarker Signature for Adult Diffuse Glioma Diagnostics.

Title:
Multivariate Analysis of RNA Chemistry Marks Uncovers Epitranscriptomics-Based Biomarker Signature for Adult Diffuse Glioma Diagnostics.
Authors:
Relier S; IGF, Univ. Montpellier, CNRS, INSERM, Montpellier, Hérault 34094, France., Amalric A; IGF, Univ. Montpellier, CNRS, INSERM, Montpellier, Hérault 34094, France.; IRMB-PPC, INM, Univ Montpellier, CHU Montpellier, INSERM CNRS, Montpellier 34295, France., Attina A; IRMB-PPC, INM, Univ Montpellier, CHU Montpellier, INSERM CNRS, Montpellier 34295, France., Koumare IB; Neurosurgery Department, Montpellier University Medical Center, Montpellier, Hérault 34295, France.; Neurosurgery Department, CHU Gabriel Toure, Bamako, Mali., Rigau V; Department of Pathology and Oncobiology, Montpellier University Medical Center, Montpellier, Hérault 34295, France., Burel Vandenbos F; Central Laboratory of Pathology, Univ. Côte d'Azur, CHU Nice, CNRS, INSERM, Nice, Alpes-Maritimes 06000, France., Fontaine D; Neurosurgery Department, Univ. Côte d'Azur, CHU Nice, Nice, Alpes-Maritimes 06000, France., Baroncini M; Neurosurgery Department, CHU Lille, Univ. of Lille, Lille, Nord 59037, France., Hugnot JP; IGF, Univ. Montpellier, CNRS, INSERM, Montpellier, Hérault 34094, France., Duffau H; IGF, Univ. Montpellier, CNRS, INSERM, Montpellier, Hérault 34094, France.; Neurosurgery Department, Montpellier University Medical Center, Montpellier, Hérault 34295, France., Bauchet L; IGF, Univ. Montpellier, CNRS, INSERM, Montpellier, Hérault 34094, France.; Neurosurgery Department, Montpellier University Medical Center, Montpellier, Hérault 34295, France., Hirtz C; IRMB-PPC, INM, Univ Montpellier, CHU Montpellier, INSERM CNRS, Montpellier 34295, France., Rivals E; LIRMM, Univ. Montpellier, CNRS, Montpellier, Hérault 34095, France., David A; IGF, Univ. Montpellier, CNRS, INSERM, Montpellier, Hérault 34094, France.; IRMB-PPC, INM, Univ Montpellier, CHU Montpellier, INSERM CNRS, Montpellier 34295, France.
Source:
Analytical chemistry [Anal Chem] 2022 Sep 06; Vol. 94 (35), pp. 11967-11972. Date of Electronic Publication: 2022 Aug 23.
Publication Type:
Journal Article; Research Support, Non-U.S. Gov't
Language:
English
Journal Info:
Publisher: American Chemical Society Country of Publication: United States NLM ID: 0370536 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1520-6882 (Electronic) Linking ISSN: 00032700 NLM ISO Abbreviation: Anal Chem Subsets: MEDLINE
Imprint Name(s):
Original Publication: Washington, American Chemical Society.
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Substance Nomenclature:
0 (Biomarkers)
63231-63-0 (RNA)
Entry Date(s):
Date Created: 20220823 Date Completed: 20220908 Latest Revision: 20250728
Update Code:
20260130
PubMed Central ID:
PMC9453740
DOI:
10.1021/acs.analchem.2c01526
PMID:
35998076
Database:
MEDLINE

*Further Information*

*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 conventional therapy. In this study, we have designed a unique pipeline combining multiplex analysis of the epitranscriptomic landscape by high-performance liquid chromatography coupled to tandem mass spectrometry with statistical multivariate analysis and machine learning approaches in order to identify biomarker signatures that could guide precision medicine and improve disease diagnosis. We applied this approach to analyze a cohort of adult diffuse glioma patients and demonstrate the existence of an "epitranscriptomics-based signature" that permits glioma grades to be discriminated and predicted with unmet accuracy. This study demonstrates that epitranscriptomics (co)evolves along cancer progression and opens new prospects in the field of omics molecular profiling and personalized medicine.*