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Epitranscriptomics & Cancer Adaptation : A.David

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Our research work focuses on the contribution of post-transcriptional mechanisms on cancer cell adaptation, in particular RNA epigenetic & translational control.

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Added by mollevi
Last modified by standudu
Group name EquipeAT
Item Type Journal Article
Title Innovative methodology for the identification of soluble biomarkers in fresh tissues
Creator Costanza et al.
Author Brunella Costanza
Author Andrei Turtoi
Author Akeila Bellahcène
Author Touko Hirano
Author Olivier Peulen
Author Arnaud Blomme
Author Vincent Hennequière
Author Eugene Mutijima
Author Jacques Boniver
Author Marie-Alice Meuwis
Author Claire Josse
Author Benjamin Koopmansch
Author Karin Segers
Author Takehiko Yokobori
Author Karim Fahmy
Author Marc Thiry
Author Carla Coimbra
Author Nancy Garbacki
Author Alain Colige
Author Dominique Baiwir
Author Vincent Bours
Author Edouard Louis
Author Olivier Detry
Author Philippe Delvenne
Author Masahiko Nishiyama
Author Vincent Castronovo
Abstract The identification of diagnostic and prognostic biomarkers from early lesions, measurable in liquid biopsies remains a major challenge, particularly in oncology. Fresh human material of high quality is required for biomarker discovery but is often not available when it is totally required for clinical pathology investigation. Hence, all OMICs studies are done on residual and less clinically relevant biological samples. Here after, we present an innovative, simple, and non-destructive, procedure named EXPEL that uses rapid, pressure-assisted, interstitial fluid extrusion, preserving the specimen for full routine clinical pathology investigation. In the meantime, the technique allows a comprehensive OMICs analysis (proteins, metabolites, miRNAs and DNA). As proof of concept, we have applied EXPEL on freshly collected human colorectal cancer and liver metastases tissues. We demonstrate that the procedure efficiently allows the extraction, within a few minutes, of a wide variety of biomolecules holding diagnostic and prognostic potential while keeping both tissue morphology and antigenicity unaltered. Our method enables, for the first time, both clinicians and scientists to explore identical clinical material regardless of its origin and size, which has a major positive impact on translation to the clinic.
Publication Oncotarget
Volume 9
Issue 12
Pages 10665-10680
Date Feb 13, 2018
Journal Abbr Oncotarget
Language eng
DOI 10.18632/oncotarget.24366
ISSN 1949-2553
Library Catalog PubMed
Extra PMID: 29535834 PMCID: PMC5828218
Tags metabolomic, miRNAs, original, proteomic, tDNA
Date Added 2019/01/18 - 16:11:02
Date Modified 2019/05/29 - 13:57:34
Notes and Attachments PubMed entry (Attachment)


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