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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 standudu
Group name EquipeAT
Item Type Journal Article
Title Intratumoral heterogeneity and consequences for targeted therapies
Creator Turtoi et al.
Author Andrei Turtoi
Author Arnaud Blomme
Author Vincent Castronovo
Abstract According to the clonal model and Darwinian evolution, cancer cell evolves through new mutations helping it to proliferate, migrate, invade and metastasize. Recent genetic studies have clearly shown that tumors, when diagnosed, consist of a large number of mutations distributed in different cells. This heterogeneity translates in substantial genetic plasticity enabling cancer cells to adapt to any hostile environment. As targeted therapy focuses only on one pathway or protein, there will always be a cell with the "right" genetic background to survive the treatment and cause tumor relapse. Because today's targeted therapies never took tumor heterogeneity into account, nearly all novel drugs fail to provide patients with a considerable improvement of the survival. However, emerging proteomic studies guided by the idea that Darwinian selection is governed by the phenotype and not genotype, show that heterogeneity at the protein level is much less complex, then it could be expected from genetic studies. This information together with the recent trend to switch from functional to cytotoxic targeting may offer an entirely new strategy to efficiently combat cancer.
Publication Bulletin Du Cancer
Volume 102
Issue 1
Pages 17-23
Date Jan 2015
Journal Abbr Bull Cancer
Language eng
DOI 10.1016/j.bulcan.2014.12.006
ISSN 1769-6917
Library Catalog PubMed
Extra PMID: 25609489
Tags Adaptation, Physiological, Cell Survival, Evolution, Molecular, first-last-corresponding, Gene mutation, Humans, MALDI-imaging, MALDI-TOF, Molecular Targeted Therapy, Mutation, Mutation génétique, Neoplasms, original, Phenotype, Protéomique, Receptor Protein-Tyrosine Kinases, Receptors, Growth Factor, Rechute tumorale, Résistance aux médicaments, Tumor relapse
Date Added 2019/05/29 - 16:15:59
Date Modified 2019/05/29 - 16:16:21
Notes and Attachments PubMed entry (Attachment)
Texte intégral (Attachment)


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